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
125681842 12568184 2 F 20160728 20160718 20160810 EXP US-ACTELION-A-US2016-139173 ACTELION 75.00 YR E M Y 0.00000 20160811 PH 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
125681842 12568184 1 PS TRACLEER BOSENTAN 1 Oral 125 MG, UNK OP023P0101 21290 125 MG TABLET
125681842 12568184 2 C GABAPENTIN. GABAPENTIN 1 300 MG, UNK U 0 300 MG
125681842 12568184 3 C SIMVASTATIN. SIMVASTATIN 1 80 MG, UNK U 0 80 MG
125681842 12568184 4 C METOPROLOL. METOPROLOL 1 100 MG, UNK U 0 100 MG
125681842 12568184 5 C CLOPIDOGREL CLOPIDOGREL BISULFATE 1 75 MG, UNK U 0 75 MG
125681842 12568184 6 C RANITIDINE. RANITIDINE 1 150 MG, UNK U 0 150 MG
125681842 12568184 7 C OMEPRAZOLE. OMEPRAZOLE 1 20 MG, UNK U 0 20 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125681842 12568184 1 Pulmonary arterial hypertension

Outcome of event

Event ID CASEID OUTC COD
125681842 12568184 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
125681842 12568184 Pulmonary arterial hypertension

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
125681842 12568184 1 20140926 0