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Index of reports
> Cases with Incorrect Drug Administration Duration (8)
Below is the selection of side effect reports (a.k.a. adverse event reports) related to Azasite (Azithromycin Ophthalmic) where reactions include incorrect drug administration duration. The selected reports were submitted to the FDA during the sample period of about a year.
Possible Azasite side effects in
Reported by a physician from United States on 2012-08-27
Patient:
Reactions: Product Quality Issue, Incorrect Drug Administration Duration
Drug(s) suspected as cause:
Azasite
Dosage: 1 df, qd
Indication: Conjunctivitis Bacterial
Start date: 2012-06-28
Azasite
Indication: Eye Inflammation
Possible Azasite side effects in
Reported by a physician from United States on 2012-08-23
Patient:
Reactions: Product Quality Issue, Wrong Technique in Drug Usage Process, Incorrect Drug Administration Duration, Eyelid Disorder, Eye Pain
Drug(s) suspected as cause:
Azasite
Possible Azasite side effects in
Reported by a physician from United States on 2012-08-23
Patient:
Reactions: Incorrect Drug Administration Duration, Overdose, NO Adverse Event
Drug(s) suspected as cause:
Azasite
Possible Azasite side effects in
Reported by a pharmacist from United States on 2012-08-23
Patient:
Reactions: NO Adverse Event, Incorrect Drug Administration Duration, Product Packaging Quantity Issue
Drug(s) suspected as cause:
Azasite
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 pharmacist from United States on 2012-07-31
Patient:
Reactions: Incorrect Drug Administration Duration, NO Adverse Event, Product Packaging Quantity Issue
Drug(s) suspected as cause:
Azasite
Possible Azasite side effects in
Reported by a health professional (non-physician/pharmacist) from United States on 2012-07-31
Patient:
Reactions: Incorrect Drug Administration Duration, Eye Irritation
Drug(s) suspected as cause:
Azasite
Dosage: 2 gtt, qd
Azasite
Dosage: 2 gtt, bid
Indication: Blepharitis
Start date: 2012-07-09
Possible Azasite side effects in
Reported by a physician from United States on 2012-07-26
Patient:
Reactions: Product Quality Issue, Drug Dose Omission, Inappropriate Schedule of Drug Administration, NO Adverse Event, Incorrect Drug Administration Duration
Drug(s) suspected as cause:
Azasite
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