The Safety Rates Drug Report

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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
105622643 10562264 3 F 2014 20150107 20141104 20160907 EXP SA-UNITED THERAPEUTICS-UNT-2014-010006 UNITED THERAPEUTICS 75.00 YR M Y 76.00000 KG 20160907 AT SA

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
105622643 10562264 1 PS REMODULIN TREPROSTINIL 1 Intravenous drip 0.068 ?G/KG, CONTINUING U 21272 .068 UG/KG INJECTION
105622643 10562264 2 C VIAGRA SILDENAFIL CITRATE 1 Oral 80 MG, TID U 0 80 MG TID
105622643 10562264 3 C TRACLEER BOSENTAN 1 Oral 125 MG, BID U 0 125 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
105622643 10562264 1 Pulmonary arterial hypertension
105622643 10562264 2 Product used for unknown indication
105622643 10562264 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
105622643 10562264 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
105622643 10562264 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
105622643 10562264 1 20130918 20141018 0
105622643 10562264 2 20141018 0
105622643 10562264 3 20141018 0