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
125940961 12594096 1 I 201601 20160106 20160726 20160726 EXP US-UNITED THERAPEUTICS-UNT-2016-000240 UNITED THERAPEUTICS 71.59 YR M Y 102.99000 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
125940961 12594096 1 PS TYVASO TREPROSTINIL 1 18-54 ?G, QID U U 2100695 22387 INHALATION GAS QID
125940961 12594096 2 SS TYVASO TREPROSTINIL 1 UNK U U 2100716 22387 INHALATION GAS
125940961 12594096 3 C REVATIO SILDENAFIL CITRATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125940961 12594096 1 Pulmonary arterial hypertension
125940961 12594096 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125940961 12594096 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125940961 12594096 Cough
125940961 12594096 Decreased appetite
125940961 12594096 Dizziness
125940961 12594096 Dyspnoea
125940961 12594096 Headache
125940961 12594096 Nasal congestion
125940961 12594096 Nausea
125940961 12594096 Oedema peripheral
125940961 12594096 Retching
125940961 12594096 Syncope
125940961 12594096 Vomiting

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
125940961 12594096 1 20160104 0