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Azantac adverse events reported to FDA.

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Summary

FDA Adverse Reports: 10. View All

Azantac FDA safety alerts: No

Reported deaths: 2

Reported hospitalizations: 9

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Often additional risks of using a medication, such as Azantac, become known after product is used by a larger number of patients, for a longer period of time, and by patients with different health characteristics from those studied before drug approval. This page allows You to Find answers and discuss health symptoms with other Azantac users, Learn more about unwanted side effects & find ways to reduce them. Browse Azantac Adverse Reports reported to FDA and participate in Azantac discussion, find alternative treatments and find ways to avoid or reduce risks associated with using Azantac. You can also Post a question to users community or Ask a Doctor. PatientsVille.com is Your Complete Guide to all common, undocumented and undisclosed side effects associated with drugs and vaccines. Browse More Drug Reports Here: A  B  C  D  E  F  G  H  I  J  K  L  M  N  O  P  Q  R  S  T  U  V  W  X  Y  Z

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Azantac Adverse Effect Reports (FDA)

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4920290-6 | Abdominal Pain, Agitation, Anoxic Encephalopathy, Circulatory Collapse, Electrocardiogram Qrs Complex Prolonged, Feeling Cold, Hypotension, Loss Of Consciousness
on Feb 16, 2006 Female patient from FRANCE , 43 years of age, weighting 352.7 lb, was diagnosed with prophylaxis and was treated with Azantac (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal pain (What is abdominal pain?), agitation, anoxic encephalopathy, circulatory collapse, electrocardiogram qrs complex prolonged, feeling cold, hypotension, loss of consciousness. Azantac dosage: 50mg Single Dose. During the same period patient was treated with ACUPAN (20mg Single Dose) (View Acupan Review and Acupan Label ), DROLEPTAN (1.25mg Single Dose) (View Droleptan Review and Droleptan Label ), CLINDAMYCIN HCL (600mg Single Dose) (View Clindamycin Hcl Review and Clindamycin Hcl Label ), DIPRIVAN (130mg Single Dose) (View Diprivan Review and Diprivan Label ), SUFENTA (15unit Single Dose) (View Sufenta Review and Sufenta Label ), GENTAMYCIN SULFATE (120mg Single Dose) (View Gentamycin Sulfate Review and Gentamycin Sulfate Label ), PROFENID (100mg Single Dose) (View Profenid Review and Profenid Label ), SYNTOCINON (5iu Single Dose) (View Syntocinon Review and Syntocinon Label ).

4808585-8 | Decreased Appetite, Somnolence, Transaminases Increased, Weight Decreased
Patient was taking Azantac (View Usage). Patient had the following side effects: decreased appetite, somnolence, transaminases increased, weight decreased on Oct 13, 2005 from FRANCE Additional patient health information: Male patient , weighting 6.39 lb, . Azantac dosage: .6ml Twice Per Day. During the same period patient was treated with PHOSPHALUGEL (View Phosphalugel Review and Phosphalugel Label ). Patient was hospitalized.

4743758-4 | Abdominal Pain, Blood Amylase Increased, Pancreatitis Acute, Pyrexia, White Blood Cell Count Increased
Adverse event was reported on Aug 03, 2005 by a Male patient taking Azantac (View Usage) (Dosage: ) was diagnosed with anaesthesia and. Location: FRANCE , 50 years of age, After Azantac was administered, patient had the following side effects: abdominal pain (What is abdominal pain?), blood amylase increased, pancreatitis acute, pyrexia, white blood cell count increased. During the same period patient was treated with DIPRIVAN (View Diprivan Review and Diprivan Label ), SUFENTA (View Sufenta Review and Sufenta Label ), SEVORANE (View Sevorane Review and Sevorane Label ). Patient was hospitalized.

4738410-5 | Acinetobacter Infection, Anaemia Macrocytic, Fistula, Haemophilus Infection, Multi-organ Failure, Pneumococcal Infection, Respiratory Distress, Respiratory Failure, Septic Shock
on Aug 03, 2005 Female patient from FRANCE , 72 years of age, was diagnosed with resuscitation and was treated with Azantac (View Usage). Patient experienced the following unwanted or unexpected effects: acinetobacter infection, anaemia macrocytic, fistula (What is fistula?), haemophilus infection, multi-organ failure, pneumococcal infection, respiratory distress, respiratory failure, septic shock. Azantac dosage: . During the same period patient was treated with LOVENOX (40mg Per Day) (View Lovenox Review and Lovenox Label ), TIENAM (500mg Four Times Per Day) (View Tienam Review and Tienam Label ), SANDOSTATIN (100mcg Three Times Per Day) (View Sandostatin Review and Sandostatin Label ), TRIFLUCAN (800mg Per Day) (View Triflucan Review and Triflucan Label ), VANCOMYCIN (1.5mg Per Day) (View Vancomycin Review and Vancomycin Label ), ACTRAPID (View Actrapid Review and Actrapid Label ), HYDROCORTISONE (200mg Per Day) (View Hydrocortisone Review and Hydrocortisone Label ), SOLU MEDROL (View Solu-medrol Review and Solu-medrol Label ). Patient was hospitalized.


4735646-4 | Anuria, Cough, Cyanosis, Dyspnoea, Hypoxia, Meningitis Pneumococcal, Metabolic Acidosis, Pericardial Effusion, Pigmentation Disorder
on Jul 26, 2005 Male patient from FRANCE , 54 years of age, weighting 187.4 lb, was treated with Azantac (View Usage). Patient had the following side effects: anuria, cough, cyanosis, dyspnoea, hypoxia, meningitis pneumococcal, metabolic acidosis, pericardial effusion, pigmentation disorder. Azantac dosage: . During the same period patient was treated with APRANAX (View Apranax Review and Apranax Label ), DI ANTALVIC (View Di Antalvic Review and Di Antalvic Label ), MYOLASTAN (View Myolastan Review and Myolastan Label ), PROPOFOL (View Propofol Review and Propofol Label ), THIOCOLCHICOSIDE (View Thiocolchicoside Review and Thiocolchicoside Label ). Patient was hospitalized.

