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
123902562 12390256 2 F 20130401 20160624 20160520 20160704 EXP US-009507513-1605USA007657 MERCK 66.00 YR M Y 93.88000 KG 20160704 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
123902562 12390256 1 PS JANUMET METFORMIN HYDROCHLORIDESITAGLIPTIN PHOSPHATE 1 UNK U 22044 FILM-COATED TABLET
123902562 12390256 2 C DIURETIC (UNSPECIFIED) UNSPECIFIED INGREDIENT 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123902562 12390256 1 Drug therapy

Outcome of event

Event ID CASEID OUTC COD
123902562 12390256 OT
123902562 12390256 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
123902562 12390256 Flank pain
123902562 12390256 Hallucination
123902562 12390256 Headache
123902562 12390256 Seizure
123902562 12390256 Vitreous floaters
123902562 12390256 Weight decreased

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

no results found

Therapies reported

no results found