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
125917371 12591737 1 I 201601 20160128 20160726 20160726 PER US-UNITED THERAPEUTICS-UNT-2016-001495 UNITED THERAPEUTICS 64.20 YR M Y 82.54000 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
125917371 12591737 1 PS REMODULIN TREPROSTINIL 1 Intravenous drip 0.12 ?G/KG, CONTINUING 2100666 21272 .12 UG/KG INJECTION
125917371 12591737 2 SS LETAIRIS AMBRISENTAN 1 Unknown 5 MG, QD SBFP 0 5 MG TABLET QD
125917371 12591737 3 SS LETAIRIS AMBRISENTAN 1 UNK 0 TABLET
125917371 12591737 4 SS LETAIRIS AMBRISENTAN 1 UNK 0 TABLET
125917371 12591737 5 SS ADCIRCA TADALAFIL 1 Unknown U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125917371 12591737 1 Pulmonary arterial hypertension
125917371 12591737 2 Product used for unknown indication
125917371 12591737 5 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125917371 12591737 Nasal congestion
125917371 12591737 Sinus disorder

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
125917371 12591737 1 20130805 0
125917371 12591737 2 20150929 0