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
121527582 12152758 2 F 20160719 20160304 20160725 EXP US-ACTELION-A-US2015-119042 ACTELION 69.00 YR E M Y 0.00000 20160725 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
121527582 12152758 1 PS VENTAVIS ILOPROST 1 Respiratory (inhalation) 2.5 MCG, UNK MA0233E, MA02A59 21779 2.5 UG INHALATION VAPOUR, SOLUTION
121527582 12152758 2 SS VENTAVIS ILOPROST 1 Respiratory (inhalation) 5 MCG, 6-9 TIMES A DAY MA02A59 21779 5 UG INHALATION VAPOUR, SOLUTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121527582 12152758 1 Pulmonary arterial hypertension

Outcome of event

Event ID CASEID OUTC COD
121527582 12152758 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
121527582 12152758 Blood pressure decreased
121527582 12152758 Cough
121527582 12152758 Dyspnoea
121527582 12152758 Eye irritation
121527582 12152758 Headache
121527582 12152758 Heart rate decreased
121527582 12152758 Heart rate irregular
121527582 12152758 Myalgia
121527582 12152758 Neuropathy peripheral
121527582 12152758 Pain in jaw
121527582 12152758 Scrotal swelling

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
121527582 12152758 1 20150430 0