The Safety Rates Drug Report

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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
125909602 12590960 2 F 20151130 20160129 20160726 20160726 PER US-UNITED THERAPEUTICS-UNT-2015-015253 UNITED THERAPEUTICS 54.32 YR F Y 111.11000 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
125909602 12590960 1 PS REMODULIN TREPROSTINIL 1 Intravenous drip 0.102 ?G/KG, CONTINUING U U 2100665 21272 .102 UG/KG INJECTION
125909602 12590960 2 SS REMODULIN TREPROSTINIL 1 UNK U U 2100666 21272 INJECTION
125909602 12590960 3 C ADCIRCA TADALAFIL 1 Unknown 0
125909602 12590960 4 C OPSUMIT MACITENTAN 1 Unknown 0
125909602 12590960 5 C DILTIZEM 2 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125909602 12590960 1 Pulmonary arterial hypertension
125909602 12590960 3 Product used for unknown indication
125909602 12590960 4 Product used for unknown indication
125909602 12590960 5 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125909602 12590960 Drug dose omission
125909602 12590960 Dyspnoea
125909602 12590960 Headache
125909602 12590960 Sinusitis

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
125909602 12590960 1 20151105 0