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
124887972 12488797 2 F 20160719 20160622 20160802 PER US-ACTELION-A-NJ2016-137729 ACTELION 66.00 YR E F Y 0.00000 20160802 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
124887972 12488797 1 PS UPTRAVI SELEXIPAG 1 Oral UNK MCG, UNK U U 207947 TABLET
124887972 12488797 2 SS AMBRISENTAN AMBRISENTAN 1 Unknown 10 MG, QD 1504767A 0 10 MG QD
124887972 12488797 3 SS ADCIRCA TADALAFIL 1 Unknown U U 0
124887972 12488797 4 C VITAMIN D CHOLECALCIFEROL 1 U 0
124887972 12488797 5 C CALCIUM CITRATE CALCIUM CITRATE 1 U 0
124887972 12488797 6 C IRON IRON 1 U 0
124887972 12488797 7 C BACTRIM SULFAMETHOXAZOLETRIMETHOPRIM 1 U 0
124887972 12488797 8 C KLOR-CON POTASSIUM CHLORIDE 1 U 0
124887972 12488797 9 C LASIX FUROSEMIDE 1 U 0
124887972 12488797 10 C COUMADIN WARFARIN SODIUM 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124887972 12488797 1 Pulmonary hypertension
124887972 12488797 2 Pulmonary hypertension
124887972 12488797 3 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
124887972 12488797 Headache
124887972 12488797 Myalgia
124887972 12488797 Pain

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
124887972 12488797 2 20120617 0