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
5384854 6355067 I 5384854-0 20070510 20070702 20070711 EXP GB-ALLERGAN-0707299US 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
5384854 1008688410 PS OCUFEN 1 OPHTHALMIC E47165
5384854 1008688411 SS OCUFEN 1 F47065
5384854 1008688412 SS OCUFEN 1 E46628
5384854 1008688413 SS CHLORAMPHENICOL 1
5384854 1008688414 SS CYCLOPENTOLATE HCL 1
5384854 1008688415 SS PHENYLEPHRINE 2
5384854 1008688416 SS LIDOCAINE 1
5384854 1008688417 SS POVIDONE IODINE 1
5384854 1008688418 SS BALANCED SALT SOLUTION 1
5384854 1008688419 SS HEALON 2
5384854 1008688420 SS BETAMETHASONE/NEOMYCIN 2

Indications of drugs used

Event ID DRUG SEQ INDI PT
5384854 1008688410 PREOPERATIVE CARE
5384854 1008688413 PREOPERATIVE CARE
5384854 1008688414 PREOPERATIVE CARE
5384854 1008688415 PREOPERATIVE CARE
5384854 1008688416 PREOPERATIVE CARE
5384854 1008688417 PREOPERATIVE CARE
5384854 1008688418 PREOPERATIVE CARE
5384854 1008688419 PREOPERATIVE CARE
5384854 1008688420 POSTOPERATIVE CARE

Outcome of event

Event ID OUTC COD
5384854 OT

Reactions reported

Event ID PT
5384854 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
5384854 1008688410 20070501