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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125876221 | 12587622 | 1 | I | 20160414 | 20160725 | 20160725 | PER | US-MYLANLABS-2016M1016044 | MYLAN | 48.00 | YR | F | Y | 0.00000 | 20160725 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125876221 | 12587622 | 1 | PS | HALOPERIDOL. | HALOPERIDOL | 1 | Oral | 10 MG, AM | 70278 | 10 | MG | TABLET | QD | ||||||
125876221 | 12587622 | 2 | SS | HALOPERIDOL. | HALOPERIDOL | 1 | Oral | 5 MG, HS | 70278 | 5 | MG | TABLET | QD | ||||||
125876221 | 12587622 | 3 | SS | HALOPERIDOL. | HALOPERIDOL | 1 | UNK UNK, Q2W | 0 | INJECTION | QOW | |||||||||
125876221 | 12587622 | 4 | SS | LORAZEPAM. | LORAZEPAM | 1 | Oral | 1 MG, BID | 0 | 1 | MG | TABLET | BID | ||||||
125876221 | 12587622 | 5 | SS | COGENTIN | BENZTROPINE MESYLATE | 1 | Oral | UNK UNK, BID | 0 | BID |
Indications of drugs used
no results found |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125876221 | 12587622 | Depressed mood | |
125876221 | 12587622 | Lethargy | |
125876221 | 12587622 | Limb discomfort | |
125876221 | 12587622 | Malaise |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |