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Cimetidine adverse events reported to FDA.

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Summary

FDA Adverse Reports: 64. View All

Cimetidine FDA safety alerts: No

Reported deaths: 9

Reported hospitalizations: 25

Cimetidine Dosage, Warnings, Usage.

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Often additional risks of using a medication, such as Cimetidine, 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 Cimetidine users, Learn more about unwanted side effects & find ways to reduce them. Browse Cimetidine Adverse Reports reported to FDA and participate in Cimetidine discussion, find alternative treatments and find ways to avoid or reduce risks associated with using Cimetidine. 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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Cimetidine Adverse Effect Reports (FDA)

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7018917-0 | Lactic Acidosis, Pancreatitis Acute
on Sep 14, 2010 Female patient from UNITED STATES , 59 years of age, was diagnosed with gastrooesophageal reflux disease and was treated with Cimetidine (View Usage). Patient experienced the following unwanted or unexpected effects: lactic acidosis, pancreatitis acute. Cimetidine dosage: . During the same period patient was treated with METFORMIN (View Metformin Review and Metformin Label ), FENOFIBRATE (View Fenofibrate Review and Fenofibrate Label ), LISINOPRIL (View Lisinopril Review and Lisinopril Label ), FLUVASTATIN (View Fluvastatin Review and Fluvastatin Label ), ATENOLOL (View Atenolol Review and Atenolol Label ). Patient was hospitalized.

7018916-9 | Lactic Acidosis, Pancreatitis Acute
Patient was taking Cimetidine (View Usage). Patient had the following side effects: lactic acidosis, pancreatitis acute on Sep 14, 2010 from UNITED STATES Additional patient health information: Female patient , 59 years of age, was diagnosed with gastrooesophageal reflux disease and. Cimetidine dosage: . During the same period patient was treated with METFORMIN (View Metformin Review and Metformin Label ), FENOFIBRATE (View Fenofibrate Review and Fenofibrate Label ), LISINOPRIL (View Lisinopril Review and Lisinopril Label ), FLUVASTATIN (View Fluvastatin Review and Fluvastatin Label ), ATENOLOL (View Atenolol Review and Atenolol Label ). Patient was hospitalized.

7018915-7 | Lactic Acidosis, Pancreatitis Acute
Adverse event was reported on Sep 14, 2010 by a Female patient taking Cimetidine (View Usage) (Dosage: ) was diagnosed with gastrooesophageal reflux disease and. Location: UNITED STATES , 59 years of age, After Cimetidine was administered, patient had the following side effects: lactic acidosis, pancreatitis acute. During the same period patient was treated with METFORMIN (View Metformin Review and Metformin Label ), FENOFIBRATE (View Fenofibrate Review and Fenofibrate Label ), LISINOPRIL (View Lisinopril Review and Lisinopril Label ), FLUVASTATIN (View Fluvastatin Review and Fluvastatin Label ), ATENOLOL (View Atenolol Review and Atenolol Label ). Patient was hospitalized.

6946202-1 | Alanine Aminotransferase Increased, Anion Gap Increased, Aspartate Aminotransferase Increased, Blood Lactate Dehydrogenase Increased, Blood Phosphorus Increased, Blood Potassium Increased, Blood Pressure Decreased, Cardiac Murmur, Dialysis
on Aug 10, 2010 Female patient from UNITED STATES , 59 years of age, was diagnosed with gastrooesophageal reflux disease, type 2 diabetes mellitus and was treated with Cimetidine (View Usage). Patient experienced the following unwanted or unexpected effects: alanine aminotransferase increased, anion gap increased, aspartate aminotransferase increased, blood lactate dehydrogenase increased, blood phosphorus increased, blood potassium increased, blood pressure decreased, cardiac murmur, dialysis (What is dialysis?). Cimetidine dosage: Oral. During the same period patient was treated with METFORMIN HCL (Oral) (View Metformin Hcl Review and Metformin Hcl Label ), FENOFIBRATE (View Fenofibrate Review and Fenofibrate Label ), LISINOPRIL (View Lisinopril Review and Lisinopril Label ), FLUVASTATIN SODIUM (View Fluvastatin Sodium Review and Fluvastatin Sodium Label ), ATENOLOL (View Atenolol Review and Atenolol Label ). Patient was hospitalized.


