Thursday, 29 September 2016

Macular Degeneration Medications


Definition of Macular Degeneration: Macular degeneration is a disorder that affects the macula (the central part of the retina of the eye) causing decreased visual acuity and possible loss of central vision.

Drugs associated with Macular Degeneration

The following drugs and medications are in some way related to, or used in the treatment of Macular Degeneration. This service should be used as a supplement to, and NOT a substitute for, the expertise, skill, knowledge and judgment of healthcare practitioners.

Learn more about Macular Degeneration





Drug List:

Myxedema Coma Medications


Drugs associated with Myxedema Coma

The following drugs and medications are in some way related to, or used in the treatment of Myxedema Coma. This service should be used as a supplement to, and NOT a substitute for, the expertise, skill, knowledge and judgment of healthcare practitioners.





Drug List:

Apo-Medroxy




Apo-Medroxy may be available in the countries listed below.


Ingredient matches for Apo-Medroxy



Medroxyprogesterone

Medroxyprogesterone 17α-acetate (a derivative of Medroxyprogesterone) is reported as an ingredient of Apo-Medroxy in the following countries:


  • Canada

International Drug Name Search

PMS-Terbinafine




PMS-Terbinafine may be available in the countries listed below.


Ingredient matches for PMS-Terbinafine



Terbinafine

Terbinafine hydrochloride (a derivative of Terbinafine) is reported as an ingredient of PMS-Terbinafine in the following countries:


  • Canada

International Drug Name Search

Clamoxyl Mucolitico




Clamoxyl Mucolitico may be available in the countries listed below.


Ingredient matches for Clamoxyl Mucolitico



Amoxicillin

Amoxicillin trihydrate (a derivative of Amoxicillin) is reported as an ingredient of Clamoxyl Mucolitico in the following countries:


  • Spain

Bromhexine

Bromhexine hydrochloride (a derivative of Bromhexine) is reported as an ingredient of Clamoxyl Mucolitico in the following countries:


  • Spain

International Drug Name Search

Buflomédil Mylan




Buflomédil Mylan may be available in the countries listed below.


Ingredient matches for Buflomédil Mylan



Buflomedil

Buflomedil hydrochloride (a derivative of Buflomedil) is reported as an ingredient of Buflomédil Mylan in the following countries:


  • France

International Drug Name Search

Mucolloid




Mucolloid may be available in the countries listed below.


Ingredient matches for Mucolloid



Chondroitin Polysulfate

Chondroitin Polysulfate sodium salt (a derivative of Chondroitin Polysulfate) is reported as an ingredient of Mucolloid in the following countries:


  • Japan

International Drug Name Search

Pentamon




Pentamon may be available in the countries listed below.


Ingredient matches for Pentamon



Pentoxifylline

Pentoxifylline is reported as an ingredient of Pentamon in the following countries:


  • Croatia (Hrvatska)

International Drug Name Search

Myelofibrosis Medications


Definition of Myelofibrosis:

Myelofibrosis is a disorder of the bone marrow, in which the marrow is replaced by scar (fibrous) tissue.

Drugs associated with Myelofibrosis

The following drugs and medications are in some way related to, or used in the treatment of Myelofibrosis. This service should be used as a supplement to, and NOT a substitute for, the expertise, skill, knowledge and judgment of healthcare practitioners.

Learn more about Myelofibrosis





Drug List:

Axetine




Axetine may be available in the countries listed below.


Ingredient matches for Axetine



Cefuroxime

Cefuroxime sodium salt (a derivative of Cefuroxime) is reported as an ingredient of Axetine in the following countries:


  • Bulgaria

  • China

  • Czech Republic

  • Estonia

  • Latvia

  • Lithuania

  • Malta

  • Romania

  • Russian Federation

  • Slovakia

  • Sri Lanka

International Drug Name Search

Meibomian Cyst Medications


There are currently no drugs listed for "Meibomian Cyst".

Learn more about Meibomian Cyst





Drug List:

Multiple Myeloma Medications


Definition of Multiple Myeloma: Multiple myeloma is a cancer of the plasma cells in bone marrow.

Drugs associated with Multiple Myeloma

The following drugs and medications are in some way related to, or used in the treatment of Multiple Myeloma. This service should be used as a supplement to, and NOT a substitute for, the expertise, skill, knowledge and judgment of healthcare practitioners.

See sub-topics

Topics under Multiple Myeloma

  • Osteolytic Bone Lesions of Multiple Myeloma (4 drugs)

Learn more about Multiple Myeloma





Drug List:

Hypoparathyroidism Medications


Definition of Hypoparathyroidism: Hypoparthyroidism is a deficiency of parathyroid hormone that causes abnormal metabolism of calcium and phosphorus.

Drugs associated with Hypoparathyroidism

The following drugs and medications are in some way related to, or used in the treatment of Hypoparathyroidism. This service should be used as a supplement to, and NOT a substitute for, the expertise, skill, knowledge and judgment of healthcare practitioners.

See sub-topics

Topics under Hypoparathyroidism

  • Pseudohypoparathyroidism (4 drugs)

Learn more about Hypoparathyroidism





Drug List:

Coumarin




Scheme

DCF

CAS registry number (Chemical Abstracts Service)

0000091-64-5

Chemical Formula

C9-H6-O2

Molecular Weight

146

Therapeutic Categories

Agent for antivaricose therapy

Vasoprotective agent

Chemical Name

2H-1-Benzopyran-2-one

Foreign Names

  • Cumarinum (Latin)
  • Cumarin (German)
  • Coumarine (French)
  • Cumarina (Spanish)

Generic Names

  • Coumarine (OS: DCF)
  • Tonka Bean Camphor (IS)
  • Cumarin (PH: DAB 1999)

Brand Names

  • Esberiven
    Craveri, Argentina


  • Venalot mono
    Schaper & Brümmer, Luxembourg


  • Venalot (Coumarin and Troxerutin)
    Schaper & Brümmer, Germany

International Drug Name Search

Glossary

DCFDénomination Commune Française
ISInofficial Synonym
OSOfficial Synonym
PHPharmacopoeia Name

Click for further information on drug naming conventions and International Nonproprietary Names.

Nitrazepam Merck




Nitrazepam Merck may be available in the countries listed below.


Ingredient matches for Nitrazepam Merck



Nitrazepam

Nitrazepam is reported as an ingredient of Nitrazepam Merck in the following countries:


  • Netherlands

International Drug Name Search

Hyperkalemia Medications


Definition of Hyperkalemia: Hyperkalemia is a condition caused by higher than normal levels of potassium in the bloodstream.

