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
125915282 12591528 2 F 201601 20160222 20160726 20160726 PER US-UNITED THERAPEUTICS-UNT-2016-000867 UNITED THERAPEUTICS 60.30 YR F Y 51.47000 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
125915282 12591528 1 PS REMODULIN TREPROSTINIL 1 Intravenous drip 0.090 ?G/KG, CONTINUING U U 926117 21272 .09 UG/KG INJECTION
125915282 12591528 2 SS LETAIRIS AMBRISENTAN 1 Oral 10 MG, QD 1500226A 0 10 MG TABLET QD
125915282 12591528 3 SS ADEMPAS RIOCIGUAT 1 Unknown U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125915282 12591528 1 Pulmonary hypertension
125915282 12591528 2 Product used for unknown indication
125915282 12591528 3 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125915282 12591528 Bronchitis
125915282 12591528 Malaise

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
125915282 12591528 1 20090108 0
125915282 12591528 2 20080326 0