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
82327482 8232748 2 F 19981120 20121018 20111107 20121029 EXP US-ROCHE-784615 ROCHE 18.89 YR F Y 89.89000 KG 20121029 LW US US

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
82327482 8232748 1 PS Accutane 1 UNKNOWN D 18662

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
82327482 8232748 1 Acne

Outcome of event

Event ID CASEID OUTC COD
82327482 8232748 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
82327482 8232748 Blood cholesterol increased
82327482 8232748 Colitis ulcerative
82327482 8232748 Crohn's disease
82327482 8232748 Depression
82327482 8232748 Emotional distress
82327482 8232748 Inflammatory bowel disease
82327482 8232748 Irritable bowel syndrome
82327482 8232748 Suicidal ideation

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
82327482 8232748 1 19981119 19990406 0