This is an index of side effect / adverse reaction reports (a.k.a. adverse event reports) related to Azasite (Azithromycin 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 (55)
Disability (2)
Reports by Reaction Type
NO Adverse Event (31),
Drug Dose Omission (24),
Product Quality Issue (19),
Product Packaging Quantity Issue (13),
Eye Irritation (10),
Inappropriate Schedule of Drug Administration (9),
Incorrect Drug Administration Duration (8),
Eye Pain (5),
Drug Ineffective (4),
Off Label Use (4),
Wrong Technique in Drug Usage Process (3),
Overdose (2)
Below are a few examples of reports where side effects / adverse reactions may be related to Azasite (Azithromycin Ophthalmic). For a complete list or a specific selection of reports, please use the links above.
Possible Azasite side effects in
Reported by a consumer/non-health professional from United States on 2012-08-27
Patient:
Reactions: NO Adverse Event, Expired Drug Administered
Drug(s) suspected as cause:
Azasite
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 health professional (non-physician/pharmacist) from United States on 2012-08-23
Patient:
Reactions: Wrong Technique in Drug Usage Process, Eye Swelling, Ocular Rosacea, Eye Pain
Drug(s) suspected as cause:
Azasite
Possible Azasite side effects in
Reported by a pharmacist from United States on 2012-08-23
Patient:
Reactions: Drug Dose Omission, NO Adverse Event, Product Packaging Quantity Issue
Drug(s) suspected as cause:
Azasite
Possible Azasite side effects in
Reported by a pharmacist from United States on 2012-08-23
Patient:
Reactions: Drug Dose Omission, NO Adverse Event, Product Packaging Quantity Issue
Drug(s) suspected as cause:
Azasite
Possible Azasite side effects in
Reported by a physician from United States on 2012-08-23
Patient:
Reactions: Product Quality Issue, Drug Dose Omission, Eye Irritation
Drug(s) suspected as cause:
Azasite
Possible Azasite side effects in
Reported by a pharmacist from United States on 2012-08-23
Patient:
Reactions: Urticaria
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 2012-08-23
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: Inappropriate Schedule of Drug Administration, NO Adverse Event
Drug(s) suspected as cause:
Azasite
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 pharmacist from United States on 2012-08-23
Patient:
Reactions: Product Quality Issue, Drug Dose Omission, NO Adverse Event
Drug(s) suspected as cause:
Azasite
Possible Azasite side effects in
Reported by a consumer/non-health professional from United States on 2012-08-23
Patient:
Reactions: Product Quality Issue, Drug Dose Omission, NO Adverse Event
Drug(s) suspected as cause:
Azasite
Possible Azasite side effects in
Reported by a consumer/non-health professional from United States on 2012-08-23
Patient:
Reactions: Product Quality Issue, Drug Dose Omission, NO Adverse Event
Drug(s) suspected as cause:
Azasite
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 pharmacist from United States on 2012-08-22
Patient:
Reactions: Inappropriate Schedule of Drug Administration, NO Adverse Event
Drug(s) suspected as cause:
Azasite
Possible Azasite side effects in
Reported by a pharmacist from United States on 2012-08-22
Patient:
Reactions: Drug Dose Omission, Product Quality Issue, NO Adverse Event
Drug(s) suspected as cause:
Azasite
Dosage: unk
Azasite
Dosage: unk
Possible Azasite side effects in
Reported by a consumer/non-health professional from United States on 2012-08-22
Patient:
Reactions: Inappropriate Schedule of Drug Administration, NO Adverse Event, Product Packaging Quantity Issue, Underdose
Drug(s) suspected as cause:
Azasite
Possible Azasite side effects in
Reported by a physician from United States on 2012-08-13
Patient:
Reactions: Drug Dose Omission, Product Quality Issue, NO Adverse Event
Drug(s) suspected as cause:
Azasite
Possible Azasite side effects in
Reported by a consumer/non-health professional from United States on 2012-08-13
Patient:
Reactions: Burning Sensation, Product Packaging Issue, Wrong Technique in Drug Usage Process, Erythema
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 consumer/non-health professional from United States on 2012-08-10
Patient:
Reactions: NO Adverse Event, Accidental Overdose
Drug(s) suspected as cause:
Azasite
Possible Azasite side effects in
Reported by a pharmacist from United States on 2012-08-10
Patient:
Reactions: NO Adverse Event, Product Packaging Quantity Issue, Drug Prescribing Error
Drug(s) suspected as cause:
Azasite
Dosage: 1 drop in each eye, qd
Azasite
Dosage: 1 drop in each eye, bid
Possible Azasite side effects in
Reported by a physician from United States on 2012-08-10
Patient:
Reactions: Drug Dose Omission, Product Quality Issue, NO Adverse Event
Drug(s) suspected as cause:
Azasite
Possible Azasite side effects in
Reported by a consumer/non-health professional from United States on 2012-08-10
Patient:
Reactions: Pain
Drug(s) suspected as cause:
Azasite
Other drugs received by patient: Propylene Glycol; Minocycline HCL
Possible Azasite side effects in
Reported by a pharmacist from United States on 2012-08-10
Patient:
Reactions: Inappropriate Schedule of Drug Administration, NO Adverse Event
Drug(s) suspected as cause:
Azasite
Possible Azasite side effects in
Reported by a physician from United States on 2012-08-06
Patient:
Reactions: Product Quality Issue, Drug Dose Omission, NO Adverse Event
Drug(s) suspected as cause:
Azasite
Possible Azasite side effects in
Reported by a physician from United States on 2012-08-06
Patient:
Reactions: Inappropriate Schedule of Drug Administration, Eye Irritation, Drug Ineffective, Product Packaging Quantity Issue
Drug(s) suspected as cause:
Azasite
Other drugs received by patient: Warfarin Sodium; Metoprolol Tartrate; Thyroid TAB
Possible Azasite side effects in
Reported by a physician from United States on 2012-08-05
Patient:
Reactions: Product Quality Issue, Vision Blurred
Drug(s) suspected as cause:
Azasite
Other drugs received by patient: Coumadin
Possible Azasite side effects in
Reported by a pharmacist from United States on 2012-08-05
Patient:
Reactions: Drug Dose Omission, Product Quality Issue, NO Adverse Event
Drug(s) suspected as cause:
Azasite
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