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Tagamet Drug Description

TAGAMET®
(cimetidine) Tablets
(cimetidine hydrochloride) Liquid
(cimetidine hydrochloride) Injection


DRUG DESCRIPTION



What are the possible side effects of cimetidine (Tagamet, Tagamet HB)?

Stop using cimetidine and 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.
Call your doctor at once if you have any of these serious side effects:

cough, fever, chest congestion, trouble breathing;
red or blistering skin rash;
jaundice (yellowing of the skin or eyes);
easy bruising or bleeding, unusual weakness;
feeling...
Read All Potential Side Effects for Tagamet »




Tagamet (cimetidine) is a histamine H2-receptor antagonist. Chemically it is N?-cyano-N-methyl N'-[2-[[(5-methyl-1H-imidazol-4-yl)methyl]thio]-ethyl]-guanidine.
The empirical formula for cimetidine is C10H16N6S and for cimetidine hydrochloride, C10H16N6SHCl; these represent molecular weights of 252.34 and 288.80, respectively.

Cimetidine contains an imidazole ring, and is chemically related to histamine.
(The liquid and injection dosage forms contain cimetidine as the hydrochloride.)
Cimetidine has a bitter taste and characteristic odor. Solubility Characteristics : Cimetidine is soluble in alcohol, slightly soluble in water, very slightly soluble in chloroform and insoluble in ether. Cimetidine hydrochloride is freely soluble in water, soluble in alcohol, very slightly soluble in chloroform and practically insoluble in ether. Tablets for Oral Administration : Each light green, film-coated tablet contains cimetidine as follows: 300 mg-round, debossed with the product name TAGAMET, SB and 300; 400 mg-oval Tiltab® tablets, debossed with the product name TAGAMET, SB and 400; 800 mg-oval Tiltab® tablets, debossed with the product name TAGAMET, SB and 800. Inactive ingredients consist of cellulose, D&C Yellow No. 10, FD&C Blue No. 2, FD&C Red No. 40, FD&C Yellow No. 6, hydroxypropyl methylcellulose, iron oxides, magnesium stearate, povidone, propylene glycol, sodium lauryl sulfate, sodium starch glycolate, starch, titanium dioxide and trace amounts of other inactive ingredients. Liquid for Oral Administration : Each 5 mL (1 teaspoonful) of clear, light orange, mint-peach flavored liquid contains cimetidine hydrochloride equivalent to cimetidine, 300 mg; alcohol, 2.8%. Inactive ingredients consist of FD&C Yellow No. 6, flavors, methylparaben, polyoxyethylene polyoxypropylene glycol, propylene glycol, propylparaben, saccharin sodium, sodium chloride, sodium phosphate, sorbitol and water. Injection Single-Dose Vials for Intramuscular or Intravenous Administration : Each 2 mL contains, in sterile aqueous solution (pH range 3.8 to 6), cimetidine hydrochloride equivalent to cimetidine, 300 mg; phenol, 10 mg. Multi-Dose Vials for Intramuscular or Intravenous Administration : 8 mL (300 mg/2 mL): Each 2 mL contains, in sterile aqueous solution (pH range 3.8 to 6), cimetidine hydrochloride equivalent to cimetidine, 300 mg; phenol, 10 mg. Single-Dose Premixed Plastic Containers for Intravenous Administration : Each 50 mL of sterile aqueous solution (pH range 5 to 7) contains cimetidine hydrochloride equivalent to 300 mg cimetidine and 0.45 grams sodium chloride. No preservative has been added. The plastic container is fabricated from specially formulated polyvinyl chloride. The amount of water that can permeate from inside the container into the overwrap is insufficient to affect the solution significantly. Solutions in contact with the plastic container can leach out certain of its chemical components in very small amounts within the expiration period, e.g., di 2-ethylhexyl phthalate (DEHP), up to 5 parts per million. However, the safety of the plastic has been confirmed in tests in animals according to the USP biological tests for plastic containers as well as by tissue culture toxicity studies. ADD-Vantage®* Vials for Intravenous Administration : Each 2 mL contains, in sterile aqueous solution (pH range 3.8 to 6), cimetidine hydrochloride equivalent to cimetidine, 300 mg; phenol, 10 mg. All of the above injection formulations are pyrogen free, and sodium hydroxide N.F. is used as an ingredient to adjust the pH.
*ADD-Vantage® is a trademark of Abbott Laboratories.Last reviewed on RxList: 1/12/2005




