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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
98713233 | 9871323 | 3 | F | 20160812 | 20140205 | 20160822 | EXP | JP-ASTRAZENECA-2014SE07663 | ASTRAZENECA | 26.00 | YR | F | Y | 0.00000 | 20160822 | OT | JP | JP |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
98713233 | 9871323 | 1 | PS | SEROQUEL | QUETIAPINE FUMARATE | 1 | Oral | 1550.0MG ONCE/SINGLE ADMINISTRATION | U | U | 22047 | 1550 | MG | TABLET | |||||
98713233 | 9871323 | 2 | SS | ABILIFY | ARIPIPRAZOLE | 1 | Oral | 60 MG | U | U | 0 | TABLET | |||||||
98713233 | 9871323 | 3 | SS | SODIUM VALPROATE | VALPROATE SODIUM | 1 | Oral | 2000.0MG ONCE/SINGLE ADMINISTRATION | U | U | 0 | 2000 | MG | TABLET | |||||
98713233 | 9871323 | 4 | SS | LEVOMEPROMAZINE MALEATE | LEVOMEPROMAZINE MALEATE | 1 | Oral | 20.0MG ONCE/SINGLE ADMINISTRATION | U | U | 0 | 20 | MG | TABLET | |||||
98713233 | 9871323 | 5 | SS | LORAZEPAM. | LORAZEPAM | 1 | Oral | 0.5 MG | U | U | 0 | TABLET | |||||||
98713233 | 9871323 | 6 | SS | METLIGINE | MIDODRINE HYDROCHLORIDE | 1 | Oral | 20.0MG ONCE/SINGLE ADMINISTRATION | U | U | 0 | 20 | MG | TABLET | |||||
98713233 | 9871323 | 7 | C | CONTRACEPTIVES | UNSPECIFIED INGREDIENT | 1 | Unknown | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
98713233 | 9871323 | 1 | Product used for unknown indication |
98713233 | 9871323 | 2 | Schizophrenia |
98713233 | 9871323 | 3 | Product used for unknown indication |
98713233 | 9871323 | 4 | Product used for unknown indication |
98713233 | 9871323 | 5 | Product used for unknown indication |
98713233 | 9871323 | 6 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
98713233 | 9871323 | HO |
98713233 | 9871323 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
98713233 | 9871323 | Altered state of consciousness | |
98713233 | 9871323 | Overdose | |
98713233 | 9871323 | Rhabdomyolysis |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |