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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125990441 | 12599044 | 1 | I | 20160126 | 20160727 | 20160727 | PER | US-MYLANLABS-2016M1004244 | MYLAN | 0.00 | F | Y | 0.00000 | 20160727 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125990441 | 12599044 | 1 | PS | Tramadol Hydrochloride Tablets, USP | TRAMADOL HYDROCHLORIDE | 1 | Oral | 100 MG, TID | 75986 | 100 | MG | TABLET | TID | ||||||
125990441 | 12599044 | 2 | SS | Tramadol Hydrochloride Tablets, USP | TRAMADOL HYDROCHLORIDE | 1 | 50MG TABLET SEVERAL TIMES A DAY | 75986 | 50 | MG | TABLET | ||||||||
125990441 | 12599044 | 3 | SS | Tramadol Hydrochloride Tablets, USP | TRAMADOL HYDROCHLORIDE | 1 | 250 MG, QD | 75986 | 250 | MG | TABLET | QD | |||||||
125990441 | 12599044 | 4 | SS | LYRICA | PREGABALIN | 1 | UNK | U | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125990441 | 12599044 | 1 | Neck pain |
125990441 | 12599044 | 2 | Pain in extremity |
125990441 | 12599044 | 4 | Fibromyalgia |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125990441 | 12599044 | Somnolence | |
125990441 | 12599044 | Weight increased |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |