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
126619562 12661956 2 F 20160805 20160810 20160817 20160817 PER US-ACTELION-A-US2016-140780 ACTELION 57.00 YR A F Y 0.00000 20160817 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
126619562 12661956 1 PS VENTAVIS ILOPROST 1 Respiratory (inhalation) UNK, 6 TREATMENTS DAILY 21779 INHALATION VAPOUR, SOLUTION
126619562 12661956 2 SS TRACLEER BOSENTAN 1 Oral 125 MG, BID 21290 125 MG TABLET BID
126619562 12661956 3 C ADCIRCA TADALAFIL 1 U 0
126619562 12661956 4 C COUMADIN WARFARIN SODIUM 1 U 0
126619562 12661956 5 C PROTONIX PANTOPRAZOLE SODIUM 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126619562 12661956 1 Pulmonary arterial hypertension
126619562 12661956 2 Pulmonary arterial hypertension

Outcome of event

Event ID CASEID OUTC COD
126619562 12661956 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126619562 12661956 Blood count abnormal
126619562 12661956 Dizziness
126619562 12661956 Fall
126619562 12661956 Haemorrhage

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
126619562 12661956 1 20140206 0
126619562 12661956 2 20140305 0