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This is an index of reports of adverse events (side effects, adverse reactions, etc.) related to Ranitidine. Click on the relevant link below to view a selection of reports according to the event's seriousness level and/or the nature of the side effect / adverse reaction. Or scroll down to view a sample of recent reports further on this page.
Our database includes reports from Jan 2007 to Dec 2007. The information is not vetted and should not be cosidered as verified clinical evidence.
All cases (94)
Cases resulting in a serious event (88)
Cases resulting in death (5)
Cases resulting in life threatening events (13)
Cases resulting in hospitalization (49)
Cases resulting in disability (7)
Cases resulting in other serious reactions (41)
Below is a sample of reports where side effects / adverse reactions may be related to Ranitidine. For a complete list and/or a specific selection of reports, please use the links in the index above.
Adverse event in 56 year old female receiving Ranitidine
Reported by a consumer/non-health professional from United Kingdom on 2007-10-30
Patient: 56 year old female
Adverse reactions / side effects: Cardio-Respiratory Arrest, Anaphylactic Reaction
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Ranitidine
Adverse event in female receiving Ranitidine
Reported by a pharmacist from Germany on 2007-10-29
Patient: female
Adverse reactions / side effects: Dysgeusia, Neurotoxicity, Malaise, Nail Disorder, Abdominal Pain Upper
Suspect drug(s):
Gabapentin
Dosage: text:0.5 tablet
Administration route: Oral
Indication: Neurotoxicity
Carboplatin
Dosage: daily dose:500mg
Indication: Chemotherapy
Paclitaxel
Dosage: daily dose:294mg
Indication: Fallopian Tube Cancer
Start date: 2007-06-20
End date: 2007-10-04
Ranitidine
Indication: Prophylactic Chemotherapy
Start date: 2007-06-20
End date: 2007-10-04
Adverse event in female receiving Ranitidine
Reported by a pharmacist from Germany on 2007-10-26
Patient: female
Adverse reactions / side effects: Neurotoxicity, Dysgeusia, Malaise, Nail Disorder, Abdominal Pain Upper
Suspect drug(s):
Ranitidine
Dosage: see image
Indication: Prophylaxis
Start date: 2007-06-20
End date: 2007-06-20
Ranitidine
Dosage: see image
Indication: Prophylaxis
Start date: 2007-07-11
End date: 2007-07-11
Ranitidine
Dosage: see image
Indication: Prophylaxis
Start date: 2007-08-01
End date: 2007-08-01
Ranitidine
Dosage: see image
Indication: Prophylaxis
Start date: 2007-08-22
End date: 2007-08-22
Ranitidine
Dosage: see image
Indication: Prophylaxis
Start date: 2007-09-12
End date: 2007-09-12
Ranitidine
Dosage: see image
Indication: Prophylaxis
Start date: 2007-10-04
End date: 2007-10-04
Carboplatin
Dosage: see image
Indication: Chemotherapy
Start date: 2007-06-20
End date: 2007-06-20
Carboplatin
Dosage: see image
Indication: Chemotherapy
Start date: 2007-07-11
End date: 2007-07-11
Carboplatin
Dosage: see image
Indication: Chemotherapy
Start date: 2007-08-01
End date: 2007-08-01
Carboplatin
Dosage: see image
Indication: Chemotherapy
Start date: 2007-08-22
End date: 2007-08-22
Carboplatin
Dosage: see image
Indication: Chemotherapy
Start date: 2007-09-12
End date: 2007-09-12
Carboplatin
Dosage: see image
Indication: Chemotherapy
Start date: 2007-10-04
End date: 2007-10-04
Gabapentin
Dosage: oral
Administration route: Oral
Indication: Neurotoxicity
Paclitaxel
Dosage: see image
Indication: Fallopian Tube Cancer
Start date: 2007-06-20
End date: 2007-06-20
Paclitaxel
