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
121853262 12185326 2 F 20160906 20160316 20160915 EXP US-ACTELION-A-US2016-130314 ACTELION 66.00 YR E F Y 0.00000 20160915 OT 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
121853262 12185326 1 PS TRACLEER BOSENTAN 1 Oral 125 MG, BID IP060P0101, OP021P0101, OP026P0101 21290 125 MG TABLET BID
121853262 12185326 2 C TREPROSTINIL DIOLAMIN TREPROSTINIL DIOLAMINE 1 U 0
121853262 12185326 3 C WARFARIN WARFARIN 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121853262 12185326 1 Pulmonary arterial hypertension

Outcome of event

Event ID CASEID OUTC COD
121853262 12185326 HO
121853262 12185326 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
121853262 12185326 Bronchitis
121853262 12185326 Cardiac disorder
121853262 12185326 Dialysis
121853262 12185326 Diarrhoea
121853262 12185326 Dyspnoea exertional
121853262 12185326 Headache
121853262 12185326 Lung disorder
121853262 12185326 Pneumonia

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
121853262 12185326 1 20141120 0