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Acidosh (Famotidine)

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Acidosh is a histamine H2 antagonist. It works by reducing the amount of stomach acid secreted by glands in the lining of your stomach. The most common side effects of using Acidosh include headache, dizziness, constipation, and diarrhea.

Other names for this medication:
Acilo, Acipep, Advantac, Andic, Autidine, Blocacid, Diclosef, Dipal, Dompon, Emetec, Fadine, Fagene, Faltidin, Famiron, Famit, Famodil, Famodin, Famokan, Famolite, Famopril, Famorila, Famostan, Famotic, Famotidine, Famotin, Famowal, Fampep, Famtac, Febcid, Femidin, Femoact, Nilacid, Nocid, Noctin, Pedin, Pepdin, Recid, Ronid, Sprain, Symotin, Topcid, Ulcimax, Yekin, Zactane, Zorbin

Similar Products:
Yasmin, Indocin, Naprosyn, Catapres, Claritin, Cymbalta, Singulair, Strattera, Atoris, Terazosin, Chlotrip, Anvistat, Glimet, Gentrip, Viramune, Linaris,

Also known as: Famotidine


Famotidine is used to treat stomach ulcers (gastric and duodenal), erosive esophagitis (heartburn or acid indigestion), and gastroesophageal reflux disease (GERD). GERD is a condition where the acid in the stomach washes back up into the esophagus. It is also used to treat certain conditions where there is too much acid in the stomach (eg, Zollinger-Ellison syndrome, multiple endocrine neoplasia).

Famotidine belongs to the group of medicines known as histamine H2-receptor antagonists or H2-blockers. It works by decreasing the amount of acid produced by the stomach.

This medicine is available with your doctor's prescription and also without a prescription. For the prescription form, there is more medicine in each tablet. Your doctor will have special instructions on the proper use and dose for your medical problem.


Use Acidosh exactly as directed on the label, or as prescribed by your doctor.

You may take this medicine with or without food.

Measure liquid medicine carefully. Use the dosing syringe provided, or use a medicine dose-measuring device (not a kitchen spoon).

Most ulcers heal within 4 weeks of famotidine treatment, but it may take up to 8 weeks of using this medicine before your ulcer heals. Keep using the medication as directed.

Call your doctor if the condition you are treating with famotidine does not improve, or if it gets worse.

Acidosh may be only part of a complete program of treatment that also includes changes in diet or lifestyle habits. Follow all instructions of your doctor or dietitian.

Store at room temperature away from moisture, heat, and light. Do not allow the liquid medicine to freeze.

Throw away any unused liquid that is older than 30 days.

Detailed Acidosh dosage information


If you overdose Generic Acidosh and you don't feel good you should visit your doctor or health care provider immediately.


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.

Throw away any unused oral liquid after 30 days.

Detailed Acidosh AC dosage information

Side effects

The most common side effects associated with Acidosh are:

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Side effect occurrence does not only depend on medication you are taking, but also on your overall health and other factors.


Drinking alcohol may increase the risk of damage to your stomach.

Avoid taking other stomach acid reducers unless your doctor has told you to. However, you may take an antacid (such as Maalox, Mylanta, Gaviscon, Milk of Magnesia, Rolaids, or Tums) with famotidine.

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Consolidation with high-dose melphalan, etoposide, TBI, and autologous stem-cell support failed to improve the probability of EFS in this cohort of patients with newly diagnosed metastatic ES. The preoperative FNA findings of eight surgically excised hibernomas from seven patients (three men and four women, ages 24-60 years) were reviewed. A series of N-substituted analogs based upon the spiropiperidine core of 1 was synthesized and exhibited high binding affinity to the nociceptin (NOP) receptor. Treatment of heterozygous familial hypercholesterolemia: atorvastatin vs simvastatin. Significant amounts of CE transfer activity were detected in conditioned media of cultured adipose tissues from human, hamster and transgenic mice expressing CETP. Na,K-ATPase activity in the gill and intestine was inhibited by all the metal exposures, except 20 microM Pb exposure that resulted in an increase in the activity in the gill. Moreover, statistical analysis performed on major factors that may influence the final determination supported the validity of the optimized protocol. This Letter describes the synthesis and properties of double-stranded antisense oligonucleotides connected with a pentaerythritol linker.

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DIGESTIVE COMPLICATIONS INITIATED BY ASPIRIN ADMINISTERED BY THE ORAL ROUTE. RETROPNEUMOPERITONEUM AS A METHOD OF MORPHOLOGICAL INVESTIGATION IN 40 PATIENTS WITH MEDICAL NEPHROPATHIES. SEPARATION OF AN ANTIBODY MOLECULE BY A SPECIFIC REACTION WITH AN ANTIGEN-COATED LATEX PARTICLE. Our clinical impression of cholangiocarcinoma (Klatskin tumor), was confirmed by ultrasound, abdominal CT scan, and percutaneous transhepatic cholangiography. Beside the most frequently occurring common SCC with variable degree of differentiation, the following tumor forms can be identified microscopically: Bowen-SCC, acantholytic SCC, clear cell SCC, spindle cell SCC, keratoacanthoma-like SCC, desmoplastic SCC, neurotrophic SCC, verrucous SCC, adenosquamous carcinoma and basosquamous cell carcinoma. A 69-kDa proteinase (P69), a member of the pathogenesis-related proteins, is induced and accumulates in tomato (Lycopersicon esculentum) plants as a consequence of pathogen attack. Role of the System L permease LAT1 in amino acid and iodothyronine transport in placenta.

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Using RNAi to knock out the genes of Igk and/or Iglambda, Bcl-xL expression in HT29 cells was significantly suppressed and the cells became apoptotic. Energy coupling in Salmonella typhimurium nicotinic acid phosphoribosyltransferase: identification of His-219 as site of phosphorylation. This pattern could explain the evolution of the mental health field over the last four decades. By their use the survival times can be directly modelled, so that the interpretation of the fixed and random effects is straightforward. Follice-stimulating hormone receptor forms oligomers and shows evidence of carboxyl-terminal proteolytic processing. Properties of a system of public idiotypes of lupus autoantibodies. To account for the primary products in the above reactions, a mechanism is proposed in which the key step of the carbon--carbon bond cleavage occurs via concerted electronic transfer in dimetallacyclopentane intermediate. Although enteric nerves and smooth muscle cells have been described, it is unknown if ICC are present in the zebrafish. Monte Carlo and experimental dosimetry of an 1251 brachytherapy seed. A survey of tracheostomy practice in a cardiothoracic intensive care unit.

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