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
119149402 11914940 2 F 20160728 20160113 20160802 EXP US-GILEAD-2016-0192410 GILEAD 58.00 YR A F Y 0.00000 20160802 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
119149402 11914940 1 PS AMBRISENTAN AMBRISENTAN 1 Unknown 10 MG, QD SBFQ 22081 10 MG TABLET QD
119149402 11914940 2 SS AMBRISENTAN AMBRISENTAN 1 22081 TABLET
119149402 11914940 3 SS ADCIRCA TADALAFIL 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119149402 11914940 1 Pulmonary arterial hypertension
119149402 11914940 2 Systemic scleroderma
119149402 11914940 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
119149402 11914940 OT
119149402 11914940 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
119149402 11914940 Pulmonary arterial hypertension
119149402 11914940 Pulmonary fibrosis
119149402 11914940 Systemic scleroderma

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
119149402 11914940 1 20141027 20151231 0