Drugs associated with Hyperkalemia

The following drugs and medications are in some way related to, or used in the treatment of Hyperkalemia. This service should be used as a supplement to, and NOT a substitute for, the expertise, skill, knowledge and judgment of healthcare practitioners.

Learn more about Hyperkalemia





Drug List:

Diclocil




Diclocil may be available in the countries listed below.


Ingredient matches for Diclocil



Dicloxacillin

Dicloxacillin sodium salt (a derivative of Dicloxacillin) is reported as an ingredient of Diclocil in the following countries:


  • Australia

  • Colombia

  • Denmark

  • Finland

  • Greece

  • Iceland

  • New Zealand

  • Norway

  • Peru

  • Portugal

  • Thailand

  • Venezuela

International Drug Name Search

Hemorrhagic Nephrosonephritis Medications


There are currently no drugs listed for "Hemorrhagic Nephrosonephritis". See Renal Dysfunction.





Drug List:

Huntington's Disease Medications


Definition of Huntington's Disease: Huntington's disease is a disorder passed down through families in which nerve cells in the brain waste away, or degenerate.

Drugs associated with Huntington's Disease

The following drugs and medications are in some way related to, or used in the treatment of Huntington's Disease. This service should be used as a supplement to, and NOT a substitute for, the expertise, skill, knowledge and judgment of healthcare practitioners.

Learn more about Huntington's Disease





Drug List:

Hydatid Disease Medications


Drugs associated with Hydatid Disease

The following drugs and medications are in some way related to, or used in the treatment of Hydatid Disease. This service should be used as a supplement to, and NOT a substitute for, the expertise, skill, knowledge and judgment of healthcare practitioners.





Drug List:

Hyperphosphatemia of Renal Failure Medications


Drugs associated with Hyperphosphatemia of Renal Failure

The following drugs and medications are in some way related to, or used in the treatment of Hyperphosphatemia of Renal Failure. This service should be used as a supplement to, and NOT a substitute for, the expertise, skill, knowledge and judgment of healthcare practitioners.





Drug List:

Jutadilat




Jutadilat may be available in the countries listed below.


Ingredient matches for Jutadilat



Nifedipine

Nifedipine is reported as an ingredient of Jutadilat in the following countries:


  • Germany

International Drug Name Search

Glucophage



Generic Name: metformin (Oral route)


met-FOR-min hye-droe-KLOR-ide


Oral route(Tablet;Tablet, Extended Release;Solution)

Fortamet(R), Glucophage(R), Glucophage XR(R), Riomet(R): Lactic acidosis is a rare, but serious, metabolic complication that can occur due to metformin accumulation during treatment with metformin hydrochloride; when it occurs, it is fatal in approximately 50% of cases. Lactic acidosis may also occur in association with pathophysiologic conditions, including diabetes mellitus, characterized by significant tissue hypoperfusion and hypoxemia. The risk of lactic acidosis increases with renal impairment, increased age, congestive heart failure, and hepatic insufficiency. Treatment with metformin should not be initiated in patients 80 years old or older, unless measurement of creatinine clearance demonstrates that renal function is normal. Therapy should temporarily be discontinued prior to any intravascular radiocontrast study or surgical procedure. Excessive alcohol use should be avoided, because alcohol potentiates the effects of metformin on lactate metabolism. Discontinue therapy immediately and institute supportive measures promptly for suspected lactic acidosis .


Oral route(Tablet, Extended Release)

Glumetza(R): Lactic acidosis is a rare, but serious, complication that can occur due to metformin accumulation. The risk of lactic acidosis increases with renal or hepatic impairment, acute congestive heart failure, sepsis, dehydration, and excess alcohol intake. Onset may be subtle and include nonspecific symptoms such as malaise, myalgia, respiratory distress, somnolence, and abdominal distress; laboratory abnormalities include low pH, increased anion gap and elevated blood lactate. If lactic acidosis is suspected, Glumetza(R) should be discontinued and the patient immediately hospitalized .



Commonly used brand name(s)

In the U.S.


  • Fortamet

  • Glucophage

  • Glucophage XR

  • Glumetza

  • Riomet

Available Dosage Forms:


  • Tablet

  • Tablet, Extended Release

  • Solution

Therapeutic Class: Hypoglycemic


Chemical Class: Metformin


Uses For Glucophage


Metformin is used to treat high blood sugar levels that are caused by a type of diabetes mellitus or sugar diabetes called type 2 diabetes. With this type of diabetes, insulin produced by the pancreas is not able to get sugar into the cells of the body where it can work properly. Using metformin alone, with a type of oral antidiabetic medicine called a sulfonylurea, or with insulin, will help to lower blood sugar when it is too high and help restore the way you use food to make energy.


Many people can control type 2 diabetes with diet and exercise. Following a specially planned diet and exercise will always be important when you have diabetes, even when you are taking medicines. To work properly, the amount of metformin you take must be balanced against the amount and type of food you eat and the amount of exercise you do. If you change your diet or exercise, you will want to test your blood sugar to find out if it is too low. Your doctor will teach you what to do if this happens.


Metformin does not help patients does not help patients who have insulin-dependent or type 1 diabetes because they cannot produce insulin from their pancreas gland. Their blood glucose is best controlled by insulin injections.


This medicine is available only with your doctor's prescription.


Once a medicine has been approved for marketing for a certain use, experience may show that it is also useful for other medical problems. Although this use is not included in product labeling, metformin is used in certain patients with the following medical conditions:


  • Polycystic ovary syndrome.

Before Using Glucophage


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 this medicine, the following should be considered:


Allergies


Tell your doctor if you have ever had any unusual or allergic reaction to this medicine 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 performed to date have not demonstrated pediatric-specific problems that would limit the usefulness of metformin oral solution and tablets in children 10 to 16 years of age. However, safety and efficacy of metformin extended-release tablets in the pediatric population have not been established.


Geriatric


Although appropriate studies on the relationship of age to the effects of metformin have not been performed in the geriatric population, geriatric-specific problems are not expected to limit the usefulness of metformin in the elderly. However, elderly patients are more likely to have age-related kidney problems, which may require caution in patients receiving metformin. This medicine is not recommended in patients 80 years of age and older who have kidney problems.


Pregnancy








Pregnancy CategoryExplanation
All TrimestersBAnimal studies have revealed no evidence of harm to the fetus, however, there are no adequate studies in pregnant women OR animal studies have shown an adverse effect, but adequate studies in pregnant women have failed to demonstrate a risk to the fetus.

