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
125941591 12594159 1 I 201512 20151218 20160726 20160726 EXP US-UNITED THERAPEUTICS-UNT-2015-016162 UNITED THERAPEUTICS 57.17 YR F Y 81.63000 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
125941591 12594159 1 PS REMODULIN TREPROSTINIL 1 Intravenous drip 0.114 ?G/KG, CONTINUING U U 2100665 21272 .114 UG/KG INJECTION
125941591 12594159 2 SS REMODULIN TREPROSTINIL 1 Intravenous drip UNK U U 2100666 21272 INJECTION
125941591 12594159 3 C SILDENAFIL. SILDENAFIL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125941591 12594159 1 Pulmonary arterial hypertension
125941591 12594159 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125941591 12594159 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125941591 12594159 Device related infection
125941591 12594159 Injection site haemorrhage

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
125941591 12594159 1 20120411 0