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
121657212 12165721 2 F 20121025 20160701 20160309 20160711 EXP US-009507513-1603USA002761 MERCK 0.00 F Y 54.42000 KG 20160711 MD 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
121657212 12165721 1 PS NUVARING ETHINYL ESTRADIOLETONOGESTREL 1 Vaginal 3 WEEKS IN, 1 WEEK OUT 21187 1 DF VAGINAL RING
121657212 12165721 2 SS NUVARING ETHINYL ESTRADIOLETONOGESTREL 1 Vaginal 3 WEEKS IN, 1 WEEK OUT 21187 1 DF VAGINAL RING

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121657212 12165721 1 Contraception
121657212 12165721 2 Menstrual cycle management

Outcome of event

Event ID CASEID OUTC COD
121657212 12165721 HO
121657212 12165721 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
121657212 12165721 Acne
121657212 12165721 Cholelithiasis
121657212 12165721 Deep vein thrombosis
121657212 12165721 Infection
121657212 12165721 Lyme disease
121657212 12165721 Off label use
121657212 12165721 Pulmonary infarction

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
121657212 12165721 1 20120216 20130709 0
121657212 12165721 2 20131231 20140310 0