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
125419952 12541995 2 F 20160515 20160816 20160708 20160826 EXP US-ACTELION-A-US2016-139092 ACTELION 69.00 YR E F Y 0.00000 20160826 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
125419952 12541995 1 PS TRACLEER BOSENTAN 1 Oral 125 MG, BID 21290 125 MG TABLET BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125419952 12541995 1 Pulmonary arterial hypertension

Outcome of event

Event ID CASEID OUTC COD
125419952 12541995 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125419952 12541995 Fall
125419952 12541995 Foot fracture
125419952 12541995 Hip fracture
125419952 12541995 Lower limb fracture
125419952 12541995 Pain
125419952 12541995 Sciatica

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
125419952 12541995 1 20090118 0