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
125354613 12535461 3 F 20160627 20160729 20160707 20160808 EXP US-UNITED THERAPEUTICS-UNT-2016-010496 UNITED THERAPEUTICS 57.66 YR F Y 52.61000 KG 20160808 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
125354613 12535461 1 PS REMODULIN TREPROSTINIL 1 Subcutaneous 0.075 ?G/KG, CONTINUING U U 2100701 21272 .075 UG/KG INJECTION
125354613 12535461 2 SS REMODULIN TREPROSTINIL 1 UNK U U 21272 INJECTION
125354613 12535461 3 C ADCIRCA TADALAFIL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125354613 12535461 1 Pulmonary hypertension
125354613 12535461 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125354613 12535461 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125354613 12535461 Cellulitis
125354613 12535461 Hypotension
125354613 12535461 Oxygen saturation decreased
125354613 12535461 Thyroid disorder
125354613 12535461 Varicose vein
125354613 12535461 Vasculitis

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
125354613 12535461 1 20150515 0