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
125898071 12589807 1 I 20160713 20160713 20160725 20160725 PER US-ACTELION-A-US2016-139442 ACTELION 57.00 YR A F Y 0.00000 20160725 MD 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
125898071 12589807 1 PS TRACLEER BOSENTAN 1 Oral 125 MG, BID 0P026P0101 21290 125 MG TABLET BID
125898071 12589807 2 C REMODULIN TREPROSTINIL 1 U 0
125898071 12589807 3 C AMOXICILLIN. AMOXICILLIN 1 U 0
125898071 12589807 4 C OXYCODONE OXYCODONE 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125898071 12589807 1 Pulmonary arterial hypertension

Outcome of event

Event ID CASEID OUTC COD
125898071 12589807 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125898071 12589807 Condition aggravated
125898071 12589807 Pulmonary arterial hypertension
125898071 12589807 Pulmonary arterial pressure increased

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
125898071 12589807 1 20081205 0