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
125914382 12591438 2 F 201604 20160506 20160726 20160727 PER US-UNITED THERAPEUTICS-UNT-2016-006670 UNITED THERAPEUTICS 49.63 YR F Y 86.17000 KG 20160727 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
125914382 12591438 1 PS REMODULIN TREPROSTINIL 1 Subcutaneous 0.076 ?G/KG, CONTINUING U U 2100701 21272 .076 UG/KG INJECTION
125914382 12591438 2 SS LETAIRIS AMBRISENTAN 1 Unknown 0
125914382 12591438 3 C ADCIRCA TADALAFIL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125914382 12591438 1 Pulmonary hypertension
125914382 12591438 2 Product used for unknown indication
125914382 12591438 3 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125914382 12591438 Bronchitis
125914382 12591438 Influenza
125914382 12591438 Localised oedema
125914382 12591438 Oedema peripheral
125914382 12591438 Palpitations

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
125914382 12591438 1 20120717 0