This AIOS Adverse Events Committee has been created to receive reports, analyze, investigate, alert, sensitize and suggest preventive or remedial measures for adverse events arising out of use of ophthalmic drugs, devices, implants etc, including Endophthalmitis and TASS.

Upon submission of reports of adverse events by AIOS Members, the committee performs a detailed root cause analysis, visits the location of adverse events if needed, collates similar information nationwide followed by appropriate alleviation measures.

Please report adverse events in confidence at the link below:

AlOS Adverse Events Committee: