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Index of reports
> Cases resulting in a serious event (88)
Below is the selection of adverse event reports related to Ranitidine that includes cases resulting in a serious event.
Reports 1 - 25 of 88 Next >>
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 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 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)
Adverse event in 88 year old female receiving Ranitidine
Reported by a consumer/non-health professional from United Kingdom on 2007-06-11
Patient: 88 year old female
Adverse reactions / side effects: Mania, Paranoia, Cerebellar Ataxia
Adverse event resulted in: hospitalization, disablity
Suspect drug(s):
Ranitidine
Dosage: 150mg twice per day
Administration route: Oral
Start date: 2007-03-27
End date: 2007-04-10
Gabapentin
Administration route: Oral
Start date: 2006-09-06
End date: 2007-04-13
Other drugs received by patient: Bendroflumethiazide; Diclofenac; Domperidone; Levothyroxine Sodium; Movicol; Oxycontin
Adverse event in 48 year old female receiving Ranitidine
Reported by a health professional (non-physician/pharmacist) from Italy on 2007-06-09
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 26 year old male receiving Ranitidine
Reported by a pharmacist from Germany on 2007-06-07
Patient: 26 year old male
Adverse reactions / side effects: Myoclonus
Adverse event resulted in: hospitalization
Suspect drug(s):
Ultiva
Indication: Nasal Septal Operation
Start date: 2007-03-13
End date: 2007-03-13
Atropine Sulfate
Dosage: 1mg single dose
Start date: 2007-03-13
End date: 2007-03-13
Promethazine
Dosage: 50mg single dose
Start date: 2007-03-13
End date: 2007-03-13
Clindamycin HCL
Dosage: 300mg single dose
Administration route: Oral
Start date: 2007-03-13
End date: 2007-03-13
Ranitidine
Dosage: 300mg single dose
Administration route: Oral
Start date: 2007-03-12
End date: 2007-03-12
Dormicum
Dosage: 3mg per day
Indication: Sedation
Start date: 2007-03-13
Ultracain
Dosage: 5ml four times per day
Diclofenac
Dosage: 100mg single dose
Administration route: Oral
Start date: 2007-03-12
End date: 2007-03-12
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