Tandamol

Tandamol may be available in the countries listed below.

Ingredient matches for Tandamol

Paracetamol

Paracetamol is reported as an ingredient of Tandamol in the following countries:

• Bangladesh

International Drug Name Search

Resco

Resco may be available in the countries listed below.

Ingredient matches for Resco

Risperidone

Risperidone is reported as an ingredient of Resco in the following countries:

• Bangladesh

International Drug Name Search

A-Lennon Fluoxetine

A-Lennon Fluoxetine may be available in the countries listed below.

Ingredient matches for A-Lennon Fluoxetine

Fluoxetine

Fluoxetine hydrochloride (a derivative of Fluoxetine) is reported as an ingredient of A-Lennon Fluoxetine in the following countries:

• South Africa

International Drug Name Search

Prodolina

Prodolina may be available in the countries listed below.

Ingredient matches for Prodolina

Metamizole

Metamizole sodium anhydrous (a derivative of Metamizole) is reported as an ingredient of Prodolina in the following countries:

• Mexico

International Drug Name Search

Midazolam Panpharma

Midazolam Panpharma may be available in the countries listed below.

Ingredient matches for Midazolam Panpharma

Midazolam

Midazolam is reported as an ingredient of Midazolam Panpharma in the following countries:

• France


• Sweden

International Drug Name Search

Demi-Regroton

Generic Name: chlorthalidone and reserpine (klor THAL i done and re SER peen)

Brand Names: Demi-Regroton, Regroton

What is Demi-Regroton (chlorthalidone and reserpine)?

Reserpine lowers blood pressure by decreasing the levels of certain chemicals in your blood. This allows your blood vessels (veins and arteries) to relax and your heart to beat more slowly and easily.

Chlorthalidone is a thiazide diuretic (water pill). It helps to lower your blood pressure and decrease edema (swelling) by increasing the amount of salt and water you lose in your urine.

Together, chlorthalidone and reserpine are used to lower high blood pressure.

Chlorthalidone and reserpine may also be used for purposes other than those listed in this medication guide.

What is the most important information I should know about Demi-Regroton (chlorthalidone and reserpine)?

Stand up slowly from a sitting or lying position. Chlorthalidone and reserpine may make you feel dizzy. Do not stop taking chlorthalidone and reserpine suddenly. Even if you feel better, you need this medication to control your condition. Stopping suddenly could cause severe high blood pressure, anxiety, and other dangerous side effects.

Tell your doctor and dentist that you are taking this medication before having surgery.

Who should not take Demi-Regroton (chlorthalidone and reserpine)?

Do not take chlorthalidone and reserpine if you have an allergy to sulfa-based drugs such as sulfa antibiotics. You may have an allergic reaction to chlorthalidone.

You must not take chlorthalidone and reserpine if you

• 
  

  have peptic ulcer disease (stomach ulcers);

  
  


• 
  

  have ulcerative colitis;

  
  


• 
  

  are suffering from depression (especially if you have suicidal thoughts);

  
  


• 
  

  are receiving electroconvulsive shock therapy; or

  
  


• 
  

  are receiving a monoamine oxidase inhibitor such as isocarboxazid (Marplan), phenelzine (Nardil), or tranylcypromine (Parnate).

  
  

Before taking this medication, tell your doctor if you have

• 
  

  gallstones or other stomach problems,

  
  


• kidney or liver disease,


• 
  

  diabetes,

  
  


• 
  

  gout,

  
  


• 
  

  a collagen vascular disease such as systemic lupus erythematosus,

  
  


• 
  

  high cholesterol or triglyceride levels,

  
  


• 
  

  pancreatitis,

  
  


• 
  

  asthma, or

  
  


• 
  

  any type of heart disease.

  
  

You may require a lower dose or special monitoring during therapy with chlorthalidone and reserpine if you have any of the conditions listed above.

Chlorthalidone and reserpine is in the FDA pregnancy category C. This means that it is not known whether chlorthalidone and reserpine will harm an unborn baby. Do not take this medication without first talking to your doctor if you are pregnant. Chlorthalidone and reserpine passes into breast milk and may harm a nursing infant. Do not take this medication without first talking to your doctor if you are breast-feeding a baby. If you are over 60 years of age, you may be more likely to experience side effects from chlorthalidone and reserpine therapy. You may require a lower dose of this medication. Chlorthalidone and reserpine has not been approved for use by children.

How should I take Demi-Regroton (chlorthalidone and reserpine)?

Take chlorthalidone and reserpine exactly as directed. If you do not understand these directions, ask your pharmacist, nurse, or doctor to explain them to you.

Take each dose with a full glass of water. Take chlorthalidone and reserpine with food or milk if it upsets your stomach.

Do not stop taking chlorthalidone and reserpine suddenly. Stopping suddenly could make your condition much worse or cause very serious side effects.

Store this medication at room temperature away from moisture and heat.

What happens if I miss a dose?

Take the missed dose as soon as you remember. However, if it is almost time for your next dose, skip the dose you missed and take only your next regularly scheduled dose. Do not take a double dose of this medication.

What happens if I overdose?

Seek emergency medical treatment.

Symptoms of a chlorthalidone and reserpine overdose include low blood pressure (fainting, dizziness, weakness); sleepiness; uncontrollable hand, arm, or leg movements; a slow pulse; low body temperature; diarrhea; increased urination; vomiting; and slow breathing.

What should I avoid while taking Demi-Regroton (chlorthalidone and reserpine)?

Avoid a diet high in salt. Too much salt will cause your body to retain water and will decrease the effects of chlorthalidone.

Use caution when arising from a sitting or lying position, especially first thing in the morning. You may become dizzy while taking chlorthalidone and reserpine, and you may fall and injure yourself if you get up quickly.

Do not let yourself become overheated in hot weather or during exercise, and use caution if you have a fever. These situations increase the effects of chlorthalidone and reserpine in your body, and you may become very dizzy.

Also, chlorthalidone may increase the sensitivity of your skin to sunlight. Use a sunscreen and wear protective clothing when exposure to the sun is unavoidable. Avoid alcohol while taking chlorthalidone and reserpine. Alcohol, which will further lower your blood pressure, will also increase the drowsiness caused by chlorthalidone and reserpine and may increase dizziness. Use caution even with small amounts of alcohol.

Do not take any over-the-counter cough, cold, allergy, sleep, or diet medications without first asking your doctor or pharmacist. These medicines will interfere with your chlorthalidone and reserpine therapy.

Use caution when you are driving, operating machinery, or performing other hazardous activities until you know how chlorthalidone and reserpine affects you. If it makes you dizzy or drowsy, avoid these activities.

Tell your doctor and dentist that you are taking this medication before having surgery.

Demi-Regroton (chlorthalidone and reserpine) side effects

If you experience any of the following serious side effects, stop taking chlorthalidone and reserpine and seek emergency medical attention:

• 
  

  an allergic reaction (difficulty breathing; closing of your throat; swelling of your lips, tongue, or face; or hives);

  
  


• 
  

  a very irregular heartbeat;

  
  


• 
  

  chest pain;

  
  


• 
  

  heart failure (shortness of breath, swelling of ankles or legs, sudden weight gain of 5 pounds or more);

  
  


• 
  

  unusual fatigue;

  
  


• 
  

  abnormal bleeding or bruising;

  
  


• 
  

  yellow skin or eyes;

  
  


• 
  

  confusion;

  
  


• 
  

  fainting;

  
  


• 
  

  uncontrollable hand, arm, or leg movements; or

  
  


• 
  

  little or no urine.

  
  

Other, less serious side effects are more likely to occur. Continue to take chlorthalidone and reserpine and talk to your doctor if you experience

• 
  

  fatigue or drowsiness;

  
  


• 
  

  dizziness (avoid standing up too quickly and use caution when performing hazardous activities);

  
  


• 
  

  anxiety, depression, or nightmares;

  
  


• 
  

  diarrhea, nausea, vomiting, or acid stomach (take chlorthalidone and reserpine with food or milk if it upsets your stomach);

  
  


• 
  

  abdominal pain;

  
  


• 
  

  stuffy nose or a dry mouth (sucking on ice chips or sugarless hard candy may relieve a dry mouth);

  
  


• 
  

  blurred vision;

  
  


• 
  

  headache;

  
  


• 
  

  tingling or numbness in your arms, legs, hands, or feet;

  
  


• 
  

  excessive urination;

  
  


• 
  

  muscle weakness or cramps;

  
  


• 
  

  increased hunger or thirst;

  
  


• 
  

  weight gain;

  
  


• 
  

  sensitivity to sunlight; or

  
  


• impotence or difficulty ejaculating.

Side effects other than those listed here may also occur. Talk to your doctor about any side effect that seems unusual or that is especially bothersome.

What other drugs will affect Demi-Regroton (chlorthalidone and reserpine)?

Do not take chlorthalidone and reserpine if you are taking a monoamine oxidase inhibitor (MAOI), or if you have taken one in the last 14 days. MAOIs, used to treat depression, include isocarboxazid (Marplan), phenelzine (Nardil), and tranylcypromine (Parnate).

