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
124984514 12498451 4 F 20160611 20160715 20160627 20160720 EXP US-ACTELION-A-NJ2016-138377 ACTELION 66.00 YR E M Y 0.00000 20160720 PH 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
124984514 12498451 1 PS VENTAVIS ILOPROST 1 Respiratory (inhalation) 5 MCG, 6-9X/DAILY U MA02BP4 21779 5 UG INHALATION VAPOUR, SOLUTION
124984514 12498451 2 SS TRACLEER BOSENTAN 1 Oral 62.5 MG, Q12HRS U 21290 62.5 MG TABLET BID
124984514 12498451 3 C ADCIRCA TADALAFIL 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124984514 12498451 1 Pulmonary arterial hypertension
124984514 12498451 2 Pulmonary arterial hypertension

Outcome of event

Event ID CASEID OUTC COD
124984514 12498451 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
124984514 12498451 Acute respiratory failure
124984514 12498451 Condition aggravated
124984514 12498451 Interstitial lung disease
124984514 12498451 Pulmonary arterial hypertension

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
124984514 12498451 1 20130403 0
124984514 12498451 2 20150721 0