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Index of reports
> Cases resulting in a serious event (23)
> Cases with Drug Hypersensitivity (4)
Below is the selection of adverse event reports related to Keflex (Cephalexin) that includes cases resulting in a serious event where reactions include drug hypersensitivity.
Adverse event in female receiving Keflex (Cephalexin)
Reported by a individual with unspecified qualification from United States on 2007-07-24
Patient: female, weighing 63.5 kg (139.7 pounds)
Adverse reactions / side effects: Dyspnoea, Drug Hypersensitivity, Urticaria, Swollen Tongue
Adverse event resulted in: life threatening event
Suspect drug(s):
Keflex
Dosage: keflex 250mg 4 times a day by mouth within last 5 years
Administration route: Oral
Indication: Kidney Infection
Penicillin
Dosage: penicillin 250mg 4 times a day by mouth within last 1 year
Administration route: Oral
Indication: Ear Infection
Ampicillin
Generic Steroid Dose,pack, Generic Muscle Relaxant
Adverse event in female receiving Keflex (Cephalexin)
Reported by a individual with unspecified qualification from United States on 2007-05-04
Patient: female
Adverse reactions / side effects: Pharyngeal Oedema, Drug Hypersensitivity, LIP Oedema
Suspect drug(s):
Keflex (Cephalexin)
Adverse event in 54 year old female receiving Keflex (Cephalexin)
Reported by a physician from United Kingdom on 2007-04-03
Patient: 54 year old female
Adverse reactions / side effects: Vomiting, Dyspnoea, Viral Infection, Nausea, Urinary Tract Infection, Hypotension, Drug Hypersensitivity, Neutrophilia, Headache, Pyrexia, Myalgia, Acute Generalised Exanthematous Pustulosis, Malaise, Arthralgia, Dysuria
Adverse event resulted in: hospitalization
Suspect drug(s):
Keflex
Dosage: 500 mg; tid;
Indication: Urinary Tract Infection
Azathioprine
Dosage: 50 mg; qd
Indication: Pemphigus
Prochlorperazine Maleate
Indication: Nausea
Other drugs received by patient: Prednisolone; Metformin HCL
Adverse event in 58 year old female receiving Keflex (Cephalexin)
Reported by a physician from United States on 2007-01-29
Patient: 58 year old female
Adverse reactions / side effects: Oral Intake Reduced, Drug Dose Omission, Application Site Reaction, Staphylococcal Infection, Drug Hypersensitivity, Toxic Epidermal Necrolysis, Erythema Multiforme, Herpes Zoster
Suspect drug(s):
Aldara
Dosage: 0.5 scahet, 5 in 1 weeks (s)), topical
Administration route: Topical
Indication: Actinic Keratosis
Start date: 2006-01-01
End date: 2006-01-01
Aldara
Dosage: 0.5 scahet, 5 in 1 weeks (s)), topical
Administration route: Topical
Indication: Basal Cell Carcinoma
Start date: 2006-01-01
End date: 2006-01-01
Aldara
Dosage: 0.5 scahet, 5 in 1 weeks (s)), topical
Administration route: Topical
Indication: Actinic Keratosis
Start date: 2006-12-25
End date: 2007-01-13
Aldara
Dosage: 0.5 scahet, 5 in 1 weeks (s)), topical
Administration route: Topical
Indication: Basal Cell Carcinoma
Start date: 2006-12-25
End date: 2007-01-13
Altace
Hydrochlorothiazide
Zetia
Folic Acid
Aspirin
Fish OIL
Keflex
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