6917124-7 | Ascites, Blood Culture Positive, Candida Test Positive, Dyspnoea, Erythema Multiforme, Haemorrhage, Hypoxia, Increased Bronchial Secretion, Mucosal Erosion
on Jul 26, 2010 Male patient from JAPAN , 66 years of age, weighting 119.0 lb, was diagnosed with hepatic cirrhosis and was treated with Cimetidine (View Usage). Patient had the following side effects: ascites, blood culture positive, candida test positive, dyspnoea, erythema multiforme, haemorrhage, hypoxia, increased bronchial secretion, mucosal erosion. Cimetidine dosage: . During the same period patient was treated with URSODIOL (View Ursodiol Review and Ursodiol Label ), LORMETAZEPAM (View Lormetazepam Review and Lormetazepam Label ), ESTAZOLAM (View Estazolam Review and Estazolam Label ), HALOPERIDOL (View Haloperidol Review and Haloperidol Label ), LIMAPROST (View Limaprost Review and Limaprost Label ), FUROSEMIDE (View Furosemide Review and Furosemide Label ), SPIRONOLACTONE (View Spironolactone Review and Spironolactone Label ), LOXOPROFEN (View Loxoprofen Review and Loxoprofen Label ). Patient was hospitalized.

6883669-1 | Confusional State, Crying, Depressed Mood, Dizziness, Dry Mouth, Hallucination, Hypoaesthesia, Impaired Healing, Off Label Use
Patient was taking Cimetidine (View Usage). After Cimetidine was administered, patient had the following side effects: confusional state, crying, depressed mood, dizziness (What is dizziness?), dry mouth, hallucination, hypoaesthesia, impaired healing, off label use on Jul 22, 2010 from UNITED STATES Additional patient health information: Male patient , 31 years of age, . Cimetidine dosage: 600mg Four Times Per Day. During the same period patient was treated with ASTELIN (View Astelin Review and Astelin Label ).

6756938-3 | Haematoma, Small Intestinal Haemorrhage
Adverse event was reported on May 24, 2010 by a Female patient taking Cimetidine (View Usage) (Dosage: Unk) was diagnosed with cerebral infarction and. Location: JAPAN , 77 years of age, Patient experienced the following unwanted or unexpected effects: haematoma, small intestinal haemorrhage. During the same period patient was treated with CILOSTAZOL (Unk) (View Cilostazol Review and Cilostazol Label ). Patient was hospitalized.

6740608-1 | Intra-abdominal Haematoma
on May 11, 2010 Female patient from JAPAN , 77 years of age, was treated with Cimetidine (View Usage). Patient had the following side effects: intra-abdominal haematoma. Cimetidine dosage: . During the same period patient was treated with CILOSTAZOL (View Cilostazol Review and Cilostazol Label ). Patient was hospitalized.

6740607-X | Anaemia, Intra-abdominal Haematoma, Nausea, Small Intestinal Obstruction
on May 11, 2010 Female patient from JAPAN , 77 years of age, was treated with Cimetidine (View Usage). After Cimetidine was administered, patient had the following side effects: anaemia, intra-abdominal haematoma, nausea (What is nausea?), small intestinal obstruction. Cimetidine dosage: . During the same period patient was treated with CILOSTAZOL (View Cilostazol Review and Cilostazol Label ). Patient was hospitalized.

6740606-8 | Intra-abdominal Haematoma
Patient was taking Cimetidine (View Usage). Patient experienced the following unwanted or unexpected effects: intra-abdominal haematoma on May 11, 2010 from JAPAN Additional patient health information: Female patient , 77 years of age, . Cimetidine dosage: . During the same period patient was treated with CILOSTAZOL (View Cilostazol Review and Cilostazol Label ). Patient was hospitalized.

6740200-9 | Confusional State, Crying, Depressed Mood, Dizziness, Dry Mouth, Hallucination, Hypoaesthesia, Impaired Healing, Off Label Use
Adverse event was reported on May 19, 2010 by a Male patient taking Cimetidine (View Usage) (Dosage: 600mg Four Times Per Day) . Location: UNITED STATES , 31 years of age, Patient had the following side effects: confusional state, crying, depressed mood, dizziness (What is dizziness?), dry mouth, hallucination, hypoaesthesia, impaired healing, off label use. During the same period patient was treated with ASTELIN (View Astelin Review and Astelin Label ).

6735477-X | Activated Partial Thromboplastin Time Prolonged, Anaemia, Blood Acid Phosphatase Increased, Gamma-glutamyltransferase Increased, Inflammation, Intestinal Haematoma, Nausea, Platelet Count Decreased, Pneumonia Aspiration
on May 11, 2010 Female patient from JAPAN , 77 years of age, was treated with Cimetidine (View Usage). After Cimetidine was administered, patient had the following side effects: activated partial thromboplastin time prolonged, anaemia, blood acid phosphatase increased, gamma-glutamyltransferase increased, inflammation, intestinal haematoma, nausea (What is nausea?), platelet count decreased, pneumonia aspiration. Cimetidine dosage: . During the same period patient was treated with CILOSTAZOL (View Cilostazol Review and Cilostazol Label ). Patient was hospitalized.

