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
125919021 12591902 1 I 201602 20160229 20160726 20160726 PER US-UNITED THERAPEUTICS-UNT-2016-003623 UNITED THERAPEUTICS 0.00 F Y 0.00000 20160726 PH 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
125919021 12591902 1 PS ORENITRAM TREPROSTINIL 1 Oral 20 MG, ONE TIME DOSE U U 203496 20 MG TABLET
125919021 12591902 2 SS ADCIRCA TADALAFIL 1 Unknown 0
125919021 12591902 3 SS SILDENAFIL. SILDENAFIL 1 Unknown 20 MG, TID U U 0 20 MG TID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125919021 12591902 1 Pulmonary arterial hypertension
125919021 12591902 2 Product used for unknown indication
125919021 12591902 3 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125919021 12591902 Arthralgia
125919021 12591902 Back pain
125919021 12591902 Bone pain
125919021 12591902 Chest pain
125919021 12591902 Headache
125919021 12591902 Pain

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found