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
116256082 11625608 2 F 20150923 20160913 20151013 20160926 EXP US-ACTELION-A-US2015-125051 ACTELION 61.00 YR A F Y 0.00000 20160926 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
116256082 11625608 1 PS TRACLEER BOSENTAN 1 Oral 125 MG, BID 21290 125 MG TABLET BID
116256082 11625608 2 C ADCIRCA TADALAFIL 1 U 0
116256082 11625608 3 C FUROSEMIDE. FUROSEMIDE 1 U 0
116256082 11625608 4 C PLAQUENIL HYDROXYCHLOROQUINE SULFATE 1 U 0
116256082 11625608 5 C HUMIRA ADALIMUMAB 1 U 0
116256082 11625608 6 C GABAPENTIN. GABAPENTIN 1 U 0
116256082 11625608 7 C CYMBALTA DULOXETINE HYDROCHLORIDE 1 U 0
116256082 11625608 8 C POTASSIUM POTASSIUM 1 U 0
116256082 11625608 9 C WARFARIN WARFARIN 1 U 0
116256082 11625608 10 C METHOTREXATE. METHOTREXATE 1 U 0
116256082 11625608 11 C PREDNISONE. PREDNISONE 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
116256082 11625608 1 Pulmonary arterial hypertension

Outcome of event

Event ID CASEID OUTC COD
116256082 11625608 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
116256082 11625608 Anaemia
116256082 11625608 Dizziness
116256082 11625608 Intestinal haemorrhage
116256082 11625608 Transfusion

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
116256082 11625608 1 20120720 0