The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
5384654 6354917 I 5384654-1 20070616 20070702 20070711 EXP GB-ALLERGAN-0707300US ALLERGAN F Y 20070711 PH UNITED KINGDOM

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
5384654 1008687689 PS OCUFEN 1 OPHTHALMIC F47065
5384654 1008687690 SS OCUFEN 1 E47165
5384654 1008687691 SS OCUFEN 1 E46628
5384654 1008687692 SS CHLORAMPHENICOL 1
5384654 1008687693 SS CYCLOPENTOLATE HCL 1
5384654 1008687694 SS PHENYLEPHRINE 2
5384654 1008687695 SS LIDOCAINE 1
5384654 1008687696 SS POVIDONE IODINE 1
5384654 1008687697 SS BALANCED SALT SOLUTION 1
5384654 1008687698 SS HEALON 2
5384654 1008687699 SS BETAMETHASONE/NEOMYCIN 2

Indications of drugs used

Event ID DRUG SEQ INDI PT
5384654 1008687689 PREOPERATIVE CARE
5384654 1008687692 PREOPERATIVE CARE
5384654 1008687693 PREOPERATIVE CARE
5384654 1008687694 PREOPERATIVE CARE
5384654 1008687695 PREOPERATIVE CARE
5384654 1008687696 PREOPERATIVE CARE
5384654 1008687697 PREOPERATIVE CARE
5384654 1008687698 PREOPERATIVE CARE
5384654 1008687699 POSTOPERATIVE CARE

Outcome of event

Event ID OUTC COD
5384654 OT

Reactions reported

Event ID PT
5384654 TOXIC ANTERIOR SEGMENT SYNDROME

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
5384654 1008687689 20070605
5384654 1008687692 20070605
5384654 1008687693 20070605
5384654 1008687694 20070605
5384654 1008687695 20070605
5384654 1008687696 20070605
5384654 1008687697 20070605
5384654 1008687698 20070605
5384654 1008687699 20070605