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
125947911 12594791 1 I 201603 20160311 20160726 20160726 PER US-UNITED THERAPEUTICS-UNT-2016-004152 UNITED THERAPEUTICS 43.00 YR F Y 0.00000 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
125947911 12594791 1 PS TYVASO TREPROSTINIL 1 U U 22387 INHALATION GAS
125947911 12594791 2 SS AMBRISENTAN AMBRISENTAN 1 Unknown 10 MG, QD 1500227A 0 10 MG TABLET QD
125947911 12594791 3 SS VENTAVIS ILOPROST 1 Unknown U U 0
125947911 12594791 4 C ADCIRCA TADALAFIL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125947911 12594791 1 Product used for unknown indication
125947911 12594791 2 Product used for unknown indication
125947911 12594791 3 Product used for unknown indication
125947911 12594791 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125947911 12594791 Chest discomfort
125947911 12594791 Dyspnoea
125947911 12594791 Gastrooesophageal reflux disease
125947911 12594791 Malaise

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
125947911 12594791 2 20121025 0