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
125640821 12564082 1 I 20160713 0 20160715 20160715 DIR 41.00 YR F N 190.00000 LBS 20160714 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
125640821 12564082 1 PS MEDROXYPROGESTERONE MEDROXYPROGESTERONE 1 90 DAYS INJECTION N D 0 SUSPENSION FOR INJECTION
125640821 12564082 3 C ZYRTEC CETIRIZINE HYDROCHLORIDE 1 0
125640821 12564082 5 C WELLBUTRIN BUPROPION HYDROCHLORIDE 1 0
125640821 12564082 7 C VITAMIN C ASCORBIC ACID 1 0
125640821 12564082 9 C IRON IRON 1 0
125640821 12564082 11 C FLONASE FLUTICASONE PROPIONATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125640821 12564082 1 Menstrual disorder

Outcome of event

Event ID CASEID OUTC COD
125640821 12564082 DS
125640821 12564082 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125640821 12564082 Dizziness
125640821 12564082 Menorrhagia
125640821 12564082 Muscle spasms
125640821 12564082 Nausea
125640821 12564082 Paraesthesia
125640821 12564082 Vision blurred

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
125640821 12564082 1 20160126 20160426 90 DAY