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
121678394 12167839 4 F 20160219 20160725 20160310 20160804 EXP US-UNITED THERAPEUTICS-UNT-2016-003584 UNITED THERAPEUTICS 42.33 YR M Y 66.58000 KG 20160804 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
121678394 12167839 1 PS REMODULIN TREPROSTINIL 1 Intravenous drip 0.017 ?G/KG, CONTINUING U U 2100579 21272 .017 UG/KG INJECTION
121678394 12167839 2 C ADEMPAS RIOCIGUAT 1 0
121678394 12167839 3 C COUMADIN WARFARIN SODIUM 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121678394 12167839 1 Pulmonary hypertension
121678394 12167839 2 Product used for unknown indication
121678394 12167839 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
121678394 12167839 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
121678394 12167839 Cardiac discomfort
121678394 12167839 Cardiac failure
121678394 12167839 Decubitus ulcer
121678394 12167839 Dyspnoea
121678394 12167839 Nausea
121678394 12167839 Oedema
121678394 12167839 Pain in jaw
121678394 12167839 Pulmonary arterial hypertension
121678394 12167839 Pulmonary oedema
121678394 12167839 Septic shock
121678394 12167839 Staphylococcal sepsis

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
121678394 12167839 1 20131206 0