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
104813944 10481394 4 F 20160628 20140929 20160708 EXP US-ACTELION-A-US2014-105494 ACTELION 42.00 YR A M Y 0.00000 20160708 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
104813944 10481394 1 PS TRACLEER BOSENTAN 1 Oral 62.5 MG, BID HP015P0101, NP013P0402 21290 62.5 MG TABLET BID
104813944 10481394 2 C SILDENAFIL. SILDENAFIL 1 U 0
104813944 10481394 3 C TYVASO TREPROSTINIL 1 U 0
104813944 10481394 4 C ELIQUIS APIXABAN 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
104813944 10481394 1 Pulmonary hypertension

Outcome of event

Event ID CASEID OUTC COD
104813944 10481394 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
104813944 10481394 Cardiac failure congestive
104813944 10481394 Chest discomfort
104813944 10481394 Dyspnoea
104813944 10481394 Fatigue
104813944 10481394 Fibrin D dimer increased
104813944 10481394 Heart valve replacement
104813944 10481394 Mental fatigue
104813944 10481394 Panic attack
104813944 10481394 Procedural complication

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
104813944 10481394 1 20121030 0