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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126480622 | 12648062 | 2 | F | 20160812 | 20160812 | 20160816 | EXP | NL-JNJFOC-20160800268 | JOHNSON AND JOHNSON | 9.00 | YR | C | M | Y | 21.00000 | KG | 20160816 | CN | NL | NL |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126480622 | 12648062 | 1 | PS | TYLENOL | ACETAMINOPHEN | 1 | Unknown | N | 19872 | UNSPECIFIED | |||||||||
| 126480622 | 12648062 | 2 | SS | TYLENOL | ACETAMINOPHEN | 1 | Unknown | 3 X PER DAY | N | 19872 | 500 | MG | UNSPECIFIED | TID | |||||
| 126480622 | 12648062 | 3 | SS | PARACETAMOL | ACETAMINOPHEN | 1 | Unknown | U | 0 | 500 | MG | UNSPECIFIED | TID |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126480622 | 12648062 | 2 | Product used for unknown indication |
| 126480622 | 12648062 | 3 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126480622 | 12648062 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126480622 | 12648062 | Abnormal faeces | |
| 126480622 | 12648062 | Seizure | |
| 126480622 | 12648062 | Toxicity to various agents |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |