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
113188812 11318881 2 F 20150508 20160901 20150729 20160912 PER US-ACTELION PHARMACEUTICALS US, INC.-A-NJ2015-118037 ACTELION 27.00 YR A F Y 0.00000 20160912 MD 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
113188812 11318881 1 PS OPSUMIT MACITENTAN 1 Oral 10 MG, QD 204410 10 MG TABLET QD
113188812 11318881 2 SS REMODULIN TREPROSTINIL 1 Unknown U U 0
113188812 11318881 3 C TRAMADOL. TRAMADOL 1 U 0
113188812 11318881 4 C TRIAMCINOLONE TRIAMCINOLONE 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
113188812 11318881 1 Pulmonary arterial hypertension
113188812 11318881 2 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
113188812 11318881 Headache
113188812 11318881 Pain in extremity
113188812 11318881 Pain in jaw

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
113188812 11318881 1 201412 0