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
125940951 12594095 1 I 20151227 20160112 20160726 20160726 EXP US-UNITED THERAPEUTICS-UNT-2016-000603 UNITED THERAPEUTICS 45.71 YR F Y 55.78000 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
125940951 12594095 1 PS TYVASO TREPROSTINIL 1 18-54 ?G, QID U U 2100705 22387 INHALATION GAS
125940951 12594095 2 SS REVATIO SILDENAFIL CITRATE 1 Unknown U U 0
125940951 12594095 3 SS LETAIRIS AMBRISENTAN 1 Unknown 10 MG, QD SBFW 0 10 MG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125940951 12594095 1 Pulmonary hypertension
125940951 12594095 2 Product used for unknown indication
125940951 12594095 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125940951 12594095 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125940951 12594095 Blood pressure decreased
125940951 12594095 Dyspnoea
125940951 12594095 Dyspnoea exertional
125940951 12594095 Fatigue
125940951 12594095 Fluid retention
125940951 12594095 Oedema
125940951 12594095 Oedema peripheral
125940951 12594095 Pneumonia
125940951 12594095 Sinus congestion
125940951 12594095 Snoring

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
125940951 12594095 1 20150518 0
125940951 12594095 3 20130430 0