The Safety Rates Drug Report

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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
125919391 12591939 1 I 201603 20160318 20160726 20160726 PER US-UNITED THERAPEUTICS-UNT-2016-004590 UNITED THERAPEUTICS 48.14 YR F Y 95.24000 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
125919391 12591939 1 PS ORENITRAM TREPROSTINIL 1 Oral 7.25 MG, BID U U 2100397 203496 7.25 MG TABLET BID
125919391 12591939 2 SS ORENITRAM TREPROSTINIL 1 Oral UNK U U 2100398 203496 TABLET
125919391 12591939 3 SS ORENITRAM TREPROSTINIL 1 Oral UNK U U 2100679 203496 TABLET
125919391 12591939 4 SS LETAIRIS AMBRISENTAN 1 Oral 10MG 0 TABLET
125919391 12591939 5 C REVATIO SILDENAFIL CITRATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125919391 12591939 1 Pulmonary arterial hypertension
125919391 12591939 4 Product used for unknown indication
125919391 12591939 5 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125919391 12591939 Drug dose omission
125919391 12591939 Malaise

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
125919391 12591939 1 20140520 0