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
113316793 11331679 3 F 2013 20160627 20150803 20160708 EXP US-GLAXOSMITHKLINE-US2015108727 GLAXOSMITHKLINE 0.00 M Y 0.00000 20160708 CN 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
113316793 11331679 1 PS CARVEDILOL. CARVEDILOL 1 Oral Y 20297
113316793 11331679 2 SS CARVEDILOL PHOSPHATE. CARVEDILOL PHOSPHATE 1 7.5 MG, U Y 0 7.5 MG MODIFIED-RELEASE TABLET
113316793 11331679 3 SS COREG CR CARVEDILOL PHOSPHATE 1 20 MG, U U 0 20 MG PROLONGED-RELEASE CAPSULE
113316793 11331679 4 C ALDACTONE SPIRONOLACTONE 1 0
113316793 11331679 5 C ALLEGRA-D FEXOFENADINEPSEUDOEPHEDRINE 1 0
113316793 11331679 6 C DIOVAN VALSARTAN 1 0
113316793 11331679 7 C LANOXIN DIGOXIN 1 0
113316793 11331679 8 C LIBRIUM CHLORDIAZEPOXIDE HYDROCHLORIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
113316793 11331679 1 Product used for unknown indication
113316793 11331679 2 Product used for unknown indication
113316793 11331679 3 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
113316793 11331679 Asthenia
113316793 11331679 Drug ineffective
113316793 11331679 Fatigue

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
113316793 11331679 1 2013 2013 0
113316793 11331679 2 2013 0