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
124327853 12432785 3 F 201605 20160609 20160603 20160728 EXP IL-UNITED THERAPEUTICS-UNT-2016-008640 UNITED THERAPEUTICS 57.00 YR F Y 0.00000 20160728 CN IL IL

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
124327853 12432785 1 PS REMODULIN TREPROSTINIL 1 Intravenous drip UNK U U 21272 INJECTION
124327853 12432785 2 SS REMODULIN TREPROSTINIL 1 Intravenous drip UNK U U 21272 INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124327853 12432785 1 Pulmonary arterial hypertension
124327853 12432785 2 Scleroderma

Outcome of event

Event ID CASEID OUTC COD
124327853 12432785 HO
124327853 12432785 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
124327853 12432785 Asthenia
124327853 12432785 Dehydration
124327853 12432785 Gastrointestinal haemorrhage
124327853 12432785 Pain
124327853 12432785 Product use issue

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
124327853 12432785 1 20150910 0
124327853 12432785 2 2014 0