Tagamet Drug Description

TAGAMET®
(cimetidine) Tablets
(cimetidine hydrochloride) Liquid
(cimetidine hydrochloride) Injection


DRUG DESCRIPTION



What are the possible side effects of cimetidine (Tagamet, Tagamet HB)?

Stop using cimetidine and 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.
Call your doctor at once if you have any of these serious side effects:

cough, fever, chest congestion, trouble breathing;
red or blistering skin rash;
jaundice (yellowing of the skin or eyes);
easy bruising or bleeding, unusual weakness;
feeling...
Read All Potential Side Effects for Tagamet »




Tagamet (cimetidine) is a histamine H2-receptor antagonist. Chemically it is N?-cyano-N-methyl N'-[2-[[(5-methyl-1H-imidazol-4-yl)methyl]thio]-ethyl]-guanidine.
The empirical formula for cimetidine is C10H16N6S and for cimetidine hydrochloride, C10H16N6SHCl; these represent molecular weights of 252.34 and 288.80, respectively.

Cimetidine contains an imidazole ring, and is chemically related to histamine.
(The liquid and injection dosage forms contain cimetidine as the hydrochloride.)
Cimetidine has a bitter taste and characteristic odor. Solubility Characteristics : Cimetidine is soluble in alcohol, slightly soluble in water, very slightly soluble in chloroform and insoluble in ether. Cimetidine hydrochloride is freely soluble in water, soluble in alcohol, very slightly soluble in chloroform and practically insoluble in ether. Tablets for Oral Administration : Each light green, film-coated tablet contains cimetidine as follows: 300 mg-round, debossed with the product name TAGAMET, SB and 300; 400 mg-oval Tiltab® tablets, debossed with the product name TAGAMET, SB and 400; 800 mg-oval Tiltab® tablets, debossed with the product name TAGAMET, SB and 800. Inactive ingredients consist of cellulose, D&C Yellow No. 10, FD&C Blue No. 2, FD&C Red No. 40, FD&C Yellow No. 6, hydroxypropyl methylcellulose, iron oxides, magnesium stearate, povidone, propylene glycol, sodium lauryl sulfate, sodium starch glycolate, starch, titanium dioxide and trace amounts of other inactive ingredients. Liquid for Oral Administration : Each 5 mL (1 teaspoonful) of clear, light orange, mint-peach flavored liquid contains cimetidine hydrochloride equivalent to cimetidine, 300 mg; alcohol, 2.8%. Inactive ingredients consist of FD&C Yellow No. 6, flavors, methylparaben, polyoxyethylene polyoxypropylene glycol, propylene glycol, propylparaben, saccharin sodium, sodium chloride, sodium phosphate, sorbitol and water. Injection Single-Dose Vials for Intramuscular or Intravenous Administration : Each 2 mL contains, in sterile aqueous solution (pH range 3.8 to 6), cimetidine hydrochloride equivalent to cimetidine, 300 mg; phenol, 10 mg. Multi-Dose Vials for Intramuscular or Intravenous Administration : 8 mL (300 mg/2 mL): Each 2 mL contains, in sterile aqueous solution (pH range 3.8 to 6), cimetidine hydrochloride equivalent to cimetidine, 300 mg; phenol, 10 mg. Single-Dose Premixed Plastic Containers for Intravenous Administration : Each 50 mL of sterile aqueous solution (pH range 5 to 7) contains cimetidine hydrochloride equivalent to 300 mg cimetidine and 0.45 grams sodium chloride. No preservative has been added. The plastic container is fabricated from specially formulated polyvinyl chloride. The amount of water that can permeate from inside the container into the overwrap is insufficient to affect the solution significantly. Solutions in contact with the plastic container can leach out certain of its chemical components in very small amounts within the expiration period, e.g., di 2-ethylhexyl phthalate (DEHP), up to 5 parts per million. However, the safety of the plastic has been confirmed in tests in animals according to the USP biological tests for plastic containers as well as by tissue culture toxicity studies. ADD-Vantage®* Vials for Intravenous Administration : Each 2 mL contains, in sterile aqueous solution (pH range 3.8 to 6), cimetidine hydrochloride equivalent to cimetidine, 300 mg; phenol, 10 mg. All of the above injection formulations are pyrogen free, and sodium hydroxide N.F. is used as an ingredient to adjust the pH.
*ADD-Vantage® is a trademark of Abbott Laboratories.Last reviewed on RxList: 1/12/2005




Tagamet Drug Description

TAGAMET®
(cimetidine) Tablets
(cimetidine hydrochloride) Liquid
(cimetidine hydrochloride) Injection


DRUG DESCRIPTION



What are the possible side effects of cimetidine (Tagamet, Tagamet HB)?

Stop using cimetidine and 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.
Call your doctor at once if you have any of these serious side effects:

cough, fever, chest congestion, trouble breathing;
red or blistering skin rash;
jaundice (yellowing of the skin or eyes);
easy bruising or bleeding, unusual weakness;
feeling...
Read All Potential Side Effects for Tagamet »




Tagamet (cimetidine) is a histamine H2-receptor antagonist. Chemically it is N?-cyano-N-methyl N'-[2-[[(5-methyl-1H-imidazol-4-yl)methyl]thio]-ethyl]-guanidine.
The empirical formula for cimetidine is C10H16N6S and for cimetidine hydrochloride, C10H16N6SHCl; these represent molecular weights of 252.34 and 288.80, respectively.

Cimetidine contains an imidazole ring, and is chemically related to histamine.
(The liquid and injection dosage forms contain cimetidine as the hydrochloride.)
Cimetidine has a bitter taste and characteristic odor. Solubility Characteristics : Cimetidine is soluble in alcohol, slightly soluble in water, very slightly soluble in chloroform and insoluble in ether. Cimetidine hydrochloride is freely soluble in water, soluble in alcohol, very slightly soluble in chloroform and practically insoluble in ether. Tablets for Oral Administration : Each light green, film-coated tablet contains cimetidine as follows: 300 mg-round, debossed with the product name TAGAMET, SB and 300; 400 mg-oval Tiltab® tablets, debossed with the product name TAGAMET, SB and 400; 800 mg-oval Tiltab® tablets, debossed with the product name TAGAMET, SB and 800. Inactive ingredients consist of cellulose, D&C Yellow No. 10, FD&C Blue No. 2, FD&C Red No. 40, FD&C Yellow No. 6, hydroxypropyl methylcellulose, iron oxides, magnesium stearate, povidone, propylene glycol, sodium lauryl sulfate, sodium starch glycolate, starch, titanium dioxide and trace amounts of other inactive ingredients. Liquid for Oral Administration : Each 5 mL (1 teaspoonful) of clear, light orange, mint-peach flavored liquid contains cimetidine hydrochloride equivalent to cimetidine, 300 mg; alcohol, 2.8%. Inactive ingredients consist of FD&C Yellow No. 6, flavors, methylparaben, polyoxyethylene polyoxypropylene glycol, propylene glycol, propylparaben, saccharin sodium, sodium chloride, sodium phosphate, sorbitol and water. Injection Single-Dose Vials for Intramuscular or Intravenous Administration : Each 2 mL contains, in sterile aqueous solution (pH range 3.8 to 6), cimetidine hydrochloride equivalent to cimetidine, 300 mg; phenol, 10 mg. Multi-Dose Vials for Intramuscular or Intravenous Administration : 8 mL (300 mg/2 mL): Each 2 mL contains, in sterile aqueous solution (pH range 3.8 to 6), cimetidine hydrochloride equivalent to cimetidine, 300 mg; phenol, 10 mg. Single-Dose Premixed Plastic Containers for Intravenous Administration : Each 50 mL of sterile aqueous solution (pH range 5 to 7) contains cimetidine hydrochloride equivalent to 300 mg cimetidine and 0.45 grams sodium chloride. No preservative has been added. The plastic container is fabricated from specially formulated polyvinyl chloride. The amount of water that can permeate from inside the container into the overwrap is insufficient to affect the solution significantly. Solutions in contact with the plastic container can leach out certain of its chemical components in very small amounts within the expiration period, e.g., di 2-ethylhexyl phthalate (DEHP), up to 5 parts per million. However, the safety of the plastic has been confirmed in tests in animals according to the USP biological tests for plastic containers as well as by tissue culture toxicity studies. ADD-Vantage®* Vials for Intravenous Administration : Each 2 mL contains, in sterile aqueous solution (pH range 3.8 to 6), cimetidine hydrochloride equivalent to cimetidine, 300 mg; phenol, 10 mg. All of the above injection formulations are pyrogen free, and sodium hydroxide N.F. is used as an ingredient to adjust the pH.
*ADD-Vantage® is a trademark of Abbott Laboratories.Last reviewed on RxList: 1/12/2005




Tagamet Drug Description

TAGAMET®
(cimetidine) Tablets
(cimetidine hydrochloride) Liquid
(cimetidine hydrochloride) Injection


DRUG DESCRIPTION



What are the possible side effects of cimetidine (Tagamet, Tagamet HB)?

Stop using cimetidine and 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.
Call your doctor at once if you have any of these serious side effects:

cough, fever, chest congestion, trouble breathing;
red or blistering skin rash;
jaundice (yellowing of the skin or eyes);
easy bruising or bleeding, unusual weakness;
feeling...
Read All Potential Side Effects for Tagamet »




Tagamet (cimetidine) is a histamine H2-receptor antagonist. Chemically it is N?-cyano-N-methyl N'-[2-[[(5-methyl-1H-imidazol-4-yl)methyl]thio]-ethyl]-guanidine.
The empirical formula for cimetidine is C10H16N6S and for cimetidine hydrochloride, C10H16N6SHCl; these represent molecular weights of 252.34 and 288.80, respectively.

Cimetidine contains an imidazole ring, and is chemically related to histamine.
(The liquid and injection dosage forms contain cimetidine as the hydrochloride.)
Cimetidine has a bitter taste and characteristic odor. Solubility Characteristics : Cimetidine is soluble in alcohol, slightly soluble in water, very slightly soluble in chloroform and insoluble in ether. Cimetidine hydrochloride is freely soluble in water, soluble in alcohol, very slightly soluble in chloroform and practically insoluble in ether. Tablets for Oral Administration : Each light green, film-coated tablet contains cimetidine as follows: 300 mg-round, debossed with the product name TAGAMET, SB and 300; 400 mg-oval Tiltab® tablets, debossed with the product name TAGAMET, SB and 400; 800 mg-oval Tiltab® tablets, debossed with the product name TAGAMET, SB and 800. Inactive ingredients consist of cellulose, D&C Yellow No. 10, FD&C Blue No. 2, FD&C Red No. 40, FD&C Yellow No. 6, hydroxypropyl methylcellulose, iron oxides, magnesium stearate, povidone, propylene glycol, sodium lauryl sulfate, sodium starch glycolate, starch, titanium dioxide and trace amounts of other inactive ingredients. Liquid for Oral Administration : Each 5 mL (1 teaspoonful) of clear, light orange, mint-peach flavored liquid contains cimetidine hydrochloride equivalent to cimetidine, 300 mg; alcohol, 2.8%. Inactive ingredients consist of FD&C Yellow No. 6, flavors, methylparaben, polyoxyethylene polyoxypropylene glycol, propylene glycol, propylparaben, saccharin sodium, sodium chloride, sodium phosphate, sorbitol and water. Injection Single-Dose Vials for Intramuscular or Intravenous Administration : Each 2 mL contains, in sterile aqueous solution (pH range 3.8 to 6), cimetidine hydrochloride equivalent to cimetidine, 300 mg; phenol, 10 mg. Multi-Dose Vials for Intramuscular or Intravenous Administration : 8 mL (300 mg/2 mL): Each 2 mL contains, in sterile aqueous solution (pH range 3.8 to 6), cimetidine hydrochloride equivalent to cimetidine, 300 mg; phenol, 10 mg. Single-Dose Premixed Plastic Containers for Intravenous Administration : Each 50 mL of sterile aqueous solution (pH range 5 to 7) contains cimetidine hydrochloride equivalent to 300 mg cimetidine and 0.45 grams sodium chloride. No preservative has been added. The plastic container is fabricated from specially formulated polyvinyl chloride. The amount of water that can permeate from inside the container into the overwrap is insufficient to affect the solution significantly. Solutions in contact with the plastic container can leach out certain of its chemical components in very small amounts within the expiration period, e.g., di 2-ethylhexyl phthalate (DEHP), up to 5 parts per million. However, the safety of the plastic has been confirmed in tests in animals according to the USP biological tests for plastic containers as well as by tissue culture toxicity studies. ADD-Vantage®* Vials for Intravenous Administration : Each 2 mL contains, in sterile aqueous solution (pH range 3.8 to 6), cimetidine hydrochloride equivalent to cimetidine, 300 mg; phenol, 10 mg. All of the above injection formulations are pyrogen free, and sodium hydroxide N.F. is used as an ingredient to adjust the pH.
*ADD-Vantage® is a trademark of Abbott Laboratories.Last reviewed on RxList: 1/12/2005




Tagamet Drug Description

TAGAMET®
(cimetidine) Tablets
(cimetidine hydrochloride) Liquid
(cimetidine hydrochloride) Injection


DRUG DESCRIPTION



What are the possible side effects of cimetidine (Tagamet, Tagamet HB)?

Stop using cimetidine and 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.
Call your doctor at once if you have any of these serious side effects:

cough, fever, chest congestion, trouble breathing;
red or blistering skin rash;
jaundice (yellowing of the skin or eyes);
easy bruising or bleeding, unusual weakness;
feeling...
Read All Potential Side Effects for Tagamet »




Tagamet (cimetidine) is a histamine H2-receptor antagonist. Chemically it is N?-cyano-N-methyl N'-[2-[[(5-methyl-1H-imidazol-4-yl)methyl]thio]-ethyl]-guanidine.
The empirical formula for cimetidine is C10H16N6S and for cimetidine hydrochloride, C10H16N6SHCl; these represent molecular weights of 252.34 and 288.80, respectively.

Cimetidine contains an imidazole ring, and is chemically related to histamine.
(The liquid and injection dosage forms contain cimetidine as the hydrochloride.)
Cimetidine has a bitter taste and characteristic odor. Solubility Characteristics : Cimetidine is soluble in alcohol, slightly soluble in water, very slightly soluble in chloroform and insoluble in ether. Cimetidine hydrochloride is freely soluble in water, soluble in alcohol, very slightly soluble in chloroform and practically insoluble in ether. Tablets for Oral Administration : Each light green, film-coated tablet contains cimetidine as follows: 300 mg-round, debossed with the product name TAGAMET, SB and 300; 400 mg-oval Tiltab® tablets, debossed with the product name TAGAMET, SB and 400; 800 mg-oval Tiltab® tablets, debossed with the product name TAGAMET, SB and 800. Inactive ingredients consist of cellulose, D&C Yellow No. 10, FD&C Blue No. 2, FD&C Red No. 40, FD&C Yellow No. 6, hydroxypropyl methylcellulose, iron oxides, magnesium stearate, povidone, propylene glycol, sodium lauryl sulfate, sodium starch glycolate, starch, titanium dioxide and trace amounts of other inactive ingredients. Liquid for Oral Administration : Each 5 mL (1 teaspoonful) of clear, light orange, mint-peach flavored liquid contains cimetidine hydrochloride equivalent to cimetidine, 300 mg; alcohol, 2.8%. Inactive ingredients consist of FD&C Yellow No. 6, flavors, methylparaben, polyoxyethylene polyoxypropylene glycol, propylene glycol, propylparaben, saccharin sodium, sodium chloride, sodium phosphate, sorbitol and water. Injection Single-Dose Vials for Intramuscular or Intravenous Administration : Each 2 mL contains, in sterile aqueous solution (pH range 3.8 to 6), cimetidine hydrochloride equivalent to cimetidine, 300 mg; phenol, 10 mg. Multi-Dose Vials for Intramuscular or Intravenous Administration : 8 mL (300 mg/2 mL): Each 2 mL contains, in sterile aqueous solution (pH range 3.8 to 6), cimetidine hydrochloride equivalent to cimetidine, 300 mg; phenol, 10 mg. Single-Dose Premixed Plastic Containers for Intravenous Administration : Each 50 mL of sterile aqueous solution (pH range 5 to 7) contains cimetidine hydrochloride equivalent to 300 mg cimetidine and 0.45 grams sodium chloride. No preservative has been added. The plastic container is fabricated from specially formulated polyvinyl chloride. The amount of water that can permeate from inside the container into the overwrap is insufficient to affect the solution significantly. Solutions in contact with the plastic container can leach out certain of its chemical components in very small amounts within the expiration period, e.g., di 2-ethylhexyl phthalate (DEHP), up to 5 parts per million. However, the safety of the plastic has been confirmed in tests in animals according to the USP biological tests for plastic containers as well as by tissue culture toxicity studies. ADD-Vantage®* Vials for Intravenous Administration : Each 2 mL contains, in sterile aqueous solution (pH range 3.8 to 6), cimetidine hydrochloride equivalent to cimetidine, 300 mg; phenol, 10 mg. All of the above injection formulations are pyrogen free, and sodium hydroxide N.F. is used as an ingredient to adjust the pH.
*ADD-Vantage® is a trademark of Abbott Laboratories.Last reviewed on RxList: 1/12/2005





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Other reviews about Tagamet on web:

Learn about the prescription medication Tagamet (Cimetidine), drug uses, dosage, side effects, drug interactions, warnings, reviews and patient labeling. Tagamet (Cimetidine) Drug Information: Uses, Side Effects, Drug ...


It is marketed by GlaxoSmithKline under the trade name Tagamet (sometimes Tagamet HB or Tagamet HB200). Cimetidine was approved in the UK in 1976 and was approved in the US by the Food ... Cimetidine - Wikipedia, the free encyclopedia


Tagamet information from Drugs.com. Tagamet is prescribed for the treatment of certain kinds of stomach and intestinal ulcers and related conditions. These include: active ... Tagamet patient advice including side effects


Physician reviewed Tagamet patient information - includes Tagamet description, dosage and directions. Tagamet (cimetidine) medical facts from Drugs.com


Home; About Tagamet; About Heartburn; Heartburn Relief; Recipes; Living Well; Learn more about the Advantage Brands and the Essentials for Living Well Choose TAGAMET® for Heartburn Relief.


Definition of Tagamet – Our online dictionary has Tagamet information from A Dictionary of Nursing dictionary. Encyclopedia.com: English, psychology and medical dictionaries Tagamet – Dictionary definition of Tagamet | Encyclopedia.com ...


Tagamet is a drug that is used to treat conditions related to the esophagus, stomach, and intestines. This eMedTV article features an overview of Tagamet, including information ... Tagamet


Explains the medication cimetidine (Tagamet), a drug used in promoting the healing of active stomach and duodenal ulcers, and in reducing ulcer pain. cimetidine (Tagamet) - drug class, medical uses, medication side ...


Tagamet Tagamet is used for treating and preventing ulcers of the stomach and small intestine, and treating gastroesophageal reflux disease (GERD). Buy Tagamet


Learn about Tagamet from the publishers of the Physicians Desk Reference. Find prescription drug information resources including interactions, side effects, symptoms, treatment ... Tagamet | Prescription Drug Information, Side Effects | PDRHealth





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