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
87850825 8785082 5 F 20140318 20160902 20120914 20160913 EXP US-ACTELION-A-NJ2012-71244 ACTELION 58.00 YR A F Y 0.00000 20160913 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
87850825 8785082 1 PS TRACLEER BOSENTAN 1 Oral 125 MG, BID IP015P0101, IP044P0101, IP051P0101 21290 125 MG TABLET BID
87850825 8785082 2 C ADCIRCA TADALAFIL 1 U 0
87850825 8785082 3 C ASPIRIN. ASPIRIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
87850825 8785082 1 Pulmonary hypertension

Outcome of event

Event ID CASEID OUTC COD
87850825 8785082 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
87850825 8785082 Acute kidney injury
87850825 8785082 Blood disorder
87850825 8785082 Cardiogenic shock
87850825 8785082 Dizziness
87850825 8785082 Dyspnoea
87850825 8785082 Endotracheal intubation
87850825 8785082 Flank pain
87850825 8785082 Haemodialysis
87850825 8785082 Hypotension
87850825 8785082 Leukocytosis
87850825 8785082 Myelofibrosis
87850825 8785082 Pain in extremity
87850825 8785082 Peripheral swelling
87850825 8785082 Respiratory failure
87850825 8785082 Septic shock
87850825 8785082 Splenomegaly
87850825 8785082 Thrombocytosis
87850825 8785082 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
87850825 8785082 1 20100629 0