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
125911652 12591165 2 F 201603 20160617 20160726 20160727 PER US-UNITED THERAPEUTICS-UNT-2016-003960 UNITED THERAPEUTICS 50.68 YR F Y 70.30000 KG 20160727 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
125911652 12591165 1 PS REMODULIN TREPROSTINIL 1 Subcutaneous 0.036 ?G/KG, CONTINUING 926118 21272 .036 UG/KG INJECTION
125911652 12591165 2 SS LETAIRIS AMBRISENTAN 1 Unknown 10 MG, QD 1500227A 0 10 MG TABLET QD
125911652 12591165 3 SS LETAIRIS AMBRISENTAN 1 Unknown UNK 1503901A 0 TABLET
125911652 12591165 4 SS LETAIRIS AMBRISENTAN 1 Unknown UNK 1504768A 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125911652 12591165 1 Pulmonary arterial hypertension
125911652 12591165 2 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125911652 12591165 Diarrhoea
125911652 12591165 Oedema peripheral

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
125911652 12591165 1 20090624 0
125911652 12591165 2 20141121 0