Before taking this medication, tell your doctor if you are taking any of the following medicines:

• tricyclic antidepressants such as amitriptyline (Elavil, Endep) or doxepin (Sinequan), which may decrease the effects of chlorthalidone and reserpine;


• other commonly used tricyclic antidepressants, including amoxapine (Ascendin), clomipramine (Anafranil), desipramine (Norpramin), imipramine (Tofranil), nortriptyline (Pamelor), and protriptyline (Vivactil);


• 
  

  digoxin (Lanoxin) or quinidine (Cardioquin, Quinidex, Quinora, Quinaglute), which will increase the risk that you will experience an irregular heartbeat when it is taken with chlorthalidone and reserpine;

  
  


• 
  

  barbiturates such as phenobarbital (Luminal, Solfoton), amobarbital (Amytal), and secobarbital (Seconal), which may cause extreme sleepiness or dizziness if taken with chlorthalidone and reserpine;

  
  


• 
  

  narcotic pain relievers such as codeine (Tylenol #3, Tylenol #4, others), propoxyphene (Darvon, Darvocet, Wygesic), oxycodone (Percodan, Percocet, Tylox), meperidine (Demerol), morphine (MS Contin, Duramorph, others), and others also may cause extreme sleepiness or dizziness if taken with chlorthalidone and reserpine;

  
  


• 
  

  steroid medications such as hydrocortisone (Hydrocortone, Cortef), prednisone (Deltasone, Orasone), prednisolone (Delta Cortef, Prelone), methylprednisolone (Medrol), betamethasone (Celestone), dexamethasone (Decadron, Hexadrol), and others, which may increase the side effects of chlorthalidone;

  
  


• 
  

  prescription and over-the-counter cough, cold, allergy, diet, and sleeping pills, any of which may contain drugs that increase your blood pressure and heart rate and thus decrease the effects of reserpine;

  
  


• 
  

  the cholesterol-lowering drugs cholestyramine (Questran) and colestipol (Colestid), which may decrease the effects of;

  
  


• 
  

  nonsteroidal anti-inflammatory drugs (NSAIDs) such as ibuprofen (Motrin, Advil), ketoprofen (Orudis, Orudis, KT, Oruvail), and naproxen (Naprosyn, Anaprox, Aleve), which may also decrease the effects of chlorthalidone;

  
  


• 
  

  other commonly used NSAIDs, including diclofenac (Cataflam, Voltaren), etodolac (Lodine), fenoprofen (Nalfon), flurbiprofen (Ansaid), indomethacin (Indocin), ketorolac (Toradol), mefenamic acid (Ponstel), nabumetone (Relafen), oxaprozin (Daypro), piroxicam (Feldene), sulindac (Clinoril), and tolmetin (Tolectin);

  
  


• 
  

  oral antidiabetic drugs such as Glipizide (Glucotrol), glyburide (Micronase, Glynase, Diabeta), chlorpropamide (Diabinese), tolazamide (Tolinase) and tolbutamide (Orinase), which may not lower your blood sugar as well (your diabetes therapy may have to be adjusted);

  
  


• 
  

  lithium (Lithobid, Eskalith), should not be taken with chlorthalidone because serious side effects may result; or

  
  


• 
  

  other drugs that also lower blood pressure, including acebutolol (Sectral), atenolol (Tenormin), bisoprolol (Zebeta), carteolol (Cartrol), labetalol (Trandate, Normodyne), propranolol (Inderal), pindolol (Visken), timolol (Blocadren), benazepril (Lotensin), enalapril (Vasotec), captopril (Capoten), fosinopril (Monopril), lisinopril (Prinivil, Zestril), moexipril (Univasc), quinapril (Accupril), ramipril (Altace), amlodipine (Norvasc), bepridil (Vascor), diltiazem (Cardizem, Dilacor), felodipine (Plendil), isradipine (Dynacirc), nicardipine (Cardene), nifedipine (Adalat, Procardia), nimodipine (Nimotop), and verapamil (Calan, Verelan, Isoptin).

  
  

Drugs other than those listed here may also interact with chlorthalidone and reserpine or affect your condition. Talk to your doctor and pharmacist before taking any prescription or over-the-counter medicines.

More Demi-Regroton resources

• Demi-Regroton Side Effects (in more detail)
• Demi-Regroton Use in Pregnancy & Breastfeeding
• Drug Images
• Demi-Regroton Drug Interactions
• Demi-Regroton Support Group
• 0 Reviews for Demi-Regroton - Add your own review/rating

Compare Demi-Regroton with other medications

• High Blood Pressure

Where can I get more information?

• Your pharmacist has additional information about chlorthalidone and reserpine written for health professionals that you may read.

What does my medication look like?

Chlorthalidone and reserpine is available with a prescription under the brand names Regroton and Demi-Regroton. Other brand or generic formulations may also be available. Ask your pharmacist any questions you have about this medication, especially if it is new to you.

See also: Demi-Regroton side effects (in more detail)

Ezator

Ezator may be available in the countries listed below.

Ingredient matches for Ezator

Atorvastatin

Atorvastatin is reported as an ingredient of Ezator in the following countries:

• Peru

Ezetimibe

Ezetimibe is reported as an ingredient of Ezator in the following countries:

• Peru

International Drug Name Search

Penciclovir

Pronunciation: pen-SEYE-kloe-veer
Generic Name: Penciclovir
Brand Name: Denavir

Penciclovir is used for:

Treating recurring cold sores associated with the herpes simplex virus. It may also be used for other conditions as determined by your doctor.

Penciclovir is an antiviral. It works by preventing the herpes simplex virus from growing.

Do NOT use Penciclovir if:

• you are allergic to any ingredient in Penciclovir

Contact your doctor or health care provider right away if any of these apply to you.

Before using Penciclovir:

Some medical conditions may interact with Penciclovir. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

• if you are pregnant, planning to become pregnant, or are breast-feeding


• if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement


• if you have allergies to medicines, foods, or other substances


• if you have a weakened immune system

Some MEDICINES MAY INTERACT with Penciclovir. Because little, if any, of Penciclovir is absorbed into the blood, the risk of it interacting with another medicine is low.

Ask your health care provider if Penciclovir may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

How to use Penciclovir:

Use Penciclovir as directed by your doctor. Check the label on the medicine for exact dosing instructions.

• Start treatment as soon as lesions or signs of cold sores (tingling, redness, itching, or a bump) appear.


• Before using Penciclovir, wash your hands, clean your face, and pat dry.


• Apply enough of Penciclovir to cover only the cold sore area of tingling (or other symptoms) before the cold sores appear. Rub the cream in until it disappears.


• Wash your hands with soap and water immediately after using Penciclovir.


• To clear up your infection completely, use Penciclovir for the full course of treatment. Keep using it even if your symptoms improve in a few days.


• If you miss a dose of Penciclovir, use it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not use 2 doses at once.

Ask your health care provider any questions you may have about how to use Penciclovir.

Important safety information:

• Use Penciclovir only on cold sores on the lips or face. Avoid applying in or near the eyes as irritation may occur.


• Penciclovir is not a cure for cold sores and all patients may not respond to it, especially patients with weakened immune systems.


• Penciclovir should not be used in CHILDREN younger than 12 years old; safety and effectiveness in these children have not been confirmed.


• PREGNANCY and BREAST-FEEDING: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Penciclovir while you are pregnant. It is not known if Penciclovir is found in breast milk. Do not breast-feed while taking Penciclovir.

Possible side effects of Penciclovir:

All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:

Bad taste in mouth; burning, pain, flushing, or itching at the application site; headache.

Seek medical attention right away if any of these SEVERE side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue).

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA.

See also: Penciclovir side effects (in more detail)

If OVERDOSE is suspected:

Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately. Penciclovir may be harmful if swallowed.

Proper storage of Penciclovir:

Store Penciclovir at room temperature, between 68 and 77 degrees F (20 and 25 degrees C). Store away from heat, light, and moisture. Keep Penciclovir out of the reach of children and away from pets.

General information:

• If you have any questions about Penciclovir, please talk with your doctor, pharmacist, or other health care provider.


• Penciclovir is to be used only by the patient for whom it is prescribed. Do not share it with other people.


• If your symptoms do not improve or if they become worse, check with your doctor.


• Check with your pharmacist about how to dispose of unused medicine.

This information is a summary only. It does not contain all information about Penciclovir. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.

Issue Date: February 1, 2012

Database Edition 12.1.1.002

Copyright © 2012 Wolters Kluwer Health, Inc.

More Penciclovir resources

• Penciclovir Side Effects (in more detail)
• Penciclovir Use in Pregnancy & Breastfeeding
• Penciclovir Support Group
• 7 Reviews for Penciclovir - Add your own review/rating

Compare Penciclovir with other medications

• Cold Sores

degarelix Subcutaneous

deg-a-REL-ix

Available Dosage Forms:

• Powder for Solution

Pharmacologic Class: Luteinizing Hormone Releasing Hormone Antagonist

Uses For degarelix

Degarelix is used in men to treat advanced prostate cancer. Degarelix is a type of medicine called a gonadotropin-releasing hormone (GnRH) antagonist. It helps treat prostate cancer by lowering the amount of testosterone hormone in the blood. In some patients, testosterone will cause prostate cancer to grow larger.

degarelix is available only with your doctor's prescription.

