The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
125227431 12522743 1 I 2011 20160622 20160701 20160701 EXP BR-BAUSCH-BL-2016-015271 BAUSCH AND LOMB 71.00 YR M Y 70.00000 KG 20160701 CN BR BR

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
125227431 12522743 1 PS TIMOPTOL TIMOLOL 1 Ophthalmic Y 18086 EYE DROPS, SOLUTION QD
125227431 12522743 2 SS MESALAMINE. MESALAMINE 1 Oral 1 TABLET FOR 7 DAYS AND A FREE INTERVAL DURING 21 DAYS U 22301 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125227431 12522743 1 Glaucoma
125227431 12522743 2 Prophylaxis

Outcome of event

Event ID CASEID OUTC COD
125227431 12522743 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125227431 12522743 Diverticulitis
125227431 12522743 Drug ineffective

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

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
125227431 12522743 1 2009 2011 0
125227431 12522743 2 2009 0