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
125942811 12594281 1 I 201605 20160513 20160726 20160726 PER US-UNITED THERAPEUTICS-UNT-2016-007911 UNITED THERAPEUTICS 73.96 YR F Y 62.00000 KG 20160726 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
125942811 12594281 1 PS REMODULIN TREPROSTINIL 1 Intravenous drip 0.01 ?G/KG, CONTINUING U U 926617 21272 .01 UG/KG INJECTION
125942811 12594281 2 SS TORSEMIDE. TORSEMIDE 1 Unknown UNK 0
125942811 12594281 3 SS TORSEMIDE. TORSEMIDE 1 Unknown 40 MG, Q12H 0 40 MG BID
125942811 12594281 4 C ADEMPAS RIOCIGUAT 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125942811 12594281 1 Pulmonary hypertension
125942811 12594281 2 Product used for unknown indication
125942811 12594281 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125942811 12594281 Dizziness
125942811 12594281 Nausea
125942811 12594281 Weight decreased

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
125942811 12594281 1 20160426 0