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
121326625 12132662 5 F 20150826 20160706 20160301 20160718 EXP US-ACTELION-A-NJ2015-124200 ACTELION 64.00 YR A F Y 0.00000 20160718 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
121326625 12132662 1 PS TRACLEER BOSENTAN 1 Oral 125 MG, UNK Y NP013P0402 21290 125 MG TABLET
121326625 12132662 2 SS TRACLEER BOSENTAN 1 Oral 62.5 MG, BID Y NP013P0402 21290 62.5 MG TABLET BID
121326625 12132662 3 C IMDUR ISOSORBIDE MONONITRATE 1 Y U 0
121326625 12132662 4 C ASA ASPIRIN 1 U 0
121326625 12132662 5 C PLAVIX CLOPIDOGREL BISULFATE 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121326625 12132662 1 Pulmonary arterial hypertension

Outcome of event

Event ID CASEID OUTC COD
121326625 12132662 HO
121326625 12132662 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
121326625 12132662 Abdominal pain upper
121326625 12132662 Back pain
121326625 12132662 Blood pressure decreased
121326625 12132662 Chest pain
121326625 12132662 Condition aggravated
121326625 12132662 Dialysis
121326625 12132662 Fluid retention
121326625 12132662 Flushing
121326625 12132662 Gastrooesophageal reflux disease
121326625 12132662 Headache
121326625 12132662 Renal transplant
121326625 12132662 Underdose

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
121326625 12132662 1 20150515 0
121326625 12132662 2 20160219 0