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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126930751 | 12693075 | 1 | I | 201608 | 20160815 | 20160829 | 20160829 | EXP | US-JNJFOC-20160814749 | JOHNSON AND JOHNSON | 27.00 | YR | A | M | Y | 0.00000 | 20160829 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126930751 | 12693075 | 1 | PS | TYLENOL PM EXTRA STRENGTH | ACETAMINOPHENDIPHENHYDRAMINE HYDROCHLORIDE | 1 | Oral | 12 DOSES IN TOTAL | U | U | JFC218 | 999999 | 12 | DF | TABLET | ||||
| 126930751 | 12693075 | 2 | SS | TYLENOL | ACETAMINOPHEN | 1 | Unknown | U | U | 19872 | UNSPECIFIED | ||||||||
| 126930751 | 12693075 | 3 | SS | TYLENOL | ACETAMINOPHEN | 1 | Unknown | IN 24 HOURS | U | U | 19872 | 1000 | MG | UNSPECIFIED | |||||
| 126930751 | 12693075 | 4 | C | NEXIUM | ESOMEPRAZOLE MAGNESIUM | 1 | Unknown | 0 | UNSPECIFIED | ||||||||||
| 126930751 | 12693075 | 5 | C | ADDERALL | AMPHETAMINE ASPARTATEAMPHETAMINE SULFATEDEXTROAMPHETAMINE SACCHARATEDEXTROAMPHETAMINE SULFATE | 1 | Unknown | 0 | UNSPECIFIED |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126930751 | 12693075 | 1 | Insomnia |
| 126930751 | 12693075 | 3 | Product used for unknown indication |
| 126930751 | 12693075 | 4 | Product used for unknown indication |
| 126930751 | 12693075 | 5 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126930751 | 12693075 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126930751 | 12693075 | Accidental overdose | |
| 126930751 | 12693075 | Drug administration error | |
| 126930751 | 12693075 | Drug ineffective for unapproved indication | |
| 126930751 | 12693075 | Fatigue | |
| 126930751 | 12693075 | Lethargy | |
| 126930751 | 12693075 | Off label use | |
| 126930751 | 12693075 | Palpitations | |
| 126930751 | 12693075 | Somnolence | |
| 126930751 | 12693075 | Tachycardia | |
| 126930751 | 12693075 | Wrong technique in product usage process |
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 |
|---|---|---|---|---|---|---|
| 126930751 | 12693075 | 1 | 20160815 | 0 | ||
| 126930751 | 12693075 | 3 | 201608 | 0 |