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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 107556245 | 10755624 | 5 | F | 2014 | 20160810 | 20150202 | 20160823 | EXP | BR-ABBVIE-15K-020-1339874-00 | ABBVIE | 75.70 | YR | M | Y | 68.00000 | KG | 20160823 | CN | COUNTRY NOT SPECIFIED | BR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 107556245 | 10755624 | 1 | PS | HUMIRA | ADALIMUMAB | 1 | Subcutaneous | UNKNOWN | 125057 | 40 | MG | SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE | |||||||
| 107556245 | 10755624 | 2 | SS | HUMIRA | ADALIMUMAB | 1 | Subcutaneous | UNKNOWN | 125057 | 40 | MG | SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE | |||||||
| 107556245 | 10755624 | 3 | C | ATENOLOL. | ATENOLOL | 1 | Oral | 0 | TABLET | ||||||||||
| 107556245 | 10755624 | 4 | C | ATENOLOL. | ATENOLOL | 1 | 0 | ||||||||||||
| 107556245 | 10755624 | 5 | C | TRAMAL | TRAMADOL | 1 | Oral | 0 | 50 | MG | TABLET | Q12H | |||||||
| 107556245 | 10755624 | 6 | C | ATORVASTATIN | ATORVASTATIN | 1 | Oral | 0 | TABLET |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 107556245 | 10755624 | 1 | Rheumatoid arthritis |
| 107556245 | 10755624 | 3 | Blood pressure management |
| 107556245 | 10755624 | 4 | Hypertension |
| 107556245 | 10755624 | 5 | Arthritis |
| 107556245 | 10755624 | 6 | Blood cholesterol increased |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 107556245 | 10755624 | HO |
| 107556245 | 10755624 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 107556245 | 10755624 | Anaemia | |
| 107556245 | 10755624 | Arthralgia | |
| 107556245 | 10755624 | Arthritis infective | |
| 107556245 | 10755624 | Device dislocation | |
| 107556245 | 10755624 | Device related infection | |
| 107556245 | 10755624 | Escherichia infection | |
| 107556245 | 10755624 | Fall | |
| 107556245 | 10755624 | Gastric disorder | |
| 107556245 | 10755624 | Immunodeficiency | |
| 107556245 | 10755624 | Joint swelling | |
| 107556245 | 10755624 | Malaise | |
| 107556245 | 10755624 | Pain | |
| 107556245 | 10755624 | Pathogen resistance | |
| 107556245 | 10755624 | Patient-device incompatibility | |
| 107556245 | 10755624 | Phlebitis | |
| 107556245 | 10755624 | Secretion discharge | |
| 107556245 | 10755624 | Somnolence | |
| 107556245 | 10755624 | Staphylococcal infection |
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 |
|---|---|---|---|---|---|---|
| 107556245 | 10755624 | 1 | 20110103 | 201403 | 0 | |
| 107556245 | 10755624 | 2 | 201601 | 0 |