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
125442081 12544208 1 I 20160622 20160705 20160711 20160711 EXP GB-009507513-1606GBR012775 GB-GLENMARK GENERICS (EUROPE) LTD.-2016GMK023564 GLENMARK 0.00 Y 0.00000 20160711 OT GB GB

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
125442081 12544208 1 PS EZETIMIBE. EZETIMIBE 1 Oral UNK U 78560 TABLET
125442081 12544208 2 SS ATORVASTATIN ATORVASTATIN 1 Unknown UNK U 0
125442081 12544208 3 SS CLEXANE ENOXAPARIN SODIUM 1 Unknown UNK U 0
125442081 12544208 4 SS INSULIN INSULIN NOS 1 Unknown UNK U 0
125442081 12544208 5 SS METRONIDAZOLE. METRONIDAZOLE 1 Unknown UNK U 0
125442081 12544208 6 SS OMEPRAZOLE. OMEPRAZOLE 1 Oral UNK U 0
125442081 12544208 7 SS RAMIPRIL. RAMIPRIL 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125442081 12544208 1 Product used for unknown indication
125442081 12544208 2 Product used for unknown indication
125442081 12544208 3 Product used for unknown indication
125442081 12544208 4 Product used for unknown indication
125442081 12544208 5 Product used for unknown indication
125442081 12544208 6 Product used for unknown indication
125442081 12544208 7 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125442081 12544208 OT
125442081 12544208 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125442081 12544208 Acute kidney injury

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

no results found

Therapies reported

no results found