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
125828432 12582843 2 F 20160715 20160822 20160722 20160829 EXP US-UNITED THERAPEUTICS-UNT-2016-011572 UNITED THERAPEUTICS 40.71 YR F Y 160.54000 KG 20160829 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
125828432 12582843 1 PS REMODULIN TREPROSTINIL 1 Intravenous drip 0.026 ?G/KG, CONTINUING U U 2100956 21272 .026 UG/KG INJECTION
125828432 12582843 2 C LETAIRIS AMBRISENTAN 1 0
125828432 12582843 3 C COUMADIN WARFARIN SODIUM 1 0
125828432 12582843 4 C REVATIO SILDENAFIL CITRATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125828432 12582843 1 Pulmonary arterial hypertension
125828432 12582843 2 Product used for unknown indication
125828432 12582843 3 Product used for unknown indication
125828432 12582843 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125828432 12582843 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125828432 12582843 Blood potassium decreased
125828432 12582843 Malaise

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
125828432 12582843 1 20150805 0