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
86194337 8619433 7 F 20110222 20160711 20120618 20160719 EXP FR-BAYER-2012-057968 BAYER 30.00 YR A F Y 71.00000 KG 20160719 CN FR FR

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
86194337 8619433 1 PS YAZ DROSPIRENONEETHINYL ESTRADIOL 1 Oral 1 DF, UNK 21676 1 DF FILM-COATED TABLET
86194337 8619433 2 SS Jasmine DROSPIRENONEETHINYL ESTRADIOL 1 Oral UNK 0 FILM-COATED TABLET
86194337 8619433 3 SS AMOXICILLIN. AMOXICILLIN 1 UNK 0
86194337 8619433 4 SS PARACETAMOL ACETAMINOPHEN 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
86194337 8619433 1 Oral contraception
86194337 8619433 3 Tonsillitis
86194337 8619433 4 Tonsillitis

Outcome of event

Event ID CASEID OUTC COD
86194337 8619433 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
86194337 8619433 Nausea
86194337 8619433 Pulmonary embolism

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
86194337 8619433 1 201102 20110704 0
86194337 8619433 2 20030728 20110222 0