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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 107300683 | 10730068 | 3 | F | 20160915 | 20150122 | 20160919 | EXP | US-PFIZER INC-2015022746 | PFIZER | 37.00 | YR | F | Y | 0.00000 | 20160919 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 107300683 | 10730068 | 1 | PS | LYRICA | PREGABALIN | 1 | 300 MG, 2X/DAY | U | 21446 | 300 | MG | CAPSULE, HARD | BID | ||||||
| 107300683 | 10730068 | 2 | SS | LYRICA | PREGABALIN | 1 | 150 MG, 3X/DAY | U | 21446 | 150 | MG | CAPSULE, HARD | TID | ||||||
| 107300683 | 10730068 | 3 | C | ADDERALL | AMPHETAMINE ASPARTATEAMPHETAMINE SULFATEDEXTROAMPHETAMINE SACCHARATEDEXTROAMPHETAMINE SULFATE | 1 | 30 MG, 2X/DAY | 0 | 30 | MG | TABLET | BID | |||||||
| 107300683 | 10730068 | 4 | C | PERCOCET | ACETAMINOPHENOXYCODONE HYDROCHLORIDE | 1 | 1 DF (5/325), AS NEEDED | 0 | 1 | DF | |||||||||
| 107300683 | 10730068 | 5 | C | PERCOCET | ACETAMINOPHENOXYCODONE HYDROCHLORIDE | 1 | 0 | ||||||||||||
| 107300683 | 10730068 | 6 | C | PRENATAL MV AND MIN/ FE-FA TABS | 2 | UNK UNK, 1X/DAY | 0 | TABLET | QD | ||||||||||
| 107300683 | 10730068 | 7 | C | PROTONIX | PANTOPRAZOLE SODIUM | 1 | 40 MG, 2X/DAY | 0 | 40 | MG | PROLONGED-RELEASE TABLET | BID | |||||||
| 107300683 | 10730068 | 8 | C | PROTONIX | PANTOPRAZOLE SODIUM | 1 | 40 MG, 1X/DAY | 0 | 40 | MG | PROLONGED-RELEASE TABLET | QD | |||||||
| 107300683 | 10730068 | 9 | C | DAILY MULTIVITAMIN | VITAMINS | 1 | 2/DAY | 0 | 2 | DF |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 107300683 | 10730068 | 1 | Nystagmus |
| 107300683 | 10730068 | 2 | Eye disorder |
| 107300683 | 10730068 | 4 | Pain |
| 107300683 | 10730068 | 5 | Arthralgia |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 107300683 | 10730068 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 107300683 | 10730068 | Abasia | |
| 107300683 | 10730068 | Cerebrovascular accident | |
| 107300683 | 10730068 | Product use issue | |
| 107300683 | 10730068 | Visual impairment |
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 |
|---|---|---|---|---|---|---|
| 107300683 | 10730068 | 1 | 20150105 | 0 | ||
| 107300683 | 10730068 | 3 | 20160405 | 0 | ||
| 107300683 | 10730068 | 6 | 20160405 | 0 | ||
| 107300683 | 10730068 | 7 | 20160405 | 0 |