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Index of reports
> Cases resulting in life threatening events (20)
Below is the selection of adverse event reports related to Acyclovir that includes cases resulting in life threatening events.
Adverse event in 57 year old female receiving Acyclovir
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-07-31
Patient: 57 year old female
Adverse reactions / side effects: Transplant Rejection, Renal Failure Chronic, Haemodialysis
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Acyclovir
Dosage: 200 mg iv
Indication: Herpes Zoster
Start date: 2007-06-12
End date: 2007-06-15
Acyclovir
Dosage: 200 mg
Indication: Herpes Zoster
Start date: 2007-03-22
End date: 2007-03-29
Other drugs received by patient: Bisoprolol Fumarate; Calcichew; Calcium Acetate; Cyclosporine; Omeprazole; Acetaminophen; Prednisolone; Valproate Sodium; Titralac; Vancomycin
Adverse event in 57 year old female receiving Acyclovir
Reported by a consumer/non-health professional from United Kingdom on 2007-07-30
Patient: 57 year old female
Adverse reactions / side effects: Transplant Rejection, Renal Failure Chronic
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Acyclovir
Other drugs received by patient: Bisoprolol Fumarate; Calcichew; Calcium Acetate; Cyclosporine; Omeprazole; Paracetamol; Prednisolone; Valproate Sodium; Titralac; Vancomycin; EPO; ONE-Alpha; Aqueous Cream
Adverse event in 57 year old female receiving Acyclovir
Reported by a consumer/non-health professional from United Kingdom on 2007-07-27
Patient: 57 year old female
Adverse reactions / side effects: Transplant Rejection, Renal Failure Chronic
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Acyclovir
Other drugs received by patient: Bisoprolol Fumarate; Calcichew; Calcium Acetate; Cyclosporine; Omeprazole; Acetaminophen; Prednisolone; Valproate Sodium; Titralac; Vancomycin; EPO; ONE-Alpha; Aqueous Cream
Adverse event in 57 year old female receiving Acyclovir
Reported by a individual with unspecified qualification from United Kingdom on 2007-07-26
Patient: 57 year old female
Adverse reactions / side effects: Transplant Rejection, Renal Failure Chronic
Adverse event resulted in: life threatening event
Suspect drug(s):
Acyclovir
Other drugs received by patient: Acyclovir; Prednisolone; Cyclosporine; Vancomycin; Valproic Acid; Prednisclone; Calcium Acetate; Acetaminophen; Bisoprolol Fumarate; Omeprazole; Titralac; Calcichew
Adverse event in 51 year old female receiving Acyclovir
Reported by a individual with unspecified qualification from United States on 2007-05-11
Patient: 51 year old female, weighing 63.5 kg (139.7 pounds)
Adverse reactions / side effects: Dyspnoea, Blood Urine Present, Nausea, Urticaria, Urine Output Decreased, Swollen Tongue, Headache, Paraesthesia, Pharyngeal Oedema, Joint Swelling, Dysphonia
Adverse event resulted in: life threatening event
Suspect drug(s):
Acyclovir
Other drugs received by patient: Benadryl
Adverse event in 51 year old female receiving Acyclovir
Reported by a individual with unspecified qualification from United States on 2007-05-11
Patient: 51 year old female, weighing 63.5 kg (139.7 pounds)
Adverse reactions / side effects: Dyspnoea, Nausea, Urticaria, Haematuria, Urine Output Decreased, Swollen Tongue, Headache, Paraesthesia, Pharyngeal Oedema, Joint Swelling, Dysphonia
Adverse event resulted in: life threatening event
Suspect drug(s):
Acyclovir
Adverse event in 61 year old male receiving Acyclovir
Reported by a physician from Germany on 2007-05-07
Patient: 61 year old male, weighing 79.0 kg (173.8 pounds)
Adverse reactions / side effects: Pulmonary Embolism, Cholestasis, Hepatic Failure, Constipation, Disease Progression, Acute Graft Versus Host Disease in Skin, Acute Graft Versus Host Disease in Intestine, Right Ventricular Failure, Refusal of Treatment by Patient, Pneumonia, Hepatic Fibrosis, Nephropathy Toxic, Gastric Ulcer Haemorrhage, Renal Cyst, DRY Skin, Cystitis, Convulsion, Hepatocellular Damage, Cholelithiasis, Epstein-Barr Virus Infection, Syncope, Renal Failure, NO Therapeutic Response, Hepatic Congestion, Dehydration, Sepsis, Cytomegalovirus Infection, Hepatic Siderosis, Human Herpesvirus 6 Infection, Leukopenia
Adverse event resulted in: death, life threatening event, hospitalization
Suspect drug(s):
Posaconazole
Dosage: 200 mg; qid; po
Administration route: Oral
Indication: Fungal Infection
