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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127979151 | 12797915 | 1 | I | 20160604 | 20160609 | 20160930 | 20160930 | PER | US-LUPIN PHARMACEUTICALS INC.-E2B_00005648 | LUPIN | 67.75 | YR | F | Y | 30.87000 | KG | 20160930 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127979151 | 12797915 | 1 | PS | Cephalexin capsules USP 500mg | CEPHALEXIN | 1 | Oral | N | UNKNOWN | 65229 | 500 | MG | Q6H | ||||||
| 127979151 | 12797915 | 2 | SS | Cephalexin capsules USP 500mg | CEPHALEXIN | 1 | Oral | N | UNKNOWN | 65229 | 500 | MG | Q6H |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127979151 | 12797915 | 1 | Product used for unknown indication |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127979151 | 12797915 | Abdominal discomfort | |
| 127979151 | 12797915 | Product odour abnormal |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|---|
| 127979151 | 12797915 | 1 | 20160604 | 20160609 | 0 | |
| 127979151 | 12797915 | 2 | 20160609 | 0 |