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
125911492 12591149 2 F 20160212 20160328 20160726 20160727 PER US-UNITED THERAPEUTICS-UNT-2016-003728 UNITED THERAPEUTICS 0.00 A F Y 0.00000 20160727 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
125911492 12591149 1 PS REMODULIN TREPROSTINIL 1 Intravenous drip 0.005 ?G/KG, CONTINUING 926618 21272 .005 UG/KG INJECTION
125911492 12591149 2 SS REMODULIN TREPROSTINIL 1 Intravenous drip 0.008 ?G/KG, EVERY 48 HOURS 21272 .008 UG/KG INJECTION
125911492 12591149 3 SS REMODULIN TREPROSTINIL 1 Intravenous drip 0.01 ?G/KG, CONTINUING 926618 21272 .01 UG/KG INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125911492 12591149 1 Pulmonary arterial hypertension

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125911492 12591149 Back pain
125911492 12591149 Decreased appetite
125911492 12591149 Diarrhoea
125911492 12591149 Dizziness
125911492 12591149 Faeces discoloured
125911492 12591149 Headache
125911492 12591149 Nausea
125911492 12591149 Pain in extremity
125911492 12591149 Vomiting

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
125911492 12591149 1 20160212 0
125911492 12591149 3 20160223 0