Before Using degarelix

In deciding to use a medicine, the risks of taking the medicine must be weighed against the good it will do. This is a decision you and your doctor will make. For degarelix, the following should be considered:

Allergies

Tell your doctor if you have ever had any unusual or allergic reaction to degarelix or any other medicines. Also tell your health care professional if you have any other types of allergies, such as to foods, dyes, preservatives, or animals. For non-prescription products, read the label or package ingredients carefully.

Pediatric

Appropriate studies have not been performed on the relationship of age to the effects of degarelix in the pediatric population. Safety and efficacy have not been established.

Geriatric

Appropriate studies performed to date have not demonstrated geriatric-specific problems that would limit the usefulness of degarelix in the elderly.

Pregnancy

	Pregnancy Category	Explanation
All Trimesters	X	Studies in animals or pregnant women have demonstrated positive evidence of fetal abnormalities. This drug should not be used in women who are or may become pregnant because the risk clearly outweighs any possible benefit.

Breast Feeding

There are no adequate studies in women for determining infant risk when using this medication during breastfeeding. Weigh the potential benefits against the potential risks before taking this medication while breastfeeding.

Interactions with Medicines

Although certain medicines should not be used together at all, in other cases two different medicines may be used together even if an interaction might occur. In these cases, your doctor may want to change the dose, or other precautions may be necessary. Tell your healthcare professional if you are taking any other prescription or nonprescription (over-the-counter [OTC]) medicine.

Interactions with Food/Tobacco/Alcohol

Certain medicines should not be used at or around the time of eating food or eating certain types of food since interactions may occur. Using alcohol or tobacco with certain medicines may also cause interactions to occur. Discuss with your healthcare professional the use of your medicine with food, alcohol, or tobacco.

Other Medical Problems

The presence of other medical problems may affect the use of degarelix. Make sure you tell your doctor if you have any other medical problems, especially:

• Congestive heart failure or


• Heart rhythm problems (e.g., prolonged QT interval) or


• Mineral imbalance (low calcium, magnesium, potassium, or sodium in the blood)—May increase risk for more serious side effects.

• Kidney disease, severe or


• Liver disease, severe—Use with caution. The effects of degarelix may be increased because of slower removal from the body.

Proper Use of degarelix

A nurse or other trained health professional will give you degarelix. degarelix is given as a shot under your skin in the stomach area.

degarelix comes with a patient information leaflet. Read and follow the instructions in the leaflet carefully. Ask your doctor if you have any questions.

Missed Dose

degarelix needs to be given on a fixed schedule. If you miss a dose, call your doctor, home health caregiver, or treatment clinic for instructions.

Precautions While Using degarelix

It is very important that your doctor check your progress at regular visits to make sure that degarelix is working properly. Blood tests may be needed to check for unwanted effects.

degarelix can cause a change in heart rhythm called prolongation of the QT interval. This condition may change the way your heart beats (faster or slower) and can cause chest pain, dizziness, fainting, or shortness of breath. Contact your doctor right away if you have any of these symptoms or any questions.

degarelix may decrease bone mineral density when used for a long time. A low bone mineral density can cause weak bones or osteoporosis. If you have any questions about this ask your doctor.

degarelix Side Effects

Along with its needed effects, a medicine may cause some unwanted effects. Although not all of these side effects may occur, if they do occur they may need medical attention.

Check with your doctor or nurse immediately if any of the following side effects occur:

More common

• Back pain


• blurred vision


• dizziness


• fever


• flushing or redness of the skin


• hard lump


• headache


• nervousness


• pain


• pounding in the ears


• slow or fast heartbeat


• small lumps under the skin


• swelling


• unusually warm skin

Less common

• Bladder pain


• bloody or cloudy urine


• chills


• decrease in testicle size


• decreased interest in sexual intercourse


• difficult, burning, or painful urination


• difficulty in moving


• frequent urge to urinate


• inability to have or keep an erection


• increased sweating


• loss in sexual ability, desire, drive, or performance


• lower back or side pain


• muscle pain or stiffness


• pain in the joints

Rare

• Chest pain or discomfort


• fainting


• irregular heartbeat


• pounding heartbeat


• shortness of breath

Some side effects may occur that usually do not need medical attention. These side effects may go away during treatment as your body adjusts to the medicine. Also, your health care professional may be able to tell you about ways to prevent or reduce some of these side effects. Check with your health care professional if any of the following side effects continue or are bothersome or if you have any questions about them:

More common

• Difficulty having a bowel movement (stool)


• feeling of warmth


• increased weight


• redness of the face, neck, arms, and occasionally, upper chest


• sudden sweating


• unusual tiredness or weakness

Less common

• Diarrhea


• lack or loss of strength


• nausea


• night sweats


• sleeplessness


• swelling of the breasts or breast soreness


• trouble sleeping


• unable to sleep

Other side effects not listed may also occur in some patients. If you notice any other effects, check with your healthcare professional.

Call your doctor for medical advice about side effects. You may report side effects to the FDA at 1-800-FDA-1088.

See also: degarelix Subcutaneous side effects (in more detail)

The information contained in the Thomson Reuters Micromedex products as delivered by Drugs.com is intended as an educational aid only. It is not intended as medical advice for individual conditions or treatment. It is not a substitute for a medical exam, nor does it replace the need for services provided by medical professionals. Talk to your doctor, nurse or pharmacist before taking any prescription or over the counter drugs (including any herbal medicines or supplements) or following any treatment or regimen. Only your doctor, nurse, or pharmacist can provide you with advice on what is safe and effective for you.

The use of the Thomson Reuters Healthcare products is at your sole risk. These products are provided "AS IS" and "as available" for use, without warranties of any kind, either express or implied. Thomson Reuters Healthcare and Drugs.com make no representation or warranty as to the accuracy, reliability, timeliness, usefulness or completeness of any of the information contained in the products. Additionally, THOMSON REUTERS HEALTHCARE MAKES NO REPRESENTATION OR WARRANTIES AS TO THE OPINIONS OR OTHER SERVICE OR DATA YOU MAY ACCESS, DOWNLOAD OR USE AS A RESULT OF USE OF THE THOMSON REUTERS HEALTHCARE PRODUCTS. ALL IMPLIED WARRANTIES OF MERCHANTABILITY AND FITNESS FOR A PARTICULAR PURPOSE OR USE ARE HEREBY EXCLUDED. Thomson Reuters Healthcare does not assume any responsibility or risk for your use of the Thomson Reuters Healthcare products.

More degarelix Subcutaneous resources

• Degarelix Subcutaneous Side Effects (in more detail)
• Degarelix Subcutaneous Use in Pregnancy & Breastfeeding
• Degarelix Subcutaneous Drug Interactions
• Degarelix Subcutaneous Support Group
• 0 Reviews for Degarelix Subcutaneous - Add your own review/rating

Compare degarelix Subcutaneous with other medications

• Prostate Cancer

Roceron

Roceron may be available in the countries listed below.

Ingredient matches for Roceron

Interferon alfa

Interferon alfa Interferon alfa-2a (Lys-23; His-34) (a derivative of Interferon alfa) is reported as an ingredient of Roceron in the following countries:

• Norway

International Drug Name Search

Cerisa Wash

sulfacetamide sodium and sulfur

Dosage Form: lotion
CERISA™ WASH

(Sodium Sulfacetamide 10% and Sulfur 1%)

Rx only

Cerisa Wash Description

Each gram of CERISA™ WASH contains 100mg of Sodium Sulfacetamide and 10mg of Sulfur in a wash containing Butylated Hydroxytolulene, Cetyl Alcohol, Disodium EDTA, Glyceryl Stearate and PEG-l00 Stearate, Lactic Acid, Magnesium Aluminum Silicate, Methyl Paraben, Propyl Paraben, Purified Water, Sodium C14-16 Olefin Sulfonate, Sodium Hydroxide, Sodium Thiosulfate, Stearyl alcohol, White Petrolatum and Xanthan Gum.

Sodium Sulfacetamide is a sulfonamide with antibacterial activity while sulfur acts as a keratolytic agent. Chemically, Sodium Sulfacetamide is N-{(4-aminophenyl) sulfony}-acetamide, monosodium salt, monohydrate.

The structural formula is:

Cerisa Wash - Clinical Pharmacology

The most widely accepted mechanism of action of sulfonamides in the Woods-Fildes theory which is based on the fact that sulfonamides act as competitive antagonists to para-aminobenzoic acid (PABA), an essential component for bacterial growth. While absorption through intact skin has not been determined, Sodium Sulfacetamide is readily absorbed from the gastrointestinal tract when taken orally and excreted in the urine, largely unchanged. The biological half-life has variously been reported as 7 to 12.8 hours.

The exact mode of action of sulfur in the treatment of acne is unknown, but it has been reported that it inhibits the growth of Propionibacterium acnes and the formation of free fatty acids.

Indications and Usage for Cerisa Wash

CERISA™ WASH is indicated in the topical control of acne vulgaris, acne rosacea and seborrheic dermatitis.

Contraindications

CERISA™ WASH is contraindicated for use by patients having known hypersensitivity to sulfonamides, sulfur or any other component of this preparation. CERISA™ WASH is not to be used by patients with kidney disease.

Warnings

Although rare, sensitivity to Sodium Sulfacetamide may occur. Therefore, caution and careful supervision should be observed when prescribing this drug for patients who may be prone to hypersensitivity to topical sulfonamides. Systemic toxic reactions such as agranulocytosis, acute hemolytic anemia, purpura hemorrhagica, drug fever, jaundice, and contact dermatitis indicate hypersensitivity to sulfonamides. Particular caution should be employed if areas of denuded or abraded skin are involved. FOR EXTERNAL USE ONLY. Keep out of reach of children. Keep tube tightly closed.

Precautions

General

If irritation develops, use of the product should be discontinued and appropriate therapy instituted. Patients should be very carefully observed for possible local irritation or sensitization during long-term therapy. The object of this therapy is to achieve desquamation without irritation, but sodium sulfacetamide and sulfur can cause reddening and scaling of the epidermis. These side effects are not unusual in the treatment of acne vulgaris, but patients should be cautioned about the possibility.

Carcinogenesis, Mutagenesis an Impairment of Fertility

Long-term studies in animals have not been performed to evaluate carcinogenic potential.

Pregnancy

Category C

Animal reproduction studies have not been conducted with CERISA™ WASH. It is also not known whether CERISA™ WASH can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. CERISA™ WASH should be given to a pregnant woman only if clearly needed.

Nursing Mothers

It is not known whether sodium sulfacetamide is excreted in human milk following topical use of CERISA™ WASH. However, small amounts of orally administered sulfonamides have been reported to be eliminated in human milk. In view of this and because many drugs are excreted in human milk, caution should be exercised when CERISA™ WASH is administered to a nursing woman.

Pediatric Use

Safety and effectiveness in children under the age of 12 have not been established.

Adverse Reactions

Although rare, sodium sulfacetamide may cause local irritation.

Cerisa Wash Dosage and Administration

Wash affected areas once or twice daily, or as directed by your physician. Avoid contact with eyes or mucous membranes. Wet skin and liberally apply to areas to be treated, massage gently into skin for 10-20 seconds working into a full lather, rinse thoroughly and pat dry. If dying occurs, it may be controlled by rinsing wash off sooner or using less often.

How is Cerisa Wash Supplied

CERISA™ WASH is available in 170.1g (6.0 oz) tubes,NDC 58980-330-61.

Store at controlled room temperature: 15°-30° C (59°-86° F)

Distributed by

STRATUS

PHARMACEUTICALS INC

Manufactured by

Sonar Products Inc.

Carlstadt, NJ 07072

exclusively for

Stratus Pharmaceuticals Inc.

12379 Southwest 130th Street

Miami, Florida 33186-6727

Customer Service

Telephone: 1-800-442-7882

Fax: 305-254-6875

©2008 Stratus Pharmaceuticals Inc.

JG-CW-IN200811.

PRINCIPAL DISPLAY PANEL - 170.1 g Carton

NDC 58980-330-61

Net WT. 6.0 oz. (170.1g)

CERISA™ WASH

(Sodium Sulfacetamide 10% and Sulfur Wash 1%)

STRATUS

PHARMACEUTICALS INC

Rx only

Manufactured for Stratus Pharmaceuticals Inc., 12379 Southwest 130th Street, Miami, Florida 33186-6208

CERISA  sulfacetamide sodium and sulfur  lotion

Product Information Product Type HUMAN PRESCRIPTION DRUG NDC Product Code (Source) 58980-330 Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SULFACETAMIDE SODIUM (SULFACETAMIDE) SULFACETAMIDE SODIUM 100 mg  in 1 g SULFUR (SULFUR) SULFUR 10 mg  in 1 g

Inactive Ingredients Ingredient Name Strength No Inactive Ingredients Found

Product Characteristics Color WHITE (off white) Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 58980-330-61 1 TUBE In 1 BOX contains a TUBE 1 170.1 g In 1 TUBE This package is contained within the BOX (58980-330-61)

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Unapproved other		04/06/2009

Labeler - Stratus Pharamceuticals, Inc (789001641)

Registrant - Sonar Products, Inc (104283945)

Establishment
Name	Address	ID/FEI	Operations
Sonar Products, Inc		104283945	MANUFACTURE

Revised: 10/2009Stratus Pharamceuticals, Inc

More Cerisa Wash resources

• Cerisa Wash Side Effects (in more detail)
• Cerisa Wash Use in Pregnancy & Breastfeeding
• Cerisa Wash Drug Interactions
• 0 Reviews for Cerisa - Add your own review/rating

Compare Cerisa Wash with other medications

• Acne
• Rosacea
• Seborrheic Dermatitis

Dicel DM

Generic Name: chlorpheniramine, dextromethorphan, and pseudoephedrine (klor feh NEER a meen, dex tro meh THOR fan, and soo doe eh FEH drin)

Brand Names: AccuHist PDX Drops, Atuss DS, Children's NyQuil, Creomulsion Cough/Cold/Allergy, Creomulsion Pediatric, Dicel DM, Dicel DM Chewables, Entre-S, Esocor P, Kidcare Cough and Cold, M-End DM, Mesehist DM, Neutrahist PDX Drops, Nyquil Child Cough and Cold, Pediatric Cough & Cold Medicine, Rescon-DM, Robitussin Pediatric Night Relief, Robitussin PM Cough & Cold, Triaminic Cold and Cough, Triaminic Multi-Sympton, Triaminic Night Time, Triaminic Softchew Cold and Cough, Triaminic-D Multi-Symptom Cold, Vicks 44M Pediatric, Vicks Pediatric Formula 44M

What is Dicel DM (chlorpheniramine, dextromethorphan, and pseudoephedrine)?

Chlorpheniramine is an antihistamine that reduces the effects of natural chemical histamine in the body. Histamine can produce symptoms of sneezing, itching, watery eyes, and runny nose.

Dextromethorphan is a cough suppressant. It affects the signals in the brain that trigger cough reflex.

Pseudoephedrine is a decongestant that shrinks blood vessels in the nasal passages. Dilated blood vessels can cause nasal congestion (stuffy nose).

The combination of chlorpheniramine, dextromethorphan, and pseudoephedrine is used to treat runny or stuffy nose, sneezing, itching, watery eyes, cough, and sinus congestion caused by allergies, the common cold, or the flu.

Dextromethorphan will not treat a cough that is caused by smoking, asthma, or emphysema.

Chlorpheniramine, dextromethorphan, and pseudoephedrine may also be used for purposes not listed in this medication guide.

What is the most important information I should know about Dicel DM (chlorpheniramine, dextromethorphan, and pseudoephedrine)?

Do not give this medication to a child younger than 4 years old. Always ask a doctor before giving a cough or cold medicine to a child. Death can occur from the misuse of cough and cold medicines in very young children. Do not use a cough or cold medicine if you have used an MAO inhibitor such as furazolidone (Furoxone), isocarboxazid (Marplan), phenelzine (Nardil), rasagiline (Azilect), selegiline (Eldepryl, Emsam, Zelapar), or tranylcypromine (Parnate) in the last 14 days. A dangerous drug interaction could occur, leading to serious side effects.

Ask a doctor or pharmacist before taking this medicine if you have heart disease, high blood pressure, kidney disease, diabetes, glaucoma, a thyroid disorder, emphysema or bronchitis, an enlarged prostate, or urination problems.

Do not use cold or cough medicine without your doctor's advice if you are pregnant or breast-feeding. Ask a doctor or pharmacist before using any other cold, cough, or allergy medicine. Chlorpheniramine, dextromethorphan, and pseudoephedrine are contained in many combination medicines. Taking certain products together can cause you to get too much of a certain drug. Check the label to see if a medicine contains an antihistamine, cough suppressant, or decongestant. Do not take this medicine for longer than 7 days in a row. Talk with your doctor if your symptoms do not improve after 7 days of treatment, or if you have a fever with a headache, cough, or skin rash.

What should I discuss with my healthcare provider before taking Dicel DM (chlorpheniramine, dextromethorphan, and pseudoephedrine)?

Do not use a cough or cold medicine if you have used an MAO inhibitor such as furazolidone (Furoxone), isocarboxazid (Marplan), phenelzine (Nardil), rasagiline (Azilect), selegiline (Eldepryl, Emsam, Zelapar), or tranylcypromine (Parnate) in the last 14 days. A dangerous drug interaction could occur, leading to serious side effects.

Ask a doctor or pharmacist if it is safe for you to take this medicine if you have:

• 
  

  heart disease or high blood pressure;

  
  


• 
  

  kidney disease;

  
  


• 
  

  diabetes;

  
  


• 
  

  glaucoma;

  
  


• 
  

  a thyroid disorder;

  
  


• 
  

  emphysema or chronic bronchitis;

  
  


• 
  

  an enlarged prostate; or

  
  


• 
  

  problems with urination.

  
  

FDA pregnancy category C. It is not known whether chlorpheniramine, dextromethorphan, and pseudoephedrine will harm an unborn baby. Do not use this medication without medical advice if you are pregnant. Chlorpheniramine, dextromethorphan, and pseudoephedrine may pass into breast milk and may harm a nursing baby. Do not use cold or cough medicine without medical advice if you are breast-feeding a baby.

Artificially sweetened liquid cough or cold medicine may contain phenylalanine. If you have phenylketonuria (PKU), check the medication label to see if the product contains phenylalanine.

How should I take Dicel DM (chlorpheniramine, dextromethorphan, and pseudoephedrine)?

