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
126954502 12695450 2 F 2016 20160915 20160829 20160919 EXP BR-JNJFOC-20160822924 JANSSEN 0.00 A F Y 0.00000 20160919 CN BR BR

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
126954502 12695450 1 PS ORTHO EVRA ETHINYL ESTRADIOLNORELGESTROMIN 1 Transdermal N UNKNOWN 21180 PATCH

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126954502 12695450 1 Contraception

Outcome of event

Event ID CASEID OUTC COD
126954502 12695450 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126954502 12695450 Acne
126954502 12695450 Application site reaction
126954502 12695450 Chromaturia
126954502 12695450 Ephelides
126954502 12695450 Medication error
126954502 12695450 Polydipsia
126954502 12695450 Product adhesion issue
126954502 12695450 Renal disorder
126954502 12695450 Skin disorder

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found