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Index of reports
> Cases resulting in a serious event (6)
Below is the selection of adverse event reports related to Ceftin (Cefuroxime) that includes cases resulting in a serious event.
Adverse event in 39 year old female receiving Ceftin (Cefuroxime)
Reported by a physician from France on 2007-06-05
Patient: 39 year old female
Adverse reactions / side effects: Angioedema, Myocardial Ischaemia, Drug Hypersensitivity, Anaphylactic Shock
Adverse event resulted in: hospitalization
Suspect drug(s):
Ceftin (Cefuroxime)
Other drugs received by patient: Deanxit; Trazodone HCL; Lormetazepam; Aspirin
Adverse event in 11 year old female receiving Ceftin (Cefuroxime)
Reported by a physician from United States on 2007-04-13
Patient: 11 year old female, weighing 52.3 kg (115.1 pounds)
Adverse reactions / side effects: Back Pain, Viral Infection, Pruritus, Escherichia Urinary Tract Infection, Drug Hypersensitivity, Urinary Tract Infection, Rash, Pyrexia, Neutropenia
Adverse event resulted in: hospitalization
Suspect drug(s):
Menactra
Start date: 2007-02-26
End date: 2007-02-26
Ceftin
Dosage: 250mg twice per day
Administration route: Oral
Indication: Urinary Tract Infection
Start date: 2007-03-05
End date: 2007-03-12
Cefzil
Dosage: 500mg twice per day
Administration route: Oral
Indication: Urinary Tract Infection
Start date: 2007-03-16
End date: 2007-03-18
Rocephin
Dosage: 500mg continuous
Indication: Disease Recurrence
Start date: 2007-03-18
End date: 2007-03-20
Rocephin
Dosage: 500mg continuous
Indication: Urinary Tract Infection
Start date: 2007-03-18
End date: 2007-03-20
Adverse event in 11 year old female receiving Ceftin (Cefuroxime)
Reported by a physician from United States on 2007-04-10
Patient: 11 year old female, weighing 52.2 kg (114.9 pounds)
Adverse reactions / side effects: Back Pain, Viral Infection, Escherichia Urinary Tract Infection, Drug Hypersensitivity, Neutropenia
Adverse event resulted in: hospitalization
Suspect drug(s):
Menactra Injection (Menactra)
Dosage: single dose / intramuscular
Start date: 2007-02-26
End date: 2007-02-26
Ceftin
Dosage: 250 mg / twice per day / oral
Administration route: Oral
Indication: Urinary Tract Infection
Start date: 2007-03-05
End date: 2007-03-15
Adverse event in 67 year old female receiving Ceftin (Cefuroxime)
Reported by a individual with unspecified qualification from China on 2007-03-29
Patient: 67 year old female
Adverse reactions / side effects: Dyspnoea, Anaphylactic Shock, Erythema, Loss of Consciousness, Respiratory Rate Decreased, Heart Rate Decreased, Choking, Rhythm Idioventricular
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Zinacef
Dosage: unk, see dosage text, intraderm
Indication: Cough
Start date: 2005-07-21
End date: 2005-07-21
Ceftin
Dosage: oral
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Other drugs received by patient: Ambroxol; Liquorice; Diprophylline; Sulperazon; Clindamycin; Levofloxacin
Adverse event in 32 year old female receiving Ceftin (Cefuroxime)
Reported by a consumer/non-health professional from United States on 2007-02-05
Patient: 32 year old female, weighing 68.2 kg (150.0 pounds)
Adverse reactions / side effects: Skin Exfoliation, Corneal Scar, Blindness, Stevens-Johnson Syndrome
Adverse event resulted in: hospitalization, disablity
Suspect drug(s):
Ceftin (Cefuroxime)
Other drugs received by patient: Ibuprofen; Dexamethasone; Rocephin; Excedrin (Migraine)
Adverse event in 88 year old female receiving Ceftin (Cefuroxime)
Reported by a consumer/non-health professional from United States on 2007-01-31
Patient: 88 year old female, weighing 54.4 kg (119.7 pounds)
Adverse reactions / side effects: Blood Urine Present, Vomiting, Wheezing, Rash Erythematous, Faecal Incontinence, Oedema, Asthenia, Faeces Discoloured
Adverse event resulted in: hospitalization
Suspect drug(s):
Ceftin
Dosage: one twice daily orally
Administration route: Oral
Indication: Bronchitis
Start date: 2007-01-01
End date: 2007-01-15
Ceftin
Dosage: one twice daily orally
Administration route: Oral
Indication: Chronic Obstructive Pulmonary Disease
Start date: 2007-01-01
End date: 2007-01-15
Avelox
Dosage: one tablet once daily orally
Administration route: Oral
Indication: Bronchitis
Start date: 2007-01-16
End date: 2007-01-23
Other drugs received by patient: Oxygen
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