RANITIDINE Side Effects

6995149-3 | Anaemia, Haemorrhage
on Sep 07, 2010 Female patient from UNITED STATES , 50 years of age, was treated with Ranitidine (View Usage). Patient experienced the following unwanted or unexpected effects: anaemia, haemorrhage. Ranitidine dosage: 150 Mg, Two Tabs 4-5 Times A Day.

6992864-2 | Abdominal Pain, Anaphylactic Reaction, Angioedema, Dizziness, Dyspnoea, Face Oedema, Hypotension, Pruritus, Rash
Patient was taking Ranitidine (View Usage). Patient had the following side effects: abdominal pain (What is abdominal pain?), anaphylactic reaction, angioedema, dizziness (What is dizziness?), dyspnoea, face oedema, hypotension, pruritus, rash (What is rash?) on Sep 08, 2010 from KOREA, REPUBLIC OF Additional patient health information: Male patient , 56 years of age, . Ranitidine dosage: 150mg Per Day. During the same period patient was treated with PINAVERIUM (50mg Per Day) (View Pinaverium Review and Pinaverium Label ).

6978688-0 | Depressed Level Of Consciousness, Oxygen Saturation Decreased
Adverse event was reported on Aug 31, 2010 by a Male patient taking Ranitidine (View Usage) (Dosage: ) was diagnosed with non-small cell lung cancer and. Location: CANADA , 76 years of age, weighting 180.3 lb, After Ranitidine was administered, patient had the following side effects: depressed level of consciousness, oxygen saturation decreased. During the same period patient was treated with ZOFRAN (View Zofran Review and Zofran Label ), PACLITAXEL (200mgm2 Every 3 Weeks) (View Paclitaxel Review and Paclitaxel Label ), FENTANYL CITRATE (View Fentanyl Citrate Review and Fentanyl Citrate Label ), DILAUDID (View Dilaudid Review and Dilaudid Label ), DECADRON (View Decadron Review and Decadron Label ), BENADRYL (View Benadryl Review and Benadryl Label ), GABAPENTIN (View Gabapentin Review and Gabapentin Label ), METOPROLOL TARTRATE (View Metoprolol Tartrate Review and Metoprolol Tartrate Label ). Patient was hospitalized.

6978035-4 | Chest Pain, Dyspnoea, Heart Rate Increased
on Aug 27, 2010 Female patient from UNITED KINGDOM , 23 years of age, weighting 127.9 lb, was diagnosed with hyperchlorhydria and was treated with Ranitidine (View Usage). Patient experienced the following unwanted or unexpected effects: chest pain (What is chest pain?), dyspnoea, heart rate increased. Ranitidine dosage: 150 Mg, Unk.


6973572-0 | Chest Pain, Dyspnoea, Heart Rate Increased
on Aug 27, 2010 Female patient from UNITED KINGDOM , 23 years of age, weighting 127.9 lb, was diagnosed with hyperchlorhydria and was treated with Ranitidine (View Usage). Patient had the following side effects: chest pain (What is chest pain?), dyspnoea, heart rate increased. Ranitidine dosage: .

6973559-8 | Chest Pain, Dyspnoea, Heart Rate Increased
Patient was taking Ranitidine (View Usage). After Ranitidine was administered, patient had the following side effects: chest pain (What is chest pain?), dyspnoea, heart rate increased on Aug 30, 2010 from Additional patient health information: Female patient , 23 years of age, weighting 61.73 lb, was diagnosed with hyperchlorhydria and. Ranitidine dosage: 150mg, Daily, Oral.

6972924-2 | Ballismus
Adverse event was reported on Aug 27, 2010 by a Male patient taking Ranitidine (View Usage) (Dosage: Unk) was diagnosed with abdominal discomfort and. Location: NETHERLANDS , 17 years of age, Patient experienced the following unwanted or unexpected effects: ballismus.

6971731-4 | Chest Pain, Dyspnoea, Heart Rate Increased
on Aug 27, 2010 Female patient from DENMARK , 23 years of age, was diagnosed with hyperchlorhydria and was treated with Ranitidine (View Usage). Patient had the following side effects: chest pain (What is chest pain?), dyspnoea, heart rate increased. Ranitidine dosage: 150 Mg; Po. During the same period patient was treated with CON MEDS (View Con Meds Review and Con Meds Label ), PREV MEDS (View Prev Meds Review and Prev Meds Label ).

