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
126869201 12686920 1 I 20160727 20160729 20160826 20160826 PER US-TEVA-682041ACC TEVA 22.21 YR F Y 81.72000 KG 20160826 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
126869201 12686920 1 PS PLAN B ONE-STEP LEVONORGESTREL 1 21998 1.5 MOL TABLET
126869201 12686920 2 C JOLESSA ETHINYL ESTRADIOLLEVONORGESTREL 1 0
126869201 12686920 3 C TOPIRAMATE. TOPIRAMATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126869201 12686920 1 Post coital contraception
126869201 12686920 2 Contraception
126869201 12686920 3 Migraine

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126869201 12686920 Abdominal distension
126869201 12686920 Abdominal pain upper
126869201 12686920 Diarrhoea
126869201 12686920 Dysmenorrhoea
126869201 12686920 Nausea
126869201 12686920 Vaginal discharge

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
126869201 12686920 1 20160714 20160714 0