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
126017451 12601745 1 I 201601 20160115 20160728 20160728 PER US-UNITED THERAPEUTICS-UNT-2016-000760 UNITED THERAPEUTICS 74.34 YR M Y 92.97000 KG 20160728 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
126017451 12601745 1 PS TYVASO TREPROSTINIL 1 54 MICROGRAMS, QID U U 2100716 22387 54 UG INHALATION GAS QID
126017451 12601745 2 SS LETAIRIS AMBRISENTAN 1 Unknown 10 MG, QD 1500226A 0 10 MG TABLET QD
126017451 12601745 3 SS ADCIRCA TADALAFIL 1 Unknown U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126017451 12601745 1 Pulmonary arterial hypertension
126017451 12601745 2 Product used for unknown indication
126017451 12601745 3 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126017451 12601745 Dizziness
126017451 12601745 Dysgeusia
126017451 12601745 Flushing
126017451 12601745 Headache

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
126017451 12601745 1 20141125 0
126017451 12601745 2 20131105 0