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Index of reports
> Cases with Drug Dose Omission (24)
Below is the selection of side effect reports (a.k.a. adverse event reports) related to Azasite (Azithromycin Ophthalmic) where reactions include drug dose omission. The selected reports were submitted to the FDA during the sample period of about a year.
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 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: Drug Dose Omission, NO Adverse Event, Product Packaging Quantity Issue
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 2012-08-23
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 2012-08-23
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 2012-08-22
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: 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 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 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 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 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
Possible Azasite side effects in
Reported by a physician from United States on 2012-08-03
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 2012-08-02
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 2012-07-31
Patient:
Reactions: Drug Dose Omission, 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: Drug Dose Omission, Inappropriate Schedule of Drug Administration, Drug Ineffective, Product Packaging Quantity Issue
Drug(s) suspected as cause:
Azasite
Dosage: 2 df, bid
Indication: Blepharitis
Start date: 2012-06-29
Azasite
Indication: Conjunctivitis
Possible Azasite side effects in
Reported by a consumer/non-health professional from United States on 2012-07-30
Patient:
Reactions: Drug Dose Omission, NO Adverse Event, Drug Prescribing Error, Product Container Issue
Drug(s) suspected as cause:
Azasite
Dosage: 2 drops, bid
Azasite
Dosage: 2 drops, qd
Possible Azasite side effects in
Reported by a physician from United States on 2012-07-27
Patient:
Reactions: Drug Dose Omission, Product Quality Issue, Eye Irritation
Drug(s) suspected as cause:
Azasite
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
Possible Azasite side effects in
Reported by a pharmacist from United States on 2012-07-19
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 consumer/non-health professional from United States on 2012-07-18
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 2012-07-18
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 2012-07-18
Patient:
Reactions: Product Quality Issue, Drug Dose Omission, NO Adverse Event, Intentional Drug Misuse
Drug(s) suspected as cause:
Azasite
Possible Azasite side effects in
Reported by a consumer/non-health professional from United States on 2012-07-17
Patient:
Reactions: Drug Dose Omission, NO Adverse Event, Product Packaging Quantity Issue
Drug(s) suspected as cause:
Azasite
Indication: Episcleritis
Azasite
Indication: Blepharitis
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