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
126126301 12612630 1 I 20160707 20160726 20160801 20160801 EXP US-ACTELION-A-NJ2016-140111 ACTELION 76.00 YR E F Y 0.00000 20160802 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
126126301 12612630 1 PS TRACLEER BOSENTAN 1 Oral 125 MG, BID 403250 MG OP023P0101 21290 125 MG TABLET BID
126126301 12612630 2 SS VENTAVIS ILOPROST 1 Respiratory (inhalation) 5 MCG, 6X DAY MA02BP4 21779 5 UG INHALATION VAPOUR, SOLUTION
126126301 12612630 3 C SILDENAFIL. SILDENAFIL 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126126301 12612630 1 Pulmonary hypertension
126126301 12612630 2 Pulmonary hypertension

Outcome of event

Event ID CASEID OUTC COD
126126301 12612630 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
126126301 12612630 Death

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
126126301 12612630 1 20120206 20160707 0
126126301 12612630 2 20100917 20160707 0