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Index of reports
> Cases resulting in disability (7)
Below is the selection of adverse event reports related to Ranitidine that includes cases resulting in disability.
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 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):
Gabapentin
Administration route: Oral
Start date: 2006-09-06
End date: 2007-04-13
Ranitidine
Dosage: 150mg twice per day
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 80 year old female receiving Ranitidine
Reported by a individual with unspecified qualification from United Kingdom on 2007-01-30
Patient: 80 year old female
Adverse reactions / side effects: Respiratory Arrest, Cardiac Arrest, Hypoxic Encephalopathy, Electromechanical Dissociation
Adverse event resulted in: life threatening event, hospitalization, disablity
Suspect drug(s):
Chlorpheniramine Maleate
Dosage: 10 mg, intravenous
Indication: Drug USE FOR Unknown Indication
Start date: 2006-01-02
Ranitidine
Dosage: 50 mg, intravenous
Indication: Drug USE FOR Unknown Indication
Start date: 2006-01-02
Adverse event in 80 year old female receiving Ranitidine
Reported by a consumer/non-health professional from United Kingdom on 2007-01-29
Patient: 80 year old female
Adverse reactions / side effects: Respiratory Arrest, Cardiac Arrest, Hypoxic Encephalopathy, Electromechanical Dissociation
Adverse event resulted in: life threatening event, hospitalization, disablity
Suspect drug(s):
Chlorpheniramine Maleate
Dosage: 10mg unknown
Indication: Drug USE FOR Unknown Indication
Start date: 2006-01-02
Ranitidine
Dosage: 50mg unknown
Indication: Drug USE FOR Unknown Indication
Start date: 2006-01-02
Adverse event in female receiving Ranitidine
Reported by a consumer/non-health professional from United Kingdom on 2007-01-17
Patient: female
Adverse reactions / side effects: Back Pain, Physical Disability
Adverse event resulted in: disablity
Suspect drug(s):
Atenolol
Administration route: Oral
Bendroflumethiazide
Administration route: Oral
Lipitor
Administration route: Oral
Raloxifene HCL
Administration route: Oral
Ramipril
Administration route: Oral
Ranitidine
Administration route: Oral
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