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Acular (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 (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 (3)

Reports by Reaction Type

Pain (1)Eye Infection (1)Dermatitis Contact (1)Eye Pain (1)Visual Impairment (1)Lacrimation Increased (1)

Possible Acular side effects in 65 year old female

Reported by a consumer/non-health professional from United Kingdom on 2012-08-24

Patient: 65 year old female, weighing 48.0 kg (105.6 pounds)

Reactions: Lacrimation Increased, Eye Pain

Drug(s) suspected as cause:
Acular

Other drugs received by patient: Oftaquix; Maxidex



Possible Acular side effects in male

Reported by a consumer/non-health professional from Australia on 2012-07-13

Patient: male

Reactions: Pain, Visual Impairment, Eye Infection

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Acular



Possible Acular side effects in 49 year old female

Reported by a health professional (non-physician/pharmacist) from United States on 2012-01-20

Patient: 49 year old female

Reactions: Dermatitis Contact

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

Fluorescite
    Indication: Product Used FOR Unknown Indication

Restasis
    Indication: Product Used FOR Unknown Indication

Xalatan
    Indication: Glaucoma

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