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
124956782 12495678 2 F 20160616 20160701 20160624 20160711 EXP US-UNITED THERAPEUTICS-UNT-2016-010011 UNITED THERAPEUTICS 36.21 YR M Y 68.27000 KG 20160711 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
124956782 12495678 1 PS REMODULIN TREPROSTINIL 1 Intravenous drip 0.109 ?G/KG, CONTINUING U U 2100910 21272 .109 UG/KG INJECTION
124956782 12495678 2 C LETAIRIS AMBRISENTAN 1 0
124956782 12495678 3 C ADCIRCA TADALAFIL 1 0
124956782 12495678 4 C OPSUMIT MACITENTAN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124956782 12495678 1 Pulmonary hypertension
124956782 12495678 2 Product used for unknown indication
124956782 12495678 3 Product used for unknown indication
124956782 12495678 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
124956782 12495678 DE
124956782 12495678 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124956782 12495678 Ascites
124956782 12495678 Death
124956782 12495678 Drug dose omission
124956782 12495678 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
124956782 12495678 1 20140813 0