Breast Feeding


Studies in women suggest that this medication poses minimal risk to the infant when used during 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. When you are taking this medicine, it is especially important that your healthcare professional know if you are taking any of the medicines listed below. The following interactions have been selected on the basis of their potential significance and are not necessarily all-inclusive.


Using this medicine with any of the following medicines is not recommended. Your doctor may decide not to treat you with this medication or change some of the other medicines you take.


  • Acetrizoic Acid

  • Diatrizoate

  • Ethiodized Oil

  • Iobenzamic Acid

  • Iobitridol

  • Iocarmic Acid

  • Iocetamic Acid

  • Iodamide

  • Iodipamide

  • Iodixanol

  • Iodohippuric Acid

  • Iodopyracet

  • Iodoxamic Acid

  • Ioglicic Acid

  • Ioglycamic Acid

  • Iohexol

  • Iomeprol

  • Iopamidol

  • Iopanoic Acid

  • Iopentol

  • Iophendylate

  • Iopromide

  • Iopronic Acid

  • Ioseric Acid

  • Iosimide

  • Iotasul

  • Iothalamate

  • Iotrolan

  • Iotroxic Acid

  • Ioversol

  • Ioxaglate

  • Ioxitalamic Acid

  • Ipodate

  • Metrizamide

  • Metrizoic Acid

  • Tyropanoate Sodium

Using this medicine with any of the following medicines is usually not recommended, but may be required in some cases. If both medicines are prescribed together, your doctor may change the dose or how often you use one or both of the medicines.


  • Acetazolamide

  • Alatrofloxacin

  • Balofloxacin

  • Cimetidine

  • Ciprofloxacin

  • Clinafloxacin

  • Dichlorphenamide

  • Dofetilide

  • Enoxacin

  • Fleroxacin

  • Flumequine

  • Gatifloxacin

  • Gemifloxacin

  • Grepafloxacin

  • Levofloxacin

  • Lomefloxacin

  • Moxifloxacin

  • Norfloxacin

  • Ofloxacin

  • Pefloxacin

  • Prulifloxacin

  • Rufloxacin

  • Sparfloxacin

  • Temafloxacin

  • Topiramate

  • Tosufloxacin

  • Trovafloxacin Mesylate

  • Zonisamide

Using this medicine with any of the following medicines may cause an increased risk of certain side effects, but using both drugs may be the best treatment for you. If both medicines are prescribed together, your doctor may change the dose or how often you use one or both of the medicines.


  • Acebutolol

  • Alprenolol

  • Atenolol

  • Betaxolol

  • Bevantolol

  • Bisoprolol

  • Bitter Melon

  • Bucindolol

  • Carteolol

  • Carvedilol

  • Celiprolol

  • Cephalexin

  • Clorgyline

  • Dilevalol

  • Enalaprilat

  • Enalapril Maleate

  • Esmolol

  • Fenugreek

  • Glucomannan

  • Guar Gum

  • Iproniazid

  • Isocarboxazid

  • Labetalol

  • Levobunolol

  • Mepindolol

  • Metipranolol

  • Metoprolol

  • Moclobemide

  • Nadolol

  • Nebivolol

  • Nialamide

  • Oxprenolol

  • Pargyline

  • Penbutolol

  • Phenelzine

  • Pindolol

  • Procarbazine

  • Propranolol

  • Psyllium

  • Rifampin

  • Selegiline

  • Sotalol

  • Talinolol

  • Tertatolol

  • Timolol

  • Toloxatone

  • Tranylcypromine

  • Trospium

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. The following interactions have been selected on the basis of their potential significance and are not necessarily all-inclusive.


Other Medical Problems


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


  • Alcohol, excessive use or

  • Underactive adrenal glands or

  • Underactive pituitary gland or

  • Undernourished condition or

  • Weakened physical condition or

  • Any other condition that causes low blood sugar—Patients with these conditions may be more likely to develop low blood sugar while taking metformin.

  • Anemia (low levels of red blood cells) or

  • Vitamin B12 deficiency—Use with caution. May make these conditions worse.

  • Congestive heart failure, acute or unstable or

  • Dehydration or

  • Heart attack, acute or

  • Hypoxemia (decreased oxygen in the blood) or

  • Kidney disease or

  • Liver disease or

  • Sepsis (blood poisoning) or

  • Shock (low blood pressure, blood circulation is poor)—A rare condition called lactic acidosis can occur. Talk with your doctor if you have concerns about this.

  • Diabetic ketoacidosis (ketones in the blood) or

  • Kidney disease, severe or

  • Metabolic acidosis (extra acids in the blood) or

  • Type 1 diabetes—Should not be used in patients with these conditions.

  • Fever or

  • Infection or

  • Surgery or

  • Trauma—These conditions may cause temporary problems with blood sugar control and your doctor may want to treat you with insulin.

Proper Use of metformin

This section provides information on the proper use of a number of products that contain metformin. It may not be specific to Glucophage. Please read with care.


This medicine usually comes with a patient information insert. Read the information carefully and make sure you understand it before taking this medicine. If you have any questions, ask your doctor.


Carefully follow the special meal plan your doctor gave you. This is a very important part of controlling your condition, and is necessary if the medicine is to work properly. Also, exercise regularly and test for sugar in your blood or urine as directed.


Metformin should be taken with meals to help reduce stomach or bowel side effects that may occur during the first few weeks of treatment.


Swallow the extended-release tablet whole with a full glass of water. Do not crush, break, or chew it.


While taking the extended-release tablet, part of the tablet may pass into your stool after your body has absorbed the medicine. This is normal and nothing to worry about.


Measure the oral liquid with a marked measuring spoon, oral syringe, or medicine cup. The average household teaspoon may not hold the right amount of liquid.


Use only the brand of this medicine that your doctor prescribed. Different brands may not work the same way.


You may notice improvement in your blood glucose control in 1 to 2 weeks, but the full effect of blood glucose control may take up to 2 to 3 months. Ask your doctor if you have any questions about this.


Dosing


The dose of this medicine will be different for different patients. Follow your doctor's orders or the directions on the label. The following information includes only the average doses of this medicine. If your dose is different, do not change it unless your doctor tells you to do so.


The amount of medicine that you take depends on the strength of the medicine. Also, the number of doses you take each day, the time allowed between doses, and the length of time you take the medicine depend on the medical problem for which you are using the medicine.


  • For type 2 diabetes:
    • For oral dosage form (extended-release tablets):
      • Adults—
        • Metformin alone (Fortamet®): At first, 1000 milligrams (mg) once a day taken with the evening meal. Your doctor may increase your dose if needed until your blood sugar is controlled. However, the dose is usually not more than 2500 mg per day.

        • Metformin alone (Glucophage® XR): At first, 500 mg once daily with the evening meal. Your doctor may increase your dose if needed until your blood sugar is controlled. However, the dose is usually not more than 2000 mg per day.

        • Metformin alone (Glumetza®): At first, 500 mg once a day taken with the evening meal. Then, your doctor may increase your dose if needed until your blood sugar is controlled. However, the dose is usually not more than 2000 mg per day.

        • Metformin with a sulfonylurea: Your doctor will determine the dose of each medicine.

        • Metformin with insulin: At first, 500 mg once a day. Then, your doctor may increase your dose by 500 mg every week if needed until your blood sugar is controlled. However, the dose is usually not more than 2500 mg per day.


      • Children—Use and dose must be determined by your doctor.


    • For oral dosage form (solution):
      • Adults—
        • Metformin alone: At first, 5 milliliters (mL) two times a day, or 8.5 mL once a day with meals. Your doctor may increase your dose if needed until your blood sugar is controlled. However, the dose is usually not more than 25.5 mL per day.

        • Metformin with a sulfonylurea: Your doctor will determine the dose of each medicine.

        • Metformin with insulin: At first, 5 mL once a day. Your doctor may increase your dose if needed until your blood sugar is controlled. However, the dose is usually not more than 25 mL per day.


      • Children 10 to 16 years of age—At first, 5 mL two times a day with meals. Your doctor may increase your dose if needed until your blood sugar is controlled. However, the dose is usually not more than 20 mL per day.

      • Children younger than 10 years of age—Use and dose must be determined by your doctor.


    • For oral dosage form (tablets):
      • Adults—
        • Metformin alone: At first, 500 milligrams (mg) two times a day taken with the morning and evening meals, or 850 mg a day taken with the morning meal. Your doctor may increase your dose if needed until your blood sugar is controlled. Later, your doctor may want you to take 500 or 850 mg two to three times a day with meals. However, the dose is usually not more than 2550 mg per day.

        • Metformin with a sulfonylurea: Your doctor will determine the dose of each medicine.

        • Metformin with insulin: At first, 500 mg a day. Your doctor may increase your dose by 500 mg every week if needed until your blood sugar is controlled. However, the dose is usually not more than 2500 mg per day.


      • Children 10 to 16 years of age—At first, 500 mg two times a day taken with the morning and evening meals. Your doctor may increase your dose if needed until your blood sugar is controlled. However, the dose is usually not more than 2000 mg per day.

      • Children younger than 10 years of age—Use and dose must be determined by your doctor.



Missed Dose


If you miss a dose of this medicine, take it as soon as possible. However, if it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not double doses.


Storage


Store the medicine in a closed container at room temperature, away from heat, moisture, and direct light. Keep from freezing.


Keep out of the reach of children.


Do not keep outdated medicine or medicine no longer needed.


Ask your healthcare professional how you should dispose of any medicine you do not use.


Precautions While Using Glucophage


It is very important that your doctor check your progress at regular visits, especially during the first few weeks that you take this medicine. Blood and urine tests may be needed to check for unwanted effects.


This medicine may interact with the dye used for an X-ray or CT scan. Your doctor should advise you to stop taking it before you have any medical exams or diagnostic tests that might cause less urine output than usual. You may be advised to start taking the medicine again 48 hours after the exams or tests if your kidney function is tested and found to be normal.


Make sure any doctor or dentist who treats you knows that you are using this medicine. You may need to stop using this medicine several days before having surgery or medical tests.


It is very important to carefully follow any instructions from your health care team about:


  • Alcohol—Drinking alcohol may cause severe low blood sugar. Discuss this with your health care team.

  • Other medicines—Do not take other medicines unless they have been discussed with your doctor. This especially includes nonprescription medicines such as aspirin, and medicines for appetite control, asthma, colds, cough, hay fever, or sinus problems.

  • Counseling—Other family members need to learn how to prevent side effects or help with side effects if they occur. Also, patients with diabetes may need special counseling about diabetes medicine dosing changes that might occur with lifestyle changes, such as changes in exercise or diet. Counseling on birth control and pregnancy may be needed because of the problems that can occur in pregnancy for patients with diabetes.

  • Travel—Keep a recent prescription and your medical history with you. Be prepared for an emergency as you would normally. Make allowances for changing time zones and keep your meal times as close as possible to your usual meal times.

  • In case of emergency—There may be a time when you need emergency help for a problem caused by your diabetes. You need to be prepared for these emergencies. It is a good idea to wear a medical identification (ID) bracelet or neck chain at all times. Also, carry an ID card in your wallet or purse that says that you have diabetes and a list of all of your medicines.

Under certain conditions, too much metformin can cause lactic acidosis. The symptoms of lactic acidosis are severe and quick to appear, and usually occur when other health problems not related to the medicine are present and are very severe, such as a heart attack or kidney failure. Symptoms of lactic acidosis include abdominal or stomach discomfort, decreased appetite; diarrhea; fast or shallow breathing; a general feeling of discomfort; severe muscle pain or cramping; and unusual sleepiness, tiredness, or weakness.


If symptoms of lactic acidosis occur, you should get immediate emergency medical help.


Metformin can cause low blood sugar (hypoglycemia). However, this can also occur if you delay or miss a meal or snack, drink alcohol, exercise more than usual, cannot eat because of nausea or vomiting, take certain medicines, or take metformin with another type of diabetes medicine. The symptoms of low blood sugar must be treated before they lead to unconsciousness (passing out). Different people feel different symptoms of low blood sugar. It is important that you learn which symptoms of low blood sugar you usually have so that you can treat it quickly.


Symptoms of hypoglycemia (low blood sugar) include anxiety; behavior change similar to being drunk; blurred vision; cold sweats; confusion; cool, pale skin; difficulty with thinking; drowsiness; excessive hunger; fast heartbeat; headache (continuing); nausea; nervousness; nightmares; restless sleep; shakiness; slurred speech; or unusual tiredness or weakness.


If symptoms of low blood sugar occur, eat glucose tablets or gel, corn syrup, honey, or sugar cubes; or drink fruit juice, non-diet soft drink, or sugar dissolved in water. Also, check your blood for low blood sugar. Glucagon is used in emergency situations when severe symptoms such as seizures (convulsions) or unconsciousness occur. Have a glucagon kit available, along with a syringe or needle, and know how to use it. The members of your household also should know how to use it.


High blood sugar (hyperglycemia) is another problem related to uncontrolled diabetes. Symptoms of mild high blood sugar appear more slowly than those of low blood sugar. These may include blurred vision; drowsiness; dry mouth; flushed, dry skin; fruit-like breath odor; increased urination (frequency and volume); ketones in the urine; loss of appetite; sleepiness; stomachache, nausea or vomiting; tiredness; troubled breathing (rapid and deep); unconsciousness; or unusual thirst.


High blood sugar may occur if you do not exercise as much as usual, have a fever or infection, do not take enough or skip a dose of your diabetes medicine, or overeat or do not follow your meal plan.


If symptoms of high blood sugar occur, check your blood sugar level and then call your doctor for instructions.


This medicine is only part of a complete program for controlling diabetes. It is important that you always eat a healthy diet, watch your weight, and get regular exercise.


Glucophage 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 immediately if any of the following side effects occur:


More common
  • Abdominal or stomach discomfort

  • cough or hoarseness

  • decreased appetite

  • diarrhea

  • fast or shallow breathing

  • fever or chills

  • general feeling of discomfort

  • lower back or side pain

  • muscle pain or cramping

  • painful or difficult urination

  • sleepiness

Less common
  • Anxiety

  • blurred vision

  • chest discomfort

  • cold sweats

  • coma

  • confusion

  • cool, pale skin

  • depression

  • difficult or labored breathing

  • dizziness

  • fast, irregular, pounding, or racing heartbeat or pulse

  • feeling of warmth

  • headache

  • increased hunger

  • increased sweating

  • nausea

  • nervousness

  • nightmares

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

  • seizures

  • shakiness

  • shortness of breath

  • slurred speech

  • tightness in the chest

  • unusual tiredness or weakness

  • wheezing

Rare
  • Behavior change similar to being drunk

  • difficulty with concentrating

  • drowsiness

  • lack or loss of strength

  • restless sleep

  • unusual sleepiness

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
  • Acid or sour stomach

  • belching

  • bloated

  • excess air or gas in the stomach or intestines

  • full feeling

  • heartburn

  • indigestion

  • loss of appetite

  • metallic taste in the mouth

  • passing of gas

  • stomachache

  • stomach upset or pain

  • vomiting

  • weight loss

Less common
  • Abnormal stools

  • bad, unusual, or unpleasant (after) taste

  • change in taste

  • difficulty with moving

  • discoloration of the fingernails or toenails

  • flu-like symptoms

  • joint pain

  • rash

  • runny nose

  • sneezing

  • stuffy nose

  • swollen joints

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: Glucophage 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 Glucophage resources


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


  • Glucophage MedFacts Consumer Leaflet (Wolters Kluwer)

  • Glucophage Prescribing Information (FDA)

  • Glucophage Consumer Overview

  • Fortamet Prescribing Information (FDA)

  • Glucophage XR Extended-Release Tablets MedFacts Consumer Leaflet (Wolters Kluwer)

  • Glucophage XR Prescribing Information (FDA)

  • Glumetza Prescribing Information (FDA)

  • Metformin Prescribing Information (FDA)

  • Metformin Hydrochloride Monograph (AHFS DI)

  • Riomet Prescribing Information (FDA)

  • Riomet Consumer Overview

  • Riomet Solution MedFacts Consumer Leaflet (Wolters Kluwer)



Compare Glucophage with other medications


  • Diabetes, Type 2
  • Insulin Resistance Syndrome

Herpes Zoster Peripheral Neuropathy Medications


There are currently no drugs listed for "Herpes Zoster Peripheral Neuropathy".

Learn more about Herpes Zoster Peripheral Neuropathy





Drug List:

Delestrogen




In the US, Delestrogen (estradiol systemic) is a member of the drug class estrogens and is used to treat Atrophic Urethritis, Atrophic Vaginitis, Hypoestrogenism, Oophorectomy, Postmenopausal Symptoms, Primary Ovarian Failure and Prostate Cancer.

US matches:

  • Delestrogen

Ingredient matches for Delestrogen



Estradiol

Estradiol 17ß-valerate (a derivative of Estradiol) is reported as an ingredient of Delestrogen in the following countries:


  • United States

International Drug Name Search

Histiocytosis Medications


Definition of Histiocytosis: "Histiocytosis" is a generic name for syndromes characterized by an abnormal increase in the number of histiocyte cells (also called monocytes, macrophages, or dendritic cells) in the body. It is separated broadly into 3 classes of histiocytoses: (1) Langerhans cell histiocytosis (histiocytosis X); (2) Non-Langerhans cell histiocytosis (hemophagocytic syndromes); (3) malignant histiocytosis syndrome (not discussed here).

Drugs associated with Histiocytosis

The following drugs and medications are in some way related to, or used in the treatment of Histiocytosis. This service should be used as a supplement to, and NOT a substitute for, the expertise, skill, knowledge and judgment of healthcare practitioners.

Learn more about Histiocytosis





Drug List:

Geratam




Geratam may be available in the countries listed below.


Ingredient matches for Geratam



Piracetam

Piracetam is reported as an ingredient of Geratam in the following countries:


  • Belgium

  • Czech Republic

  • Luxembourg

International Drug Name Search

Hyperadrenocorticism Medications


There are currently no drugs listed for "Hyperadrenocorticism".

Definition of Hyperadrenocorticism:

Excess hormone called cortisol. Often called cushing's syndrome, it is an extremely complex condition that involves many areas of the body. It results from an excess of cortisol and its effects on the human body.


Common symptoms are thinning of the skin, weakness, weight gain, bruising, hypertension, diabetes, weak bones (osteoporosis), facial puffiness, and in women cessation of periods. One of the commonest causes of cushing's syndrome is the administration of cortisol-like medications for the treatment of diverse diseases.


All other cases of cushing's syndrome are due to excess production of cortisol by the adrenal gland including 1) an abnormal growth of the pituitary gland, which stimulates the adrenal gland, 2) a benign or malignant growth within the adrenal gland itself, which produces cortisol and 3) production within another part of the body (ectopic production) of a hormone that directly or indirectly stimulates the adrenal gland to make cortisol. Harvey cushing (1869-1939), a neurosurgeon, described hyperadrenocorticism due specifically to an acth-secreting basophilic pituitary adenoma, a benign pituitary tumour that puts out acth (adrenocorticotropic hormone) that, in turn, drives (or overdrives) the adrenal gland.

Learn more about Hyperadrenocorticism





Drug List:

Lidocorit




Lidocorit may be available in the countries listed below.


