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
125972731 12597273 1 I 201512 20151216 20160726 20160726 PER US-UNITED THERAPEUTICS-UNT-2015-015926 UNITED THERAPEUTICS 69.20 YR M Y 116.10000 KG 20160726 OT 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
125972731 12597273 1 PS TYVASO TREPROSTINIL 1 54-108 MICROGRAMS, QID N 2100687 22387 INHALATION GAS QID
125972731 12597273 2 SS LETAIRIS AMBRISENTAN 1 Oral 10 MG, QD 1500226A 0 10 MG TABLET QD
125972731 12597273 3 SS ADCIRCA TADALAFIL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125972731 12597273 1 Pulmonary arterial hypertension
125972731 12597273 2 Product used for unknown indication
125972731 12597273 3 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125972731 12597273 Back pain
125972731 12597273 Chest pain
125972731 12597273 Constipation
125972731 12597273 Decreased activity
125972731 12597273 Eructation
125972731 12597273 Gait disturbance
125972731 12597273 Memory impairment
125972731 12597273 Pain in extremity
125972731 12597273 Treatment noncompliance
125972731 12597273 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
125972731 12597273 1 20130930 201512 0
125972731 12597273 2 20131009 0