6967283-5 | Chest Pain, Gastrooesophageal Reflux Disease
on Aug 25, 2010 Female patient from UNITED KINGDOM , 87 years of age, was diagnosed with gastrooesophageal reflux disease and was treated with Ranitidine (View Usage). After Ranitidine was administered, patient had the following side effects: chest pain (What is chest pain?), gastrooesophageal reflux disease. Ranitidine dosage: 150 Mg; Bid; Po. During the same period patient was treated with DIGOXIN (View Digoxin Review and Digoxin Label ), FOLIC ACID (View Folic Acid Review and Folic Acid Label ), FUROSEMIDE (View Furosemide Review and Furosemide Label ), LISINOPRIL (View Lisinopril Review and Lisinopril Label ).

6965487-9 | Abdominal Pain, Anaphylactic Reaction, Angioedema, Dizziness, Face Oedema, Hypotension, Skin Test Positive, Urticaria
Patient was taking Ranitidine (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal pain (What is abdominal pain?), anaphylactic reaction, angioedema, dizziness (What is dizziness?), face oedema, hypotension, skin test positive, urticaria on Aug 30, 2010 from KOREA, REPUBLIC OF Additional patient health information: Male patient , 56 years of age, . Ranitidine dosage: .

6956432-0 | Chest Pain, Dyspnoea, Heart Rate Increased
Adverse event was reported on Aug 27, 2010 by a Female patient taking Ranitidine (View Usage) (Dosage: ) . Location: UNITED KINGDOM , 23 years of age, weighting 127.9 lb, Patient had the following side effects: chest pain (What is chest pain?), dyspnoea, heart rate increased.

6942578-X | Circulatory Collapse, Loss Of Consciousness, Pulse Absent, Torsade De Pointes
on Aug 17, 2010 Female patient from , 36 years of age, was diagnosed with gastrooesophageal reflux disease, dyspepsia, abdominal wall haematoma, abdominal wall infection, torsade de pointes and was treated with Ranitidine (View Usage). After Ranitidine was administered, patient had the following side effects: circulatory collapse, loss of consciousness, pulse absent, torsade de pointes. Ranitidine dosage: 300 Mg. During the same period patient was treated with CISAPRIDE (30 Mg) (View Cisapride Review and Cisapride Label ), METRONIDAZOLE (View Metronidazole Review and Metronidazole Label ), AMIODARONE (View Amiodarone Review and Amiodarone Label ), LOPERAMIDE (View Loperamide Review and Loperamide Label ), NITROFURANTOIN (View Nitrofurantoin Review and Nitrofurantoin Label ).

6938173-9 | Anaphylactic Reaction, Skin Test Positive
on Aug 05, 2010 Female patient from SPAIN , 36 years of age, was diagnosed with dyspepsia and was treated with Ranitidine (View Usage). Patient experienced the following unwanted or unexpected effects: anaphylactic reaction, skin test positive. Ranitidine dosage: 300 Mg; 1x; Po. During the same period patient was treated with IBUPROFEN (600 Mg;1x; Po) (View Ibuprofen Review and Ibuprofen Label ).

6936079-2 | Dysgeusia
Patient was taking Ranitidine (View Usage). Patient had the following side effects: dysgeusia on Aug 05, 2010 from DENMARK Additional patient health information: Male patient , 66 years of age, was diagnosed with dyspepsia and. Ranitidine dosage: 150 Mg Unk Po.

6933734-5 | Product Taste Abnormal
Adverse event was reported on Aug 05, 2010 by a Male patient taking Ranitidine (View Usage) (Dosage: 150mg, Oral) was diagnosed with dyspepsia and. Location: , 66 years of age, After Ranitidine was administered, patient had the following side effects: product taste abnormal.

6933014-8 | Fatigue, Headache, Pain, Product Odour Abnormal
on Aug 18, 2010 Female patient from UNITED STATES , 54 years of age, weighting 130.0 lb, was diagnosed with hyperchlorhydria and was treated with Ranitidine (View Usage). Patient experienced the following unwanted or unexpected effects: fatigue, headache (What is headache?), pain (What is pain?), product odour abnormal. Ranitidine dosage: 1 Tablet Twice A Day Po.

6932831-8 | Disease Recurrence, Dysgeusia
on Aug 05, 2010 Male patient from UNITED KINGDOM , 66 years of age, was diagnosed with dyspepsia and was treated with Ranitidine (View Usage). Patient had the following side effects: disease recurrence, dysgeusia. Ranitidine dosage: .

