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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 862264811 | 8622648 | 11 | F | 201005 | 20160719 | 20120619 | 20160727 | EXP | US-JNJFOC-20120606087 | JOHNSON AND JOHNSON | 41.28 | YR | A | F | Y | 68.04000 | KG | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 862264811 | 8622648 | 1 | SS | TYLENOL EXTRA STRENGTH | ACETAMINOPHEN | 1 | Oral | U | U | 0 | 500 | MG | GELCAPS | ||||||
| 862264811 | 8622648 | 2 | PS | TYLENOL EXTRA STRENGTH | ACETAMINOPHEN | 1 | Oral | U | U | 19872 | 500 | MG | GELCAPS | ||||||
| 862264811 | 8622648 | 3 | SS | TYLENOL EXTRA STRENGTH | ACETAMINOPHEN | 1 | Oral | U | U | 19872 | 500 | MG | GELCAPS | ||||||
| 862264811 | 8622648 | 4 | SS | TYLENOL | ACETAMINOPHEN | 1 | Oral | 2 GRAMS EVERY 3 HOURS (MORE THAN OR EQUAL TO 18-24 HOURS). | U | U | 0 | 2 | G | TABLET | |||||
| 862264811 | 8622648 | 5 | SS | TYLENOL | ACETAMINOPHEN | 1 | Oral | 2 GRAMS EVERY 3 HOURS (MORE THAN OR EQUAL TO 18-24 HOURS). | U | U | 19872 | 2 | G | TABLET | |||||
| 862264811 | 8622648 | 6 | SS | TYLENOL | ACETAMINOPHEN | 1 | Oral | 2 GRAMS EVERY 3 HOURS (MORE THAN OR EQUAL TO 18-24 HOURS). | U | U | 19872 | 2 | G | TABLET | |||||
| 862264811 | 8622648 | 7 | SS | ALCOHOL. | ALCOHOL | 1 | Unknown | U | 0 | UNSPECIFIED | |||||||||
| 862264811 | 8622648 | 8 | C | CLARITIN | LORATADINE | 1 | Unknown | 0 | UNSPECIFIED |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 862264811 | 8622648 | 1 | Back pain |
| 862264811 | 8622648 | 2 | Chills |
| 862264811 | 8622648 | 3 | Pyrexia |
| 862264811 | 8622648 | 4 | Back pain |
| 862264811 | 8622648 | 5 | Chills |
| 862264811 | 8622648 | 6 | Pyrexia |
| 862264811 | 8622648 | 7 | Product used for unknown indication |
| 862264811 | 8622648 | 8 | Multiple allergies |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 862264811 | 8622648 | OT |
| 862264811 | 8622648 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 862264811 | 8622648 | Accidental overdose | |
| 862264811 | 8622648 | Acute hepatic failure | |
| 862264811 | 8622648 | Renal failure | |
| 862264811 | 8622648 | Toxicity to various agents | |
| 862264811 | 8622648 | Urinary tract infection |
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 |
|---|---|---|---|---|---|---|
| 862264811 | 8622648 | 1 | 20100527 | 0 | ||
| 862264811 | 8622648 | 2 | 20100527 | 0 | ||
| 862264811 | 8622648 | 3 | 20100527 | 0 | ||
| 862264811 | 8622648 | 4 | 20100528 | 201005 | 0 | |
| 862264811 | 8622648 | 5 | 20100528 | 201005 | 0 | |
| 862264811 | 8622648 | 6 | 20100528 | 201005 | 0 |