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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 94676192 | 9467619 | 2 | F | 20160715 | 20130821 | 20160729 | EXP | US-RANBAXY-2013US-72321 | RANBAXY | LEUCKER TM, SINGH S, MOFFETT BK. FLUOXETINE INHIBITION OF CYP3A4 POTENTIATING ADRENAL SUPPRESSION AND PEPTIC ULCER DISEASE FROM INTRA-ARTICULAR TRIAMCINOLONE INJECTIONS. PAIN MED. 2013;JUN;14(6):952-3 | 35.00 | YR | F | Y | 0.00000 | 20160729 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 94676192 | 9467619 | 1 | PS | FLUOXETINE | FLUOXETINE HYDROCHLORIDE | 1 | Unknown | UNK | U | 76990 | |||||||||
| 94676192 | 9467619 | 2 | I | Triamcinolone | TRIAMCINOLONE | 1 | Intra-articular | UNK, 3 MONTHLY | 0 | INJECTION | |||||||||
| 94676192 | 9467619 | 3 | C | LACTULOSE. | LACTULOSE | 1 | Unknown | UNK | U | 0 | |||||||||
| 94676192 | 9467619 | 4 | C | ZOLPIDEM | ZOLPIDEMOLPIDEM TARTRATE | 1 | Unknown | UNK | U | 0 | |||||||||
| 94676192 | 9467619 | 5 | C | POTASSIUM CHLORIDE. | POTASSIUM CHLORIDE | 1 | Unknown | UNK | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 94676192 | 9467619 | 1 | Product used for unknown indication |
| 94676192 | 9467619 | 2 | Product used for unknown indication |
| 94676192 | 9467619 | 3 | Product used for unknown indication |
| 94676192 | 9467619 | 4 | Product used for unknown indication |
| 94676192 | 9467619 | 5 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 94676192 | 9467619 | HO |
| 94676192 | 9467619 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 94676192 | 9467619 | Alkalosis | |
| 94676192 | 9467619 | Cushing's syndrome | |
| 94676192 | 9467619 | Drug interaction | |
| 94676192 | 9467619 | Drug level increased | |
| 94676192 | 9467619 | Hypokalaemia | |
| 94676192 | 9467619 | Peptic ulcer |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |