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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125924742 | 12592474 | 2 | F | 20160714 | 20160726 | 20160729 | EXP | GB-JNJFOC-20160712495 | JOHNSON AND JOHNSON | 57.00 | YR | A | F | Y | 49.80000 | KG | 20160729 | PH | GB | GB |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125924742 | 12592474 | 1 | PS | PARACETAMOL | ACETAMINOPHEN | 1 | Unknown | Y | N | 19872 | TABLET | ||||||||
| 125924742 | 12592474 | 2 | SS | PARACETAMOL | ACETAMINOPHEN | 1 | Unknown | DOSE: 500 (UNITS UNSPECIFIED). 15/20 TABLETS FOR A COUPLE OF WEEKS. | Y | N | 19872 | TABLET | |||||||
| 125924742 | 12592474 | 3 | C | LIBRIUM | CHLORDIAZEPOXIDE HYDROCHLORIDE | 1 | Unknown | DOSAGE: REDUCING REGIME | 0 | UNSPECIFIED | |||||||||
| 125924742 | 12592474 | 4 | C | LANSOPRAZOLE. | LANSOPRAZOLE | 1 | Unknown | 30 DOSE (UNITS UNSPECIFIED), ONCE A DAY IN THE MORNING | 0 | CAPSULE | |||||||||
| 125924742 | 12592474 | 5 | C | THIAMIN | THIAMINE | 1 | Unknown | DOSE: 100 (UNITS UNSPECIFIED), TWICE A DAY. | 0 | UNSPECIFIED |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125924742 | 12592474 | 2 | Pain |
| 125924742 | 12592474 | 3 | Alcohol abuse |
| 125924742 | 12592474 | 4 | Product used for unknown indication |
| 125924742 | 12592474 | 5 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125924742 | 12592474 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125924742 | 12592474 | Blood potassium decreased | |
| 125924742 | 12592474 | Gamma-glutamyltransferase increased | |
| 125924742 | 12592474 | Overdose | |
| 125924742 | 12592474 | Vomiting |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |