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
125974931 12597493 1 I 20151230 20160107 20160726 20160726 PER US-UNITED THERAPEUTICS-UNT-2016-000295 UNITED THERAPEUTICS 0.00 E F Y 0.00000 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
125974931 12597493 1 PS TYVASO TREPROSTINIL 1 54 ?G, QID 22387 54 UG INHALATION GAS QID
125974931 12597493 2 SS ALENDRONATE ALENDRONATE SODIUM 1 Unknown UNK U U 0
125974931 12597493 3 SS ADCIRCA TADALAFIL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125974931 12597493 1 Pulmonary arterial hypertension
125974931 12597493 2 Product used for unknown indication
125974931 12597493 3 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125974931 12597493 Dizziness
125974931 12597493 Nasal congestion
125974931 12597493 Nausea
125974931 12597493 Ocular hyperaemia
125974931 12597493 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
125974931 12597493 1 20151217 0