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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