The Safety Rates Drug Report

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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
125940051 12594005 1 I 201511 20151120 20160726 20160726 PER US-UNITED THERAPEUTICS-UNT-2015-014869 UNITED THERAPEUTICS 42.61 YR F Y 63.49000 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
125940051 12594005 1 PS TYVASO TREPROSTINIL 1 18-54 MICROGRAMS, QID 2100695 22387 INHALATION GAS QID
125940051 12594005 2 SS TYVASO TREPROSTINIL 1 UNK 2100705 22387 INHALATION GAS
125940051 12594005 3 SS LETAIRIS AMBRISENTAN 1 Oral 10 MG, QD SBFW 0 10 MG TABLET QD
125940051 12594005 4 SS REVATIO SILDENAFIL CITRATE 1 Unknown U U 0
125940051 12594005 5 C COUMADIN WARFARIN SODIUM 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125940051 12594005 1 Pulmonary arterial hypertension
125940051 12594005 3 Product used for unknown indication
125940051 12594005 4 Product used for unknown indication
125940051 12594005 5 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125940051 12594005 Cough
125940051 12594005 Headache
125940051 12594005 Hypotension
125940051 12594005 Seasonal allergy
125940051 12594005 Sinusitis
125940051 12594005 Vertigo

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
125940051 12594005 1 20151109 0
125940051 12594005 3 20150601 0