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
123329693 12332969 3 F 20160229 20160705 20160504 20160715 EXP GB-WATSON-2016-08716 WATSON 60.00 YR F Y 0.00000 20160715 CN 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
123329693 12332969 1 PS TRIMETHOPRIM. TRIMETHOPRIM 1 Oral 200 MG, UNK Y 15169 70049 200 MG TABLET
123329693 12332969 2 C KEPPRA LEVETIRACETAM 1 Unknown UNK U 0
123329693 12332969 3 C LAMOTRIGINE. LAMOTRIGINE 1 Unknown 1 QAM/ 1 QPM U 0 BID
123329693 12332969 4 C SELENIUM SELENIUM 1 Unknown UNK U 0
123329693 12332969 5 C ZINC ZINCINC CHLORIDE 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123329693 12332969 1 Cystitis
123329693 12332969 2 Product used for unknown indication
123329693 12332969 3 Epilepsy
123329693 12332969 4 Product used for unknown indication
123329693 12332969 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
123329693 12332969 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123329693 12332969 Fall
123329693 12332969 Loss of consciousness

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
123329693 12332969 1 20160229 0