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Advantac (Famotidine)

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Advantac is in a class of medications called H2 blockers. It works by decreasing the amount of acid made in the stomach. Over-the-counter Advantac is used to prevent and treat heartburn due to acid indigestion and sour stomach caused by eating or drinking certain foods or drinks.

Other names for this medication:
Acilo, Acipep, Acredin, Advantac, Andic, Autidine, Avifam, Diclofam, Dipal, Dumotin, Emetec, Fadine, Fagene, Faltidin, Famit, Famocid, Famodil, Famodin, Famolite, Famopril, Famostan, Famot, Famotidine, Famotin, Famowal, Febcid, Femidin, Femotidine, Femspas, Fudone, Mahagesic, Motinac, Neutracaine, Nocid, Noctin, Pedin, Pepdin, Recid, Ronid, Tobur, Ulcimax, Zactane

Similar Products:
Micardis, Cozaar, Lunesta, Rhinocort, Arimidex, Keflex, Neurontin, Diflucan, Klomicina, Sleecalm, Deviry, Rivasmine, Ancofex, Glimpid,

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.


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

Take this medicine exactly as directed by your doctor or as directed on the package. Do not take more of it, do not take it more often, and do not take it for a longer time than your doctor ordered. To do so may increase the chance of side effects.

Keep using this medicine for the full time of treatment, even if you begin to feel better.

You may take this medicine with or without food.

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

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 oral dosage forms (suspension, tablets): To prevent an ulcer from coming back: Adults—20 milligrams (mg) once a day. Children—Use and dose must be determined by your doctor. To treat erosive esophagitis (heartburn): Adults and children weighing 40 kilograms (kg) or more—20 milligrams (mg) 1 or 2 times per day, at the morning and at bedtime, or 40 mg once a day at bedtime for up to 12 weeks. Children weighing less than 40 kg—Use and dose be determined by your doctor. To treat gastroesophageal reflux disease (GERD): Adults and children weighing 40 kilograms (kg) or more—20 milligrams (mg) 2 times per day, in the morning and at bedtime for up to 6 weeks. Children weighing less than 40 kg—Use and dose be determined by your doctor. To treat stomach ulcers: Adults and children weighing 40 kilograms (kg) or more—20 milligrams (mg) 2 times per day, at the morning and at bedtime, or 40 mg once a day at bedtime for up to 8 weeks. Children weighing less than 40 kg—Use and dose be determined by your doctor. To treat too much stomach acid (Zollinger-Ellison syndrome): Adults—20 milligrams (mg) every 6 hours. Your doctor may adjust your dose as needed. Children—Use and dose must be determined by your doctor.


If you overdose Generic Advantac 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 Advantac AC dosage information

Side effects

The most common side effects associated with Advantac 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.


Heartburn can mimic early symptoms of a heart attack. Get emergency medical help if you have chest pain that spreads to your jaw or shoulder and you feel anxious or light-headed.

You should not use this medicine if you are allergic to famotidine or similar stomach acid reducers, such as ranitidine, cimetidine, Zantac, Tagamet, and others.

Do not use Advantac Complete if you have:

trouble swallowing food, or pain when swallowing; vomiting with blood; or black, bloody, or tarry stools.

Ask a doctor or pharmacist if this medicine is safe to use if you have ever had:

wheezing or trouble breathing when you have heartburn; nausea, vomiting, or stomach pain; unusual weight loss; kidney disease; or if you have had heartburn for longer than 3 months.

This medicine may contain phenylalanine. Check the medication label if you have phenylketonuria (PKU).

Ask a doctor before using this medicine if you are pregnant or breastfeeding.

Do not give this medicine to a child younger than 12 years old without medical advice.

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Prevalence of sleepiness and its relation to autonomic evidence of arousals and increased inspiratory effort in a community based population of men and women. This will enable clinicians to distinguish NDMs from myotonic dystrophy, thus allowing them to inform patients promptly about the disease, perform genetic counseling, and orient therapy (Vicart et al. Technology assessment status evaluation: disposable endoscopic accessories. A study of mandible chewing movement in patients with developmental lateral jaw deformity. Characteristic of SBMP was the identification of an amorphous phase deposited at the outer surface of the hybrid layer. Effect of hypertension on aortic root size and prevalence of aortic regurgitation. With inappropriate glycemic or blood pressure control, most patients will only seek care once micro- or macrovascular complications have already developed. The ratios of stable isotopes in albacore (Thunnus alalunga), amberjack (Seriola dumerili), blue butterfish (Stromaeus fiatola), bullet tuna (Auxis rochei), dolphinfish (Coryphaena hyppurus), horse mackerel (Trachurus trachurus), mackerel (Scomber scombrus) and pompano (Trachinotus ovatus) were consistent with mixed diets revealed by stomach content analysis, including nekton and crustaceans, but the consumption of gelatinous plankton could not be ruled out completely.

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Functional correlation of NMDA receptor epsilon subunits expression with the properties of single-channel and synaptic currents in the developing cerebellum. Alexander Nikolaevich Ogilvi--the first director of the first balneological institute. Mitochondria were isolated from rat dorsal root ganglia or brain and exposed to glucose or dinitrobenzene (DNB) to simulate the cellular environment of a diabetic animal that has been exposed to excess glucose or to DNB. Thus, we performed dosimetric measurements with iodine-123 (123I)-rituximab to evaluate rituximab uptake in PCNSL after systemic intravenous administration. Authors report the case of a 9 years old girl who was hit by a car.

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Sport- and recreation-related injuries are a major source of morbidity in the paediatric population. Interactions between genes are realized as gene regulatory networks (GRNs). This paper describes and quantitatively evaluates sources of uncertainty and variability in estimating the risk to an ecological receptor (osprey) from the trophic transfer of polychlorinated biphenyls (PCBs) in sediments from the New York-New Jersey (NY-NJ) Harbor. The treatment of human peripheral blood mononuclear cells with an inflammatory lysophospholipid induced beta-galactosidase and sialidase activity of lymphocytes, leading to the generation of macrophage-activating factor and activation of monocytes/macrophages. In this study, we developed a relatively small and simple SPR system, using optical fibers of 250 microm diameter to detect the activation of living cells attached to the fiber tip. Suppression of cell motility by cytotoxic doses of EMP (0.5-10 microM) group was attributed by the cyto-reductive effect, relating to apoptosis. Analysis of the autocorrelation histogram shapes showed that in both structures phenibut increased bursts of neuronal discharges, decreased the interspike intervals within the burst, increased the number of neurons with delta-frequency oscillation and decreased the number of neurons with theta-1 oscillation. We used a biochemical genomics approach to elucidate the pathway leading to synthesis of methylketones in the glandular trichomes of the wild tomato Lycopersicon hirsutum f glabratum (accession PI126449). Trichogin inhibited HIV-1 reverse transcriptase with an IC50 of 83 nM. The neurokinin A receptor activates calcium and cAMP responses through distinct conformational states.

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