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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126851861 | 12685186 | 1 | I | 201606 | 20160815 | 20160825 | 20160825 | EXP | US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-069958 | BRISTOL MYERS SQUIBB | 62.00 | YR | F | Y | 0.00000 | 20160825 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126851861 | 12685186 | 1 | PS | ABILIFY | ARIPIPRAZOLE | 1 | Oral | 1 DF, QD | 21436 | 1 | DF | QD | |||||||
| 126851861 | 12685186 | 2 | SS | ABILIFY | ARIPIPRAZOLE | 1 | Oral | 25 MG, QD | 21436 | 25 | MG | QD | |||||||
| 126851861 | 12685186 | 3 | SS | ABILIFY | ARIPIPRAZOLE | 1 | Oral | 20 MG, QD | 21436 | 20 | MG | QD | |||||||
| 126851861 | 12685186 | 4 | C | SYNTHROID | LEVOTHYROXINE SODIUM | 1 | Unknown | U | 0 | ||||||||||
| 126851861 | 12685186 | 5 | C | ATORVASTATIN | ATORVASTATIN | 1 | Unknown | U | 0 | ||||||||||
| 126851861 | 12685186 | 6 | C | MIDODRINE | MIDODRINE | 1 | Unknown | U | 0 | ||||||||||
| 126851861 | 12685186 | 7 | C | OXYCODONE | OXYCODONE | 1 | Unknown | 10 MG, BID | U | 0 | 10 | MG | BID | ||||||
| 126851861 | 12685186 | 8 | C | KLONOPIN | CLONAZEPAM | 1 | Unknown | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126851861 | 12685186 | 1 | Affective disorder |
| 126851861 | 12685186 | 4 | Product used for unknown indication |
| 126851861 | 12685186 | 5 | Blood cholesterol |
| 126851861 | 12685186 | 6 | Product used for unknown indication |
| 126851861 | 12685186 | 7 | Product used for unknown indication |
| 126851861 | 12685186 | 8 | Anxiety |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126851861 | 12685186 | OT |
| 126851861 | 12685186 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126851861 | 12685186 | Blood pressure decreased | |
| 126851861 | 12685186 | Fatigue | |
| 126851861 | 12685186 | Hospitalisation | |
| 126851861 | 12685186 | Musculoskeletal stiffness | |
| 126851861 | 12685186 | Pain | |
| 126851861 | 12685186 | Poor quality sleep | |
| 126851861 | 12685186 | Product use issue |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |