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
125743222 12574322 2 F 201607 20160728 20160720 20160804 EXP US-UNITED THERAPEUTICS-UNT-2016-011319 UNITED THERAPEUTICS 65.21 YR F Y 58.50000 KG 20160804 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
125743222 12574322 1 PS REMODULIN TREPROSTINIL 1 Subcutaneous 0.065 ?G/KG, CONTINUING 2100701 21272 .065 UG/KG INJECTION
125743222 12574322 2 C COUMADIN WARFARIN SODIUM 1 0
125743222 12574322 3 C SILDENAFIL. SILDENAFIL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125743222 12574322 1 Pulmonary arterial hypertension
125743222 12574322 2 Product used for unknown indication
125743222 12574322 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125743222 12574322 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125743222 12574322 Gout
125743222 12574322 Pain in extremity

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
125743222 12574322 1 20111007 0