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
125214722 12521472 2 F 20160622 20160630 20160701 20160712 EXP US-ACTELION-A-NJ2016-138626 ACTELION 55.00 YR A F Y 0.00000 20160712 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
125214722 12521472 1 PS TRACLEER BOSENTAN 1 Oral 125 MG, BID 959250 MG OP023P0101 21290 125 MG TABLET BID
125214722 12521472 2 C TREPROSTINIL DIOLAMIN TREPROSTINIL DIOLAMINE 1 U 0
125214722 12521472 3 C REVATIO SILDENAFIL CITRATE 1 U 0
125214722 12521472 4 C METOLAZONE. METOLAZONE 1 U 0
125214722 12521472 5 C MIDODRINE MIDODRINE 1 U 0
125214722 12521472 6 C TORSEMIDE. TORSEMIDE 1 U 0
125214722 12521472 7 C COUMADIN WARFARIN SODIUM 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125214722 12521472 1 Pulmonary hypertension

Outcome of event

Event ID CASEID OUTC COD
125214722 12521472 HO
125214722 12521472 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
125214722 12521472 Death
125214722 12521472 Malaise
125214722 12521472 Pain

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
125214722 12521472 1 20051220 20160622 0