Ingredient matches for Lidocorit



Lidocaine

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


  • Austria

International Drug Name Search

Adagen


Generic Name: pegademase bovine (peg AD e mase BOE vine)

Brand Names: Adagen


What are Adagen (pegademase bovine)?

Pegademase bovine is the enzyme called adenosine deaminase (ADA). Without ADA, certain proteins accumulate that harm white blood cells. White blood cells are important for protecting the body from infection.


Pegademase bovine is used to replenish ADA which allows an increase in white blood cells and decreases the risk of infection in conditions such as severe combined immunodeficiency disease (SCID).


Pegademase bovine may also be used for purposes other than those listed in this medication guide.


What is the most important information I should know about Adagen (pegademase bovine)?


Do not administer an injection if you are unsure how to properly do so, how much to inject, or how often to inject the medication. Call your doctor, nurse, or pharmacist to go over the instructions with you. Contact your doctor if you develop a fever; chills; sore throat; congestion; or redness, pain, or swelling around a wound or sore while using pegademase bovine. These may be signs of infection.

What should I discuss with my healthcare provider before using a Adagen (pegademase bovine)?


Before using pegademase bovine, tell your doctor if you



  • are undergoing radiation or receiving chemotherapy; or




  • have a bleeding disorder.



You may not be able to use pegademase bovine or you may require a dosage adjustment or special monitoring if you have any of the conditions listed above.


Pegademase bovine is in the FDA pregnancy category C. This means that it is not known whether pegademase bovine will be harmful to an unborn baby. Do not use pegademase bovine without first talking to your doctor if you are pregnant or could become pregnant during treatment. It is not known whether pegademase bovine will be harmful to a nursing baby. Do not use pegademase bovine without first talking to your doctor if you are breast-feeding a baby.

How should I use Adagen (pegademase bovine)?


Use pegademase bovine exactly as directed by your doctor. If you do not understand these instructions, ask your pharmacist, nurse, or doctor to explain them to you.


Pegademase bovine is given by intramuscular (IM) injection. Your doctor, nurse, or pharmacist will give you specific instructions on how and where to inject the medication.


Do not administer an injection if you are unsure how to properly do so, how much to inject, or how often to inject the medication. Call your doctor, nurse, or pharmacist to go over the instructions with you.

Pegademase bovine is usually administered once every 7 days.


Do not inject a pegademase bovine that is discolored or that has particles in it.

Properly store and discard all syringes and needles.


Your doctor may want you to have regularly scheduled blood tests while using pegademase bovine to monitor effectiveness and possible side effects of the medication.


Do not stop taking pegademase bovine without talking to your doctor. It may take several weeks to 6 months to be fully effective. Stopping pegademase bovine may cause your immune system to become less effective and serious infections may occur.


Store pegademase bovine in the refrigerator between 2 and 8 degrees Celsius (36 to 46 degrees Fahrenheit) away from light, moisture, and the reach of children. Avoid freezing the medication. Do not use this product if there are any indications that it may have frozen.

What happens if I miss a dose?


Contact your doctor as soon as possible if you miss a dose of this medication.


What happens if I overdose?


Seek emergency medical attention.

Symptoms of a pegademase bovine overdose are not known.


What should I avoid while using Adagen (pegademase bovine)?


There are no restrictions regarding foods, beverages, or activities during treatment with pegademase bovine unless otherwise directed by your doctor.


Adagen (pegademase bovine) side effects


If you experience any of the following serious side effects, stop using the pegademase bovine and seek emergency medical treatment or contact your doctor immediately:

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




  • signs of infection such as sore throat, fever or congestion.



Other, less serious side effects may be more likely to occur. Continue to use the pegademase bovine and talk to your doctor if you experience:



  • headache;




  • swelling, redness, or pain at the injection site.



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 Adagen (pegademase bovine)?


Before using this medication, tell your doctor if you



  • are receiving vidarabine eye ointment (Vira-A).



You may not be able to use the pegademase bovine or you may require a dosage adjustment or special monitoring if you are taking the medication listed above.


Drugs other than those listed here may also interact with pegademase bovine. Talk to your doctor and pharmacist before taking any prescription or over-the-counter medicines, including herbal products.



More Adagen resources


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


  • Adagen Prescribing Information (FDA)

  • Adagen Advanced Consumer (Micromedex) - Includes Dosage Information

  • Adagen MedFacts Consumer Leaflet (Wolters Kluwer)



Compare Adagen with other medications


  • Immunodeficiency


Where can I get more information?


  • Your pharmacist can provide more information about pegademase bovine.

See also: Adagen side effects (in more detail)


Neo-Zol Topical



Generic Name: clotrimazole (Topical route)

kloe-TRIM-a-zole

Commonly used brand name(s)

In the U.S.


  • Clotrim Antifungal

  • Cruex Prescription Strength

  • Lotrimin

  • Lotrimin AF

  • Mycelex

In Canada


  • Canesten

  • Clotrimaderm

  • Desenex

  • Myclo-Derm

  • Neo-Zol

Available Dosage Forms:


  • Lotion

  • Solution

  • Cream

Therapeutic Class: Antifungal


Chemical Class: Imidazole


Uses For Neo-Zol


Clotrimazole topical preparations are used to treat fungus infections on the skin.


This medicine is available both over-the-counter (OTC) and with your doctor's prescription.


Before Using Neo-Zol


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 this medicine, the following should be considered:


Allergies


Tell your doctor if you have ever had any unusual or allergic reaction to this medicine 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


This medicine has been tested in children and, in effective doses, has not been shown to cause different side effects or problems than it does in adults.


Geriatric


Many medicines have not been studied specifically in older people. Therefore, it may not be known whether they work exactly the same way they do in younger adults. Although there is no specific information comparing use of topical clotrimazole in the elderly with use in other age groups, this medicine is not expected to cause different side effects or problems in older people than it does in younger adults.


Pregnancy








Pregnancy CategoryExplanation
All TrimestersCAnimal studies have shown an adverse effect and there are no adequate studies in pregnant women OR no animal studies have been conducted and there are no adequate studies in pregnant women.

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. When you are taking this medicine, it is especially important that your healthcare professional know if you are taking any of the medicines listed below. The following interactions have been selected on the basis of their potential significance and are not necessarily all-inclusive.


Using this medicine with any of the following medicines may cause an increased risk of certain side effects, but using both drugs may be the best treatment for you. If both medicines are prescribed together, your doctor may change the dose or how often you use one or both of the medicines.


  • Fentanyl

  • Tacrolimus

  • Trimetrexate

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.


Proper Use of clotrimazole

This section provides information on the proper use of a number of products that contain clotrimazole. It may not be specific to Neo-Zol. Please read with care.


Apply enough clotrimazole to cover the affected and surrounding skin areas, and rub in gently.


Keep this medicine away from the eyes.


When clotrimazole is used to treat certain types of fungus infections of the skin, an occlusive dressing (airtight covering, such as kitchen plastic wrap) should not be applied over the medicine. To do so may cause irritation of the skin. Do not apply an occlusive dressing over this medicine unless you have been directed to do so by your doctor.


To help clear up your infection completely, it is very important that you keep using this medicine for the full time of treatment , even if your symptoms begin to clear up after a few days. Since fungus infections may be very slow to clear up, you may have to continue using this medicine every day for several weeks or more. If you stop using this medicine too soon, your symptoms may return. Do not miss any doses .


Dosing


The dose of this medicine will be different for different patients. Follow your doctor's orders or the directions on the label. The following information includes only the average doses of this medicine. If your dose is different, do not change it unless your doctor tells you to do so.


The amount of medicine that you take depends on the strength of the medicine. Also, the number of doses you take each day, the time allowed between doses, and the length of time you take the medicine depend on the medical problem for which you are using the medicine.


  • For topical dosage forms (cream, lotion, and solution):
    • Fungal infections (treatment):
      • Adults and children—Use two times a day, morning and evening.



Missed Dose


If you miss a dose of this medicine, apply it as soon as possible. However, if it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule.


Storage


Store the medicine in a closed container at room temperature, away from heat, moisture, and direct light. Keep from freezing.


Keep out of the reach of children.


Do not keep outdated medicine or medicine no longer needed.


Precautions While Using Neo-Zol


If your skin problem does not improve within 4 weeks, or if it becomes worse, check with your doctor.


Neo-Zol 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 as soon as possible if any of the following side effects occur:


  • Skin rash, hives, blistering, burning, itching, peeling, redness, stinging, swelling, or other sign of skin irritation not present before use of this medicine

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.



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 Neo-Zol Topical resources


  • Neo-Zol Topical Use in Pregnancy & Breastfeeding
  • Neo-Zol Topical Support Group
  • 2 Reviews for Neo-Zol Topical - Add your own review/rating


Compare Neo-Zol Topical with other medications


  • Cutaneous Candidiasis
  • Tinea Corporis
  • Tinea Cruris
  • Tinea Pedis
  • Tinea Versicolor
  • Vaginal Yeast Infection

Angiozem




Angiozem may be available in the countries listed below.


Ingredient matches for Angiozem



Diltiazem

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


  • Philippines

International Drug Name Search

Hyperlipoproteinemia Medications


Drugs associated with Hyperlipoproteinemia

The following drugs and medications are in some way related to, or used in the treatment of Hyperlipoproteinemia. This service should be used as a supplement to, and NOT a substitute for, the expertise, skill, knowledge and judgment of healthcare practitioners.

See sub-topics

Topics under Hyperlipoproteinemia

  • Hyperlipoproteinemia Type IIa, Elevated LDL (27 drugs)

  • Hyperlipoproteinemia Type IIb, Elevated LDL VLDL (26 drugs)

  • Hyperlipoproteinemia Type III, Elevated beta-VLDL IDL (5 drugs)

  • Hyperlipoproteinemia Type IV, Elevated VLDL (20 drugs)

  • Hyperlipoproteinemia Type V, Elevated Chylomicrons VLDL (15 drugs)





Drug List:

Silvadiazin




Silvadiazin may be available in the countries listed below.


Ingredient matches for Silvadiazin



Sulfadiazine

Sulfadiazine silver (a derivative of Sulfadiazine) is reported as an ingredient of Silvadiazin in the following countries:


  • Oman

  • Turkey

International Drug Name Search

Dimenhydrinate Tablets


Pronunciation: dye-men-HYE-dri-nate
Generic Name: Dimenhydrinate
Brand Name: Examples include Dramamine and Travel-Eze


Dimenhydrinate is used for:

Preventing and treating nausea, vomiting, and dizziness caused by motion sickness. It may also be used for other conditions as determined by your doctor.


Dimenhydrinate is an antihistamine and anticholinergic. It works in the brain to decrease nausea, vomiting, and dizziness.


Do NOT use Dimenhydrinate if:


  • you are allergic to any ingredient in Dimenhydrinate or other similar medicines

  • you are taking sodium oxybate (GHB)

  • you are currently taking or have taken a monoamine oxidase (MAO) inhibitor (eg, phenelzine) in the past 14 days

  • you are breast-feeding

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



Before using Dimenhydrinate:


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


  • if you are pregnant or planning to become pregnant

  • 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 asthma, chronic obstructive pulmonary disease (COPD), chronic bronchitis, emphysema, lung disease, shortness of breath, or sleep apnea

  • if you have a blockage of the stomach, intestine, or urinary tract; difficulty urinating; diabetes; ulcers; enlargement of the prostate; glaucoma; heart disease; irregular heartbeat; high blood pressure; porphyria; or thyroid disease

Some MEDICINES MAY INTERACT with Dimenhydrinate. Tell your health care provider if you are taking any other medicines, especially any of the following:


  • Sodium oxybate (GHB) because an increase in sleep duration and a decrease in the ability to breathe are likely to occur

  • MAO inhibitors (eg, phenelzine) because serious side effects, such as high blood pressure or seizure, may occur

  • Antibiotics that may cause hearing problems (eg, gentamicin, vancomycin) because Dimenhydrinate may mask symptoms of hearing problems

This may not be a complete list of all interactions that may occur. Ask your health care provider if Dimenhydrinate 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 Dimenhydrinate:


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


  • Dimenhydrinate may be taken with or without food.

  • Use Dimenhydrinate exactly as directed on the package, unless instructed differently by your doctor. If you are taking Dimenhydrinate without a prescription, follow any warnings and precautions on the label.

  • Take the first dose at least 30 minutes before activity or travel.

  • If you miss a dose of Dimenhydrinate 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 Dimenhydrinate.



Important safety information:


  • Dimenhydrinate may cause drowsiness or dizziness. Do not drive, operate machinery, or do anything else that could be dangerous until you know how you react to Dimenhydrinate. Using Dimenhydrinate alone, with certain other medicines, or with alcohol may lessen your ability to drive or to perform other potentially dangerous tasks.

  • Avoid drinking alcohol or taking other medications that cause drowsiness (eg, sedatives, tranquilizers) while taking Dimenhydrinate. Dimenhydrinate will add to the effects of alcohol and other depressants. Ask your pharmacist if you have questions about which medicines are depressants.

