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
114418394 11441839 4 F 20160827 20150901 20160902 EXP US-ABBVIE-15P-163-1451397-00 ABBVIE 0.00 M Y 0.00000 20160902 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
114418394 11441839 1 PS HUMIRA ADALIMUMAB 1 Subcutaneous U UNKNOWN 125057 SOLUTION FOR INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
114418394 11441839 1 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
114418394 11441839 OT
114418394 11441839 CA

Reactions reported

Event ID CASEID DRUG REC ACT PT
114418394 11441839 Abdominal pain
114418394 11441839 Activities of daily living impaired
114418394 11441839 Chronic obstructive pulmonary disease
114418394 11441839 Congenital diaphragmatic hernia
114418394 11441839 Feeling abnormal
114418394 11441839 Injury
114418394 11441839 Joint range of motion decreased
114418394 11441839 Lung disorder
114418394 11441839 Mobility decreased
114418394 11441839 Rheumatoid arthritis

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

no results found

Therapies reported

no results found