Start date: 2005-11-03
Prograf
Dosage: 4 mg; po
Administration route: Oral
Indication: Prophylaxis Against Graft Versus Host Disease
Start date: 2005-12-16
End date: 2006-02-23
Acyclovir
Dosage: 200 mg; bid; po
Administration route: Oral
Indication: Antiviral Prophylaxis
Start date: 2005-12-22
End date: 2006-02-22
Other drugs received by patient: Sandimmune; Decortin; Cellcept; Ganciclovir; Beloc ZOC Comp; Decortin; Klacid; Magnesium Sulfate; Lasix; Dopamin; Calcium Chloride; Kalinor RET; Pantozol; Metoclopramide; Cymeven; Ciprofloxacin HCL; Amitriptyline HCL; Doxyciclin; Zyvox; Entocort; ..; Avelox; Albumin (Human); Fortum; Lopedum; Elobact; Entocort; Albumin (Human); Spirocomb; Perfalgan; Meronem; Omeprazole; Arternol; Kybernin; Mirtazapine; Paracetamol; .; Metoprolol Succinate; Kalinor RET
Adverse event in 67 year old female receiving Acyclovir
Reported by a consumer/non-health professional from United Kingdom on 2007-04-26
Patient: 67 year old female
Adverse reactions / side effects: Ischaemia, Abnormal Behaviour, Local Swelling, Somnolence, Viith Nerve Paralysis, Neurotoxicity, Subdural Haematoma, Nervous System Disorder, Gait Disturbance, Coordination Abnormal
Adverse event resulted in: death, life threatening event, hospitalization
Suspect drug(s):
Acyclovir
Adverse event in 67 year old female receiving Acyclovir
Reported by a consumer/non-health professional from United Kingdom on 2007-04-19
Patient: 67 year old female
Adverse reactions / side effects: Ischaemia, Abnormal Behaviour, Local Swelling, Somnolence, Viith Nerve Paralysis, Neurotoxicity, Subdural Haematoma, Nervous System Disorder, Gait Disturbance, Coordination Abnormal
Adverse event resulted in: death, life threatening event, hospitalization
Suspect drug(s):
Acyclovir
Adverse event in 49 year old male receiving Acyclovir
Reported by a physician from France on 2007-04-11
Patient: 49 year old male
Adverse reactions / side effects: Multi-Organ Failure, Venoocclusive Liver Disease, Disease Progression
Adverse event resulted in: death, life threatening event
Suspect drug(s):
Gemtuzumab Ozogamicin
Dosage: unknown
Indication: Acute Myeloid Leukaemia
Start date: 2007-02-06
End date: 2007-02-06
Acyclovir
Dosage: 250 mg total daily
Start date: 2007-02-07
End date: 2007-02-20
Vancomycin
Dosage: 2.5 g total daily
Start date: 2007-02-10
End date: 2007-02-23
Fludarabine Phosphate
Dosage: unknown
Indication: Acute Myeloid Leukaemia
Start date: 2007-02-06
End date: 2007-02-10
Idarubicin HCL
Dosage: unknown
Indication: Acute Myeloid Leukaemia
Start date: 2007-02-08
End date: 2007-02-09
Cytarabine
Dosage: unknown
Indication: Acute Myeloid Leukaemia
Start date: 2007-02-06
End date: 2007-02-10
Other drugs received by patient: Inipomp; Contramal; Ciprofloxacin HCL; Zophren; Furosemide; Perfalgan; Gentamicin
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 female receiving Acyclovir
Reported by a pharmacist from United States on 2007-04-04
Patient: female, weighing 80.0 kg (176.0 pounds)
Adverse reactions / side effects: Stevens-Johnson Syndrome
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Acyclovir
Adverse event in 48 year old male receiving Acyclovir
Reported by a physician from Switzerland on 2007-03-28
Patient: 48 year old male, weighing 98.0 kg (215.6 pounds)
Adverse reactions / side effects: Cerebral Disorder, Bradypnoea, Hypotension, Coma, Condition Aggravated, Hepatic Enzyme Increased, Liver Disorder, Respiratory Failure, Sepsis, Bradycardia, Splenomegaly
Adverse event resulted in: death, life threatening event, hospitalization
Suspect drug(s):
Posaconazole
Dosage: 400 mg;bid;po
Administration route: Oral
Indication: Fungal Infection
Start date: 2005-08-04
End date: 2005-08-07
Morphine
Dosage: iv
Indication: Pain
Start date: 2005-07-15
Morphine
Dosage: po
Administration route: Oral
Indication: Pain
Start date: 2005-07-15
Acyclovir
Dosage: 750 mg; iv
Indication: Antiviral Prophylaxis
Start date: 2005-07-09
Taxobactam / Piperacillin (NO Pref. Name)
Dosage: 4.5 gm;tid
Indication: Pneumonia
Start date: 2005-08-03
Propofol
Dosage: iv
Indication: Sedation
Start date: 2005-08-05
Other drugs received by patient: Abelcet; Voriconazole; Diflucan
Adverse event in 68 year old female receiving Acyclovir
Reported by a physician from Japan on 2007-03-23
Patient: 68 year old female, weighing 40.0 kg (88.0 pounds)
Adverse reactions / side effects: Intervertebral Disc Protrusion, Drug Eruption, Multi-Organ Failure, Skin Exfoliation, Ocular Hyperaemia, Septic Shock, Blister
