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
123474903 12347490 3 F 20160802 20160509 20160815 EXP US-ACTELION-A-US2016-135623 ACTELION 49.00 YR A F Y 117.91000 KG 20160815 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
123474903 12347490 1 PS UPTRAVI SELEXIPAG 1 Oral UNK U 030951801 207947 TABLET
123474903 12347490 2 SS UPTRAVI SELEXIPAG 1 Oral 200 MCG, BID U 030951801 207947 200 UG TABLET BID
123474903 12347490 3 SS UPTRAVI SELEXIPAG 1 Oral 800 MCG, BID U 03100401 207947 800 UG TABLET BID
123474903 12347490 4 SS UPTRAVI SELEXIPAG 1 Oral 1000 MCG, BID U 207947 1000 UG TABLET BID
123474903 12347490 5 SS AMBIEN ZOLPIDEM TARTRATE 1 Unknown U U 0
123474903 12347490 6 SS XANAX ALPRAZOLAM 1 Unknown U U 0
123474903 12347490 7 C AMLODIPINE AMLODIPINE BESYLATE 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123474903 12347490 1 Pulmonary hypertension
123474903 12347490 5 Product used for unknown indication
123474903 12347490 6 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
123474903 12347490 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
123474903 12347490 Hypotension
123474903 12347490 Hypoxia
123474903 12347490 Intentional overdose
123474903 12347490 Mechanical ventilation
123474903 12347490 Myalgia
123474903 12347490 Pneumonia
123474903 12347490 Presyncope

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
123474903 12347490 1 20160308 20160412 0
123474903 12347490 2 201604 0