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Kenalog (Triamcinolone Topical) - Disability - Suspected Cause - Side Effect Reports

 
 



Index of reports > Disability (3)

Below is the selection of side effect reports (a.k.a. adverse event reports) related to Kenalog (Triamcinolone Topical) disability. The selected reports were submitted to the FDA during the sample period of about a year.

Possible Kenalog side effects in female

Reported by a physician from United States on 2012-07-10

Patient: female

Reactions: Product Quality Issue, Endophthalmitis, Ocular Vasculitis, Eye Infection Fungal, Pseudoendophthalmitis, Retinitis, Medication Residue

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Kenalog



Possible Kenalog side effects in female

Reported by a consumer/non-health professional from United States on 2012-06-07

Patient: female, weighing 77.3 kg (170.1 pounds)

Reactions: Skin Exfoliation, Injection Site Induration

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Kenalog



Possible Kenalog side effects in female

Reported by a consumer/non-health professional from United States on 2012-04-11

Patient: female, weighing 59.9 kg (131.7 pounds)

Reactions: Nerve Injury, Pruritus, Skin Disorder, Headache, Fatigue, Injection Site Induration, Unevaluable Event, Mood Swings, Hair Disorder

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Kenalog

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