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
125390341 12539034 1 I 20160705 20160708 20160708 EXP CA-BAUSCH-BL-2016-016015 BAUSCH AND LOMB 20.00 YR M Y 0.00000 20160708 MD CA CA

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
125390341 12539034 1 PS WELLBUTRIN XL BUPROPION HYDROCHLORIDE 1 Oral U 21515 150 MG TABLET
125390341 12539034 2 SS WELLBUTRIN XL BUPROPION HYDROCHLORIDE 1 U 21515
125390341 12539034 3 C CIPRALEX ESCITALOPRAM OXALATE 1 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125390341 12539034 1 Depression
125390341 12539034 2 Anxiety
125390341 12539034 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125390341 12539034 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
125390341 12539034 Malaise
125390341 12539034 Peripheral swelling
125390341 12539034 Serum sickness-like reaction
125390341 12539034 Swelling
125390341 12539034 Temporomandibular joint syndrome
125390341 12539034 Urticaria

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

no results found

Therapies reported

no results found