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
125909012 12590901 2 F 20151125 20151221 20160726 20160726 PER US-UNITED THERAPEUTICS-UNT-2015-015079 UNITED THERAPEUTICS 53.93 YR F Y 81.63000 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
125909012 12590901 1 PS REMODULIN TREPROSTINIL 1 Subcutaneous 0.085 ?G/KG, CONTINUING U U 2100665 21272 .085 UG/KG INJECTION
125909012 12590901 2 C ADCIRCA TADALAFIL 1 0
125909012 12590901 3 C OPSUMIT MACITENTAN 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125909012 12590901 1 Pulmonary arterial hypertension
125909012 12590901 2 Product used for unknown indication
125909012 12590901 3 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125909012 12590901 Accidental overdose
125909012 12590901 Device issue
125909012 12590901 Diplopia
125909012 12590901 Dizziness
125909012 12590901 Headache
125909012 12590901 Infusion site haemorrhage
125909012 12590901 Infusion site injury

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
125909012 12590901 1 20130816 0
125909012 12590901 3 201512 0