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
123867633 12386763 3 F 20160311 20160720 20160519 20160727 EXP DE-ACTELION-A-US2016-136518 ACTELION 70.00 YR E F Y 0.00000 20160727 OT DE CO

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
123867633 12386763 1 PS VENTAVIS ILOPROST 1 Respiratory (inhalation) 5 MCG, 6-9X/DAY U 21779 5 UG INHALATION VAPOUR, SOLUTION
123867633 12386763 2 SS VENTAVIS ILOPROST 1 Respiratory (inhalation) UNK, 5/DAY U 21779 INHALATION VAPOUR, SOLUTION
123867633 12386763 3 SS VENTAVIS ILOPROST 1 Respiratory (inhalation) UNK, 6/DAY U 21779 INHALATION VAPOUR, SOLUTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123867633 12386763 1 Pulmonary hypertension

Outcome of event

Event ID CASEID OUTC COD
123867633 12386763 DE
123867633 12386763 HO
123867633 12386763 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123867633 12386763 Condition aggravated
123867633 12386763 Death
123867633 12386763 Product use issue
123867633 12386763 Renal cancer

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
123867633 12386763 1 20150511 0
123867633 12386763 2 20160507 0
123867633 12386763 3 20160519 201607 0