6711493-9 | Confusional State, Educational Problem, Fatigue, Somnolence
on May 04, 2010 Male patient from UNITED STATES , 20 years of age, weighting 170.0 lb, was diagnosed with skin papilloma and was treated with Cimetidine (View Usage). Patient experienced the following unwanted or unexpected effects: confusional state, educational problem, fatigue, somnolence. Cimetidine dosage: 800mg 3 Times A Day Po.

6707098-6 | Crying, Depressed Mood, Dizziness, Dry Mouth, Hallucination, Impaired Healing, Off Label Use, Tension, Vision Blurred
Patient was taking Cimetidine (View Usage). Patient had the following side effects: crying, depressed mood, dizziness (What is dizziness?), dry mouth, hallucination, impaired healing, off label use, tension, vision blurred on Apr 23, 2010 from UNITED STATES Additional patient health information: Male patient , 31 years of age, . Cimetidine dosage: 600mg Four Times Per Day. During the same period patient was treated with ASTELIN (View Astelin Review and Astelin Label ).

6665175-2 | Haemolytic Anaemia
Adverse event was reported on Mar 22, 2010 by a Female patient taking Cimetidine (View Usage) (Dosage: ) was diagnosed with breast cancer (What is breast cancer?) and. Location: UNITED STATES , 63 years of age, After Cimetidine was administered, patient had the following side effects: haemolytic anaemia. During the same period patient was treated with CARBOPLATIN (View Carboplatin Review and Carboplatin Label ), PACLITAXEL (View Paclitaxel Review and Paclitaxel Label ), DEXAMETHASONE (View Dexamethasone Review and Dexamethasone Label ), DIPHENHYDRAMINE HYDROCHLORIDE (View Diphenhydramine Hydrochloride Review and Diphenhydramine Hydrochloride Label ). Patient was hospitalized.

6652348-8 |
on Mar 22, 2010 Female patient from UNITED STATES , 57 years of age, was treated with Cimetidine (View Usage). . Cimetidine dosage: . During the same period patient was treated with CARISOPRODOL (WATSON LABORATORIES) (View Carisoprodol (watson Laboratories) Review and Carisoprodol (watson Laboratories) Label ), CODEINE SULFATE (View Codeine Sulfate Review and Codeine Sulfate Label ), AMPHETAMINE SULFATE (View Amphetamine Sulfate Review and Amphetamine Sulfate Label ), VITAMINS (View Vitamins Review and Vitamins Label ).

6635972-8 | Back Pain, Haemolytic Anaemia
on Mar 01, 2010 Female patient from UNITED STATES , 63 years of age, was diagnosed with breast cancer metastatic and was treated with Cimetidine (View Usage). Patient had the following side effects: back pain (What is back pain?), haemolytic anaemia. Cimetidine dosage: 300 Mg / Intravenous. During the same period patient was treated with DIPHENHYDRAMINE HCL (View Diphenhydramine Hcl Review and Diphenhydramine Hcl Label ), DEXAMETHASONE (View Dexamethasone Review and Dexamethasone Label ), CARBOPLATIN (View Carboplatin Review and Carboplatin Label ), PACLITAXEL (View Paclitaxel Review and Paclitaxel Label ). Patient was hospitalized.

6579390-X |
Patient was taking Cimetidine (View Usage). on Jan 18, 2010 from UNITED STATES Additional patient health information: Female patient , 57 years of age, . Cimetidine dosage: Oral. During the same period patient was treated with CODEINE SULFATE (Oral) (View Codeine Sulfate Review and Codeine Sulfate Label ), AMPHETAMINE SULFATE TAB (Oral) (View Amphetamine Sulfate Tab Review and Amphetamine Sulfate Tab Label ).

6361438-9 | Abnormal Behaviour, Agitation, Depression, Pruritus, Suicidal Ideation, Urticaria
Adverse event was reported on Sep 16, 2009 by a Male patient taking Cimetidine (View Usage) (Dosage: 400mg Twice Daily Oral) was diagnosed with skin papilloma and. Location: UNITED STATES , weighting 74.00 lb, Patient experienced the following unwanted or unexpected effects: abnormal behaviour, agitation, depression (What is depression?), pruritus, suicidal ideation, urticaria.

