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
126369351 12636935 1 I 20160801 20160809 20160809 EXP PHHY2016CA105950 SANDOZ 73.00 YR F Y 97.51000 KG 20160809 OT CA CA

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
126369351 12636935 1 PS METFORMIN METFORMIN HYDROCHLORIDE 1 Oral 500 MG, BID U 75985 500 MG FILM-COATED TABLET BID
126369351 12636935 2 C ADVAIR HFA FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 Unknown U 0
126369351 12636935 3 C AVAPRO IRBESARTAN 1 Unknown U 0 TABLET
126369351 12636935 4 C BISOPROLOL BISOPROLOL 1 Unknown U 0 TABLET
126369351 12636935 5 C CADUET AMLODIPINE BESYLATEATORVASTATIN CALCIUM 1 Unknown U 0 TABLET
126369351 12636935 6 C CARDURA DOXAZOSIN MESYLATE 1 Unknown U 0 TABLET
126369351 12636935 7 C ELTROXIN LEVOTHYROXINE 1 Unknown U 0 TABLET
126369351 12636935 8 C RABEPRAZOLE RABEPRAZOLE 1 Unknown U 0
126369351 12636935 9 C SPIRIVA TIOTROPIUM BROMIDE MONOHYDRATE 1 Unknown U 0 CAPSULE
126369351 12636935 10 C VENTOLIN ALBUTEROL SULFATE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126369351 12636935 1 Type 2 diabetes mellitus
126369351 12636935 2 Product used for unknown indication
126369351 12636935 3 Product used for unknown indication
126369351 12636935 4 Product used for unknown indication
126369351 12636935 5 Product used for unknown indication
126369351 12636935 6 Product used for unknown indication
126369351 12636935 7 Product used for unknown indication
126369351 12636935 8 Product used for unknown indication
126369351 12636935 9 Product used for unknown indication
126369351 12636935 10 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126369351 12636935 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126369351 12636935 Blood glucose decreased
126369351 12636935 Frequent bowel movements
126369351 12636935 Nausea
126369351 12636935 Product substitution issue

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

no results found

Therapies reported

no results found