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Index of reports
> Cases resulting in hospitalization (49)
Below is the selection of adverse event reports related to Ranitidine that includes cases resulting in hospitalization.
Reports 1 - 25 of 49 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 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 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 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
Adverse event in 52 year old female receiving Ranitidine
Reported by a physician from Argentina on 2007-05-25
Patient: 52 year old female
Adverse reactions / side effects: Renal Failure, Skin Exfoliation, Intentional Self-Injury, Rash Pruritic
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Eskalith
Dosage: 900mg per day
Administration route: Oral
Indication: Bipolar Disorder
Start date: 2007-04-27
End date: 2007-05-10
Lamotrigine
Dosage: 150mg per day
Administration route: Oral
Indication: Bipolar Disorder
Start date: 2006-07-01
End date: 2007-04-27
Ranitidine
Indication: Drug USE FOR Unknown Indication
Levothyroxine Sodium
Indication: Drug USE FOR Unknown Indication
Other drugs received by patient: NO Concurrent Medication
Adverse event in 54 year old male receiving Ranitidine
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-05-25
Patient: 54 year old male
Adverse reactions / side effects: Overdose, Blood Pressure Decreased, Haemodynamic Instability
Adverse event resulted in: hospitalization
Suspect drug(s):
Zocor
Administration route: Oral
Zocor
Administration route: Oral
Ranitidine
Administration route: Oral
Ranitidine
Administration route: Oral
Ramipril
Administration route: Oral
Ramipril
Administration route: Oral
Adverse event in 54 year old male receiving Ranitidine
Reported by a physician from United Kingdom on 2007-05-25
Patient: 54 year old male
Adverse reactions / side effects: Overdose, Hypotension, Haemodynamic Instability
Adverse event resulted in: hospitalization
Suspect drug(s):
Zocor
Administration route: Oral
Zocor
Administration route: Oral
Ramipril
Administration route: Oral
Ramipril
Administration route: Oral
Ranitidine
Administration route: Oral
Ranitidine
Administration route: Oral
Adverse event in 7 month old female receiving Ranitidine
Reported by a pharmacist from Canada on 2007-05-14
Patient: 7 month old female, weighing 4.8 kg (10.6 pounds)
Adverse reactions / side effects: Overdose, Fontanelle Bulging, Medication Error, Convulsion
Adverse event resulted in: hospitalization
Suspect drug(s):
Ranitidine
Adverse event in 49 year old male receiving Ranitidine
Reported by a health professional (non-physician/pharmacist) from United States on 2007-05-14
Patient: 49 year old male
Adverse reactions / side effects: Weight Decreased, Drug Screen Positive, Clostridial Infection, Giardiasis, Infection in AN Immunocompromised Host
Adverse event resulted in: hospitalization
Suspect drug(s):
Ranitidine
Adverse event in 53 year old male receiving Ranitidine
Reported by a health professional (non-physician/pharmacist) from Spain on 2007-05-14
Patient: 53 year old male
Adverse reactions / side effects: Acute Generalised Exanthematous Pustulosis, Erythema Multiforme
Adverse event resulted in: hospitalization
Suspect drug(s):
Ranitidine
Other drugs received by patient: Atorvastatin Calcium; Clopidogrel
Adverse event in 49 year old male receiving Ranitidine
Reported by a health professional (non-physician/pharmacist) from United States on 2007-05-09
Patient: 49 year old male
Adverse reactions / side effects: Achlorhydria, Clostridial Infection, Giardiasis
Adverse event resulted in: hospitalization
Suspect drug(s):
Ranitidine
Adverse event in male receiving Ranitidine
Reported by a pharmacist from Germany on 2007-04-24
Patient: 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
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
Adverse event in 80 year old male receiving Ranitidine
Reported by a health professional (non-physician/pharmacist) from Japan on 2007-04-19
Patient: 80 year old male
Adverse reactions / side effects: Drug Eruption, Blood Lactate Dehydrogenase Increased, Lymphocyte Stimulation Test Positive, Glycosylated Haemoglobin Increased, Skin Discolouration, Lymph Node Palpable, Pigmentation Disorder, Blood Glucose Increased, White Blood Cell Count Increased
Adverse event resulted in: hospitalization
Suspect drug(s):
Ranitidine
Other drugs received by patient: Codeine Phosphate; Trapidil
Adverse event in male receiving Ranitidine
Reported by a consumer/non-health professional from Spain on 2007-04-16
Patient: male
Adverse reactions / side effects: Urticaria, Bronchospasm, Laryngeal Oedema
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Augmentin '125'
Indication: Drug USE FOR Unknown Indication
Start date: 2007-03-05
End date: 2007-03-05
Ranitidine
Dosage: 50mg per day
Indication: Prophylaxis
Start date: 2007-03-05
End date: 2007-03-05
Perfalgan
Indication: Prophylaxis
Start date: 2007-03-05
End date: 2007-03-05
Adverse event in 31 year old male receiving Ranitidine
Reported by a health professional (non-physician/pharmacist) from Japan on 2007-04-12
Patient: 31 year old male
Adverse reactions / side effects: Atelectasis
Adverse event resulted in: hospitalization
Suspect drug(s):
Butorphanol Tartrate
Indication: Anaesthesia
Midazolam HCL
Indication: Anaesthesia
Ranitidine
Administration route: Oral
Adverse event in receiving Ranitidine
Reported by a consumer/non-health professional from United Kingdom on 2007-04-10
Patient:
Adverse reactions / side effects: Overdose, Hypotension, Blood Pressure Decreased, Haemodynamic Instability
Adverse event resulted in: hospitalization
Suspect drug(s):
Altace
Dosage: 300 mg, single
Administration route: Oral
Ranitidine
Dosage: 4500 mg, single
Administration route: Oral
Simvastatin
Dosage: 600 mg, single
Administration route: Oral
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