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
125918171 12591817 1 I 201602 20160215 20160726 20160726 PER US-UNITED THERAPEUTICS-UNT-2016-002484 UNITED THERAPEUTICS 80.64 YR F Y 57.14000 KG 20160726 CN 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
125918171 12591817 1 PS ORENITRAM TREPROSTINIL 1 Oral 2.5 MG, BID U U 2100679 203496 2.5 MG TABLET BID
125918171 12591817 2 SS ORENITRAM TREPROSTINIL 1 Oral UNK U U 2100399 203496 TABLET
125918171 12591817 3 SS VENTAVIS ILOPROST 1 Unknown Y 0
125918171 12591817 4 C LETAIRIS AMBRISENTAN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125918171 12591817 1 Pulmonary arterial hypertension
125918171 12591817 3 Product used for unknown indication
125918171 12591817 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125918171 12591817 Back pain
125918171 12591817 Headache
125918171 12591817 Migraine
125918171 12591817 Neck pain
125918171 12591817 Pain in extremity

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
125918171 12591817 1 20160113 0