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
117206193 11720619 3 F 20160810 20151110 20160817 PER US-ACTELION PHARMACEUTICALS US, INC.-A-NJ2014-107774 ACTELION 61.00 YR A F Y 0.00000 20160817 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
117206193 11720619 1 PS VENTAVIS ILOPROST 1 Respiratory (inhalation) 5 MCG, 6 TO 9X/DAY MA022UX,MA026TA,MA02DL0 21779 5 UG INHALATION VAPOUR, SOLUTION
117206193 11720619 2 C REVATIO SILDENAFIL CITRATE 1 U 0
117206193 11720619 3 C LETAIRIS AMBRISENTAN 1 U 0
117206193 11720619 4 C ADCIRCA TADALAFIL 1 U 0
117206193 11720619 5 C WARFARIN WARFARIN 1 U 0
117206193 11720619 6 C PROCARDIA NIFEDIPINE 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
117206193 11720619 1 Pulmonary hypertension

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
117206193 11720619 Bronchitis
117206193 11720619 Cough
117206193 11720619 Flushing
117206193 11720619 Pain in jaw
117206193 11720619 Pleural effusion
117206193 11720619 Pulmonary fibrosis

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
117206193 11720619 1 20071029 0