Use exactly as directed on the label, or as prescribed by your doctor. Do not use in larger or smaller amounts or for longer than recommended. Cough or cold medicine is usually taken only for a short time until your symptoms clear up.

Do not give this medication to a child younger than 4 years old. Always ask a doctor before giving a cough or cold medicine to a child. Death can occur from the misuse of cough and cold medicines in very young children.

Measure liquid medicine with a special dose-measuring spoon or medicine cup, not with a regular table spoon. If you do not have a dose-measuring device, ask your pharmacist for one.

The chewable tablet should be chewed before you swallow it.

Shake the oral suspension well just before you measure a dose. Do not take this medicine for longer than 7 days in a row. Talk with your doctor if your symptoms do not improve after 7 days of treatment, or if you have a fever with a headache, cough, or skin rash.

This medication can cause unusual results with allergy skin tests. Tell any doctor who treats you that you are taking an antihistamine.

If you need surgery, tell the surgeon ahead of time if you have taken a cough or cold medicine within the past few days. Store at room temperature away from moisture and heat.

What happens if I miss a dose?

Since cough or cold medicine is taken when needed, you may not be on a dosing schedule. If you are taking the medication regularly, take the missed dose as soon as you remember. Skip the missed dose if it is almost time for your next scheduled dose. Do not take extra medicine to make up the missed dose.

What happens if I overdose?

Seek emergency medical attention or call the Poison Help line at 1-800-222-1222.

Overdose symptoms may include severe forms of some of the side effects listed in this medication guide.

What should I avoid while taking Dicel DM (chlorpheniramine, dextromethorphan, and pseudoephedrine)?

This medication may cause blurred vision and may impair your thinking or reactions. Be careful if you drive or do anything that requires you to be alert and able to see clearly.

Avoid becoming overheated or dehydrated during exercise and in hot weather. Chlorpheniramine can decrease sweating and you may be more prone to heat stroke.

Drinking alcohol can increase certain side effects of this medication.

Avoid taking this medication if you also take diet pills, caffeine pills, or other stimulants (such as ADHD medications). Taking a stimulant together with a decongestant can increase your risk of unpleasant side effects.

Ask a doctor or pharmacist before using any other cold, cough, or allergy medicine. Chlorpheniramine, dextromethorphan, and pseudoephedrine are contained in many combination medicines. Taking certain products together can cause you to get too much of a certain drug. Check the label to see if a medicine contains an antihistamine, cough suppressant, or decongestant.

Dicel DM (chlorpheniramine, dextromethorphan, and pseudoephedrine) side effects

Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficult breathing; swelling of your face, lips, tongue, or throat. Stop using this medicine and call your doctor at once if you have a serious side effect such as:

• 
  

  fast, pounding, or uneven heartbeats;

  
  


• 
  

  slow, shallow breathing;

  
  


• 
  

  confusion, hallucinations, unusual thoughts or behavior;

  
  


• 
  

  severe dizziness, anxiety, restless feeling, or nervousness;

  
  


• 
  

  urinating less than usual or not at all;

  
  


• 
  

  easy bruising or bleeding, unusual weakness, fever, chills, body aches, flu symptoms; or

  
  


• 
  

  dangerously high blood pressure (severe headache, blurred vision, buzzing in your ears, anxiety, confusion, chest pain, shortness of breath, uneven heartbeats, seizure).

  
  

Less serious side effects may include:

• 
  

  dry mouth, nose, or throat;

  
  


• 
  

  mild stomach pain, constipation;

  
  


• 
  

  blurred vision;

  
  


• 
  

  dizziness, drowsiness, mild headache;

  
  


• 
  

  sleep problems (insomnia);

  
  


• 
  

  feeling restless or excited (especially in children);

  
  


• 
  

  problems with memory or concentration; or

  
  


• 
  

  flushing (warmth, redness, or tingly feeling).

  
  

This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.

What other drugs will affect Dicel DM (chlorpheniramine, dextromethorphan, and pseudoephedrine)?

Before using this medicine, tell your doctor if you regularly use other medicines that make you sleepy (such as sedatives, narcotic pain medicine, sleeping pills, muscle relaxers, and medicine for seizures, depression, or anxiety). They can add to sleepiness caused by chlorpheniramine, dextromethorphan, and pseudoephedrine.

Ask a doctor or pharmacist if it is safe for you to use chlorpheniramine, dextromethorphan, and pseudoephedrine if you are also using any of the following drugs:

• 
  

  glycopyrrolate (Robinul);

  
  


• 
  

  mepenzolate (Cantil);

  
  


• 
  

  atropine (Atreza, Sal-Tropine), belladonna (Donnatal, and others), benztropine (Cogentin), dimenhydrinate (Dramamine), methscopolamine (Pamine), or scopolamine (Transderm Scop);

  
  


• 
  

  bladder or urinary medications such as darifenacin (Enablex), flavoxate (Urispas), oxybutynin (Ditropan, Oxytrol), tolterodine (Detrol), or solifenacin (Vesicare);

  
  


• 
  

  bronchodilators such as ipratropium (Atrovent) or tiotropium (Spiriva);

  
  


• 
  

  a diuretic (water pill), or blood pressure medicine;

  
  


• 
  

  irritable bowel medications such as dicyclomine (Bentyl), hyoscyamine (Hyomax), or propantheline (Pro Banthine); or

  
  


• 
  

  salicylates such as aspirin, Backache Relief Extra Strength, Novasal, Nuprin Backache Caplet, Doan's Pills Extra Strength, Pepto-Bismol, Tricosal, and others.

  
  

This list is not complete and other drugs may interact with chlorpheniramine, dextromethorphan, and pseudoephedrine. Tell your doctor about all medications you use. This includes prescription, over-the-counter, vitamin, and herbal products. Do not start a new medication without telling your doctor.

More Dicel DM resources

• Dicel DM Side Effects (in more detail)
• Dicel DM Use in Pregnancy & Breastfeeding
• Dicel DM Drug Interactions
• Dicel DM Support Group
• 0 Reviews for Dicel DM - Add your own review/rating

• AccuHist PDX Drops MedFacts Consumer Leaflet (Wolters Kluwer)


• AccuHist PDX Drops Prescribing Information (FDA)


• Dicel DM Chewables Chewable Tablets MedFacts Consumer Leaflet (Wolters Kluwer)


• Entre-S Prescribing Information (FDA)

Compare Dicel DM with other medications

• Cough and Nasal Congestion

Where can I get more information?

• Your pharmacist can provide more information about chlorpheniramine, dextromethorphan, and pseudoephedrine.

See also: Dicel DM side effects (in more detail)

Nimesulide Dorom

Nimesulide Dorom may be available in the countries listed below.

Ingredient matches for Nimesulide Dorom

Nimesulide

Nimesulide is reported as an ingredient of Nimesulide Dorom in the following countries:

• Italy

International Drug Name Search

Metfor

Metfor may be available in the countries listed below.

Ingredient matches for Metfor

Metformin

Metformin hydrochloride (a derivative of Metformin) is reported as an ingredient of Metfor in the following countries:

• Myanmar


• Oman

International Drug Name Search

Dexchlorpheniramine/Methscopolamine/Pseudoephedrine Sustained-Release Tablets

Generic Name: Dexchlorpheniramine/Methscopolamine/Pseudoephedrine (DEX-klor-fen-IR-a-meen/SOO-doe-e-FED-rin/METH-skoe-POL-a-meen)
Brand Name: DuraHist D

Dexchlorpheniramine/Methscopolamine/Pseudoephedrine Sustained-Release Tablets are used for:

Relieving congestion, sneezing, runny nose, and itchy, watery eyes due to colds, flu, or hay fever. It may also be used for other conditions as determined by your doctor.

Dexchlorpheniramine/Methscopolamine/Pseudoephedrine Sustained-Release Tablets are an antihistamine, decongestant, and anticholinergic combination. The antihistamine works by blocking histamine, a substance in the body that causes sneezing, runny nose, and watery eyes. The decongestant relieves nasal congestion by shrinking the nasal mucous membranes, which promotes nasal drainage. The anticholinergic dries the chest by decreasing lung secretions.

Do NOT use Dexchlorpheniramine/Methscopolamine/Pseudoephedrine Sustained-Release Tablets if:

• you are allergic to any ingredient in Dexchlorpheniramine/Methscopolamine/Pseudoephedrine Sustained-Release Tablets


• you take sodium oxybate (GHB) or you have taken furazolidone or a monoamine oxidase inhibitor (MAOI) (eg, phenelzine) within the last 14 days


• you have severe heart blood vessel disease, severe high blood pressure, rapid heartbeat, or severe heart problems


• you have narrow-angle glaucoma, severe bleeding, severe irritation of the esophagus or other serious problems with the esophagus (eg, esophageal achalasia), peptic ulcer, a blockage of your stomach or bowel, bowel motility problems, severe bowel inflammation (eg, ulcerative colitis), certain muscle problems (eg, myasthenia gravis), or uncontrolled bleeding


• you are unable to urinate or are having an asthma attack

Contact your doctor or health care provider right away if any of these apply to you.

