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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 122238656 | 12223865 | 6 | F | 20160209 | 20160704 | 20160330 | 20160722 | EXP | PHHY2016IE039384 | SANDOZ | 63.00 | YR | F | Y | 0.00000 | 20160722 | LW | IE | IE |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 122238656 | 12223865 | 1 | PS | DICLAC | DICLOFENAC | 1 | Oral | 150 MG, QD | U | 74376 | 150 | MG | QD | ||||||
| 122238656 | 12223865 | 2 | SS | PROLIA | DENOSUMAB | 1 | Intramuscular | 60 MG, ONCE/SINGLE | 120 | MG | Y | 0 | 60 | MG | INJECTION | 1X | |||
| 122238656 | 12223865 | 3 | C | METHOTREXATE. | METHOTREXATE | 1 | Oral | 12.5 MG, QW | 0 | 12.5 | MG | /wk | |||||||
| 122238656 | 12223865 | 4 | C | FOLIC ACID. | FOLIC ACID | 1 | Oral | 10 MG, QW | 0 | 10 | MG | /wk | |||||||
| 122238656 | 12223865 | 5 | C | IDEOS | CALCIUM CARBONATECHOLECALCIFEROL | 1 | Oral | UNK | 0 | QD | |||||||||
| 122238656 | 12223865 | 6 | C | PNEUMOCOCCAL VACCINE POLYVALENT NOS | PNEUMOCOCCAL VACCINE POLYVALENT | 1 | Intramuscular | 0.5 ML, UNK | U | 0 | .5 | ML |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 122238656 | 12223865 | 1 | Arthralgia |
| 122238656 | 12223865 | 2 | Osteoporosis |
| 122238656 | 12223865 | 3 | Rheumatoid arthritis |
| 122238656 | 12223865 | 4 | Product used for unknown indication |
| 122238656 | 12223865 | 5 | Osteoporosis |
| 122238656 | 12223865 | 6 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 122238656 | 12223865 | OT |
| 122238656 | 12223865 | LT |
| 122238656 | 12223865 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 122238656 | 12223865 | Abdominal pain | |
| 122238656 | 12223865 | Abdominal pain upper | |
| 122238656 | 12223865 | Arthralgia | |
| 122238656 | 12223865 | Diarrhoea | |
| 122238656 | 12223865 | Faeces discoloured | |
| 122238656 | 12223865 | Fatigue | |
| 122238656 | 12223865 | Feeling abnormal | |
| 122238656 | 12223865 | Gait disturbance | |
| 122238656 | 12223865 | Haematemesis | |
| 122238656 | 12223865 | Injection site erythema | |
| 122238656 | 12223865 | Injection site pain | |
| 122238656 | 12223865 | Injection site swelling | |
| 122238656 | 12223865 | Internal haemorrhage | |
| 122238656 | 12223865 | Joint swelling | |
| 122238656 | 12223865 | Pain | |
| 122238656 | 12223865 | Syncope | |
| 122238656 | 12223865 | 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 |
|---|---|---|---|---|---|---|
| 122238656 | 12223865 | 1 | 20160209 | 0 | ||
| 122238656 | 12223865 | 2 | 20160208 | 20160209 | 0 | |
| 122238656 | 12223865 | 3 | 2004 | 0 | ||
| 122238656 | 12223865 | 4 | 2004 | 0 | ||
| 122238656 | 12223865 | 5 | 2004 | 0 | ||
| 122238656 | 12223865 | 6 | 20160208 | 0 |