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
126987772 12698777 2 F 201607 20160831 20160830 20160906 EXP DE-ACTELION-A-US2016-141526 ACTELION 56.00 YR A F Y 0.00000 20160907 OT DE KR

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
126987772 12698777 1 PS VENTAVIS ILOPROST 1 Respiratory (inhalation) UNK, 6X/DAY 21779 INHALATION VAPOUR, SOLUTION
126987772 12698777 2 C TRACLEER BOSENTAN 1 U 21290 TABLET
126987772 12698777 3 C FURIX FUROSEMIDE 1 U 0
126987772 12698777 4 C WARFARIN WARFARIN 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126987772 12698777 1 Pulmonary arterial hypertension
126987772 12698777 2 Pulmonary arterial hypertension

Outcome of event

Event ID CASEID OUTC COD
126987772 12698777 HO
126987772 12698777 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
126987772 12698777 Asthenia
126987772 12698777 Back pain
126987772 12698777 Death
126987772 12698777 Dizziness
126987772 12698777 Fall
126987772 12698777 Fatigue
126987772 12698777 Neck pain
126987772 12698777 Product use issue

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
126987772 12698777 1 20160718 20160725 0