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
125870212 12587021 2 F 201607 20160803 20160725 20160811 EXP US-UNITED THERAPEUTICS-UNT-2016-011298 UNITED THERAPEUTICS 44.51 YR M Y 69.98000 KG 20160811 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
125870212 12587021 1 PS REMODULIN TREPROSTINIL 1 Intravenous drip 0.003 ?G/KG, CONTINUING Y U 2100954 21272 .003 UG/KG INJECTION
125870212 12587021 2 SS REMODULIN TREPROSTINIL 1 Subcutaneous 0.005 ?G/KG, CONTINUING Y U 929005 21272 .005 UG/KG INJECTION
125870212 12587021 3 SS CEFEPIME CEFEPIME HYDROCHLORIDE 1 UNK 0
125870212 12587021 4 C ELIQUIS APIXABAN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125870212 12587021 1 Pulmonary hypertension
125870212 12587021 3 Product used for unknown indication
125870212 12587021 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125870212 12587021 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125870212 12587021 Dialysis
125870212 12587021 Dizziness
125870212 12587021 Eyelid oedema
125870212 12587021 Fatigue
125870212 12587021 Hypotension
125870212 12587021 Infection
125870212 12587021 Thrombosis in device

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
125870212 12587021 1 20160630 0
125870212 12587021 2 20160715 0
125870212 12587021 3 20160713 0