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
114924504 11492450 4 F 20160719 20150910 20160729 EXP US-ACTELION-A-NJ2015-123723 ACTELION 80.00 YR E F Y 0.00000 20160729 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
114924504 11492450 1 PS TRACLEER BOSENTAN 1 Oral 125 MG, BID IP056P0101,IP060P0101, OP023P0101 21290 125 MG TABLET BID
114924504 11492450 2 C SILDENAFIL. SILDENAFIL 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
114924504 11492450 1 Pulmonary arterial hypertension

Outcome of event

Event ID CASEID OUTC COD
114924504 11492450 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
114924504 11492450 Cardiac disorder
114924504 11492450 Cellulitis
114924504 11492450 Clostridium difficile infection
114924504 11492450 Dialysis
114924504 11492450 Pneumonia
114924504 11492450 Pyrexia

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
114924504 11492450 1 20150211 0