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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124511002 | 12451100 | 2 | F | 20160125 | 20160628 | 20160609 | 20160704 | EXP | JP-UCBSA-2016021303 | UCB | 83.00 | YR | M | Y | 0.00000 | 20160704 | MD | JP | JP |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124511002 | 12451100 | 1 | PS | CIMZIA | CERTOLIZUMAB PEGOL | 1 | Subcutaneous | 400 MG, EV 4 WEEKS | U | 125160 | 400 | MG | SOLUTION FOR INJECTION | ||||||
| 124511002 | 12451100 | 2 | SS | STARSIS | NATEGLINIDE | 1 | Oral | UNK, POR | U | 0 | |||||||||
| 124511002 | 12451100 | 3 | SS | TAMSULOSIN HYDROCHLORIDE. | TAMSULOSIN HYDROCHLORIDE | 1 | Oral | UNK | U | 0 | TABLET | ||||||||
| 124511002 | 12451100 | 4 | SS | LIVALO | PITAVASTATIN CALCIUM | 1 | Oral | UNK, POR | U | 0 | |||||||||
| 124511002 | 12451100 | 5 | SS | SPIRIVA | TIOTROPIUM BROMIDE MONOHYDRATE | 1 | Respiratory (inhalation) | UNK, INH (INHALATION) | U | 0 | |||||||||
| 124511002 | 12451100 | 6 | SS | Mucosolvan | AMBROXOL HYDROCHLORIDE | 1 | Oral | UNK, POR | U | 0 | |||||||||
| 124511002 | 12451100 | 7 | SS | Mucodyne | CARBOCYSTEINE | 1 | Oral | UNK, POR | U | 0 | |||||||||
| 124511002 | 12451100 | 8 | SS | PREDNISOLONE. | PREDNISOLONE | 1 | Oral | UNK, POR | U | 0 | |||||||||
| 124511002 | 12451100 | 9 | SS | Onbrez | INDACATEROL | 1 | Respiratory (inhalation) | UNK, INH | U | 0 | |||||||||
| 124511002 | 12451100 | 10 | SS | Meptin | PROCATEROL HYDROCHLORIDE | 1 | Respiratory (inhalation) | UNK, INH | U | 0 | |||||||||
| 124511002 | 12451100 | 11 | SS | Takepron | LANSOPRAZOLE | 1 | Oral | UNK, POR | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 124511002 | 12451100 | 1 | Rheumatoid arthritis |
| 124511002 | 12451100 | 2 | Product used for unknown indication |
| 124511002 | 12451100 | 3 | Product used for unknown indication |
| 124511002 | 12451100 | 4 | Product used for unknown indication |
| 124511002 | 12451100 | 5 | Product used for unknown indication |
| 124511002 | 12451100 | 6 | Product used for unknown indication |
| 124511002 | 12451100 | 7 | Product used for unknown indication |
| 124511002 | 12451100 | 8 | Product used for unknown indication |
| 124511002 | 12451100 | 9 | Product used for unknown indication |
| 124511002 | 12451100 | 10 | Product used for unknown indication |
| 124511002 | 12451100 | 11 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 124511002 | 12451100 | DE |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 124511002 | 12451100 | Pneumonia |
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 |
|---|---|---|---|---|---|---|
| 124511002 | 12451100 | 1 | 20140219 | 20160121 | 0 |