6236545-1 | Supraventricular Tachycardia
on Jun 09, 2009 Male patient from UNITED KINGDOM , 46 years of age, weighting 154.3 lb, was diagnosed with blood cholesterol increased and was treated with Cimetidine (View Usage). Patient had the following side effects: supraventricular tachycardia. Cimetidine dosage: 800mg Per Day. During the same period patient was treated with LISINOPRIL (View Lisinopril Review and Lisinopril Label ), SIMVASTATIN (View Simvastatin Review and Simvastatin Label ). Patient was hospitalized.

6140647-8 | Haemorrhage, Scratch
on Apr 01, 2009 Female patient from UNITED STATES , 50 years of age, weighting 200.0 lb, was diagnosed with urticaria chronic and was treated with Cimetidine (View Usage). After Cimetidine was administered, patient had the following side effects: haemorrhage, scratch. Cimetidine dosage: 400 Mg Bid Po.

6139024-5 | Diarrhoea, Flushing, Hypotonia
Patient was taking Cimetidine (View Usage). Patient experienced the following unwanted or unexpected effects: diarrhoea, flushing, hypotonia on Mar 05, 2009 from UNITED KINGDOM Additional patient health information: Female patient , child 3 years of age, . Cimetidine dosage: . During the same period patient was treated with EPINEPHRINE (View Epinephrine Review and Epinephrine Label ), ALIMEMAZINE (ALIMEMAZINE) (View Alimemazine (alimemazine) Review and Alimemazine (alimemazine) Label ), CHLORPHENIRAMINE MALEATE (View Chlorpheniramine Maleate Review and Chlorpheniramine Maleate Label ), CETIRIZINE (View Cetirizine Review and Cetirizine Label ), DISODIUM CROMOGLYCATE (CROMOGLICATE SODIUM) (View Disodium Cromoglycate (cromoglicate Sodium) Review and Disodium Cromoglycate (cromoglicate Sodium) Label ), KETOTIFEN (KETOTIFEN) (View Ketotifen (ketotifen) Review and Ketotifen (ketotifen) Label ), HYDROCORTISONE (View Hydrocortisone Review and Hydrocortisone Label ), MIDAZOLAM HCL (View Midazolam Hcl Review and Midazolam Hcl Label ).

6139021-X | Dyskinesia
Adverse event was reported on Mar 02, 2009 by a Male patient taking Cimetidine (View Usage) (Dosage: 400 Mg; Twice A Day; Oral) was diagnosed with gastritis, anxiety (What is anxiety?), depression (What is depression?) and. Location: UNITED KINGDOM , 36 years of age, Patient had the following side effects: dyskinesia. During the same period patient was treated with NEFAZODONE HCL (View Nefazodone Hcl Review and Nefazodone Hcl Label ).

6127917-4 | Diarrhoea, Endoscopy Upper Gastrointestinal Tract, Flushing, Hypotonia
on Mar 05, 2009 Female patient from UNITED KINGDOM , child 3 years of age, was treated with Cimetidine (View Usage). After Cimetidine was administered, patient had the following side effects: diarrhoea, endoscopy upper gastrointestinal tract, flushing, hypotonia. Cimetidine dosage: . During the same period patient was treated with EPINEPHRINE (View Epinephrine Review and Epinephrine Label ), ALIMEMAZINE (ALIMEMAZINE) (View Alimemazine (alimemazine) Review and Alimemazine (alimemazine) Label ), CHLORPHENIRAMINE MALEATE (View Chlorpheniramine Maleate Review and Chlorpheniramine Maleate Label ), CETIRIZINE HCL (View Cetirizine Hcl Review and Cetirizine Hcl Label ), DISODIUM CROMOGLYCATE (CROMOGLICATE SODIUM) (View Disodium Cromoglycate (cromoglicate Sodium) Review and Disodium Cromoglycate (cromoglicate Sodium) Label ), KETOFIEN (KETOFIEN) (View Ketofien (ketofien) Review and Ketofien (ketofien) Label ), HYDROCORTISONE (View Hydrocortisone Review and Hydrocortisone Label ), MIDAZOLAM HCL (View Midazolam Hcl Review and Midazolam Hcl Label ).

6127247-0 | Dyskinesia
on Mar 02, 2009 Male patient from UNITED KINGDOM , 36 years of age, was diagnosed with gastritis, anxiety (What is anxiety?), depression (What is depression?) and was treated with Cimetidine (View Usage). Patient experienced the following unwanted or unexpected effects: dyskinesia. Cimetidine dosage: 400 Mg;twice A Day;oral. During the same period patient was treated with NEFAZODONE HCL (View Nefazodone Hcl Review and Nefazodone Hcl Label ).

6108711-7 | Dyskinesia
Patient was taking Cimetidine (View Usage). Patient had the following side effects: dyskinesia on Mar 02, 2009 from UNITED KINGDOM Additional patient health information: Male patient , 36 years of age, was diagnosed with gastritis, anxiety (What is anxiety?), depression (What is depression?) and. Cimetidine dosage: 400 Mg, Bid. During the same period patient was treated with NEFAZODONE HCL (Unk) (View Nefazodone Hcl Review and Nefazodone Hcl Label ).

6025360-X | Leukocyturia, Nausea, Nephritis Allergic, Pyelonephritis Acute, Tubulointerstitial Nephritis
Adverse event was reported on Dec 12, 2008 by a Male patient taking Cimetidine (View Usage) (Dosage: ) . Location: CANADA , 45 years of age, After Cimetidine was administered, patient had the following side effects: leukocyturia, nausea (What is nausea?), nephritis allergic, pyelonephritis acute, tubulointerstitial nephritis. During the same period patient was treated with NAPROXEN (View Naproxen Review and Naproxen Label ).

6021359-8 | Back Pain, Disease Progression, International Normalised Ratio Increased
on Dec 17, 2008 Male patient from FRANCE , 61 years of age, was diagnosed with colon cancer and was treated with Cimetidine (View Usage). Patient experienced the following unwanted or unexpected effects: back pain (What is back pain?), disease progression, international normalised ratio increased. Cimetidine dosage: . During the same period patient was treated with ENZASTAURIN (375mg Twice Per Day) (View Enzastaurin Review and Enzastaurin Label ), PREVISCAN (View Previscan Review and Previscan Label ), FRAXODI (View Fraxodi Review and Fraxodi Label ), PARACETAMOL (View Paracetamol Review and Paracetamol Label ), TRAMADOL (View Tramadol Review and Tramadol Label ), KLIPAL (View Klipal Review and Klipal Label ). Patient was hospitalized.

5989768-0 | Alopecia, Cough, Myalgia
on Nov 24, 2008 Female patient from UNITED KINGDOM , 63 years of age, was diagnosed with cystitis interstitial and was treated with Cimetidine (View Usage). Patient had the following side effects: alopecia, cough, myalgia. Cimetidine dosage: 400 Mg; Daily; Oral. During the same period patient was treated with CALCIUM (View Calcium Review and Calcium Label ), COD LIVER OIL (View Cod Liver Oil Review and Cod Liver Oil Label ), SILICA (View Silica Review and Silica Label ), VITAMIN D (View Vitamin D Review and Vitamin D Label ).

5968222-6 | Alopecia, Cough, Myalgia
Patient was taking Cimetidine (View Usage). After Cimetidine was administered, patient had the following side effects: alopecia, cough, myalgia on Nov 19, 2008 from UNITED KINGDOM Additional patient health information: Female patient , 63 years of age, was diagnosed with cystitis interstitial and. Cimetidine dosage: 400mg Per Day. During the same period patient was treated with CALCIUM (View Calcium Review and Calcium Label ), COD LIVER OIL (View Cod Liver Oil Review and Cod Liver Oil Label ), VITAMIN D (View Vitamin D Review and Vitamin D Label ), SILICA (View Silica Review and Silica Label ).

5959832-0 | Back Pain, International Normalised Ratio Increased
Adverse event was reported on Nov 13, 2008 by a Male patient taking Cimetidine (View Usage) (Dosage: ) was diagnosed with colon cancer and. Location: FRANCE , 61 years of age, Patient experienced the following unwanted or unexpected effects: back pain (What is back pain?), international normalised ratio increased. During the same period patient was treated with ENZASTAURIN (375mg Twice Per Day) (View Enzastaurin Review and Enzastaurin Label ), PREVISCAN (View Previscan Review and Previscan Label ), FRAXODI (View Fraxodi Review and Fraxodi Label ). Patient was hospitalized.

5924906-7 | Erythema, Infusion Related Reaction, Rash, Vasculitis
on Oct 17, 2008 Female patient from UNITED STATES , 56 years of age, weighting 108.0 lb, was diagnosed with nausea (What is nausea?) and was treated with Cimetidine (View Usage). Patient had the following side effects: erythema, infusion related reaction, rash (What is rash?), vasculitis (What is vasculitis?). Cimetidine dosage: 300 Mg Once Iv. During the same period patient was treated with DEXAMETHASONE (View Dexamethasone Review and Dexamethasone Label ), DIPHENHYDRAMINE HCL (View Diphenhydramine Hcl Review and Diphenhydramine Hcl Label ), LORAZEPAM (View Lorazepam Review and Lorazepam Label ), PACLITAXEL (View Paclitaxel Review and Paclitaxel Label ).