Adverse event resulted in: death, life threatening event, hospitalization
Suspect drug(s):
Clarithromycin
Administration route: Oral
Indication: Pneumonia
Start date: 2006-11-17
End date: 2006-11-24
Acyclovir
Indication: Meningitis
Start date: 2006-12-01
End date: 2006-12-06
Acyclovir
Indication: Encephalitis Herpes
Phenobarbital TAB
Indication: Convulsion
Start date: 2006-11-15
End date: 2006-11-17
Cefozopran Hydrochloride
Indication: Pneumonia
Start date: 2006-11-16
End date: 2006-11-16
Piperacillin Sodium
Indication: Pneumonia
Start date: 2006-11-17
End date: 2006-11-24
Meropenem Hydrate
Indication: Septic Shock
Start date: 2006-11-29
End date: 2006-12-27
Adverse event in 48 year old male receiving Acyclovir
Reported by a physician from Switzerland on 2007-03-15
Patient: 48 year old male, weighing 98.0 kg (215.6 pounds)
Adverse reactions / side effects: Jaundice, Cerebral Disorder, Bradypnoea, Coma, Pulmonary Embolism, Liver Disorder, Ventricular Hypertrophy, Iliac Artery Thrombosis, Lipomatosis, Arteriosclerosis, Intracardiac Thrombus, Tracheobronchitis, Hypotension, Pulmonary Alveolar Haemorrhage, Condition Aggravated, Brain Stem Syndrome, Respiratory Failure, Sepsis, Bradycardia, Arteriosclerosis Coronary Artery, Cardiovascular Disorder
Adverse event resulted in: death, life threatening event, hospitalization
Suspect drug(s):
Posaconazole
Dosage: 400 mg; bid; po
Administration route: Oral
Indication: Sinusitis Fungal
Start date: 2005-08-04
End date: 2005-08-07
Morphine
Dosage: see image
Indication: Pain
Start date: 2005-07-15
Acyclovir
Dosage: 750 mg; iv
Indication: Herpes Virus Infection
Start date: 2005-07-09
Acyclovir
Dosage: 750 mg; iv
Indication: Prophylaxis
Start date: 2005-07-09
Taxobactam / Piperacillin (NO Pref. Name)
Dosage: 4.5 gm; tid
Indication: Pneumonia
Start date: 2005-08-03
Propofol
Dosage: iv
Indication: Sedation
Start date: 2005-08-05
Other drugs received by patient: Abelcet; Voriconazole; Diflucan
Adverse event in 68 year old female receiving Acyclovir
Reported by a physician from Japan on 2007-03-15
Patient: 68 year old female, weighing 40.0 kg (88.0 pounds)
Adverse reactions / side effects: Drug Eruption, Multi-Organ Failure, Skin Exfoliation, Ocular Hyperaemia, Septic Shock, Blister
Adverse event resulted in: death, life threatening event, hospitalization
Suspect drug(s):
Clarithromycin
Administration route: Oral
Indication: Pneumonia
Start date: 2006-11-17
End date: 2006-11-24
Acyclovir
Indication: Meningitis
Start date: 2006-12-01
End date: 2006-12-06
Acyclovir
Indication: Encephalitis Herpes
Phenobarbital TAB
Indication: Convulsion
Start date: 2006-11-15
End date: 2006-11-17
Cefozopran Hydrochloride
Indication: Pneumonia
Start date: 2006-11-16
End date: 2006-11-16
Piperacillin Sodium
Indication: Pneumonia
Start date: 2006-11-17
End date: 2006-11-24
Meropenem Hydrate
Indication: Septic Shock
Start date: 2006-11-29
End date: 2006-12-27
Adverse event in 63 year old female receiving Acyclovir
Reported by a physician from France on 2007-03-01
Patient: 63 year old female
Adverse reactions / side effects: Coma
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Neurontin
Dosage: daily dose:300mg
Administration route: Oral
Start date: 2006-05-06
End date: 2006-05-09
Acyclovir
Dosage: daily dose:250mg
Start date: 2006-05-04
End date: 2006-05-09
Other drugs received by patient: Duphalac; Heparin; Nexium
Adverse event in 75 year old male receiving Acyclovir
Reported by a pharmacist from United States on 2007-02-12
Patient: 75 year old male, weighing 89.2 kg (196.2 pounds)
Adverse reactions / side effects: Rash
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Acyclovir
Adverse event in 10 year old receiving Acyclovir
Reported by a consumer/non-health professional from United Kingdom on 2007-01-09
Patient: 10 year old , weighing 48.7 kg (107.1 pounds)
Adverse reactions / side effects: Renal Impairment
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Acyclovir
Adverse event in 36 year old female receiving Acyclovir
Reported by a consumer/non-health professional from United States on 2007-01-08
Patient: 36 year old female
Adverse reactions / side effects: CD4 Lymphocytes Decreased, Squamous Cell Carcinoma, Drug Ineffective
Adverse event resulted in: life threatening event, disablity
Suspect drug(s):
Acyclovir
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