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
96382969 9638296 9 F 2013 20160822 20131022 20160830 EXP US-ACTELION-A-NJ2013-89962 ACTELION 57.00 YR A F Y 0.00000 20160830 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
96382969 9638296 1 PS TRACLEER BOSENTAN 1 Oral 125 MG, BID 0P010A0102,IP050P0101,OP021P0101 21290 125 MG TABLET BID
96382969 9638296 2 SS TRACLEER BOSENTAN 1 Oral 125 MG, BID OP026P0101 21290 125 MG TABLET BID
96382969 9638296 3 C ASPIRIN. ASPIRIN 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
96382969 9638296 1 Pulmonary arterial hypertension

Outcome of event

Event ID CASEID OUTC COD
96382969 9638296 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
96382969 9638296 Knee arthroplasty
96382969 9638296 Knee operation
96382969 9638296 Malaise
96382969 9638296 Meniscus injury
96382969 9638296 Patella fracture
96382969 9638296 Therapeutic procedure

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
96382969 9638296 1 20130129 0