|
Index of reports
> Cases resulting in other serious reactions (51)
> Cases with Renal Failure Acute (8)
Below is the selection of adverse event reports related to Acyclovir that includes cases resulting in other serious reactions where reactions include renal failure acute.
Adverse event in 42 year old male receiving Acyclovir
Reported by a health professional (non-physician/pharmacist) from France on 2007-10-09
Patient: 42 year old male
Adverse reactions / side effects: Confusional State, Renal Failure Acute
Suspect drug(s):
Acyclovir
Adverse event in 50 year old female receiving Acyclovir
Reported by a physician from Hong Kong on 2007-07-23
Patient: 50 year old female
Adverse reactions / side effects: Renal Failure Acute
Suspect drug(s):
Acyclovir
Other drugs received by patient: Aspirin
Adverse event in 50 year old female receiving Acyclovir
Reported by a individual with unspecified qualification from Hong Kong on 2007-05-14
Patient: 50 year old female
Adverse reactions / side effects: Refusal of Treatment by Patient, Dehydration, Nephropathy Toxic, Scar, Renal Failure Acute
Suspect drug(s):
Acyclovir
Other drugs received by patient: Aspirin
Adverse event in 50 year old female receiving Acyclovir
Reported by a consumer/non-health professional from Hong Kong on 2007-05-10
Patient: 50 year old female
Adverse reactions / side effects: Nephrolithiasis, Back Pain, Nausea, Dehydration, Nephropathy Toxic, Blood Creatinine Increased, Renal Failure Acute
Suspect drug(s):
Acyclovir
Other drugs received by patient: Aspirin
Adverse event in male receiving Acyclovir
Reported by a physician from Japan on 2007-04-05
Patient: male, weighing 55.0 kg (121.0 pounds)
Adverse reactions / side effects: Hyperbilirubinaemia, Disseminated Intravascular Coagulation, Condition Aggravated, Chronic Graft Versus Host Disease, Sepsis, Platelet Count Decreased, Blood Pressure Decreased, Oxygen Saturation Decreased, Renal Failure Acute
Adverse event resulted in: life threatening event
Suspect drug(s):
Acyclovir
Indication: Prophylaxis
Start date: 2006-05-14
End date: 2006-05-27
Acyclovir
Start date: 2006-06-04
Cytarabine
Dosage: unknown daily dose
Indication: Acute Leukaemia
Start date: 2006-05-12
End date: 2006-05-14
Cytarabine
Dosage: unknown daily dose
Start date: 2006-06-30
End date: 2006-07-02
Gaster
Administration route: Oral
Indication: Prophylaxis
Start date: 2006-05-14
End date: 2006-05-17
Meropen
Dosage: unknown daily dose
Indication: Sepsis
Start date: 2006-05-14
End date: 2006-05-25
Mylotarg
Indication: Acute Leukaemia
Start date: 2006-05-16
End date: 2006-05-16
Prograf
Administration route: Oral
Indication: Graft Versus Host Disease
Start date: 2006-05-27
End date: 2006-06-01
Targocid
Indication: Sepsis
Start date: 2006-05-19
Vfend
Indication: Sepsis
Start date: 2006-05-16
Other drugs received by patient: Ciprofloxacin; Ganciclovir; Urso; Blopress; Blopress; Omepral; Morphine; Biofermin R; Adsorbin; Lopemin; Amlodin; Amlodin; Rebetol; Hycamtin; Hycamtin; Hycamtin; Hycamtin; Hycamtin
Adverse event in 27 year old male receiving Acyclovir
Reported by a health professional (non-physician/pharmacist) from Greece on 2007-03-27
Patient: 27 year old male
Adverse reactions / side effects: Rhabdomyolysis, Alanine Aminotransferase Increased, Blood Lactate Dehydrogenase Increased, Bone Pain, Pain, Herpes Zoster, Aspartate Aminotransferase Increased, Liver Function Test Abnormal, Renal Failure Acute
Suspect drug(s):
Acyclovir
Dosage: 10 mg/kg, q8h, intravenous
Indication: Encephalitis
Ceftriaxone
Dosage: 2 g, q12h, intravenous
Indication: Encephalitis
Adverse event in 43 year old receiving Acyclovir
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-03-01
Patient: 43 year old
Adverse reactions / side effects: Nephritis Interstitial, Sepsis, General Physical Health Deterioration, Hypoperfusion, Hypovolaemia, Renal Failure Acute
Adverse event resulted in: hospitalization
Suspect drug(s):
Acyclovir
Dosage: see image
Start date: 2006-12-31
End date: 2006-12-31
Acyclovir
Dosage: see image
Start date: 2007-01-02
End date: 2007-01-13
Ciprofloxacin
Dosage: 500 mg, bid, oral
Administration route: Oral
Start date: 2006-12-29
End date: 2006-12-31
Ciprofloxacin
Dosage: 500 mg, bid, oral
Administration route: Oral
Start date: 2007-01-11
End date: 2007-01-12
Other drugs received by patient: Adizem-XL; Allopurinol; ALL-Trans-Retinoic Acid; Candesartan; Caspofungin; Ceftazidime; Clomipramine HCL; Metronidazole; Teicoplanin
Adverse event in 43 year old female receiving Acyclovir
Reported by a consumer/non-health professional from United Kingdom on 2007-02-22
Patient: 43 year old female
Adverse reactions / side effects: Nephritis Interstitial, Sepsis, Hypoperfusion, Ill-Defined Disorder, Renal Failure Acute
Adverse event resulted in: hospitalization
Suspect drug(s):
Acyclovir
Dosage: 750mg per day
Start date: 2006-12-31
End date: 2006-12-31
Acyclovir
Dosage: 200mg three times per day
Administration route: Oral
Start date: 2007-01-02
End date: 2007-01-13
Ciprofloxacin
Dosage: 500mg twice per day
Administration route: Oral
Start date: 2006-12-29
End date: 2006-12-31
Ciprofloxacin
Dosage: 750mg twice per day
Administration route: Oral
Start date: 2007-01-11
End date: 2007-01-12
Other drugs received by patient: Adizem-XL; Allopurinol Sodium; ALL-Trans-Retinoic Acid; Candesartan; Caspofungin; Ceftazidime; Clomipramine HCL; Metronidazole; Teicoplanin; Metronidazole
|
