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
120723333 12072333 3 F 2009 20160701 20160212 20160711 EXP AT-BAYER-2015-030024 BAYER 24.00 YR A F Y 0.00000 20160711 MD AT AT

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
120723333 12072333 1 PS Yasminelle DROSPIRENONE 1 UNK Y 0 FILM-COATED TABLET
120723333 12072333 2 SS Yasminelle DROSPIRENONE 1 Oral UNK Y 0 FILM-COATED TABLET
120723333 12072333 3 SS YASMIN DROSPIRENONEETHINYL ESTRADIOL 1 UNK Y 0 FILM-COATED TABLET
120723333 12072333 4 C FLOXACILLIN FLUCLOXACILLIN 1 500 MG, UNK 0 500 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
120723333 12072333 1 Contraception
120723333 12072333 2 Contraception

Outcome of event

Event ID CASEID OUTC COD
120723333 12072333 HO
120723333 12072333 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
120723333 12072333 Abscess limb
120723333 12072333 Arthralgia
120723333 12072333 Autonomic nervous system imbalance
120723333 12072333 Cellulitis
120723333 12072333 Deep vein thrombosis
120723333 12072333 Discomfort
120723333 12072333 Erythema
120723333 12072333 Pain
120723333 12072333 Pain in extremity
120723333 12072333 Peripheral swelling
120723333 12072333 Varicose vein
120723333 12072333 Venous valve ruptured

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
120723333 12072333 1 20071029 200812 0
120723333 12072333 2 20080904 200812 0
120723333 12072333 3 200812 200906 0