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
125919881 12591988 1 I 20160309 0 20160725 20160725 DIR 19.00 YR M N 140.00000 LBS 20160723 N 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
125919881 12591988 1 PS CLARAVIS ISOTRETINOIN 1 Oral N D 34027332A 20170524 0 222 DF CAPSULE BID
125919881 12591988 3 C PROZAC FLUOXETINE HYDROCHLORIDE 1 0
125919881 12591988 5 C MELATONIN MELATONIN 1 0
125919881 12591988 7 C CITICOLINE CITICOLINE 1 0
125919881 12591988 9 C L-TYROSINE 2 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125919881 12591988 1 Acne

Outcome of event

Event ID CASEID OUTC COD
125919881 12591988 DS
125919881 12591988 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125919881 12591988 Anhedonia
125919881 12591988 Depression
125919881 12591988 Sexual dysfunction

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
125919881 12591988 1 20160117 20160520 0