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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125970241 | 12597024 | 1 | I | 20160225 | 20160727 | 20160727 | PER | US-SUN PHARMACEUTICAL INDUSTRIES LTD-2016US-112823 | RANBAXY | 0.00 | F | Y | 88.90000 | KG | 20160727 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125970241 | 12597024 | 1 | PS | TRAMADOL. | TRAMADOL | 1 | Unknown | 50 MG AT BEDTIME | 76100 | 50 | MG | ||||||||
| 125970241 | 12597024 | 2 | SS | NEURONTIN | GABAPENTIN | 1 | Unknown | 600 MG, TID | 0 | 600 | MG | Q8H | |||||||
| 125970241 | 12597024 | 3 | SS | XELJANZ | TOFACITINIB CITRATE | 1 | Unknown | 5 MG, BID | M73567 | 0 | 5 | MG | Q12H | ||||||
| 125970241 | 12597024 | 4 | SS | XELJANZ | TOFACITINIB CITRATE | 1 | 0 | ||||||||||||
| 125970241 | 12597024 | 5 | C | PROMETHAZINE | PROMETHAZINEPROMETHAZINE HYDROCHLORIDE | 1 | Unknown | 25 MG, TID | 0 | 25 | MG | Q8H | |||||||
| 125970241 | 12597024 | 6 | C | VITAMIN D | CHOLECALCIFEROL | 1 | Unknown | 400 IU, QD | 0 | 400 | IU | ||||||||
| 125970241 | 12597024 | 7 | C | PROTONIX | PANTOPRAZOLE SODIUM | 1 | Unknown | 40 MG, QD | 0 | 40 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125970241 | 12597024 | 1 | Pain |
| 125970241 | 12597024 | 2 | Pain |
| 125970241 | 12597024 | 3 | Rheumatoid arthritis |
| 125970241 | 12597024 | 4 | Systemic lupus erythematosus |
| 125970241 | 12597024 | 5 | Nausea |
| 125970241 | 12597024 | 6 | Vitamin D deficiency |
| 125970241 | 12597024 | 7 | Gastrooesophageal reflux disease |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125970241 | 12597024 | Inappropriate schedule of drug administration | |
| 125970241 | 12597024 | Weight increased |
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 |
|---|---|---|---|---|---|---|
| 125970241 | 12597024 | 3 | 201601 | 0 |