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
126334661 12633466 1 I 20160723 20160802 20160809 20160809 PER US-TEVA-682533ACC TEVA 0.00 F Y 0.00000 20160809 CN 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
126334661 12633466 1 PS PLAN B ONE-STEP LEVONORGESTREL 1 21998 1.5 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126334661 12633466 1 Menstruation delayed

Outcome of event

Event ID CASEID OUTC COD
126334661 12633466 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126334661 12633466 Exposure during pregnancy
126334661 12633466 Intentional product misuse
126334661 12633466 Intentional product use issue
126334661 12633466 Menstruation delayed
126334661 12633466 Pregnancy after post coital contraception

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
126334661 12633466 1 20160723 20160723 0