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Azasite (Azithromycin Ophthalmic) - Inappropriate Schedule of Drug Administration - Suspected Cause - Side Effect Reports

 
 



Index of reports > Cases with Inappropriate Schedule of Drug Administration (9)

Below is the selection of side effect reports (a.k.a. adverse event reports) related to Azasite (Azithromycin Ophthalmic) where reactions include inappropriate schedule of drug administration. 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 2012-08-23

Patient:

Reactions: Inappropriate Schedule of Drug Administration, NO Adverse Event

Drug(s) suspected as cause:
Azasite



Possible Azasite side effects in

Reported by a 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 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 2012-08-10

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: 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 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 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 male

Reported by a physician from United States on 2012-03-23

Patient: male

Reactions: Inappropriate Schedule of Drug Administration, Eye Irritation, Ocular Discomfort, Eye Pain

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Azasite

Other drugs received by patient: Restasis



Possible Azasite side effects in male

Reported by a physician from United States on 2012-02-27

Patient: male

Reactions: Inappropriate Schedule of Drug Administration, Eye Irritation, Ocular Discomfort, Eye Pain

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Azasite

Other drugs received by patient: Restasis

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