6931511-2 | Disease Recurrence, Dysgeusia
Patient was taking Ranitidine (View Usage). After Ranitidine was administered, patient had the following side effects: disease recurrence, dysgeusia on Aug 05, 2010 from UNITED KINGDOM Additional patient health information: Male patient , 66 years of age, was diagnosed with dyspepsia and. Ranitidine dosage: 150 Mg, Unk.

6928947-2 | Cardiac Arrest
Adverse event was reported on Aug 03, 2010 by a Female patient taking Ranitidine (View Usage) (Dosage: ) was diagnosed with prophylaxis, epidural anaesthesia and. Location: UNITED KINGDOM , 20 years of age, weighting 143.3 lb, Patient experienced the following unwanted or unexpected effects: cardiac arrest (What is cardiac arrest?). During the same period patient was treated with FENTANYL (View Fentanyl Review and Fentanyl Label ), METOCLOPRAMIDE (View Metoclopramide Review and Metoclopramide Label ), BUPIVACAINE HCL (View Bupivacaine Hcl Review and Bupivacaine Hcl Label ), ISOFLURANE (View Isoflurane Review and Isoflurane Label ), LIDOCAINE (View Lidocaine Review and Lidocaine Label ), OXYTOCIN (View Oxytocin Review and Oxytocin Label ).

6928945-9 | Cardiac Arrest
on Aug 03, 2010 Female patient from UNITED KINGDOM , 20 years of age, weighting 143.3 lb, was diagnosed with prophylaxis, epidural anaesthesia and was treated with Ranitidine (View Usage). Patient had the following side effects: cardiac arrest (What is cardiac arrest?). Ranitidine dosage: . During the same period patient was treated with FENTANYL (View Fentanyl Review and Fentanyl Label ), METOCLOPRAMIDE (View Metoclopramide Review and Metoclopramide Label ), BUPIVACAINE HCL (View Bupivacaine Hcl Review and Bupivacaine Hcl Label ), ISOFLURANE (View Isoflurane Review and Isoflurane Label ), LIDOCAINE (View Lidocaine Review and Lidocaine Label ), OXYTOCIN (View Oxytocin Review and Oxytocin Label ).

6923683-0 | Disease Recurrence, Dysgeusia
on Aug 05, 2010 Male patient from UNITED KINGDOM , 66 years of age, was treated with Ranitidine (View Usage). After Ranitidine was administered, patient had the following side effects: disease recurrence, dysgeusia. Ranitidine dosage: .

6922221-6 | Dermatitis Contact
Patient was taking Ranitidine (View Usage). Patient experienced the following unwanted or unexpected effects: dermatitis contact on Jul 29, 2010 from BELGIUM Additional patient health information: Female patient , 59 years of age, . Ranitidine dosage: . During the same period patient was treated with MYOLASTAN (View Myolastan Review and Myolastan Label ), STILNOCT (View Stilnoct Review and Stilnoct Label ), CYCLOHEXYLTHIOPHTALIMIDE (View Cyclohexylthiophtalimide Review and Cyclohexylthiophtalimide Label ).

6880616-3 | Dyspepsia, Nausea
Adverse event was reported on Jan 22, 2010 by a Female patient taking Ranitidine (View Usage) (Dosage: 300mg Twice Per Day) . Location: UNITED STATES , 80 years of age, Patient had the following side effects: dyspepsia, nausea (What is nausea?). During the same period patient was treated with ZANTAC (View Zantac Review and Zantac Label ), PRILOSEC (View Prilosec Review and Prilosec Label ), PLAVIX (View Plavix Review and Plavix Label ).

6880611-4 | Nausea
on Dec 30, 2009 Female patient from UNITED STATES , 46 years of age, was treated with Ranitidine (View Usage). After Ranitidine was administered, patient had the following side effects: nausea (What is nausea?). Ranitidine dosage: 75mg Three Times Per Day. During the same period patient was treated with ZANTAC (View Zantac Review and Zantac Label ).

6880588-1 | Abdominal Pain Upper, Agitation, Confusional State, Nervousness, Stress
on Sep 03, 2009 Female patient from UNITED STATES , 48 years of age, was treated with Ranitidine (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal pain upper, agitation, confusional state, nervousness, stress (What is stress?). Ranitidine dosage: 150mg Twice Per Day.