5924874-8 | Erythema, Infusion Related Reaction, Vasculitis
on Oct 17, 2008 Female patient from UNITED STATES , 65 years of age, weighting 120.0 lb, was diagnosed with nausea (What is nausea?) and was treated with Cimetidine (View Usage). After Cimetidine was administered, patient had the following side effects: erythema, infusion related reaction, vasculitis (What is vasculitis?). Cimetidine dosage: 300 Mg Once Iv. During the same period patient was treated with DEXAMETHASONE (View Dexamethasone Review and Dexamethasone Label ), DIPHENHYDRAMINE HCL (View Diphenhydramine Hcl Review and Diphenhydramine Hcl Label ), PACLITAXEL (View Paclitaxel Review and Paclitaxel Label ), CARBOPLATIN (View Carboplatin Review and Carboplatin Label ), PALONOSETRON (View Palonosetron Review and Palonosetron Label ).

5919396-4 | Back Pain, International Normalised Ratio Increased
Patient was taking Cimetidine (View Usage). Patient experienced the following unwanted or unexpected effects: back pain (What is back pain?), international normalised ratio increased on Oct 08, 2008 from FRANCE Additional patient health information: Male patient , 61 years of age, was diagnosed with colon cancer and. Cimetidine dosage: 400mg Twice Per Day. During the same period patient was treated with ENZASTAURIN (375mg Twice Per Day) (View Enzastaurin Review and Enzastaurin Label ), PREVISCAN (View Previscan Review and Previscan Label ). Patient was hospitalized.

5758594-X |
Adverse event was reported on May 27, 2008 by a Male patient taking Cimetidine (View Usage) (Dosage: 400mg Single Dose) was diagnosed with bile duct cancer, phlebitis and. Location: FRANCE , 59 years of age, . During the same period patient was treated with ENZASTAURIN (250mg Twice Per Day) (View Enzastaurin Review and Enzastaurin Label ), OXYCONTIN (View Oxycontin Review and Oxycontin Label ), OXYNORM (View Oxynorm Review and Oxynorm Label ), NEXIUM (View Nexium Review and Nexium Label ), INNOHEP (View Innohep Review and Innohep Label ), SUCRALFATE (View Sucralfate Review and Sucralfate Label ), LASILIX (View Lasilix Review and Lasilix Label ), DAFLON (View Daflon Review and Daflon Label ).

5739174-9 |
on May 12, 2008 Male patient from FRANCE , 59 years of age, was diagnosed with bile duct cancer, phlebitis and was treated with Cimetidine (View Usage). . Cimetidine dosage: 400mg Single Dose. During the same period patient was treated with OXYCONTIN (View Oxycontin Review and Oxycontin Label ), OXYNORM (View Oxynorm Review and Oxynorm Label ), NEXIUM (View Nexium Review and Nexium Label ), INNOHEP (View Innohep Review and Innohep Label ), SUCRALFATE (View Sucralfate Review and Sucralfate Label ), LASILIX (View Lasilix Review and Lasilix Label ), DAFLON (View Daflon Review and Daflon Label ).

5670151-2 | Antidiuretic Hormone Abnormality, Inappropriate Antidiuretic Hormone Secretion
on Feb 29, 2008 Female patient from UNITED KINGDOM , 44 years of age, weighting 56.00 lb, was diagnosed with dyspepsia and was treated with Cimetidine (View Usage). Patient experienced the following unwanted or unexpected effects: antidiuretic hormone abnormality, inappropriate antidiuretic hormone secretion. Cimetidine dosage: 400 Mg, Bid, Oral. During the same period patient was treated with LISINOPRIL (View Lisinopril Review and Lisinopril Label ), LORATADINE (View Loratadine Review and Loratadine Label ).

5663141-7 | Skin Reaction
Patient was taking Cimetidine (View Usage). Patient had the following side effects: skin reaction on Mar 12, 2008 from UNITED KINGDOM Additional patient health information: Female patient , 64 years of age, weighting 192.7 lb, was diagnosed with duodenal ulcer, metastatic renal cell carcinoma, pain (What is pain?) and. Cimetidine dosage: 800mg Per Day. During the same period patient was treated with SORAFENIB (400mg Per Day) (View Sorafenib Review and Sorafenib Label ), CO CODAMOL (View Co-codamol Review and Co-codamol Label ).