  • Dimenhydrinate may cause dizziness. Alcohol, hot weather, exercise, and fever can increase this effect. To prevent it, sit up or stand slowly, especially in the morning. Also, sit or lie down at the first sign of dizziness.

  • Do not exceed the recommended dose or use Dimenhydrinate more frequently or for longer than prescribed without first checking with your doctor.

  • Do not become overheated in hot weather or during exercise or other activities since heatstroke may occur.

  • Dimenhydrinate may cause increased sensitivity to the sun. Avoid exposure to the sun, sunlamps, or tanning booths until you know how you react to Dimenhydrinate. Use a sunscreen or protective clothing if you must be outside for a prolonged period.

  • Do not use Dimenhydrinate with any medicine that contains diphenhydramine. Before you begin taking any new prescription or nonprescription medicine, including one used on the skin, read the ingredients to see if it also contains diphenhydramine or another similar medicine (eg, antihistamine). If it does, or if you are uncertain if it does, contact your doctor or pharmacist.

  • Use Dimenhydrinate with caution in the ELDERLY because they may be more sensitive to its effects, especially dizziness, sedation, and lightheadedness upon standing.

  • Safe use and instructions for use in CHILDREN differs according to the brand used. Talk to your doctor or pharmacist if you have any questions about the brand you are using.

  • Use of Dimenhydrinate is not recommended in CHILDREN younger than 2 years of age without first talking with the child's doctor. Safety and effectiveness in this age group have not been confirmed.

  • PREGNANCY and BREAST-FEEDING: If you become pregnant, discuss with your doctor the benefits and risks of using Dimenhydrinate during pregnancy. Dimenhydrinate is excreted in breast milk. Do not breast-feed while taking Dimenhydrinate.


Possible side effects of Dimenhydrinate:


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:



Dizziness; drowsiness; dry mouth, throat, and nose; thickening of mucus in nose or throat.



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

Severe allergic reactions (rash; hives; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); chest pain; convulsions; decreased alertness; difficulty urinating; excessive excitability; fast or irregular heartbeat; fever, chills, or sore throat; hallucinations; mental or mood changes; pounding in the chest; seizures; tremor; unusual bruising or bleeding; wheezing; yellowing of the eyes or skin.



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: Dimenhydrinate 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 coma; excitement; hallucinations; loss of consciousness; muscle twitching; seizures; severe drowsiness; tremor; weakness.


Proper storage of Dimenhydrinate:

Store Dimenhydrinate at room temperature, between 68 and 77 degrees F (20 and 25 degrees C), or according to directions on the package label. Store in the original package or container. Store away from heat, moisture, and light. Do not store in the bathroom. Keep Dimenhydrinate out of the reach of children and away from pets.


General information:


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

  • Dimenhydrinate 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 Dimenhydrinate. 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 Dimenhydrinate resources


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


Compare Dimenhydrinate with other medications


  • Motion Sickness
  • Nausea/Vomiting

History, Tuberculosis Medications


There are currently no drugs listed for "History, Tuberculosis".

Definition of History, Tuberculosis:

An infection caused by a species of Mycobacterium, still remains a major worldwide health problem. Although deaths from this disease have declined since the 1950's there has been some increase in tuberculosis incidence.


Tuberculosis is transmitted from person to person by an aerosol of organisms suspended in tiny droplets that are inhaled.

Learn more about History, Tuberculosis





Drug List:

Gabapentin Hersil




Gabapentin Hersil may be available in the countries listed below.


Ingredient matches for Gabapentin Hersil



Gabapentin

Gabapentin is reported as an ingredient of Gabapentin Hersil in the following countries:


  • Peru

International Drug Name Search

Kripton




Kripton may be available in the countries listed below.


Ingredient matches for Kripton



Bromocriptine

Bromocriptine mesilate (a derivative of Bromocriptine) is reported as an ingredient of Kripton in the following countries:


  • Australia

International Drug Name Search

Nilutamide




In the US, Nilutamide (nilutamide systemic) is a member of the following drug classes: antiandrogens, hormones/antineoplastics and is used to treat Prostate Cancer.

US matches:

  • Nilutamide

Scheme

Rec.INN

ATC (Anatomical Therapeutic Chemical Classification)

L02BB02

CAS registry number (Chemical Abstracts Service)

0063612-50-0

Chemical Formula

C12-H10-F3-N3-O4

Molecular Weight

317

Therapeutic Categories

Antineoplastic agent

Antiandrogen

Chemical Name

2,4-Imidazolidinedione, 5,5-dimethyl-3-[4-nitro-3-(trifluoromethyl)phenyl]-

Foreign Names

  • Nilutamidum (Latin)
  • Nilutamid (German)
  • Nilutamide (French)
  • Nilutamida (Spanish)

Generic Names

  • Nilutamide (OS: BAN, DCF, USAN)
  • RU 23908 (IS: RousselUclaf)
  • Nilutamide (PH: Ph. Eur. 6, BP 2010)
  • Nilutamidum (PH: Ph. Eur. 6)

Brand Names

  • Anandron
    Aventis, Czech Republic; Aventis, Peru; Aventis, Serbia; EU-Pharma, Netherlands; Sanofi-Aventis, Australia; Sanofi-Aventis, Brazil; Sanofi-Aventis, Canada; Sanofi-Aventis, France; Sanofi-Aventis, Hungary; Sanofi-Aventis, Mexico; Sanofi-Aventis, Netherlands; Sanofi-Aventis - Produtos farmacêuticos, S.A., Portugal


  • Nilandron
    Sanofi-Aventis, United States

International Drug Name Search

Glossary

BANBritish Approved Name
DCFDénomination Commune Française
ISInofficial Synonym
OSOfficial Synonym
PHPharmacopoeia Name
Rec.INNRecommended International Nonproprietary Name (World Health Organization)
USANUnited States Adopted Name

Click for further information on drug naming conventions and International Nonproprietary Names.

Hypertensive Renal Disease Medications


Topics under Hypertensive Renal Disease

  • Hypertensive Heart with CHF and Renal Disease (0 drugs)

  • Hypertensive Heart without CHF and Renal Disease (0 drugs)

Learn more about Hypertensive Renal Disease





Drug List:

Lidocaine and Tetracaine




Ingredient matches for Lidocaine and Tetracaine



Lidocaine

Lidocaine is reported as an ingredient of Lidocaine and Tetracaine in the following countries:


  • United States

Tetracaine

Tetracaine is reported as an ingredient of Lidocaine and Tetracaine in the following countries:


  • United States

International Drug Name Search