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
126019281 12601928 1 I 201604 20160726 20160728 20160728 EXP FR-ROCHE-1803182 ROCHE 59.00 YR F Y 0.00000 20160728 MD 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
126019281 12601928 1 PS MABTHERA RITUXIMAB 1 Intravenous drip DAY 1 U 103705 1 DF SOLUTION FOR INFUSION QD
126019281 12601928 2 SS MABTHERA RITUXIMAB 1 Intravenous drip DAY 15 U 103705 1 DF SOLUTION FOR INFUSION QD
126019281 12601928 3 SS SOLUPRED (FRANCE) PREDNISOLONE 1 Oral U 0 30 MG QD
126019281 12601928 4 C KARDEGIC ASPIRIN LYSINE 1 0
126019281 12601928 5 C LANSOPRAZOLE. LANSOPRAZOLE 1 0
126019281 12601928 6 C ALTEIS OLMESARTAN MEDOXOMIL 1 0
126019281 12601928 7 C FOSAVANCE ALENDRONATE SODIUMCHOLECALCIFEROL 1 0
126019281 12601928 8 C METFORMIN METFORMIN HYDROCHLORIDE 1 Unknown 0
126019281 12601928 9 C LANTUS INSULIN GLARGINE 1 0
126019281 12601928 10 C NOVORAPID INSULIN ASPART 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126019281 12601928 1 Limbic encephalitis
126019281 12601928 2 Systemic lupus erythematosus
126019281 12601928 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126019281 12601928 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126019281 12601928 Neuropathy peripheral
126019281 12601928 Off label use

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
126019281 12601928 1 20160111 20160111 0
126019281 12601928 2 20160116 20160116 0