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
124564943 12456494 3 F 20160531 20160705 20160610 20160712 EXP US-UNITED THERAPEUTICS-UNT-2016-008873 UNITED THERAPEUTICS 47.47 YR M Y 0.00000 20160712 OT 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
124564943 12456494 1 PS REMODULIN TREPROSTINIL 1 Intravenous drip 0.102 ?G/KG, CONTINUING U U 2100701 21272 .102 UG/KG INJECTION
124564943 12456494 2 C TRACLEER BOSENTAN 1 0
124564943 12456494 3 C SILDENAFIL. SILDENAFIL 1 0
124564943 12456494 4 C COUMADIN WARFARIN SODIUM 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124564943 12456494 1 Pulmonary arterial hypertension
124564943 12456494 2 Product used for unknown indication
124564943 12456494 3 Product used for unknown indication
124564943 12456494 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
124564943 12456494 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124564943 12456494 Abdominal pain upper
124564943 12456494 Back pain
124564943 12456494 Dyspnoea
124564943 12456494 Localised oedema
124564943 12456494 Oedema peripheral

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
124564943 12456494 1 20160204 0