6874967-6 | Angioedema, Pruritus
Patient was taking Ranitidine (View Usage). Patient had the following side effects: angioedema, pruritus on Jul 13, 2010 from DENMARK Additional patient health information: Female patient , 85 years of age, . Ranitidine dosage: 150 Mg;bid;po. During the same period patient was treated with CLOPIDOGREL BISULFATE (View Clopidogrel Bisulfate Review and Clopidogrel Bisulfate Label ), STRONTIUM RANELATE (View Strontium Ranelate Review and Strontium Ranelate Label ), VITAMIN TAB (View Vitamin Tab Review and Vitamin Tab Label ), LOSARTAN (View Losartan Review and Losartan Label ), PAROXETINE HCL (View Paroxetine Hcl Review and Paroxetine Hcl Label ), PROPRANOLOL (View Propranolol Review and Propranolol Label ), CALCICHEW (View Calcichew Review and Calcichew Label ). Patient was hospitalized.

6866321-8 | Blood Pressure Immeasurable, Cyanosis, Flushing, Hypersensitivity, Peripheral Circulatory Failure, Pruritus, Pulse Absent
Adverse event was reported on Jul 08, 2010 by a Female patient taking Ranitidine (View Usage) (Dosage: 50 Mg, Unk) . Location: GERMANY , 58 years of age, weighting 119.0 lb, After Ranitidine was administered, patient had the following side effects: blood pressure immeasurable, cyanosis, flushing, hypersensitivity, peripheral circulatory failure, pruritus, pulse absent. During the same period patient was treated with CLEMASTINE FUMARATE (2 Mg, Unk) (View Clemastine Fumarate Review and Clemastine Fumarate Label ). Patient was hospitalized.

6859960-1 | Abdominal Discomfort, Nausea, Product Quality Issue, Product Taste Abnormal, Tooth Disorder, Unevaluable Event
on Jul 19, 2010 Male patient from UNITED STATES , 48 years of age, weighting 209.0 lb, was treated with Ranitidine (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal discomfort, nausea (What is nausea?), product quality issue, product taste abnormal, tooth disorder (What is tooth disorder?), unevaluable event. Ranitidine dosage: .

6803618-1 | Bronchospasm, Cough
on Jun 07, 2010 Female patient from MALAYSIA , 70 years of age, was diagnosed with cardiomyopathy (What is cardiomyopathy?) and was treated with Ranitidine (View Usage). Patient had the following side effects: bronchospasm, cough. Ranitidine dosage: . During the same period patient was treated with CARBIMAZOLE (View Carbimazole Review and Carbimazole Label ), FRUSEMIDE (View Frusemide Review and Frusemide Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), AMLODIPINE (View Amlodipine Review and Amlodipine Label ), COVERSYL 2 MG TABLET (Daily Dose: 2 Milligram(s)) (View Coversyl 2 Mg Tablet Review and Coversyl 2 Mg Tablet Label ).

6797357-3 | Abdominal Pain Upper, Finger Deformity, Hypokinesia, Inflammation, Malaise, Muscle Spasms, Muscle Twitching, Muscular Weakness, Nerve Injury
Patient was taking Ranitidine (View Usage). After Ranitidine was administered, patient had the following side effects: abdominal pain upper, finger deformity, hypokinesia, inflammation, malaise, muscle spasms, muscle twitching, muscular weakness, nerve injury on Jun 08, 2010 from UNITED STATES Additional patient health information: Female patient , 61 years of age, was diagnosed with hyperchlorhydria and. Ranitidine dosage: . During the same period patient was treated with CITALOPRAM HYDROBROMIDE (View Citalopram Hydrobromide Review and Citalopram Hydrobromide Label ), ATENOLOL (View Atenolol Review and Atenolol Label ), ADVAIR DISKUS 100/50 (View Advair Diskus 100/50 Review and Advair Diskus 100/50 Label ), PACIMOL (PARACETAMOL) EYE DROPS (View Pacimol (paracetamol) Eye Drops Review and Pacimol (paracetamol) Eye Drops Label ), SINGULAIR (View Singulair Review and Singulair Label ).

