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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
114377922 | 11437792 | 2 | F | 20150630 | 20160819 | 20150831 | 20160826 | EXP | US-ABBVIE-15K-163-1453288-00 | ABBVIE | 48.62 | YR | F | Y | 97.16000 | KG | 20160826 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
114377922 | 11437792 | 1 | PS | HUMIRA | ADALIMUMAB | 1 | Subcutaneous | Y | U | 1033582 | 125057 | 40 | MG | SOLUTION FOR INJECTION IN PRE-FILLED PEN | QOW | ||||
114377922 | 11437792 | 2 | SS | HUMIRA | ADALIMUMAB | 1 | Subcutaneous | Y | U | 1033582 | 125057 | 40 | MG | SOLUTION FOR INJECTION IN PRE-FILLED PEN | QOW | ||||
114377922 | 11437792 | 3 | C | PLAQUENIL | HYDROXYCHLOROQUINE SULFATE | 1 | 0 | ||||||||||||
114377922 | 11437792 | 4 | C | HYDROCODONE | HYDROCODONE | 1 | 0 | ||||||||||||
114377922 | 11437792 | 5 | C | XANAX | ALPRAZOLAM | 1 | 0 | ||||||||||||
114377922 | 11437792 | 6 | C | FLEXERIL | CYCLOBENZAPRINE HYDROCHLORIDE | 1 | 0 | ||||||||||||
114377922 | 11437792 | 7 | C | TRAZODONE | TRAZODONE HYDROCHLORIDE | 1 | 0 | ||||||||||||
114377922 | 11437792 | 8 | C | CHLORTAB | CHLORPHENIRAMINE MALEATE | 1 | 0 | ||||||||||||
114377922 | 11437792 | 9 | C | VITAMIN B12 | CYANOCOBALAMIN | 1 | Other | 0 | |||||||||||
114377922 | 11437792 | 10 | C | VITAMIN D | CHOLECALCIFEROL | 1 | 0 | ||||||||||||
114377922 | 11437792 | 11 | C | BIOTIN | BIOTIN | 1 | 0 | ||||||||||||
114377922 | 11437792 | 12 | C | OXYCODONE | OXYCODONE | 1 | 0 | ||||||||||||
114377922 | 11437792 | 13 | C | FENTANYL. | FENTANYL | 1 | 0 | ||||||||||||
114377922 | 11437792 | 14 | C | CLARITIN | LORATADINE | 1 | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
114377922 | 11437792 | 1 | Ankylosing spondylitis |
114377922 | 11437792 | 3 | Product used for unknown indication |
114377922 | 11437792 | 4 | Product used for unknown indication |
114377922 | 11437792 | 5 | Product used for unknown indication |
114377922 | 11437792 | 6 | Product used for unknown indication |
114377922 | 11437792 | 7 | Product used for unknown indication |
114377922 | 11437792 | 8 | Product used for unknown indication |
114377922 | 11437792 | 9 | Product used for unknown indication |
114377922 | 11437792 | 10 | Product used for unknown indication |
114377922 | 11437792 | 11 | Product used for unknown indication |
114377922 | 11437792 | 12 | Product used for unknown indication |
114377922 | 11437792 | 13 | Product used for unknown indication |
114377922 | 11437792 | 14 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
114377922 | 11437792 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
114377922 | 11437792 | Adverse drug reaction | |
114377922 | 11437792 | Arthralgia | |
114377922 | 11437792 | Fatigue | |
114377922 | 11437792 | Hypotension | |
114377922 | 11437792 | Insomnia | |
114377922 | 11437792 | Neck pain | |
114377922 | 11437792 | Nephrolithiasis | |
114377922 | 11437792 | Pain in extremity | |
114377922 | 11437792 | Pyelonephritis | |
114377922 | 11437792 | Urethral ulcer |
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 |
---|---|---|---|---|---|---|
114377922 | 11437792 | 1 | 2012 | 201507 | 0 | |
114377922 | 11437792 | 2 | 2015 | 0 |