5647020-7 | Antidiuretic Hormone Abnormality
Adverse event was reported on Feb 29, 2008 by a Female patient taking Cimetidine (View Usage) (Dosage: 800mg Per Day) was diagnosed with dyspepsia, hypertension and. Location: UNITED KINGDOM , 44 years of age, weighting 123.5 lb, After Cimetidine was administered, patient had the following side effects: antidiuretic hormone abnormality. During the same period patient was treated with LISINOPRIL (View Lisinopril Review and Lisinopril Label ), LORATADINE (View Loratadine Review and Loratadine Label ).

5583123-3 | Abdominal Pain, Diarrhoea
on Aug 16, 2007 Male patient from UNITED STATES , 20 years of age, was treated with Cimetidine (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal pain (What is abdominal pain?), diarrhoea. Cimetidine dosage: 300mg Per Day.

5583122-1 | Constipation
on Jun 29, 2007 Female patient from UNITED STATES , 80 years of age, was diagnosed with prophylaxis and was treated with Cimetidine (View Usage). Patient had the following side effects: constipation (What is constipation?). Cimetidine dosage: 300mg Per Day. During the same period patient was treated with NAPROSYN (View Naprosyn Review and Naprosyn Label ).

5583119-1 | Dyspepsia
Patient was taking Cimetidine (View Usage). After Cimetidine was administered, patient had the following side effects: dyspepsia on Apr 16, 2007 from UNITED STATES Additional patient health information: Female patient , 54 years of age, was diagnosed with gastric ulcer and. Cimetidine dosage: 400mg Three Times Per Day. During the same period patient was treated with ESGIC PLUS (View Esgic-plus Review and Esgic-plus Label ).

5583117-8 | Stomach Discomfort
Adverse event was reported on Mar 12, 2007 by a Male patient taking Cimetidine (View Usage) (Dosage: 300mg Four Times Per Day) . Location: UNITED STATES , 69 years of age, Patient experienced the following unwanted or unexpected effects: stomach discomfort. During the same period patient was treated with DONNATAL (View Donnatal Review and Donnatal Label ).

5542613-X | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Alkaline Phosphatase Increased
on Dec 05, 2007 Female patient from UNITED STATES , 56 years of age, weighting 116.0 lb, was treated with Cimetidine (View Usage). Patient had the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood alkaline phosphatase increased. Cimetidine dosage: 800mg Po Bid. During the same period patient was treated with LITHIUM CARBONATE (View Lithium Carbonate Review and Lithium Carbonate Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), ESTRADIOL (View Estradiol Review and Estradiol Label ), M.V.I. (View M.v.i. Review and M.v.i. Label ).

5532998-2 | Constipation, Dry Mouth, Gastric Haemorrhage, Tremor
on Nov 27, 2007 Female patient from UNITED STATES , 80 years of age, was treated with Cimetidine (View Usage). After Cimetidine was administered, patient had the following side effects: constipation (What is constipation?), dry mouth, gastric haemorrhage, tremor. Cimetidine dosage: . During the same period patient was treated with TEKTURNA (150 Mg, Bid) (View Tekturna Review and Tekturna Label ).

5451978-9 | Balance Disorder, Dizziness, Transient Ischaemic Attack
Patient was taking Cimetidine (View Usage). Patient experienced the following unwanted or unexpected effects: balance disorder, dizziness (What is dizziness?), transient ischaemic attack on Sep 06, 2007 from UNITED KINGDOM Additional patient health information: Female patient , 68 years of age, weighting 138.9 lb, was diagnosed with dyspepsia and. Cimetidine dosage: Bid, Oral. During the same period patient was treated with DIFTAVAX(DIPHTHERIA AND TETANUS TOXOIDS) (View Diftavax(diphtheria And Tetanus Toxoids) Review and Diftavax(diphtheria And Tetanus Toxoids) Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), RANITIDINE (View Ranitidine Review and Ranitidine Label ), CINNARIZINE (View Cinnarizine Review and Cinnarizine Label ), PEPTAC(CALCIUM CARBONATE, SODIUM ALGINATE, SODIUM BICARBONATE) (View Peptac(calcium Carbonate, Sodium Alginate, Sodium Bicarbonate) Review and Peptac(calcium Carbonate, Sodium Alginate, Sodium Bicarbonate) Label ).

