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
125909482 12590948 2 F 201511 20151228 20160726 20160726 PER US-UNITED THERAPEUTICS-UNT-2015-015263 UNITED THERAPEUTICS 71.24 YR M Y 97.96000 KG 20160726 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
125909482 12590948 1 PS REMODULIN TREPROSTINIL 1 Intravenous drip 0.019 ?G/KG, CONTINUING U U 2100431 21272 .019 UG/KG INJECTION
125909482 12590948 2 SS REMODULIN TREPROSTINIL 1 Intravenous drip 0.030 ?G/KG, CONTINUING U U 926117 21272 .03 UG/KG INJECTION
125909482 12590948 3 C OPSUMIT MACITENTAN 1 0
125909482 12590948 4 C ADCIRCA TADALAFIL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125909482 12590948 1 Pulmonary arterial hypertension
125909482 12590948 3 Product used for unknown indication
125909482 12590948 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125909482 12590948 Depressed mood
125909482 12590948 Diarrhoea
125909482 12590948 Headache
125909482 12590948 Malaise
125909482 12590948 Pain in jaw
125909482 12590948 Pulmonary arterial hypertension

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
125909482 12590948 1 20150916 0
125909482 12590948 2 20150916 0