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
125723541 12572354 1 I 20160710 20160712 20160719 20160719 EXP DE-ACTELION-A-US2016-139533 ACTELION 69.00 YR E M Y 62.00000 KG 20160720 OT DE DE

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
125723541 12572354 1 PS VENTAVIS ILOPROST 1 Respiratory (inhalation) 2.5 MCG, 6-9 TIMES U 21779 2.5 UG INHALATION VAPOUR, SOLUTION
125723541 12572354 2 C ASPIRIN. ASPIRIN 1 U 0
125723541 12572354 3 C RIOCIGUAT RIOCIGUAT 1 U 0
125723541 12572354 4 C TORASEMIDE TORSEMIDE 1 U 0
125723541 12572354 5 C SERTRALINE SERTRALINE HYDROCHLORIDE 1 U 0
125723541 12572354 6 C LORAZEPAM. LORAZEPAM 1 U 0
125723541 12572354 7 C MORPHIN MORPHINE 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125723541 12572354 1 Pulmonary arterial hypertension

Outcome of event

Event ID CASEID OUTC COD
125723541 12572354 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
125723541 12572354 Death

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
125723541 12572354 1 20160421 0