4652354-9 | Asthenia, Diarrhoea, Vomiting
Patient was taking Azantac (View Usage). After Azantac was administered, patient had the following side effects: asthenia, diarrhoea, vomiting on Apr 27, 2005 from Additional patient health information: Female patient , 63 years of age, was diagnosed with gastric ulcer and. Azantac dosage: 150mg See Dosage Text. Patient was hospitalized.

4624165-1 | Haemorrhage, Idiopathic Thrombocytopenic Purpura, Petechiae, Thrombocytopenia
Adverse event was reported on Feb 21, 2005 by a Male patient taking Azantac (View Usage) (Dosage: 150mg Alternate Days) . Location: , 74 years of age, Patient experienced the following unwanted or unexpected effects: haemorrhage, idiopathic thrombocytopenic purpura, petechiae, thrombocytopenia. During the same period patient was treated with MOPRAL (10mg Per Day) (View Mopral Review and Mopral Label ), CEBUTID (100mg Per Day) (View Cebutid Review and Cebutid Label ), CIMETIDINE (1.5gk Per Day) (View Cimetidine Review and Cimetidine Label ). Patient was hospitalized.

4584218-3 | Leukopenia, Neutropenia
on Feb 01, 2005 Female patient from , 82 years of age, was treated with Azantac (View Usage). Patient had the following side effects: leukopenia, neutropenia. Azantac dosage: . During the same period patient was treated with COVERSYL (4mg Per Day) (View Coversyl Review and Coversyl Label ), AROMASIN (View Aromasin Review and Aromasin Label ), CORDARONE (200mg Per Day) (View Cordarone Review and Cordarone Label ). Patient was hospitalized.

4556042-9 | Leukopenia, Neutropenia, Respiratory Failure
on Jun 08, 2004 Female patient from , 82 years of age, was diagnosed with gastrointestinal ulcer, hypertension, breast cancer (What is breast cancer?), atrial fibrillation (What is atrial fibrillation?) and was treated with Azantac (View Usage). After Azantac was administered, patient had the following side effects: leukopenia, neutropenia, respiratory failure. Azantac dosage: 300mg Per Day. During the same period patient was treated with COVERSYL (4mg Per Day) (View Coversyl Review and Coversyl Label ), AROMASIN (25mg Per Day) (View Aromasin Review and Aromasin Label ), CORDARONE (1tab Per Day) (View Cordarone Review and Cordarone Label ), PREVISCAN (10mg Per Day) (View Previscan Review and Previscan Label ). Patient was hospitalized.

4546526-1 | Interstitial Lung Disease, Lung Disorder
Patient was taking Azantac (View Usage). Patient experienced the following unwanted or unexpected effects: interstitial lung disease, lung disorder on Dec 30, 2004 from Additional patient health information: Male patient , 66 years of age, weighting 156.5 lb, . Azantac dosage: . During the same period patient was treated with POLARAMINE (View Polaramine Review and Polaramine Label ), DEXAMETHASONE (View Dexamethasone Review and Dexamethasone Label ), TAXOL (View Taxol Review and Taxol Label ), CARBOPLATINE (View Carboplatine Review and Carboplatine Label ). Patient was hospitalized.


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To find out about documented side effects or safety concerns read either the drug label or the drug's package insert. You may also want to speak with your pharmacist or healthcare provider. All medicines have benefits and risks. The risks are the chances that something unwanted or unexpected could happen to you when you use them. You can protect yourself by searching summaries of recent safety alerts, adverse reports. Sometimes there are risks that only come to light after a medical product gets on the market and is used in a larger number of patients, for a longer period of time, and in patients whose health characteristics are different from those of the patients studied before approval.

Be aware of the following potential Azantac risks to be aware of: 1. Watch for any Serious adverse events, such as life-threatening situation, which can require an admission to hospital or longer-than-expected hospital stay, permanent disability, birth defect, miscarriage, stillbirth, or birth with serious disease requires medical care to prevent permanent damage
2. Any potential Azantac quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Azantac use error: mixing up products with similar drug names or packaging, taking wrong dose of a drug because of confusing dosing instructions on label
4. When applicable, Problems with different manufacturer of same medicine: not getting same results from a generic drug as a brand name drug, or from another generic

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Azantac Reactions
Abdominal PainWhat is Abdominal pain?
Acinetobacter Infection
Agitation
Anaemia Macrocytic
Anoxic Encephalopathy
Anuria
Asthenia
Blood Amylase Increased
Brain Death
Circulatory Collapse
Cough
Cyanosis
Death
Decreased Appetite
Diarrhoea
Dyspnoea
Electrocardiogram Qrs Complex Prolonged
Feeling Cold
FistulaWhat is Fistula?
Haemophilus Infection
Haemorrhage
Hypotension
Hypoxia
Idiopathic Thrombocytopenic Purpura
Interstitial Lung Disease
Leukopenia
Loss Of Consciousness
Lung Disorder
Neutropenia
Respiratory Failure
Azantac Side Effects Notice - The material on this site is for informational purposes only, and is not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. PatientsVille.com does not provide medical advice, diagnosis or treatment. The information regarding Azantac adverse reports, reviews and polls contained on PatientsVille.com site has not been scientifically or otherwise verified as to a cause and effect relationship and cannot be used to estimate the incidence of adverse drug reactions or for establishing or changing of patient treatments. Thank you for visiting Patientsville.com!