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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126826341 | 12682634 | 1 | I | 20160618 | 20160811 | 20160825 | 20160825 | EXP | GB-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-069981 | BRISTOL MYERS SQUIBB | 17.00 | YR | M | Y | 75.00000 | KG | 20160825 | MD | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126826341 | 12682634 | 1 | PS | ARIPIPRAZOLE. | ARIPIPRAZOLE | 1 | Oral | 5 MG, QD | 21436 | 5 | MG | QD | |||||||
126826341 | 12682634 | 2 | SS | ARIPIPRAZOLE. | ARIPIPRAZOLE | 1 | 21436 | ||||||||||||
126826341 | 12682634 | 3 | C | IBUPROFEN. | IBUPROFEN | 1 | Unknown | U | 0 | ||||||||||
126826341 | 12682634 | 4 | C | LAXIDO /06401201/ | POLYETHYLENE GLYCOL 3350POTASSIUM CHLORIDESODIUM BICARBONATESODIUM CHLORIDE | 1 | Unknown | U | 0 | ||||||||||
126826341 | 12682634 | 5 | C | MELATONIN | MELATONIN | 1 | Unknown | U | 0 | ||||||||||
126826341 | 12682634 | 6 | C | OMEPRAZOLE. | OMEPRAZOLE | 1 | Unknown | U | 0 | ||||||||||
126826341 | 12682634 | 7 | C | PARACETAMOL | ACETAMINOPHEN | 1 | Unknown | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126826341 | 12682634 | 1 | Autism |
126826341 | 12682634 | 2 | Learning disorder |
126826341 | 12682634 | 3 | Product used for unknown indication |
126826341 | 12682634 | 4 | Product used for unknown indication |
126826341 | 12682634 | 5 | Product used for unknown indication |
126826341 | 12682634 | 6 | Product used for unknown indication |
126826341 | 12682634 | 7 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126826341 | 12682634 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126826341 | 12682634 | Deep vein thrombosis | |
126826341 | 12682634 | 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 |