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
118772525 11877252 5 F 20160811 20151229 20160818 EXP US-ACTELION-A-NJ2015-129255 ACTELION 51.00 YR A F Y 0.00000 20160818 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
118772525 11877252 1 PS VENTAVIS ILOPROST 1 Respiratory (inhalation) UNK U MA026TA 21779 INHALATION VAPOUR, SOLUTION
118772525 11877252 2 SS VENTAVIS ILOPROST 1 Respiratory (inhalation) 5 MCG, 5-9X DAILY U MA02DL0 21779 5 UG INHALATION VAPOUR, SOLUTION
118772525 11877252 3 SS TRACLEER BOSENTAN 1 Oral 125 MG, BID U IP060P0101, OP019P0101 21290 125 MG TABLET BID
118772525 11877252 4 SS TRACLEER BOSENTAN 1 Oral 125 MG, BID U OP023P0101, OP026P0101 21290 125 MG TABLET BID
118772525 11877252 5 C SILDENAFIL. SILDENAFIL 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118772525 11877252 1 Pulmonary arterial hypertension
118772525 11877252 3 Pulmonary arterial hypertension

Outcome of event

Event ID CASEID OUTC COD
118772525 11877252 OT
118772525 11877252 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
118772525 11877252 Arthropathy
118772525 11877252 Cardiac failure congestive
118772525 11877252 Dysphonia
118772525 11877252 Dyspnoea
118772525 11877252 Feeling abnormal
118772525 11877252 Hypoxia
118772525 11877252 Pain
118772525 11877252 Pulmonary oedema
118772525 11877252 Rib fracture

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
118772525 11877252 1 20130617 0
118772525 11877252 3 20141106 0