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
127106731 12710673 1 I 20160825 20160902 20160902 EXP CA-PFIZER INC-2016408832 PFIZER 63.00 YR F Y 0.00000 20160902 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
127106731 12710673 1 PS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 UNK 11719
127106731 12710673 2 SS ARTHROTEC DICLOFENAC SODIUMMISOPROSTOL 1 UNK 20607 TABLET
127106731 12710673 3 SS CELEBREX CELECOXIB 1 UNK 20998 CAPSULE, HARD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127106731 12710673 1 Rheumatoid arthritis
127106731 12710673 2 Rheumatoid arthritis
127106731 12710673 3 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
127106731 12710673 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127106731 12710673 Drug ineffective
127106731 12710673 Hypoaesthesia oral
127106731 12710673 Lung disorder

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found