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
126821861 12682186 1 I 201607 20160816 20160824 20160824 EXP FR-UCBSA-2016031770 UCB 83.81 YR M Y 0.00000 20160825 OT FR FR

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
126821861 12682186 1 PS KEPPRA LEVETIRACETAM 1 Intravenous (not otherwise specified) 250 MG, 2X/DAY (BID) 2000 MG Y U 21872 250 MG CONCENTRATE FOR SOLUTION FOR INFUSION BID
126821861 12682186 2 SS Axepim CEFEPIME HYDROCHLORIDE 1 Intravenous (not otherwise specified) 2 G, 3X/DAY (TID) 42 G Y U 0 2 G POWDER FOR INJECTION TID
126821861 12682186 3 C Wellvone ATOVAQUONE 1 U 0
126821861 12682186 4 C NOXAFIL POSACONAZOLE 1 U 0
126821861 12682186 5 C METHYLPREDNISOLONE. METHYLPREDNISOLONE 1 U 0
126821861 12682186 6 C LOVENOX ENOXAPARIN SODIUM 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126821861 12682186 1 Seizure
126821861 12682186 2 Prostatism
126821861 12682186 3 Product used for unknown indication
126821861 12682186 4 Product used for unknown indication
126821861 12682186 5 Product used for unknown indication
126821861 12682186 6 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126821861 12682186 OT
126821861 12682186 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126821861 12682186 Coma
126821861 12682186 Toxic encephalopathy

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
126821861 12682186 1 20160721 20160724 0
126821861 12682186 2 20160718 20160726 0