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Index of reports
> Cases with Off Label Use (4)
Below is the selection of side effect reports (a.k.a. adverse event reports) related to Azasite (Azithromycin Ophthalmic) where reactions include off label use. The selected reports were submitted to the FDA during the sample period of about a year.
Possible Azasite side effects in
Reported by a pharmacist from United States on 2012-08-22
Patient:
Reactions: Drug Dose Omission, Off Label Use, Overdose, NO Adverse Event
Drug(s) suspected as cause:
Azasite
Indication: DRY Eye
Azasite
Dosage: 2 gtt, bid in both eyes
Indication: Meibomian Gland Dysfunction
Start date: 2012-03-23
Possible Azasite side effects in
Reported by a physician from United States on 2012-08-10
Patient:
Reactions: Off Label Use, Incorrect Drug Administration Duration, Eye Irritation
Drug(s) suspected as cause:
Azasite
Dosage: unk unk, qd
Indication: Blepharitis
Start date: 2012-05-10
End date: 2012-06-07
Azasite
Dosage: unk, bid
Indication: Rosacea
Start date: 2012-05-07
End date: 2012-05-09
Possible Azasite side effects in
Reported by a consumer/non-health professional from United States on 2012-08-03
Patient:
Reactions: Off Label Use, Eye Irritation
Drug(s) suspected as cause:
Azasite
Other drugs received by patient: Morphine Sulfate; Dilaudid; Diclofenac Sodium; Lactulose; Prednisolone Acetate; Hydrocodone Bitartrate; Zocor; Fosinopril Sodium; Bupropion Hydrochloride; Provigil; Vesicare; Zelapar
Possible Azasite side effects in
Reported by a physician from United States on 2012-07-27
Patient:
Reactions: Off Label Use, Eye Pain
Drug(s) suspected as cause:
Azasite
Dosage: 1, drop, bid
Start date: 2012-06-14
End date: 2012-06-16
Azasite
Dosage: 1 drop qd
Other drugs received by patient: Ceclor
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