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
127075891 12707589 1 I 20160624 20160503 20160901 20160901 EXP DE-ACTELION-A-NJ2016-135860 ACTELION 72.00 YR E F Y 0.00000 20160901 OT DE FR

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
127075891 12707589 1 PS VENTAVIS ILOPROST 1 Respiratory (inhalation) 5 MCG, 6/D U 21779 5 UG INHALATION VAPOUR, SOLUTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127075891 12707589 1 Pulmonary arterial hypertension

Outcome of event

Event ID CASEID OUTC COD
127075891 12707589 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
127075891 12707589 Dyspnoea
127075891 12707589 Product use issue

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
127075891 12707589 1 20130528 0