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
125947551 12594755 1 I 201602 20160202 20160726 20160726 PER US-UNITED THERAPEUTICS-UNT-2016-001679 UNITED THERAPEUTICS 32.14 YR F Y 87.53000 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
125947551 12594755 1 PS TYVASO TREPROSTINIL 1 18-54 MICROGRAMS, QID 2100758 22387 INHALATION GAS QID
125947551 12594755 2 SS TYVASO TREPROSTINIL 1 UNK 2100716 22387 INHALATION GAS
125947551 12594755 3 C OPSUMIT MACITENTAN 1 0
125947551 12594755 4 C ADCIRCA TADALAFIL 1 0
125947551 12594755 5 C SILDENAFIL. SILDENAFIL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125947551 12594755 1 Pulmonary arterial hypertension
125947551 12594755 3 Product used for unknown indication
125947551 12594755 4 Product used for unknown indication
125947551 12594755 5 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125947551 12594755 Chest pain
125947551 12594755 Dizziness
125947551 12594755 Headache
125947551 12594755 Inappropriate schedule of drug administration
125947551 12594755 Mouth haemorrhage
125947551 12594755 Nausea

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
125947551 12594755 1 20160202 0