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Keflex (Cephalexin) - Adverse Event Reports - Other Serious Reactions - Drug Dose Omission

 


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Index of reports > Cases resulting in other serious reactions (17) > Cases with Drug Dose Omission (2)

Below is the selection of adverse event reports related to Keflex (Cephalexin). that includes cases resulting in other serious reactions where reactions include drug dose omission.

Adverse event in 58 year old female receiving Keflex (Cephalexin)

Reported by a physician from United States on 2007-02-15

Patient: 58 year old female

Adverse reactions / side effects: Localised Infection, Drug Dose Omission, Application Site Reaction, Erythema Multiforme, Application Site Scab

Suspect drug(s):
Aldara
    Dosage: (0.5 sachet, 5 in 1 week(s), topical
    Administration route: Topical
    Indication: Actinic Keratosis
    Start date: 2006-01-01
    End date: 2006-01-01

Aldara
    Dosage: (0.5 sachet, 5 in 1 week(s), topical
    Administration route: Topical
    Indication: Basal Cell Carcinoma
    Start date: 2006-01-01
    End date: 2006-01-01

Aldara
    Dosage: (0.5 sachet, 5 in 1 week(s), topical
    Administration route: Topical
    Indication: Actinic Keratosis
    Start date: 2006-12-25
    End date: 2007-01-13

Aldara
    Dosage: (0.5 sachet, 5 in 1 week(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



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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