Person who experienced the adverse event (patient)
Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
4549312 | 5712410 | I | 4549312-1 | 20040525 | 20040616 | 20041230 | PER | 04-06-0859 | IVAX PHARMACEUTICALS, INC. | 47 | YR | M | N | 20040616 | OT |
Drug(s) used by person
Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
---|---|---|---|---|---|---|---|---|---|---|---|
4549312 | 1005569631 | PS | CLOZAPINE | 1 | ORAL | 100-400MG QD ORAL | D | D | 74949 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
4549312 | 1005569631 | SCHIZOPHRENIA |
Outcome of event
Event ID | OUTC COD |
---|---|
4549312 | HO |
Reactions reported
Event ID | PT |
---|---|
4549312 | CONFUSIONAL STATE |
4549312 | HALLUCINATION, AUDITORY |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | RPSR COD |
---|---|
4549312 | HP |
4549312 | OTH |
Therapies reported
Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|
4549312 | 1005569631 | 20000601 |