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
123854502 12385450 2 F 20160622 20160519 20160701 EXP US-ACTELION-A-US2016-136245 ACTELION 66.00 YR E F Y 0.00000 20160701 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
123854502 12385450 1 PS TRACLEER BOSENTAN 1 Oral UNK U U OP021P0101 21290 TABLET
123854502 12385450 2 SS FAMOTIDINE. FAMOTIDINE 1 Unknown U U 0
123854502 12385450 3 C TYVASO TREPROSTINIL 1 U 0
123854502 12385450 4 C HYDROCHLOROTHIAZIDE. HYDROCHLOROTHIAZIDE 1 Y U 0
123854502 12385450 5 C LEVOTHYROXINE. LEVOTHYROXINE 1 U 0
123854502 12385450 6 C POTASSIUM CHLORIDE. POTASSIUM CHLORIDE 1 U 0
123854502 12385450 7 C COUMADIN WARFARIN SODIUM 1 U 0
123854502 12385450 8 C LASIX FUROSEMIDE 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123854502 12385450 1 Pulmonary arterial hypertension
123854502 12385450 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
123854502 12385450 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
123854502 12385450 Feeling cold
123854502 12385450 Headache
123854502 12385450 Heart rate increased
123854502 12385450 Nausea
123854502 12385450 Oedema
123854502 12385450 Pain in extremity
123854502 12385450 Palpitations
123854502 12385450 Peripheral swelling
123854502 12385450 Pyrexia
123854502 12385450 Vomiting
123854502 12385450 Wrong drug administered

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found