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
124537803 12453780 3 F 20160629 20160609 20160715 PER US-ACTELION-A-US2016-136929 ACTELION 36.00 YR A F Y 0.00000 20160715 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
124537803 12453780 1 PS UPTRAVI SELEXIPAG 1 Oral 400 MCG, BID U U 207947 400 UG TABLET BID
124537803 12453780 2 SS UPTRAVI SELEXIPAG 1 Oral 800 UNK, UNK U U 207947 800 UG TABLET BID
124537803 12453780 3 SS REMODULIN TREPROSTINIL 1 Subcutaneous 26 NG/KG, PER MIN 0 /min

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124537803 12453780 1 Pulmonary arterial hypertension
124537803 12453780 3 Pulmonary arterial hypertension

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
124537803 12453780 Fatigue
124537803 12453780 Headache
124537803 12453780 Incorrect dose administered
124537803 12453780 Nausea

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
124537803 12453780 1 20160511 0
124537803 12453780 3 20150830 0