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
123388694 12338869 4 F 20160415 20160630 20160505 20160715 PER US-ACTELION-A-US2016-135465 ACTELION 51.00 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
123388694 12338869 1 PS OPSUMIT MACITENTAN 1 Oral 10 MG, QD 204410 10 MG TABLET QD
123388694 12338869 2 SS UPTRAVI SELEXIPAG 1 Oral 600 MCG, BID 207947 600 UG TABLET BID
123388694 12338869 3 SS UPTRAVI SELEXIPAG 1 Oral 800 MCG, UNK 207947 800 UG TABLET
123388694 12338869 4 SS VENTAVIS ILOPROST 1 Respiratory (inhalation) 5 MCG, 6-9X/DAY U U MA0199Z, MA0299Z 21779 5 UG INHALATION VAPOUR, SOLUTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123388694 12338869 1 Pulmonary arterial hypertension
123388694 12338869 2 Pulmonary arterial hypertension
123388694 12338869 4 Pulmonary arterial hypertension

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
123388694 12338869 Arthralgia
123388694 12338869 Headache
123388694 12338869 Myalgia
123388694 12338869 Therapy non-responder

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
123388694 12338869 1 20151118 0
123388694 12338869 2 20160325 0
123388694 12338869 4 20151112 0