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
98575984 9857598 4 F 20140203 20160810 20140131 20160811 EXP CA-ROCHE-1338435 ROCHE 76.71 YR F Y 65.80000 KG 20160811 CN CA CA

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
98575984 9857598 1 PS RITUXAN RITUXIMAB 1 Intravenous (not otherwise specified) FREQUENCY: DAY 1 AND 15?- LATEST RITUXIMAB INFUSION: 03/FEB/2014 103705 1000 MG SOLUTION FOR INFUSION
98575984 9857598 2 SS METHOTREXATE. METHOTREXATE 1 Unknown N 0
98575984 9857598 3 SS LIPITOR ATORVASTATIN CALCIUM 1 Unknown N 0
98575984 9857598 4 SS ELTROXIN LEVOTHYROXINE 1 Unknown N 0
98575984 9857598 5 C TYLENOL WITH CODEINE ACETAMINOPHENCODEINE PHOSPHATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
98575984 9857598 1 Rheumatoid arthritis
98575984 9857598 2 Product used for unknown indication
98575984 9857598 3 Product used for unknown indication
98575984 9857598 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
98575984 9857598 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
98575984 9857598 Arthritis
98575984 9857598 Hepatic enzyme increased
98575984 9857598 Insomnia
98575984 9857598 Nephrolithiasis
98575984 9857598 Rheumatoid arthritis

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
98575984 9857598 1 20110720 0