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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125503831 | 12550383 | 1 | I | 201606 | 20160701 | 20160712 | 20160712 | EXP | PR-ABBVIE-16K-131-1670908-00 | ABBVIE | 46.79 | YR | F | Y | 106.69000 | KG | 20160712 | CN | COUNTRY NOT SPECIFIED | PR |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125503831 | 12550383 | 1 | PS | HUMIRA | ADALIMUMAB | 1 | Subcutaneous | Y | UNKNOWN | 125057 | 40 | MG | SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE | QOW | |||||
125503831 | 12550383 | 2 | SS | HUMIRA | ADALIMUMAB | 1 | Subcutaneous | Y | UNKNOWN | 125057 | 40 | MG | SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE | QOW | |||||
125503831 | 12550383 | 3 | SS | ZOVIRAX | ACYCLOVIR | 1 | Oral | Y | UNKNOWN | 0 | |||||||||
125503831 | 12550383 | 4 | C | FOLIC ACID. | FOLIC ACID | 1 | Oral | 0 | 5 | MG | QD | ||||||||
125503831 | 12550383 | 5 | C | METHOTREXATE. | METHOTREXATE | 1 | Oral | 0 | 5 | DF | /wk | ||||||||
125503831 | 12550383 | 6 | C | IRON | IRON | 1 | Oral | 0 | 1 | DF | QD | ||||||||
125503831 | 12550383 | 7 | C | SULINDAC. | SULINDAC | 1 | Oral | 0 | 200 | MG | BID | ||||||||
125503831 | 12550383 | 8 | C | ZOLPIDEM | ZOLPIDEMOLPIDEM TARTRATE | 1 | Oral | 0 | 10 | MG | QD | ||||||||
125503831 | 12550383 | 9 | C | PROSACEA | SULFUR | 1 | Oral | 0 | 20 | MG | QD |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125503831 | 12550383 | 1 | Rheumatoid arthritis |
125503831 | 12550383 | 2 | Psoriatic arthropathy |
125503831 | 12550383 | 3 | Product used for unknown indication |
125503831 | 12550383 | 4 | Rheumatoid arthritis |
125503831 | 12550383 | 5 | Rheumatoid arthritis |
125503831 | 12550383 | 6 | Haemoglobin |
125503831 | 12550383 | 7 | Rheumatoid arthritis |
125503831 | 12550383 | 8 | Insomnia |
125503831 | 12550383 | 9 | Anxiety |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125503831 | 12550383 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125503831 | 12550383 | Dermatitis | |
125503831 | 12550383 | Dizziness | |
125503831 | 12550383 | Erythema | |
125503831 | 12550383 | Exostosis | |
125503831 | 12550383 | Migraine | |
125503831 | 12550383 | Muscle spasms | |
125503831 | 12550383 | Nausea | |
125503831 | 12550383 | Neck pain | |
125503831 | 12550383 | Pain in extremity | |
125503831 | 12550383 | Psoriasis | |
125503831 | 12550383 | Tinnitus | |
125503831 | 12550383 | Vertigo | |
125503831 | 12550383 | Vomiting |
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 |
---|---|---|---|---|---|---|
125503831 | 12550383 | 1 | 201506 | 201606 | 0 | |
125503831 | 12550383 | 2 | 201606 | 0 | ||
125503831 | 12550383 | 3 | 201606 | 201606 | 0 | |
125503831 | 12550383 | 4 | 2014 | 0 | ||
125503831 | 12550383 | 5 | 2014 | 0 | ||
125503831 | 12550383 | 7 | 2014 | 0 | ||
125503831 | 12550383 | 8 | 201501 | 0 | ||
125503831 | 12550383 | 9 | 201501 | 0 |