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Acular LS (Ketorolac Ophthalmic) - Side Effect Reports to FDA


This is an index of side effect / adverse reaction reports (a.k.a. adverse event reports) related to Acular LS (Ketorolac Ophthalmic) and submitted to the FDA during the sample period of about a year. The information is not vetted and should not be considered as verified clinical evidence.

Reports by Event Outcome

All Cases (1)

Reports by Reaction Type

Visual Acuity Reduced (1)Eye Inflammation (1)

Possible Acular LS side effects in 60 year old male

Reported by a health professional (non-physician/pharmacist) from United States on 2012-02-05

Patient: 60 year old male

Reactions: Eye Inflammation, Visual Acuity Reduced

Drug(s) suspected as cause:
Acular LS
    Indication: Product Used FOR Unknown Indication

Pred Forte
    Dosage: 1 gtt, q1hr
    Indication: Product Used FOR Unknown Indication

    Indication: Product Used FOR Unknown Indication

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