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
125666901 12566690 1 I 20160708 20160705 20160718 20160718 EXP US-UNITED THERAPEUTICS-UNT-2016-010886 UNITED THERAPEUTICS 43.22 YR M Y 111.11000 KG 20160718 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
125666901 12566690 1 PS REMODULIN TREPROSTINIL 1 Intravenous drip 0.010 ?G/KG, CONTINUING U U 2100955 21272 .01 UG/KG INJECTION
125666901 12566690 2 C ADCIRCA TADALAFIL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125666901 12566690 1 Pulmonary arterial hypertension
125666901 12566690 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125666901 12566690 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125666901 12566690 Central venous catheterisation
125666901 12566690 Dermatitis contact
125666901 12566690 Device dislocation
125666901 12566690 Injection site irritation

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
125666901 12566690 1 20160620 0