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
127438812 12743881 2 F 20160717 20160912 20160914 20160919 EXP JP-PFIZER INC-2016428242 PFIZER 80.00 YR F Y 31.40000 KG 20160919 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
127438812 12743881 1 PS RHEUMATREX METHOTREXATE SODIUM 1 Oral 4 MG WEEKLY Y 11719 4 MG CAPSULE /wk
127438812 12743881 2 C ULCERLMIN SUCRALFATE 1 UNK 0
127438812 12743881 3 C LOXONIN LOXOPROFEN SODIUM 1 0
127438812 12743881 4 C PREDNISOLONE. PREDNISOLONE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127438812 12743881 1 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
127438812 12743881 HO
127438812 12743881 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127438812 12743881 Hypokalaemia
127438812 12743881 Hyponatraemia
127438812 12743881 Pancytopenia

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
127438812 12743881 1 20160815 0
127438812 12743881 2 20160728 0