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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126789801 | 12678980 | 1 | I | 20160805 | 20160810 | 20160824 | 20160824 | EXP | US-CIPLA LTD.-2016US17385 | CIPLA | 0.00 | Y | 0.00000 | 20160824 | CN | US | US |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126789801 | 12678980 | 1 | PS | MELOXICAM. | MELOXICAM | 1 | Oral | 2.5 MG, UNK | Y | U | 0 | 2.5 | MG | TABLET | |||||
| 126789801 | 12678980 | 2 | C | ULTRAM | TRAMADOL HYDROCHLORIDE | 1 | Unknown | 50 MG, QD | U | U | 0 | 50 | MG | QD | |||||
| 126789801 | 12678980 | 3 | C | LYRICA | PREGABALIN | 1 | Unknown | UNK, QD | U | U | 0 | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126789801 | 12678980 | 2 | Pain |
| 126789801 | 12678980 | 3 | Pain |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126789801 | 12678980 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126789801 | 12678980 | Abdominal pain upper | |
| 126789801 | 12678980 | Choking sensation | |
| 126789801 | 12678980 | Dyspnoea | |
| 126789801 | 12678980 | Mouth swelling |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |