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
127702841 12770284 1 I 20160904 20160922 20160922 PER US-AMGEN-USASL2016119906 AMGEN 50.00 YR A F Y 0.00000 20160922 CN US US

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
127702841 12770284 1 PS ENBREL ETANERCEPT 1 Unknown UNK U 1067756 103795 UNKNOWN FORMULATION
127702841 12770284 2 SS TOPAMAX TOPIRAMATE 1 Unknown UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127702841 12770284 1 Rheumatoid arthritis
127702841 12770284 2 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127702841 12770284 Bladder disorder
127702841 12770284 Dry mouth
127702841 12770284 Fatigue
127702841 12770284 Hypersensitivity
127702841 12770284 Swelling face
127702841 12770284 Weight increased

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

no results found

Therapies reported

no results found