Dosage: see image
Indication: Fallopian Tube Cancer
Start date: 2007-07-11
End date: 2007-07-11
Paclitaxel
Dosage: see image
Indication: Fallopian Tube Cancer
Start date: 2007-08-01
End date: 2007-08-01
Paclitaxel
Dosage: see image
Indication: Fallopian Tube Cancer
Start date: 2007-08-22
End date: 2007-08-22
Paclitaxel
Dosage: see image
Indication: Fallopian Tube Cancer
Start date: 2007-09-12
End date: 2007-09-12
Paclitaxel
Dosage: see image
Indication: Fallopian Tube Cancer
Start date: 2007-10-04
End date: 2007-10-04
Other drugs received by patient: Sodium Chloride (Sodium Chloride) Solution FOR Infusion, 0.9%; Tropisetron (Tropisetron); Metoclopramide (Metoclopramide)
Adverse event in 16 year old male receiving Ranitidine
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-05
Patient: 16 year old male
Adverse reactions / side effects: Injection Site Erythema, Medication Error
Suspect drug(s):
Ranitidine
Adverse event in 56 year old female receiving Ranitidine
Reported by a pharmacist from Japan on 2007-10-05
Patient: 56 year old female
Adverse reactions / side effects: Anaphylactic Shock
Adverse event resulted in: life threatening event
Suspect drug(s):
Betamethasone Sodium Phosphate
Dosage: 24 mg; qd; iv
Indication: Allergy Prophylaxis
Start date: 2007-07-18
End date: 2007-07-18
Ranitidine
Dosage: 50 m;qd; iv
Start date: 2007-07-18
End date: 2007-07-18
Other drugs received by patient: Taxol; Solita-T; Veen-F
Adverse event in 45 year old male receiving Ranitidine
Reported by a consumer/non-health professional from United Kingdom on 2007-10-02
Patient: 45 year old male
Adverse reactions / side effects: Blood Creatine Phosphokinase Increased, Rhabdomyolysis
Adverse event resulted in: hospitalization
Suspect drug(s):
Flucloxacillin
Indication: Drug USE FOR Unknown Indication
Ranitidine
Indication: Drug USE FOR Unknown Indication
Other drugs received by patient: Ciprofloxacin; Hydrocortisone
Adverse event in 40 year old male receiving Ranitidine
Reported by a consumer/non-health professional from United States on 2007-07-30
Patient: 40 year old male
Adverse reactions / side effects: Drug Screen Positive, Urine Amphetamine Positive
Suspect drug(s):
Ranitidine
Adverse event in 74 year old female receiving Ranitidine
Reported by a consumer/non-health professional from United States on 2007-07-30
Patient: 74 year old female
Adverse reactions / side effects: Drug Ineffective
Suspect drug(s):
Zantac 150
Start date: 2007-01-01
End date: 2007-01-01
Ranitidine
Dosage: 75mg twice per day
Administration route: Oral
Start date: 2007-01-08
End date: 2007-01-23
Adverse event in 48 year old female receiving Ranitidine
Reported by a health professional (non-physician/pharmacist) from Italy on 2007-07-27
Patient: 48 year old female
Adverse reactions / side effects: Creatinine Renal Clearance Increased, Blood Urea, Renal Failure Acute
Adverse event resulted in: hospitalization
Suspect drug(s):
Sevorane
Indication: Drug USE FOR Unknown Indication
Rocuronium Bromide
Indication: Drug USE FOR Unknown Indication
Cefazolin
Indication: Drug USE FOR Unknown Indication
Start date: 2007-05-23
Ranitidine
Indication: Drug USE FOR Unknown Indication
Start date: 2007-05-23
End date: 2007-05-25
Ketorolac Tromethamine
Indication: Drug USE FOR Unknown Indication
Start date: 2007-05-23
End date: 2007-05-25
Tramadol Hydrochloride
Indication: Drug USE FOR Unknown Indication
Start date: 2007-05-23
End date: 2007-05-24
Metoclopramide
Indication: Drug USE FOR Unknown Indication