6790907-2 | Hypotension, Stevens-johnson Syndrome
Adverse event was reported on Jun 22, 2010 by a Male patient taking Ranitidine (View Usage) (Dosage: 300mg Per Day) . Location: UNITED KINGDOM , 56 years of age, Patient experienced the following unwanted or unexpected effects: hypotension, stevens-johnson syndrome. During the same period patient was treated with INDAPAMIDE (View Indapamide Review and Indapamide Label ), PERINDOPRIL (View Perindopril Review and Perindopril Label ), ATORVASTATIN (View Atorvastatin Review and Atorvastatin Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), EZETIMIBE (View Ezetimibe Review and Ezetimibe Label ), GLUCOSAMINE (View Glucosamine Review and Glucosamine Label ), NITROGLYCERIN (View Nitroglycerin Review and Nitroglycerin Label ). Patient was hospitalized.

6767907-1 | Abdominal Pain, Angioedema, Bronchial Obstruction, Loss Of Consciousness, Urticaria
on Jun 01, 2010 Male patient from GERMANY , 31 years of age, was diagnosed with duodenal ulcer and was treated with Ranitidine (View Usage). Patient had the following side effects: abdominal pain (What is abdominal pain?), angioedema, bronchial obstruction, loss of consciousness, urticaria. Ranitidine dosage: Oral. Patient was hospitalized.

6765386-1 | Hypersensitivity, Jaundice, Pruritus
on May 28, 2010 Male patient from NORWAY , 29 years of age, was treated with Ranitidine (View Usage). After Ranitidine was administered, patient had the following side effects: hypersensitivity, jaundice (What is jaundice?), pruritus. Ranitidine dosage: .

6755286-5 | Anaphylactic Reaction, Histamine Level Increased, Loss Of Consciousness, Pulse Absent, Respiratory Arrest, Tryptase Increased
Patient was taking Ranitidine (View Usage). Patient experienced the following unwanted or unexpected effects: anaphylactic reaction, histamine level increased, loss of consciousness, pulse absent, respiratory arrest, tryptase increased on May 18, 2010 from FRANCE Additional patient health information: Female patient , 63 years of age, . Ranitidine dosage: Intravenous. During the same period patient was treated with METHYLPREDNISOLONE (METHYLPREDNICOLONE) INJECTION (View Methylprednisolone (methylprednicolone) Injection Review and Methylprednisolone (methylprednicolone) Injection Label ), PACLITAXEL (View Paclitaxel Review and Paclitaxel Label ), CARBOPLATIN (View Carboplatin Review and Carboplatin Label ), GRANISETRON (GRANISETRON) (View Granisetron (granisetron) Review and Granisetron (granisetron) Label ).

6735968-1 | Abdominal Pain, Anaphylactic Reaction, Angioedema, Bronchial Obstruction, Conjunctivitis, Dyspnoea, Erythema, Flushing, Gastrointestinal Pain
Adverse event was reported on May 11, 2010 by a Male patient taking Ranitidine (View Usage) (Dosage: 600mg Per Day) was diagnosed with duodenal ulcer and. Location: GERMANY , 31 years of age, Patient had the following side effects: abdominal pain (What is abdominal pain?), anaphylactic reaction, angioedema, bronchial obstruction, conjunctivitis, dyspnoea, erythema, flushing, gastrointestinal pain. Patient was hospitalized.

6724796-9 | Thrombocytopenia
on May 13, 2010 Male patient from UNITED STATES , 63 years of age, was treated with Ranitidine (View Usage). After Ranitidine was administered, patient had the following side effects: thrombocytopenia. Ranitidine dosage: . Patient was hospitalized.

6696734-9 | Stevens-johnson Syndrome, Toxic Epidermal Necrolysis
on Apr 16, 2010 Female patient from FINLAND , 32 years of age, was diagnosed with pain (What is pain?), placental disorder, erythema multiforme, arthralgia and was treated with Ranitidine (View Usage). Patient experienced the following unwanted or unexpected effects: stevens-johnson syndrome, toxic epidermal necrolysis. Ranitidine dosage: . During the same period patient was treated with ACETYLSALICYLIC ACID (View Acetylsalicylic Acid Review and Acetylsalicylic Acid Label ), METAMIZOLE (View Metamizole Review and Metamizole Label ), CEPHALOSPORIN (Unit Dose: 500 Mg) (View Cephalosporin Review and Cephalosporin Label ), PREDNISOLONE (Dose Was Gradually Reduced To 15 Mg After Delivery) (View Prednisolone Review and Prednisolone Label ). Patient was hospitalized.

