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
122109035 12210903 5 F 20160804 20160325 20160816 EXP US-ACTELION-A-NJ2016-133321 ACTELION 56.00 YR A F Y 0.00000 20160816 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
122109035 12210903 1 PS TRACLEER BOSENTAN 1 Oral 125 MG, BID OP021P0101,OP023P0101 21290 125 MG TABLET BID
122109035 12210903 2 C REVATIO SILDENAFIL CITRATE 1 U 0
122109035 12210903 3 C REMODULIN TREPROSTINIL 1 0
122109035 12210903 4 C WARFARIN WARFARIN 1 U 0
122109035 12210903 5 C TREPROSTINIL DIOLAMIN TREPROSTINIL DIOLAMINE 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122109035 12210903 1 Pulmonary arterial hypertension

Outcome of event

Event ID CASEID OUTC COD
122109035 12210903 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
122109035 12210903 Cough
122109035 12210903 Dyspnoea
122109035 12210903 Pneumothorax
122109035 12210903 Pulmonary resection

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
122109035 12210903 1 20091222 0