Before using Dexchlorpheniramine/Methscopolamine/Pseudoephedrine Sustained-Release Tablets:

Some medical conditions may interact with Dexchlorpheniramine/Methscopolamine/Pseudoephedrine Sustained-Release Tablets. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

• if you are pregnant, planning to become pregnant, or breast-feeding


• if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement


• if you have allergies to medicines, foods, or other substances


• if you have a fast, slow, or irregular heartbeat or a history of other heart problems


• if you have a history of diabetes, an enlarged prostate or other prostate problems, kidney problems, high blood pressure, asthma, nerve problems, blood clots, a hiatal hernia, an adrenal gland tumor, glaucoma, breathing problems during sleep, seizures, an overactive thyroid, lung problems (eg, emphysema), severe bowel problems, trouble urinating, ulcers, stroke, bladder problems, or a blockage of your stomach, intestines, or bladder

Some MEDICINES MAY INTERACT with Dexchlorpheniramine/Methscopolamine/Pseudoephedrine Sustained-Release Tablets. Tell your health care provider if you are taking any other medicines, especially any of the following:

• Alpha-blockers (eg, guanethidine, methyldopa, prazosin), beta-blockers (eg, atenolol), diuretics (eg, furosemide, hydrochlorothiazide), furazolidone, or MAOIs (eg, phenelzine) because the risk of high or low blood pressure may be increased


• Alkalizers (eg, calcium or magnesium antacids), anticholinergics (eg, atropine, benztropine, dicyclomine), carbonic anhydrase inhibitors (eg, acetazolamide), ergotamine, sodium bicarbonate, or tricyclic antidepressants (eg, amitriptyline) because they may increase the risk of Dexchlorpheniramine/Methscopolamine/Pseudoephedrine Sustained-Release Tablets's side effects


• Bromocriptine, catechol-O-methyltransferase (COMT) inhibitors (eg, entacapone), certain stimulants (eg, doxapram, pseudoephedrine), cocaine, digoxin, droxidopa, potassium chloride, or sodium oxybate (GHB) because the risk of their side effects may be increased by Dexchlorpheniramine/Methscopolamine/Pseudoephedrine Sustained-Release Tablets


• Guanadrel, guanethidine, mecamylamine, methyldopa, or reserpine because their effectiveness may be decreased by Dexchlorpheniramine/Methscopolamine/Pseudoephedrine Sustained-Release Tablets

This may not be a complete list of all interactions that may occur. Ask your health care provider if Dexchlorpheniramine/Methscopolamine/Pseudoephedrine Sustained-Release Tablets may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

How to use Dexchlorpheniramine/Methscopolamine/Pseudoephedrine Sustained-Release Tablets:

Use Dexchlorpheniramine/Methscopolamine/Pseudoephedrine Sustained-Release Tablets as directed by your doctor. Check the label on the medicine for exact dosing instructions.

• Take Dexchlorpheniramine/Methscopolamine/Pseudoephedrine Sustained-Release Tablets by mouth with or without food. If stomach upset occurs, take with food to reduce stomach irritation.


• Do not take Dexchlorpheniramine/Methscopolamine/Pseudoephedrine Sustained-Release Tablets at the same time as an antacid, certain medicines for diarrhea (eg, attapulgite, bismuth, kaolin, pectin), or ketoconazole. Take these medicines 2 or 3 hours before or after you take Dexchlorpheniramine/Methscopolamine/Pseudoephedrine Sustained-Release Tablets.


• Swallow Dexchlorpheniramine/Methscopolamine/Pseudoephedrine Sustained-Release Tablets whole. Do not break, crush, or chew before swallowing. Some brands of Dexchlorpheniramine/Methscopolamine/Pseudoephedrine Sustained-Release Tablets may be broken in half before taking. If you have difficulty swallowing the whole tablet, ask your pharmacist if your brand of medicine may be broken in half.


• If you miss a dose of Dexchlorpheniramine/Methscopolamine/Pseudoephedrine Sustained-Release Tablets and you are taking it regularly, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.

Ask your health care provider any questions you may have about how to use Dexchlorpheniramine/Methscopolamine/Pseudoephedrine Sustained-Release Tablets.

Important safety information:

• Dexchlorpheniramine/Methscopolamine/Pseudoephedrine Sustained-Release Tablets may cause drowsiness, dizziness, or blurred vision. These effects may be worse if you take it with alcohol or certain medicines. Use Dexchlorpheniramine/Methscopolamine/Pseudoephedrine Sustained-Release Tablets with caution. Do not drive or perform other possibly unsafe tasks until you know how you react to it.


• If your symptoms do not get better within 7 days or if they get worse or you develop a high fever or persistent headache, check with your doctor.


• Dexchlorpheniramine/Methscopolamine/Pseudoephedrine Sustained-Release Tablets may cause dry mouth. To relieve dry mouth, suck on sugarless hard candy or ice chips, chew sugarless gum, drink water, or use a saliva substitute.


• Dexchlorpheniramine/Methscopolamine/Pseudoephedrine Sustained-Release Tablets may make your eyes more sensitive to sunlight. It may help to wear sunglasses.


• Dexchlorpheniramine/Methscopolamine/Pseudoephedrine Sustained-Release Tablets may reduce sweating. Do not become overheated in hot weather or while you are being active; heatstroke may occur.


• Do not take diet or appetite control medicines while you are taking Dexchlorpheniramine/Methscopolamine/Pseudoephedrine Sustained-Release Tablets without checking with your doctor.


• Dexchlorpheniramine/Methscopolamine/Pseudoephedrine Sustained-Release Tablets has dexchlorpheniramine and pseudoephedrine in it. Before you start any new medicine, check the label to see if it has dexchlorpheniramine or pseudoephedrine in it too. If it does or if you are not sure, check with your doctor or pharmacist.


• If you have trouble sleeping, ask your doctor or pharmacist about the best time of the day to take Dexchlorpheniramine/Methscopolamine/Pseudoephedrine Sustained-Release Tablets.


• Dexchlorpheniramine/Methscopolamine/Pseudoephedrine Sustained-Release Tablets may interfere with certain lab tests. Be sure your doctor and lab personnel know that you are taking Dexchlorpheniramine/Methscopolamine/Pseudoephedrine Sustained-Release Tablets.


• Tell your doctor or dentist that you take Dexchlorpheniramine/Methscopolamine/Pseudoephedrine Sustained-Release Tablets before you receive any medical or dental care, emergency care, or surgery.


• Dexchlorpheniramine/Methscopolamine/Pseudoephedrine Sustained-Release Tablets may interfere with allergy skin tests. If you are scheduled for a skin test, talk to your doctor. You may need to stop taking Dexchlorpheniramine/Methscopolamine/Pseudoephedrine Sustained-Release Tablets for a few days before the tests.


• Diabetes patients - Dexchlorpheniramine/Methscopolamine/Pseudoephedrine Sustained-Release Tablets may affect your blood sugar. Check blood sugar levels closely. Ask your doctor before you change the dose of your diabetes medicine.


• Use Dexchlorpheniramine/Methscopolamine/Pseudoephedrine Sustained-Release Tablets with caution in the ELDERLY; they may be more sensitive to its effects.


• Caution is advised when using Dexchlorpheniramine/Methscopolamine/Pseudoephedrine Sustained-Release Tablets in CHILDREN; they may be more sensitive to its effects.


• PREGNANCY and BREAST-FEEDING: It is not known if Dexchlorpheniramine/Methscopolamine/Pseudoephedrine Sustained-Release Tablets can cause harm to the fetus. If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Dexchlorpheniramine/Methscopolamine/Pseudoephedrine Sustained-Release Tablets while you are pregnant. Dexchlorpheniramine/Methscopolamine/Pseudoephedrine Sustained-Release Tablets are found in breast milk. Do not breast-feed while taking Dexchlorpheniramine/Methscopolamine/Pseudoephedrine Sustained-Release Tablets.

Possible side effects of Dexchlorpheniramine/Methscopolamine/Pseudoephedrine Sustained-Release Tablets:

All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:

Constipation; diarrhea; dizziness; drowsiness; dry mouth, nose, or throat; excitability; headache; loss of appetite; nausea; nervousness or anxiety; trouble sleeping; upset stomach; vomiting; weakness.

Seek medical attention right away if any of these SEVERE side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); difficulty urinating or inability to urinate; fast or irregular heartbeat; hallucinations; mental or mood changes; seizures; severe dizziness, lightheadedness, or headache; tremor; vision changes.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA.

See also: Dexchlorpheniramine/Methscopolamine/Pseudoephedrine side effects (in more detail)

If OVERDOSE is suspected:

Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately. Symptoms may include deep sleep or loss of consciousness; hot or cool skin; irregular heartbeat; irritability, anxiety, or panic; large pupils; numbness or tingling in the arms or legs; seizures; slowed or shallow breathing.

Proper storage of Dexchlorpheniramine/Methscopolamine/Pseudoephedrine Sustained-Release Tablets:

Store Dexchlorpheniramine/Methscopolamine/Pseudoephedrine Sustained-Release Tablets at room temperature, between 59 and 86 degrees F (15 and 30 degrees C), in a tightly closed container. Store away from heat, moisture, and light. Do not store in the bathroom. Keep Dexchlorpheniramine/Methscopolamine/Pseudoephedrine Sustained-Release Tablets out of the reach of children and away from pets.

General information:

• If you have any questions about Dexchlorpheniramine/Methscopolamine/Pseudoephedrine Sustained-Release Tablets, please talk with your doctor, pharmacist, or other health care provider.


