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
125910642 12591064 2 F 201512 20160106 20160726 20160726 PER US-UNITED THERAPEUTICS-UNT-2015-015693 UNITED THERAPEUTICS 58.19 YR F Y 61.68000 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
125910642 12591064 1 PS REMODULIN TREPROSTINIL 1 Subcutaneous 0.094 ?G/KG/MIN, CONTINUING U U 2100665 21272 .094 UG/KG INJECTION
125910642 12591064 2 SS COUMADIN WARFARIN SODIUM 1 U U 0
125910642 12591064 3 C LETAIRIS AMBRISENTAN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125910642 12591064 1 Pulmonary hypertension
125910642 12591064 2 Product used for unknown indication
125910642 12591064 3 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125910642 12591064 Drug interaction
125910642 12591064 Malaise
125910642 12591064 Nasopharyngitis

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
125910642 12591064 1 20101027 0