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
125951101 12595110 1 I 201601 20160112 20160726 20160726 PER US-UNITED THERAPEUTICS-UNT-2016-000577 UNITED THERAPEUTICS 56.13 YR M Y 104.31000 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
125951101 12595110 1 PS ORENITRAM TREPROSTINIL 1 Oral 4.625 MG, TID U U 2100684 203496 4.625 MG TABLET TID
125951101 12595110 2 SS ORENITRAM TREPROSTINIL 1 Oral UNK U U 2100398 203496 TABLET
125951101 12595110 3 SS ORENITRAM TREPROSTINIL 1 Oral UNK U U 2100399 203496 TABLET
125951101 12595110 4 SS LETAIRIS AMBRISENTAN 1 Oral 10 MG, QD 1500226A 0 10 MG TABLET QD
125951101 12595110 5 SS ADCIRCA TADALAFIL 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125951101 12595110 1 Pulmonary arterial hypertension
125951101 12595110 4 Product used for unknown indication
125951101 12595110 5 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125951101 12595110 Weight increased

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
125951101 12595110 1 20150930 0
125951101 12595110 4 20131031 0