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
125919461 12591946 1 I 201603 20160303 20160726 20160726 PER US-UNITED THERAPEUTICS-UNT-2016-003677 UNITED THERAPEUTICS 70.21 YR F Y 45.35000 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
125919461 12591946 1 PS ORENITRAM TREPROSTINIL 1 Oral 2 MG, TID U U 2100477 203496 2 MG TABLET TID
125919461 12591946 2 SS LETAIRIS AMBRISENTAN 1 10 MG, QD 1500225A 0 10 MG TABLET QD
125919461 12591946 3 C ADCIRCA TADALAFIL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125919461 12591946 1 Pulmonary arterial hypertension
125919461 12591946 2 Product used for unknown indication
125919461 12591946 3 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125919461 12591946 Abdominal distension
125919461 12591946 Drug dose omission
125919461 12591946 Dyspnoea
125919461 12591946 Fatigue
125919461 12591946 Oxygen saturation decreased
125919461 12591946 Vomiting

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
125919461 12591946 1 20150707 0
125919461 12591946 2 20130215 0