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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124761202 | 12476120 | 2 | F | 20160423 | 20160714 | 20160617 | 20160727 | EXP | GB-SA-2016SA110302 | AVENTIS | 78.00 | YR | E | F | Y | 0.00000 | 20160727 | CN | GB | GB |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124761202 | 12476120 | 1 | PS | LEFLUNOMIDE. | LEFLUNOMIDE | 1 | Oral | UNK | U | UNKNOWN | 20905 | 10 | MG | TABLET | QD | ||||
| 124761202 | 12476120 | 2 | I | MALARONE | ATOVAQUONEPROGUANIL HYDROCHLORIDE | 1 | Unknown | UNK | UNKNOWN | 0 | TABLET | ||||||||
| 124761202 | 12476120 | 3 | SS | METFORMIN | METFORMIN HYDROCHLORIDE | 1 | Unknown | U | UNKNOWN | 0 | 500 | MG | TABLET | BID | |||||
| 124761202 | 12476120 | 4 | C | ADCAL-D3 | CALCIUM CARBONATECHOLECALCIFEROL | 1 | Unknown | UNK | 0 | CHEWABLE TABLET | |||||||||
| 124761202 | 12476120 | 5 | C | AMLODIPINE | AMLODIPINE BESYLATE | 1 | Unknown | UNK | 0 | 5 | MG | CAPSULE | QD | ||||||
| 124761202 | 12476120 | 6 | C | ATORVASTATIN | ATORVASTATIN | 1 | Unknown | UNK | 0 | 20 | MG | QD | |||||||
| 124761202 | 12476120 | 7 | C | GAVISCON | ALUMINUM HYDROXIDEMAGNESIUM CARBONATE | 1 | Unknown | UNK | 0 | ||||||||||
| 124761202 | 12476120 | 8 | C | OMEPRAZOLE. | OMEPRAZOLE | 1 | Unknown | UNK | 0 | 20 | MG | CAPSULE | QD | ||||||
| 124761202 | 12476120 | 9 | C | TRAMADOL. | TRAMADOL | 1 | Unknown | UNK | 0 | 50 | MG | CAPSULE | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 124761202 | 12476120 | 1 | Arthritis |
| 124761202 | 12476120 | 2 | Prophylaxis |
| 124761202 | 12476120 | 3 | Product used for unknown indication |
| 124761202 | 12476120 | 4 | Product used for unknown indication |
| 124761202 | 12476120 | 5 | Product used for unknown indication |
| 124761202 | 12476120 | 6 | Product used for unknown indication |
| 124761202 | 12476120 | 7 | Product used for unknown indication |
| 124761202 | 12476120 | 8 | Product used for unknown indication |
| 124761202 | 12476120 | 9 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 124761202 | 12476120 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 124761202 | 12476120 | Aggression | |
| 124761202 | 12476120 | Circulatory collapse | |
| 124761202 | 12476120 | Contusion | |
| 124761202 | 12476120 | Drug interaction | |
| 124761202 | 12476120 | Eye contusion | |
| 124761202 | 12476120 | Fall | |
| 124761202 | 12476120 | Injury | |
| 124761202 | 12476120 | Memory impairment | |
| 124761202 | 12476120 | 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 |
|---|---|---|---|---|---|---|
| 124761202 | 12476120 | 2 | 20160423 | 20160423 | 0 |