• Dexchlorpheniramine/Methscopolamine/Pseudoephedrine Sustained-Release Tablets are to be used only by the patient for whom it is prescribed. Do not share it with other people.


• If your symptoms do not improve or if they become worse, check with your doctor.

This information is a summary only. It does not contain all information about Dexchlorpheniramine/Methscopolamine/Pseudoephedrine Sustained-Release Tablets. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.

Issue Date: February 1, 2012

Database Edition 12.1.1.002

Copyright © 2012 Wolters Kluwer Health, Inc.

More Dexchlorpheniramine/Methscopolamine/Pseudoephedrine resources

• Dexchlorpheniramine/Methscopolamine/Pseudoephedrine Side Effects (in more detail)
• Dexchlorpheniramine/Methscopolamine/Pseudoephedrine Use in Pregnancy & Breastfeeding
• Dexchlorpheniramine/Methscopolamine/Pseudoephedrine Drug Interactions
• Dexchlorpheniramine/Methscopolamine/Pseudoephedrine Support Group
• 0 Reviews for Dexchlorpheniramine/Methscopolamine/Pseudoephedrine - Add your own review/rating

Compare Dexchlorpheniramine/Methscopolamine/Pseudoephedrine with other medications

• Hay Fever
• Rhinitis

Zelapar

ZELAPAR 1.25 mg

Oral Lyophilisate (Tablet)

Selegiline hydrochloride

Read all of this leaflet carefully before you start taking this medicine.

• Keep this leaflet. You may need to read it again.


• If you have any further questions, ask your doctor or pharmacist.


• This medicine has been prescribed for you. Do not pass it on to others. It may harm them, even if their symptoms are the same as yours.


• If any of the side effects get serious, or if you notice any side effects not listed in this leaflet, please tell your doctor or pharmacist.

In this leaflet:

1. What ZELAPAR is and what it is used for.

2. Before you take ZELAPAR.

3. How to take ZELAPAR.

4. Possible side effects.

5. How to store ZELAPAR.

6. Further information.

What Zelapar Is And What It Is Used For

The name of this medicine is ZELAPAR 1.25 mg oral lyophilisate (tablet). The active ingredient in this medicine is selegiline hydrochloride which belongs to a group of medicines called monoamine oxidase B inhibitors.

ZELAPAR is used to treat Parkinson’s disease and can be used on its own or in combination with other medicines.

Before You Take Zelpar

Do not take ZELAPAR if you:

• Are allergic (hypersensitive) to selegiline hydrochloride or any of the other ingredients of ZELAPAR.


• Have a stomach ulcer.


• Have a condition called phenylketonuria.


• Are taking pethidine or any other opioid painkiller.


• Are taking any medicine for depression.


• Are taking any Monoamine oxidase inhibitors e.g. the antibiotic linezolid.


• Are taking any medicines for migraine e.g. rizatriptan.

If you are already taking a medicine called Levodopa for your Parkinson’s disease and suffer from any of the following conditions you should not take ZELAPAR as well:

• Major heart problems.


• Chest pain (angina).


• High blood pressure.


• An erratic or fast heartbeat.


• An overactive thyroid gland (hyperthyroid disease).


• An eye condition called narrow angle glaucoma.


• A tumour of your prostate gland.


• Major mental health problems e.g. schizophrenia.

Take special care with ZELAPAR

• If you already take Levodopa. It can cause agitation and you should tell your doctor if this happens.

If you have:

• Liver disease.


• High or low blood pressure.


• Erratic heartbeat.


• Chest pain (Angina).


• Severe dementia.


• Mental health problems.


• A history of stomach ulcers.

If any of the above apply to you, you should speak to your doctor before taking this medicine.

Taking ZELAPAR with other medicines

Please tell your doctor or pharmacist if you are taking or have recently taken any other medicines, including those obtained without a prescription. This is especially important if you are taking any of the following medicines for:

• High or low blood pressure.


• Anxiety, depression or sleep problems.


• Heart problems.


• Asthma e.g. ventolin inhalers.

or any of the following:

• Medicines to relieve congestion e.g. ephedrine.


• Medicines to relax the gut muscles.


• Medicines having antidepressant or mood elevating properties.


• Oral contraceptives (the pill).


• HRT (hormone replacement therapy).


• Amantadine (used to treat Parkinson’s).


• Altretamine (used to treat ovarian cancer).

Taking ZELAPAR with food and drink

Do not drink alcohol when you are taking ZELAPAR.

Do not eat, drink or rinse your mouth for 5 minutes after taking ZELAPAR.

Pregnancy and breast-feeding

Do not take ZELAPAR if you are pregnant, breast-feeding or planning to become pregnant.

Driving and operating machinery

ZELAPAR may make you feel slow or drowsy, if this happens to you do not drive or operate machinery.

Important information about one of the ingredients of ZELAPAR

ZELAPAR contains a source of phenylalanine. May be harmful for people with phenylketonuria.

How To Take Zelapar

Always take ZELAPAR exactly as your doctor has told you. You should check with your doctor or pharmacist if you are not sure.

The usual dose is 1.25 mg once a day.

Do not push the tablet through the foil blister. Peel back the foil and carefully remove the tablet.

Place it on your tongue in the morning and allow it to dissolve. The tablet will dissolve rapidly.

Do not eat, drink or rinse your mouth out for 5 minutes after taking it.

If you take more ZELAPAR than you should

If you take too much ZELAPAR you should contact your doctor or go to the nearest hospital emergency department immediately. Take the packet and this leaflet with you so that the doctor will know what you have taken.

If you forget to take ZELAPAR

If you forget to take your dose of ZELAPAR in the morning, ensure you take it as soon as you remember before your next dose is due. Do not take a double dose to make up for a forgotten dose.

Zelapar Side Effects

Like all medicines, ZELAPAR can cause side effects, although not everybody gets them.

Stop taking this medicine and tell your doctor immediately if you have difficulty breathing or your mouth or throat begins to swell or if you start suffering from a severe rash, itching or other skin reactions, as these may be signs of a serious allergic reaction.

The following side effects have been reported:

• Back pain, dizziness, shakes and sore throat.

Less commonly:

• Sore mouth, mouth ulcers, blocked nose.


• Falls, loss of balance, dizziness, problems sleeping, strange dreams, hallucinations, confusion.


• Muscle cramps and joint pains.


• Constipation or diarrhoea, feeling sick.

In addition, the following side effects have also been reported:

• Chest pain, headache, low blood pressure.


• Muscle aches.


• Depression, tiredness.


• Dry mouth.


• Abnormal liver tests.

Taking ZELAPAR with Levodopa

If you take ZELAPAR with Levodopa you may also notice:

• Difficulty controlling your movements or loss of balance.


• Agitation, problems sleeping, confusion, serious mental health problems, hallucinations or abnormal thoughts, anxiety, irritability, depression and tiredness.


• Dizziness or feeling faint, dry mouth, feeling sick, loss of appetite.


• High or low blood pressure, chest pains, erratic or fast heartbeat.


• Headache, blurred vision and excessive sweating.


• Shortness of breath, swollen ankles and problems passing urine.


• Skin rashes or spots.


• Low levels of white blood cells (leucocytopenia) and platelets (thrombocytopenia) in the blood which may make you more vulnerable to infections or bruising.


• Temporary liver problems.


• Hair loss.

If any of the side effects become serious, or if you notice any side effects not listed in this leaflet, please tell your doctor or pharmacist.

How To Store Zelapar

Keep out of the reach and sight of children.

Do not store above 25ºC.

Do not use after the expiry date printed on the carton and sachet.

Further Information

What ZELAPAR contains

The active ingredient is Selegiline hydrochloride (1.25 mg). It also contains gelatine, mannitol, aspartame, grapefruit flavour, glycine, anhydrous citric acid and yellow colouring (yellow iron oxide [E172] and hypromellose [E464]) as inactive ingredients.

Discard any unused medicine within 3 months of opening the sachet.

Do not take this medicine after the expiry date shown on the pack.

What ZELAPAR looks like and the contents of the pack

The tablets are pale yellow, round, and embossed with an A on one side.

They come in PVCPE/PVdC blister packs sealed with aluminium foil enclosed in a paper/PE/aluminium foil sachet.

ZELAPAR comes in packs of 10, 30, 60 and 100 tablets.

Marketing Authorisation Holder

Cephalon UK Limited

1 Albany Place

Hyde Way

Welwyn Garden City

Hertfordshire

AL7 3BT

UK

Manufacturer

Catalent UK Swindon Zydis Limited

Frankland Road

Blagrove

Swindon

Wiltshire

SN5 8RU

UK

This leaflet was last approved in June 2010

For more information please call free on

0800 783 4869 or

e-mail: UKMedInfo@cephalon.com

0122/8

11EP5536H

Erybenz

Erybenz may be available in the countries listed below.

Ingredient matches for Erybenz

Benzoyl Peroxide

Benzoyl Peroxide is reported as an ingredient of Erybenz in the following countries:

• Greece

Erythromycin

Erythromycin is reported as an ingredient of Erybenz in the following countries:

• Greece

International Drug Name Search

D-Tal

Generic Name: belladonna alkaloids and phenobarbital (BEL a DON a AL ka loids and FEEN oh BAR bi tal)

Brand Names: Bellatal, D-Tal, Donnatal

What is D-Tal (belladonna alkaloids and phenobarbital)?

