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Index of reports
> Cases resulting in life threatening events (12)
Below is the selection of adverse event reports related to Pepcid (Famotidine) that includes cases resulting in life threatening events.
Adverse event in female receiving Pepcid (Famotidine)
Reported by a physician from Japan on 2007-07-02
Patient: female
Adverse reactions / side effects: Disseminated Intravascular Coagulation, Bone Marrow Failure, Pancytopenia
Adverse event resulted in: life threatening event
Suspect drug(s):
Ciprofloxacin
Indication: Peritonitis
Start date: 2007-05-31
End date: 2007-06-05
Pepcid
Start date: 2007-05-28
End date: 2007-06-04
Other drugs received by patient: Broact; Globulin, Immune; FOY; Neuart; Diprivan; Xylocaine; Predonine
Adverse event in female receiving Pepcid (Famotidine)
Reported by a physician from Japan on 2007-06-26
Patient: female
Adverse reactions / side effects: Disseminated Intravascular Coagulation, Bone Marrow Failure, Pancytopenia
Adverse event resulted in: life threatening event
Suspect drug(s):
Ciprofloxacin
Indication: Peritonitis
Start date: 2007-05-31
End date: 2007-06-05
Pepcid
Start date: 2007-05-28
End date: 2007-06-04
Other drugs received by patient: Broact; Globulin, Immune; FOY; Neuart; Diprivan; Xylocaine; Predonine
Adverse event in 44 year old male receiving Pepcid (Famotidine)
Reported by a physician from Japan on 2007-06-26
Patient: 44 year old male
Adverse reactions / side effects: Pruritus, Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Anaphylactic Shock
Adverse event resulted in: life threatening event
Suspect drug(s):
Pepcid
Administration route: Oral
Indication: Gastritis
Start date: 2007-01-11
End date: 2007-01-13
Pepcid
Start date: 2007-01-13
End date: 2007-01-14
Adverse event in 44 year old male receiving Pepcid (Famotidine)
Reported by a physician from Japan on 2007-06-14
Patient: 44 year old male
Adverse reactions / side effects: Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Anaphylactic Shock
Adverse event resulted in: life threatening event
Suspect drug(s):
Pepcid
Administration route: Oral
Indication: Gastritis
Start date: 2007-01-11
End date: 2007-01-13
Pepcid
Start date: 2007-01-13
End date: 2007-01-14
Adverse event in 102 year old male receiving Pepcid (Famotidine)
Reported by a physician from Japan on 2007-04-30
Patient: 102 year old male
Adverse reactions / side effects: Hyperbilirubinaemia, Pneumonia, Disseminated Intravascular Coagulation, Platelet Count Decreased
Adverse event resulted in: death, life threatening event, hospitalization
Suspect drug(s):
Pepcid
Indication: Gastrointestinal Ulcer
Start date: 2007-01-22
End date: 2007-01-29
Primaxin
Indication: Pneumonia
Start date: 2007-01-22
End date: 2007-01-29
Other drugs received by patient: [therapy Unspecified]; Bisolvon; Lasix; Atarax; Meptin; Frandol
Adverse event in 44 year old male receiving Pepcid (Famotidine)
Reported by a physician from Japan on 2007-04-30
Patient: 44 year old male
Adverse reactions / side effects: Anaphylactic Shock
Adverse event resulted in: life threatening event
Suspect drug(s):
Pepcid
Indication: Gastritis
Start date: 2007-01-13
End date: 2007-01-14
Pepcid
Administration route: Oral
Start date: 2007-01-11
End date: 2007-01-13
Adverse event in female receiving Pepcid (Famotidine)
Reported by a pharmacist from United States on 2007-04-25
Patient: female
Adverse reactions / side effects: Hypersensitivity, Unresponsive TO Stimuli, Hypotension, Sepsis, Cardiogenic Shock, Acute Myocardial Infarction, Apnoea
Adverse event resulted in: life threatening event, hospitalization, disablity
Suspect drug(s):
Pepcid (Famotidine)
Other drugs received by patient: Reglan
Adverse event in female receiving Pepcid (Famotidine)
Reported by a pharmacist from United States on 2007-04-13
Patient: female
Adverse reactions / side effects: Myocardial Infarction
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Pepcid (Famotidine)
Other drugs received by patient: Reglan
Adverse event in 58 year old male receiving Pepcid (Famotidine)
Reported by a pharmacist from Japan on 2007-04-06
Patient: 58 year old male
Adverse reactions / side effects: Rhabdomyolysis
Adverse event resulted in: life threatening event
Suspect drug(s):
Pepcid
Start date: 2007-03-20
Pepcid RPD
Administration route: Oral
Start date: 2007-03-27
End date: 2007-03-29
Other drugs received by patient: Cefazolin Sodium; Unasyn; Glyceol; [therapy Unspecified]; Coniel; [therapy Unspecified]; Herbesser; Tagamet
Adverse event in 79 year old male receiving Pepcid (Famotidine)
Reported by a physician from Japan on 2007-01-23
Patient: 79 year old male
Adverse reactions / side effects: White Blood Cell Count Decreased, RED Blood Cell Count Decreased
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Pepcid (Famotidine)
Other drugs received by patient: Menesit; Alosenn
Adverse event in 70 year old female receiving Pepcid (Famotidine)
Reported by a health professional (non-physician/pharmacist) from Japan on 2007-01-22
Patient: 70 year old female
Adverse reactions / side effects: Granulocyte Count Decreased
Adverse event resulted in: life threatening event
Suspect drug(s):
Pepcid
Indication: Duodenal Ulcer
Start date: 2006-10-26
End date: 2006-11-30
Vfend
Indication: Aspergillosis
Start date: 2006-12-14
Vfend
Start date: 2006-11-09
End date: 2006-11-30
Other drugs received by patient: Denosine; Humulin 70 / 30; Solcoseryl; Predonine; Endoxan
Adverse event in 79 year old male receiving Pepcid (Famotidine)
Reported by a physician from Japan on 2007-01-18
Patient: 79 year old male
Adverse reactions / side effects: White Blood Cell Count Decreased, RED Blood Cell Count Decreased, Platelet Count Decreased
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Pepcid (Famotidine)
Other drugs received by patient: Menesit; Alosenn
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