Start date: 2007-05-23
End date: 2007-05-24
Nadroparine
Indication: Drug USE FOR Unknown Indication
Start date: 2007-05-24
End date: 2007-05-28
Adverse event in 44 year old male receiving Ranitidine
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-07-12
Patient: 44 year old male
Adverse reactions / side effects: Dermatitis Contact
Suspect drug(s):
Ranitidine
Adverse event in receiving Ranitidine
Reported by a individual with unspecified qualification on 2007-07-11
Patient:
Adverse reactions / side effects: Sepsis Neonatal
Suspect drug(s):
Ranitidine
Adverse event in receiving Ranitidine
Reported by a individual with unspecified qualification on 2007-07-11
Patient:
Adverse reactions / side effects: Sepsis Neonatal
Suspect drug(s):
Ranitidine
Adverse event in 15 month old female receiving Ranitidine
Reported by a individual with unspecified qualification on 2007-07-09
Patient: 15 month old female
Adverse reactions / side effects: Pruritus, Cardiac Failure, Drug Ineffective, Acute Respiratory Failure, Disease Progression
Adverse event resulted in: death
Suspect drug(s):
Morphine
Indication: Pain
Ranitidine
Indication: Pruritus
Codeine SUL TAB
Dosage: 1mg/kg
Indication: Pain
Hydromorphone HCL
Indication: Pain
Lorazepam
Dosage: 0.05mg/kg every 6 hours
Indication: Pain
Naloxone
Indication: Pruritus
Tricyclic Antidepressant
Indication: Pruritus
Other drugs received by patient: Paracetamol; Fentanyl; Methotrimeprazine; Diphenhydramine HCL; Anticholinergic
Adverse event in 39 year old female receiving Ranitidine
Reported by a consumer/non-health professional from Spain on 2007-06-29
Patient: 39 year old female
Adverse reactions / side effects: Dyspnoea, Dysphagia, Chest Pain
Adverse event resulted in: hospitalization
Suspect drug(s):
Taxol
Indication: Neoplasm Malignant
Start date: 2006-05-10
End date: 2006-05-10
Cisplatin
Indication: Neoplasm Malignant
Start date: 2006-05-10
End date: 2006-05-10
Ranitidine
Indication: Neoplasm Malignant
Start date: 2006-05-10
End date: 2006-05-10
Adverse event in 17 year old male receiving Ranitidine
Reported by a physician from United States on 2007-06-29
Patient: 17 year old male
Adverse reactions / side effects: Mucosal Inflammation, Bacterial Sepsis, Diverticular Perforation, Gastritis
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Decadron
Administration route: Oral
Pegaspargase
Indication: Acute Lymphocytic Leukaemia
Vincristine Sulfate
Indication: Acute Lymphocytic Leukaemia
Doxorubicin
Indication: Acute Lymphocytic Leukaemia
Ranitidine
Indication: Prophylaxis
Adverse event in 58 year old receiving Ranitidine
Reported by a pharmacist from United States on 2007-06-28
Patient: 58 year old , weighing 65.8 kg (144.7 pounds)
Adverse reactions / side effects: Chest Discomfort, Dyspnoea, Retching, Nausea, Tachycardia, Body Temperature Decreased, Tremor, Feeling Cold, Balance Disorder, Heart Rate Increased, Dizziness, Cold Sweat, Feeling Abnormal
Suspect drug(s):
Ranitidine
Adverse event in female receiving Ranitidine
Reported by a health professional (non-physician/pharmacist) from Sweden on 2007-06-28
Patient: female
Adverse reactions / side effects: Pancytopenia, Rash Maculo-Papular
Adverse event resulted in: hospitalization
Suspect drug(s):
Salazopyrin
Administration route: Oral
Indication: Colitis Ulcerative
Ranitidine
Dosage: daily dose:150mg
Administration route: Oral
Indication: Gastritis
Ranitidine
Indication: Duodenitis
Other drugs received by patient: Acetaminophen; Absenor
Adverse event in receiving Ranitidine
Reported by a pharmacist from United States on 2007-06-22
Patient:
Adverse reactions / side effects: Medication Error
Suspect drug(s):
Paroxetine
Ranitidine
Adverse event in receiving Ranitidine
Reported by a individual with unspecified qualification on 2007-06-21
Patient:
Adverse reactions / side effects: Cholestasis, Mixed Hepatocellular-Cholestatic Injury, Hepatocellular Damage
Suspect drug(s):
Nimesulide
Acetylsalicylic Acid SRT
Dosage: median 500 mg (500 - 2500 mg)
Ranitidine
Hydrochlorothiazide
Tranxene
Paracetamol
Dosage: median 650 mg (min. 500 mg, max. 3250 mg)
Metamizole
Budesonide
Naproxen
Ipratropium Bromide
Other Drugs and Herbs
Adverse event in receiving Ranitidine
Reported by a individual with unspecified qualification on 2007-06-19
Patient:
Adverse reactions / side effects: Drug Interaction, Myocarditis
Suspect drug(s):
Ranitidine
Clozapine
Adverse event in receiving Ranitidine
Reported by a individual with unspecified qualification on 2007-06-19
Patient:
Adverse reactions / side effects: Drug Interaction, Myocarditis
Suspect drug(s):
Ranitidine
Paracetamol
Sertraline
Clozapine
Adverse event in 86 year old female receiving Ranitidine
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-06-18
Patient: 86 year old female
Adverse reactions / side effects: Mania, Paranoia, Cerebellar Ataxia
Adverse event resulted in: hospitalization, disablity
Suspect drug(s):
Gabapentin
Dosage: see image
Administration route: Oral
Start date: 2006-09-06
End date: 2007-03-13
Gabapentin
Dosage: see image
Administration route: Oral
Start date: 2007-04-05
End date: 2007-04-13
Ranitidine
Dosage: 150 mg, bid, oral
Administration route: Oral
Start date: 2007-03-27
End date: 2007-04-10
Other drugs received by patient: Bendroflumethiazide (Bendroflumethiazide); Diclofenac (Diclofenac); Domperidone (Domperidone); Levothyroxine Sodium; Movicol; Oxycontin
Adverse event in 88 year old female receiving Ranitidine
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-06-15
Patient: 88 year old female
Adverse reactions / side effects: Mania, Paranoia, Cerebellar Ataxia
Adverse event resulted in: hospitalization, disablity
Suspect drug(s):
Gabapentin
Administration route: Oral
Start date: 2006-09-06
End date: 2007-04-13
Ranitidine
Administration route: Oral
Start date: 2007-03-27
End date: 2007-04-10
Other drugs received by patient: Bendroflumethiazide; Diclofenac; Domperidone; Levothyroxine Sodium; Movicol; Oxycontin
Adverse event in female receiving Ranitidine
Reported by a individual with unspecified qualification from Italy on 2007-06-14
Patient: female
Adverse reactions / side effects: Renal Failure Acute
Adverse event resulted in: hospitalization
Suspect drug(s):
Ranitidine
Adverse event in 68 year old female receiving Ranitidine
Reported by a individual with unspecified qualification from United Kingdom on 2007-06-12
Patient: 68 year old female
Adverse reactions / side effects: Mania, Paranoia, Cerebellar Ataxia, Coordination Abnormal
Adverse event resulted in: hospitalization, disablity
Suspect drug(s):
Gabapentin
Dosage: see image
Administration route: Oral
Start date: 2006-09-06
End date: 2007-03-13
Gabapentin
Dosage: see image
Administration route: Oral
Start date: 2007-04-05
End date: 2007-04-13
Ranitidine
Dosage: 150 mg, bid, oral
Administration route: Oral
Start date: 2007-03-27
End date: 2007-04-10
Other drugs received by patient: Bendroflumethiazide (Bendroflumethiazide)
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