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
123695332 12369533 2 F 20160502 20160516 20160819 PER US-GLENMARK PHARMACEUTICALS INC, USA.-2016GMK022427 GLENMARK 0.00 Y 0.00000 20160819 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
123695332 12369533 1 PS OMEPRAZOLE. OMEPRAZOLE 1 Oral 2 DF, OD Y 19150183 91672 2 DF QD
123695332 12369533 2 C POTASSIUM POTASSIUM 1 Oral UNK 0 TABLET
123695332 12369533 3 C BABY ASPIRIN ASPIRIN 1 Oral 1 DF, QD 0 1 DF TABLET
123695332 12369533 4 C VITAMIN D CHOLECALCIFEROL 1 Oral UNK 0 TABLET
123695332 12369533 5 C VITAMIN B12 CYANOCOBALAMIN 1 Oral UNK 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123695332 12369533 1 Dyspepsia
123695332 12369533 2 Product used for unknown indication
123695332 12369533 3 Product used for unknown indication
123695332 12369533 4 Product used for unknown indication
123695332 12369533 5 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
123695332 12369533 Diarrhoea
123695332 12369533 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