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
125398601 12539860 1 I 20160607 20160613 20160708 20160708 EXP US-UNITED THERAPEUTICS-UNT-2016-009596 UNITED THERAPEUTICS 81.81 YR M Y 77.78000 KG 20160708 OT 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
125398601 12539860 1 PS TYVASO TREPROSTINIL 1 18-54 ?G, QID 2100817 22387 INHALATION GAS
125398601 12539860 2 SS TYVASO TREPROSTINIL 1 18-72 ?G, QID 22387 INHALATION GAS
125398601 12539860 3 C REVATIO SILDENAFIL CITRATE 1 0
125398601 12539860 4 C LETAIRIS AMBRISENTAN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125398601 12539860 1 Pulmonary arterial hypertension
125398601 12539860 3 Product used for unknown indication
125398601 12539860 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125398601 12539860 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125398601 12539860 Hypokalaemia
125398601 12539860 Product use issue
125398601 12539860 Renal failure

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
125398601 12539860 1 20150309 0