5160246-4 | Diarrhoea, Gastrooesophageal Reflux Disease, Hyperchlorhydria, Pruritus, Vomiting
Adverse event was reported on Nov 01, 2006 by a Female patient taking Cimetidine (View Usage) (Dosage: 400mg Single Dose) . Location: UNITED STATES , 56 years of age, weighting 120.2 lb, Patient had the following side effects: diarrhoea, gastrooesophageal reflux disease, hyperchlorhydria, pruritus, vomiting. During the same period patient was treated with TAGAMET (View Tagamet Review and Tagamet Label ).

5025040-3 | Chest Discomfort, Diarrhoea, Feeling Abnormal, Feeling Cold, Hallucination, Headache, Heart Rate Increased, Middle Insomnia, Muscle Spasms
on Jun 08, 2006 Male patient from UNITED STATES , 65 years of age, weighting 159.0 lb, was diagnosed with gastrooesophageal reflux disease and was treated with Cimetidine (View Usage). After Cimetidine was administered, patient had the following side effects: chest discomfort, diarrhoea, feeling abnormal, feeling cold, hallucination, headache (What is headache?), heart rate increased, middle insomnia, muscle spasms. Cimetidine dosage: Used 200 Mg Once At Night Mouth. During the same period patient was treated with NIZATIDINE (AXID) (View Nizatidine (axid) Review and Nizatidine (axid) Label ), RANITIDINE (View Ranitidine Review and Ranitidine Label ).

4968196-0 | Antineutrophil Cytoplasmic Antibody Increased, Blood Alkaline Phosphatase Increased, Blood Immunoglobulin E Increased, Blood Immunoglobulin G Increased, Complement Factor Decreased, Hypertension, Kidney Fibrosis, Lymphocyte Stimulation Test Positive, Pyrexia
on Mar 29, 2006 Male patient from JAPAN , 75 years of age, was diagnosed with gastrointestinal disorder and was treated with Cimetidine (View Usage). Patient experienced the following unwanted or unexpected effects: antineutrophil cytoplasmic antibody increased, blood alkaline phosphatase increased, blood immunoglobulin e increased, blood immunoglobulin g increased, complement factor decreased, hypertension, kidney fibrosis, lymphocyte stimulation test positive, pyrexia. Cimetidine dosage: 800 Mg /day Po. During the same period patient was treated with LOXOPROFEN SODIUM (View Loxoprofen Sodium Review and Loxoprofen Sodium Label ), RABEPRAZOLE SODIUM (View Rabeprazole Sodium Review and Rabeprazole Sodium Label ), FAMOTIDINE (View Famotidine Review and Famotidine Label ), ACETAMINOPHEN (View Acetaminophen Review and Acetaminophen Label ). Patient was hospitalized.

4870759-8 | Cardiac Failure, Pneumonia, Toxic Epidermal Necrolysis
Patient was taking Cimetidine (View Usage). Patient had the following side effects: cardiac failure, pneumonia (What is pneumonia?), toxic epidermal necrolysis on Dec 19, 2005 from UNITED KINGDOM Additional patient health information: Male patient , 85 years of age, was diagnosed with gastritis erosive, cardiac failure and. Cimetidine dosage: 400 Mg, Bid, Oral. During the same period patient was treated with FUROSEMIDE (40 Mg, Qd, Oral) (View Furosemide Review and Furosemide Label ), FERROUS SULPHATE (FERROUS SULFATE) (View Ferrous Sulphate (ferrous Sulfate) Review and Ferrous Sulphate (ferrous Sulfate) Label ), LEVOTHYROXINE SODIUM (View Levothyroxine Sodium Review and Levothyroxine Sodium Label ). Patient was hospitalized and became disabled.

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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 Cimetidine 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 Cimetidine quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Cimetidine 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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Cimetidine can inhibit the metabolism of chloroquine, increasing its plasma level. Concomitant use of cimetidine should be avoided. Ampicillin

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Cimetidine Reactions
Abdominal PainWhat is Abdominal pain?
Agitation
Alanine Aminotransferase Increased
Alopecia
Anaemia
Antidiuretic Hormone Abnormality
Asthenia
Back PainWhat is Back pain?
Confusional State
Crying
Death
Depressed Level Of Consciousness
Depressed Mood
Diarrhoea
DizzinessWhat is Dizziness?
Dry Mouth
Dysarthria
Dyskinesia
Dyspepsia
Hallucination
Impaired Healing
International Normalised Ratio Increased
Intra-abdominal Haematoma
Lactic Acidosis
NauseaWhat is Nausea?
Off Label Use
Pancreatitis Acute
PneumoniaWhat is Pneumonia?
Toxic Epidermal Necrolysis
Vomiting
Cimetidine 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 Cimetidine 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!