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
121375854 12137585 4 F 20160713 20160728 20160302 20160801 EXP US-ACTELION-A-US2014-104806 ACTELION 57.00 YR A F Y 0.00000 20160801 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
121375854 12137585 1 PS VENTAVIS ILOPROST 1 Respiratory (inhalation) 5 MCG, 6-9X/DAY MA00ZJT,MA0259M,MA0299X,MA0299Z 21779 5 UG INHALATION VAPOUR, SOLUTION
121375854 12137585 2 SS ADCIRCA TADALAFIL 1 Unknown Y 0
121375854 12137585 3 C LETAIRIS AMBRISENTAN 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121375854 12137585 1 Pulmonary arterial hypertension
121375854 12137585 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
121375854 12137585 HO
121375854 12137585 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
121375854 12137585 Chest pain
121375854 12137585 Dyspnoea
121375854 12137585 Fluid retention
121375854 12137585 Malaise
121375854 12137585 Nephrolithiasis
121375854 12137585 Pneumonia
121375854 12137585 Pulmonary arterial hypertension
121375854 12137585 Renal surgery
121375854 12137585 Urinary tract infection
121375854 12137585 Wheezing

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
121375854 12137585 1 20110303 0