6694774-7 | Blister, Condition Aggravated, Cyst, Eating Disorder, Erythema Multiforme, Hypernatraemia, Hypokalaemia, Leukopenia
Patient was taking Ranitidine (View Usage). Patient had the following side effects: blister, condition aggravated, cyst, eating disorder (What is eating disorder?), erythema multiforme, hypernatraemia, hypokalaemia, leukopenia on Apr 16, 2010 from FINLAND Additional patient health information: Female patient , 32 years of age, was diagnosed with arthralgia, pain (What is pain?), thrombosis prophylaxis and. Ranitidine dosage: . During the same period patient was treated with PREDNISOLONE (View Prednisolone Review and Prednisolone Label ), ACETYLSALICYLIC ACID (View Acetylsalicylic Acid Review and Acetylsalicylic Acid Label ), METAMIZOLE (View Metamizole Review and Metamizole Label ), CEPHALOSPORIN (500mg Three Times Per Day) (View Cephalosporin Review and Cephalosporin Label ), IMMUNE GLOBULIN INTRAVENOUS (HUMAN) (.5gk Per Day) (View Immune Globulin Intravenous (human) Review and Immune Globulin Intravenous (human) Label ), FENTANYL (View Fentanyl Review and Fentanyl Label ), OXYCODONE HCL (View Oxycodone Hcl Review and Oxycodone Hcl Label ), DALTEPARIN (View Dalteparin Review and Dalteparin Label ). Patient was hospitalized.

6694351-8 | Finger Deformity, Hypokinesia, Malaise, Muscle Spasms, Muscle Twitching, Muscular Weakness, Product Odour Abnormal, Product Quality Issue, Tremor
Adverse event was reported on Apr 09, 2010 by a Female patient taking Ranitidine (View Usage) (Dosage: ) was diagnosed with hyperchlorhydria and. Location: UNITED STATES , 61 years of age, After Ranitidine was administered, patient had the following side effects: finger deformity, hypokinesia, malaise, muscle spasms, muscle twitching, muscular weakness, product odour abnormal, product quality issue, tremor. During the same period patient was treated with CITALOPRAM HYDROBROMIDE (View Citalopram Hydrobromide Review and Citalopram Hydrobromide Label ), ATENOLOL (View Atenolol Review and Atenolol Label ), ADVAIR DISKUS 100/50 (View Advair Diskus 100/50 Review and Advair Diskus 100/50 Label ), PACIMOL (PARACETAMOL) EYE DROPS (View Pacimol (paracetamol) Eye Drops Review and Pacimol (paracetamol) Eye Drops Label ), SINGULAIR (View Singulair Review and Singulair Label ).

6670924-3 | Dry Mouth
on Apr 06, 2010 Female patient from UNITED STATES , 71 years of age, was diagnosed with gastrooesophageal reflux disease and was treated with Ranitidine (View Usage). Patient experienced the following unwanted or unexpected effects: dry mouth. Ranitidine dosage: 1-2 Tbs Qhs Po. During the same period patient was treated with GABAPENTIN (View Gabapentin Review and Gabapentin Label ).

6641391-0 | Confusional State, Disorientation, Hallucination
on Mar 17, 2010 Male patient from UNITED STATES , 86 years of age, was treated with Ranitidine (View Usage). Patient had the following side effects: confusional state, disorientation, hallucination. Ranitidine dosage: 300 Mg Bid Po. Patient was hospitalized.

6619639-8 | Chest Pain
Patient was taking Ranitidine (View Usage). After Ranitidine was administered, patient had the following side effects: chest pain (What is chest pain?) on Feb 18, 2010 from UNITED KINGDOM Additional patient health information: Male patient , 66 years of age, was diagnosed with dyspepsia and. Ranitidine dosage: 150 Mg;bid. During the same period patient was treated with AMLODIPINE (View Amlodipine Review and Amlodipine Label ), ACETYLSALICYLIC ACID (View Acetylsalicylic Acid Review and Acetylsalicylic Acid Label ).

6616650-8 | Tubulointerstitial Nephritis
Adverse event was reported on Feb 19, 2010 by a Male patient taking Ranitidine (View Usage) (Dosage: ) was diagnosed with antifungal prophylaxis and. Location: , 58 years of age, Patient experienced the following unwanted or unexpected effects: tubulointerstitial nephritis. During the same period patient was treated with TRIMETHOPRIM + SULFAMETHOXAZOLE (View Trimethoprim + Sulfamethoxazole Review and Trimethoprim + Sulfamethoxazole Label ), FRUSEMIDE (View Frusemide Review and Frusemide Label ), TACROLIMUS (View Tacrolimus Review and Tacrolimus Label ), AZATHIOPRINE (View Azathioprine Review and Azathioprine Label ), PREDNISOLONE (View Prednisolone Review and Prednisolone Label ), GENTAMICIN (View Gentamicin Review and Gentamicin Label ), CIPROFLOXACIN (View Ciprofloxacin Review and Ciprofloxacin Label ).

6611247-8 | Hypersensitivity, Inflammation, Lung Disorder, Pain, Rhinorrhoea, Staphylococcal Scalded Skin Syndrome
on Mar 01, 2010 Male patient from UNITED STATES , 76 years of age, weighting 132.9 lb, was diagnosed with gastrointestinal haemorrhage, prophylaxis, immunisation and was treated with Ranitidine (View Usage). Patient had the following side effects: hypersensitivity, inflammation, lung disorder, pain (What is pain?), rhinorrhoea, staphylococcal scalded skin syndrome. Ranitidine dosage: 150 Mg Bid Po. During the same period patient was treated with ZOSTER VACCINE (1 Units Once Sq) (View Zoster Vaccine Review and Zoster Vaccine Label ).

6611172-2 | Blister, Circulatory Collapse, Erythema, Klebsiella Sepsis, Pyrexia, Rash, Simple Partial Seizures, Skin Erosion, Toxic Epidermal Necrolysis
on Feb 17, 2010 Female patient from FRANCE , 62 years of age, was treated with Ranitidine (View Usage). After Ranitidine was administered, patient had the following side effects: blister, circulatory collapse, erythema, klebsiella sepsis, pyrexia, rash (What is rash?), simple partial seizures, skin erosion, toxic epidermal necrolysis. Ranitidine dosage: . During the same period patient was treated with CO TRIMOXAZOLE (View Co-trimoxazole Review and Co-trimoxazole Label ), PHENYTOIN (View Phenytoin Review and Phenytoin Label ).

6611048-0 | Cardiac Failure, Circulatory Collapse, Pyrexia, Respiratory Failure, Toxic Epidermal Necrolysis
Patient was taking Ranitidine (View Usage). Patient experienced the following unwanted or unexpected effects: cardiac failure, circulatory collapse, pyrexia, respiratory failure, toxic epidermal necrolysis on Feb 17, 2010 from FRANCE Additional patient health information: Female patient , 76 years of age, . Ranitidine dosage: Unk. During the same period patient was treated with EPRAZINONE (View Eprazinone Review and Eprazinone Label ), METHOTREXATE (View Methotrexate Review and Methotrexate Label ).

6611047-9 | Anhidrosis, Asthenia, Circulatory Collapse, Dizziness, Hypotonia, Presyncope, Vomiting
Adverse event was reported on Feb 17, 2010 by a Female patient taking Ranitidine (View Usage) (Dosage: ) . Location: FRANCE , 89 years of age, Patient had the following side effects: anhidrosis, asthenia, circulatory collapse, dizziness (What is dizziness?), hypotonia, presyncope, vomiting. During the same period patient was treated with ASPIRIN (View Aspirin Review and Aspirin Label ), MADOPAR (View Madopar Review and Madopar Label ).

6611046-7 | Circulatory Collapse, Peripheral Ischaemia, Sepsis
on Feb 17, 2010 Male patient from FRANCE , 66 years of age, was treated with Ranitidine (View Usage). After Ranitidine was administered, patient had the following side effects: circulatory collapse, peripheral ischaemia, sepsis (What is sepsis?). Ranitidine dosage: 50 Mg, Unk.

6611043-1 | Anaphylactoid Reaction, Bronchospasm, Circulatory Collapse
on Feb 17, 2010 Female patient from FRANCE , 51 years of age, was treated with Ranitidine (View Usage). Patient experienced the following unwanted or unexpected effects: anaphylactoid reaction, bronchospasm, circulatory collapse. Ranitidine dosage: 50 Mg, Unk. Patient was hospitalized.

6604896-4 | Chest Pain
Patient was taking Ranitidine (View Usage). Patient had the following side effects: chest pain (What is chest pain?) on Feb 18, 2010 from UNITED KINGDOM Additional patient health information: Male patient , 66 years of age, . Ranitidine dosage: 300mg Per Day. During the same period patient was treated with AMLODIPINE (10mg Per Day) (View Amlodipine Review and Amlodipine Label ), ASPIRIN (View Aspirin Review and Aspirin Label ).