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
119523626 11952362 6 F 201606 20160706 20160126 20160713 PER US-ACTELION PHARMACEUTICALS US, INC.-A-US2016-130353 ACTELION 56.00 YR A F Y 0.00000 20160713 OT 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
119523626 11952362 1 PS TRACLEER BOSENTAN 1 Oral 125 MG, BID OP019P0101,OP021P0101, OP023P0101 21290 125 MG TABLET BID
119523626 11952362 2 SS TREPROSTINIL DIOLAMIN TREPROSTINIL DIOLAMINE 1 Unknown U U 0
119523626 11952362 3 C SILDENAFIL. SILDENAFIL 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119523626 11952362 1 Pulmonary arterial hypertension
119523626 11952362 2 Product used for unknown indication
119523626 11952362 3 Pulmonary arterial hypertension

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
119523626 11952362 Asthenia
119523626 11952362 Confusional state
119523626 11952362 Decreased appetite
119523626 11952362 Diarrhoea
119523626 11952362 Disturbance in attention
119523626 11952362 Dizziness
119523626 11952362 Fatigue
119523626 11952362 Headache
119523626 11952362 Hypotension
119523626 11952362 Influenza
119523626 11952362 Irritability
119523626 11952362 Lung infection
119523626 11952362 Malaise
119523626 11952362 Memory impairment
119523626 11952362 Nausea
119523626 11952362 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
119523626 11952362 1 20150914 0