Phenobarbital is in a group of drugs called barbiturates (bar-BIT-chur-ates). Phenobarbital slows the activity of your brain and nervous system.

Belladonna alkaloids produce many effects in the body, including reduced muscle spasms in the digestive or urinary tract, and reduced fluid secretions from certain glands or organs.

The belladonna alkaloids included in this medication include atropine, hyoscyamine, and scopolamine.

The combination of belladonna alkaloids and phenobarbital is used to treat irritable bowel syndrome and ulcers in the intestine.

Belladonna alkaloids and phenobarbital may also be used for other purposes not listed in this medication guide.

What is the most important information I should know about D-Tal (belladonna alkaloids and phenobarbital)?

Phenobarbital may be habit-forming and should be used only by the person it was prescribed for. This medication should never be shared with another person, especially someone who has a history of drug abuse or addiction. Keep the medication in a secure place where others cannot get to it.

Do not take this medication together with a potassium supplement unless your doctor has told you to.

Tell your doctor if you regularly use other medicines that make you sleepy (such as cold or allergy medicine, narcotic pain medicine, sleeping pills, muscle relaxers, and medicine for seizures, depression, or anxiety). They can add to sleepiness caused by belladonna alkaloids and phenobarbital. This medication can cause side effects that may impair your thinking or reactions. Be careful if you drive or do anything that requires you to be awake and alert. Avoid drinking alcohol while taking this medication or you could have increased dizziness and drowsiness.

Avoid becoming overheated or dehydrated during exercise and in hot weather. Belladonna alkaloids and phenobarbital can decrease perspiration and you may be more prone to heat stroke.

Call your doctor if your symptoms do not improve, or if they get worse.

What should I discuss with my healthcare provider before taking D-Tal (belladonna alkaloids and phenobarbital)?

You should not use this medication if you are allergic to atropine, hyoscyamine, scopolamine, or phenobarbital. You may not be able use this medication if you have:

• 
  

  enlarged prostate, urination problems;

  
  


• 
  

  a blockage in your intestines or digestive tract;

  
  


• 
  

  a stomach condition called paralytic ileus;

  
  


• 
  

  active bleeding;

  
  


• 
  

  severe ulcerative colitis or toxic megacolon;

  
  


• 
  

  a muscle disorder called myasthenia gravis;

  
  


• 
  

  a hiatal hernia or reflux disease; or

  
  


• 
  

  porphyria.

  
  

Before taking this medication, tell your doctor if you are allergic to any drugs or if you have:

• 
  

  a colostomy or ileostomy;

  
  


• liver disease;


• kidney disease;


• 
  

  glaucoma;

  
  


• 
  

  a thyroid disorder;

  
  


• 
  

  heart disease, high blood pressure, congestive heart failure;

  
  


• 
  

  a heart rhythm disorder; or

  
  


• 
  

  ulcerative colitis or stomach ulcer.

  
  

If you have any of these conditions, you may not be able to take belladonna alkaloids and phenobarbital, or you may need a dose adjustment or special tests during treatment.

FDA pregnancy category C. This medication may be harmful to an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant during treatment. It is not known whether this medication passes into breast milk or if it could harm a nursing baby. However, belladonna alkaloids and phenobarbital can slow breast milk production. Do not take this medication without telling your doctor if you are breast-feeding a baby. Do not give this medication to a child without the advice of a doctor. Older adults may be more likely to have side effects such as constipation, dry mouth, problems with urination, agitation, confusion, or severe memory problems.

How should I take D-Tal (belladonna alkaloids and phenobarbital)?

Take this medication exactly as prescribed by your doctor. Do not take it in larger amounts or for longer than recommended. Follow the directions on your prescription label.

Take the medicine with a full glass of water.

Measure liquid medicine with a special dose-measuring spoon or cup, not a regular table spoon. If you do not have a dose-measuring device, ask your pharmacist for one.

Call your doctor if your symptoms do not improve, or if they get worse.

This medication can cause you to have unusual results with certain medical tests. Tell any doctor who treats you that you are using belladonna alkaloids and phenobarbital.

Store belladonna alkaloids and phenobarbital at room temperature away from moisture and heat. Keep track of how much of this medicine has been used from each new bottle. Phenobarbital is a drug of abuse and you should be aware if any person in the household is using this medicine improperly or without a prescription.

What happens if I miss a dose?

Take the missed dose as soon as you remember. However, if it is almost time for your next dose, skip the missed dose and take only the next regularly scheduled dose. Do not take a double dose of this medication.

What happens if I overdose?

Seek emergency medical attention if you think you have used too much of this medicine.

Overdose symptoms may include headache, dizziness, nausea, vomiting, dry mouth, blurred vision, hot or dry skin, trouble swallowing, feeling excited or agitated,

What should I avoid while taking D-Tal (belladonna alkaloids and phenobarbital)?

Do not take this medication together with a potassium supplement unless your doctor has told you to.

Tell your doctor if you regularly use other medicines that make you sleepy (such as cold or allergy medicine, narcotic pain medicine, sleeping pills, muscle relaxers, and medicine for seizures, depression, or anxiety). They can add to sleepiness caused by belladonna alkaloids and phenobarbital. This medication can cause side effects that may impair your thinking or reactions. Be careful if you drive or do anything that requires you to be awake and alert. Avoid drinking alcohol while taking this medication or you could have increased dizziness and drowsiness.

Avoid becoming overheated or dehydrated during exercise and in hot weather. Belladonna alkaloids and phenobarbital can decrease perspiration and you may be more prone to heat stroke.

D-Tal (belladonna alkaloids and phenobarbital) side effects

Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficulty breathing; swelling of your face, lips, tongue, or throat. Stop using this medication and call your doctor at once if you have any of these serious side effects:

• 
  

  diarrhea;

  
  


• 
  

  painful or difficult urination;

  
  


• 
  

  fast or pounding heartbeats;

  
  


• 
  

  blurred vision with eye pain, or seeing halos around lights;

  
  


• 
  

  feeling like you might pass out; or

  
  


• 
  

  mouth sores, red or bleeding gums, or tooth decay (with long-term use).

  
  

Less serious side effects may include:

• 
  

  drowsiness;

  
  


• 
  

  blurred vision, increased sensitivity to light;

  
  


• 
  

  dry mouth;

  
  


• 
  

  decreased taste sensation;

  
  


• 
  

  decreased sweating or urination;

  
  


• 
  

  headache, dizziness, weakness;

  
  


• 
  

  sleep problems (insomnia);

  
  


• 
  

  nausea, vomiting, constipation, bloating;

  
  


• 
  

  feeling restless or excited; or

  
  


• 
  

  impotence, loss of interest in sex, or trouble having an orgasm.

  
  

This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.

What other drugs will affect D-Tal (belladonna alkaloids and phenobarbital)?

The following drugs can interact with belladonna alkaloids and phenobarbital. Tell your doctor if you are using any of these:

• 
  

  a blood thinner such as warfarin (Coumadin);

  
  


• 
  

  ketoconazole (Nizoral);

  
  


• 
  

  an MAO inhibitor such as isocarboxazid (Marplan), phenelzine (Nardil), rasagiline (Azilect), selegiline (Eldepryl, Emsam), or tranylcypromine (Parnate);

  
  


• 
  

  atropine (Donnatal, and others), benztropine (Cogentin), dimenhydrinate (Dramamine), methscopolamine (Pamine), or scopolamine (Transderm-Scop);

  
  


• 
  

  bronchodilators such as ipratroprium (Atrovent) or tiotropium (Spiriva);

  
  


• 
  

  glycopyrrolate (Robinul);

  
  


• 
  

  mepenzolate (Cantil);

  
  


• 
  

  bladder or urinary medications such as darifenacin (Enablex), flavoxate (Urispas), oxybutynin (Ditropan, Oxytrol), tolterodine (Detrol), or solifenacin (Vesicare); or

  
  


• 
  

  irritable bowel medications such as dicyclomine (Bentyl), hyoscyamine (Anaspaz, Cystospaz, Levsin, and others), or propantheline (Pro-Banthine).

  
  

This list is not complete and there may be other drugs that can interact with belladonna alkaloids and phenobarbital. Tell your doctor about all your prescription and over-the-counter medications, vitamins, minerals, herbal products, and drugs prescribed by other doctors. Do not start a new medication without telling your doctor.

More D-Tal resources

• D-Tal Side Effects (in more detail)
• D-Tal Use in Pregnancy & Breastfeeding
• D-Tal Drug Interactions
• D-Tal Support Group
• 0 Reviews for D-Tal - Add your own review/rating

• Alkabel-SR Controlled-Release Tablets MedFacts Consumer Leaflet (Wolters Kluwer)


• Antispasmodic Monograph (AHFS DI)


• Donnatal MedFacts Consumer Leaflet (Wolters Kluwer)


• Servira Prescribing Information (FDA)

Compare D-Tal with other medications

• Duodenal Ulcer
• Enterocolitis
• Irritable Bowel Syndrome

Where can I get more information?

• Your pharmacist can provide more information about belladonna alkaloids and phenobarbital.

See also: D-Tal side effects (in more detail)