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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127775341 | 12777534 | 1 | I | 20160525 | 20160924 | 20160924 | PER | US-TEVA-663799USA | TEVA | 0.00 | F | Y | 95.34000 | KG | 20160924 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127775341 | 12777534 | 1 | PS | CLONAZEPAM. | CLONAZEPAM | 1 | 1 MILLIGRAM DAILY; | U | 74569 | .5 | MG | TABLET | BID | ||||||
127775341 | 12777534 | 2 | C | METOPROLOL. | METOPROLOL | 1 | 0 | ||||||||||||
127775341 | 12777534 | 3 | C | HYDROXYCHLOROQUINE | HYDROXYCHLOROQUINE | 1 | 0 | ||||||||||||
127775341 | 12777534 | 4 | C | COUMADIN | WARFARIN SODIUM | 1 | 0 | ||||||||||||
127775341 | 12777534 | 5 | C | LISINOPRIL. | LISINOPRIL | 1 | 0 | ||||||||||||
127775341 | 12777534 | 6 | C | Nuvugil | 2 | 0 | |||||||||||||
127775341 | 12777534 | 7 | C | LANTUS | INSULIN GLARGINE | 1 | 0 | ||||||||||||
127775341 | 12777534 | 8 | C | amitriptyline | AMITRIPTYLINE | 1 | 0 |
Indications of drugs used
no results found |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127775341 | 12777534 | Anxiety | |
127775341 | 12777534 | False negative investigation result | |
127775341 | 12777534 | Tremor |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |