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
124821792 12482179 2 F 20160610 20160721 20160620 20160728 EXP US-UNITED THERAPEUTICS-UNT-2016-009552 UNITED THERAPEUTICS 56.29 YR F Y 99.32000 KG 20160728 PH 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
124821792 12482179 1 PS REMODULIN TREPROSTINIL 1 Intravenous drip 0.029 ?G/KG, CONTINUING U U 2100955 21272 .029 UG/KG INJECTION
124821792 12482179 2 SS REMODULIN TREPROSTINIL 1 UNK U U 929005 21272 INJECTION
124821792 12482179 3 C TRACLEER BOSENTAN 1 0
124821792 12482179 4 C ELIQUIS APIXABAN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124821792 12482179 1 Pulmonary arterial hypertension
124821792 12482179 3 Product used for unknown indication
124821792 12482179 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
124821792 12482179 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124821792 12482179 Blood creatinine increased
124821792 12482179 Blood potassium increased
124821792 12482179 Dizziness
124821792 12482179 Malaise

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
124821792 12482179 1 20140829 0