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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 93333273 | 9333327 | 3 | F | 20110909 | 20160921 | 20130606 | 20160930 | EXP | BR-JNJFOC-20130516527 | JOHNSON AND JOHNSON | 2.38 | YR | C | M | Y | 14.00000 | KG | 20160930 | CN | BR | BR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 93333273 | 9333327 | 1 | PS | TYLENOL | ACETAMINOPHEN | 1 | Oral | D | N | UNSPECIFIED | 19872 | ORAL SOLUTION |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 93333273 | 9333327 | 1 | Pyrexia |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 93333273 | 9333327 | DE |
| 93333273 | 9333327 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 93333273 | 9333327 | Acute kidney injury | |
| 93333273 | 9333327 | Adverse event | |
| 93333273 | 9333327 | Agitation | |
| 93333273 | 9333327 | Hypovolaemia | |
| 93333273 | 9333327 | Septic shock | |
| 93333273 | 9333327 | Tachycardia | |
| 93333273 | 9333327 | Thrombocytopenia |
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 |
|---|---|---|---|---|---|---|
| 93333273 | 9333327 | 1 | 20110909 | 20110909 | 0 |