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Acyclovir (Acyclovir) - Adverse Event Reports - Serious Event - Renal Failure Acute

 



Index of reports > Cases resulting in a serious event (116) > Cases with Renal Failure Acute (16)

Below is the selection of adverse event reports related to Acyclovir that includes cases resulting in a serious event 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 27 year old male receiving Acyclovir

Reported by a physician from Greece on 2007-06-13

Patient: 27 year old male

Adverse reactions / side effects: Renal Failure Acute

Adverse event resulted in: hospitalization

Suspect drug(s):
Ceftriaxone Sodium

Acyclovir



Adverse event in 36 year old male receiving Acyclovir

Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-05-25

Patient: 36 year old male

Adverse reactions / side effects: Dehydration, Renal Failure Acute

Adverse event resulted in: hospitalization

Suspect drug(s):
Acyclovir



Adverse event in 36 year old male receiving Acyclovir

Reported by a consumer/non-health professional from United Kingdom on 2007-05-22

Patient: 36 year old male

Adverse reactions / side effects: Dehydration, Renal Failure Acute

Adverse event resulted in: hospitalization

Suspect drug(s):
Acyclovir



Adverse event in 27 year old male receiving Acyclovir

Reported by a individual with unspecified qualification from Greece on 2007-05-21

Patient: 27 year old male

Adverse reactions / side effects: Blood Urine Present, Rhabdomyolysis, Encephalitis, Epstein-Barr Virus Antibody Positive, False Positive Laboratory Result, Herpes Zoster, Renal Failure Acute

Adverse event resulted in: hospitalization

Suspect drug(s):
Acyclovir
    Dosage: 10mg/kg iv q 8h
    Indication: Herpes Zoster

Ceftriaxone
    Dosage: 2 g iv q 12h
    Indication: Herpes Zoster



Adverse event in 36 year old male receiving Acyclovir

Reported by a individual with unspecified qualification from United Kingdom on 2007-05-16

Patient: 36 year old male

Adverse reactions / side effects: Dehydration, Renal Failure Acute

Adverse event resulted in: hospitalization

Suspect drug(s):
Acyclovir



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):
Mylotarg
    Indication: Acute Leukaemia
    Start date: 2006-05-16
    End date: 2006-05-16

Acyclovir
    Indication: Prophylaxis
    Start date: 2006-05-14
    End date: 2006-05-27

Acyclovir
    Start date: 2006-06-04

Meropen
    Dosage: unknown daily dose
    Indication: Sepsis
    Start date: 2006-05-14
    End date: 2006-05-25

Vfend
    Indication: Sepsis
    Start date: 2006-05-16

Targocid
    Indication: Sepsis
    Start date: 2006-05-19

Gaster
    Administration route: Oral
    Indication: Prophylaxis
    Start date: 2006-05-14
    End date: 2006-05-17

Prograf
    Administration route: Oral
    Indication: Graft Versus Host Disease
    Start date: 2006-05-27
    End date: 2006-06-01

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

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):
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

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

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 health professional (non-physician/pharmacist) from United Kingdom on 2007-02-26

Patient: 43 year old female

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

Other drugs received by patient: Adizem-XL; Tretinoin; Allopurinol; Candesartan; Caspofungin; Ceftazidime; Clomipramine HCL; Metronidazole; Teicoplanin; Metronidazole; Ciprofloxacin; Ciprofloxacin; Acyclovir



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



Adverse event in 41 year old female receiving Acyclovir

Reported by a pharmacist from United States on 2007-02-14

Patient: 41 year old female, weighing 81.6 kg (179.6 pounds)

Adverse reactions / side effects: Renal Failure Acute

Adverse event resulted in: hospitalization

Suspect drug(s):
Acyclovir



Adverse event in 45 year old male receiving Acyclovir

Reported by a pharmacist from United States on 2007-01-11

Patient: 45 year old male, weighing 84.4 kg (185.6 pounds)

Adverse reactions / side effects: Renal Tubular Disorder, Renal Failure Acute

Adverse event resulted in: hospitalization

Suspect drug(s):
Acyclovir

Other drugs received by patient: Acetaminophen; Dextrose; Glucagon; Ibuprofen; Regular Insulin; Sodium Chloride; Potassium Chloride; Promethazine; Sennosides; Temazepam

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