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
125796662 12579666 2 F 20160630 20160803 20160721 20160810 EXP US-UNITED THERAPEUTICS-UNT-2016-011400 UNITED THERAPEUTICS 0.00 A F Y 0.00000 20160810 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
125796662 12579666 1 PS TYVASO TREPROSTINIL 1 72 ?G, QID 22387 72 UG INHALATION GAS QID
125796662 12579666 2 C SILDENAFIL. SILDENAFIL 1 0
125796662 12579666 3 C AMBRISENTAN AMBRISENTAN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125796662 12579666 1 Pulmonary arterial hypertension
125796662 12579666 2 Product used for unknown indication
125796662 12579666 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125796662 12579666 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125796662 12579666 Diarrhoea infectious
125796662 12579666 Hypotension
125796662 12579666 Product use issue
125796662 12579666 Sepsis

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
125796662 12579666 1 20160127 0