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
127841811 12784181 1 I 20160626 20160706 20160927 20160927 EXP JP-PFIZER INC-2016334219 PFIZER 81.00 YR F Y 39.00000 KG 20160927 PH JP JP

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
127841811 12784181 1 PS RHEUMATREX METHOTREXATE SODIUM 1 Oral 4 MG, WEEKLY Y 11719 4 MG CAPSULE /wk
127841811 12784181 2 SS RHEUMATREX METHOTREXATE SODIUM 1 Oral 10 MG, WEEKLY Y 11719 10 MG CAPSULE /wk
127841811 12784181 3 SS ZOSYN PIPERACILLIN SODIUMTAZOBACTAM SODIUM 1 Unknown UNK U 50684
127841811 12784181 4 SS LANSOPRAZOLE. LANSOPRAZOLE 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127841811 12784181 1 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
127841811 12784181 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127841811 12784181 Overdose
127841811 12784181 White blood cell count decreased

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
127841811 12784181 2 20160626 20160628 0