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
124937362 12493736 2 F 2016 20160809 20160623 20160819 EXP US-ABBVIE-16K-163-1656496-00 ABBVIE 62.77 YR F Y 0.00000 20160819 CN COUNTRY NOT SPECIFIED 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
124937362 12493736 1 PS HUMIRA ADALIMUMAB 1 Subcutaneous U UNKNOWN 125057 40 MG SOLUTION FOR INJECTION IN PRE-FILLED PEN
124937362 12493736 2 SS GABAPENTIN. GABAPENTIN 1 Unknown UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124937362 12493736 1 Rheumatoid arthritis
124937362 12493736 2 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
124937362 12493736 Amnesia
124937362 12493736 Confusional state
124937362 12493736 Herpes zoster
124937362 12493736 Joint swelling
124937362 12493736 Neuralgia
124937362 12493736 Swelling face
124937362 12493736 Tooth impacted

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
124937362 12493736 1 2016 0