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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
90320683 | 9032068 | 3 | F | 20160825 | 20130125 | 20160830 | EXP | US-PFIZER INC-2013032670 | PFIZER | 51.00 | YR | F | Y | 127.00000 | KG | 20160830 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
90320683 | 9032068 | 1 | PS | LYRICA | PREGABALIN | 1 | Oral | 225 MG, UNK | N | 21446 | 225 | MG | CAPSULE, HARD | ||||||
90320683 | 9032068 | 2 | SS | LYRICA | PREGABALIN | 1 | Oral | 150 MG, 2X/DAY | N | 21446 | 150 | MG | CAPSULE, HARD | BID | |||||
90320683 | 9032068 | 3 | SS | LYRICA | PREGABALIN | 1 | Oral | UNK | N | 21446 | CAPSULE, HARD | ||||||||
90320683 | 9032068 | 4 | SS | LYRICA | PREGABALIN | 1 | Oral | 150 MG, ALTERNATE DAY (ONE EVERY OTHER NIGHT) | N | 21446 | 150 | MG | CAPSULE, HARD | QOD | |||||
90320683 | 9032068 | 5 | SS | METFORMIN | METFORMIN HYDROCHLORIDE | 1 | 500 MG, 2X/DAY (ONE IN THE MORNING AND AT 6PM) | 0 | 500 | MG | BID | ||||||||
90320683 | 9032068 | 6 | C | IRON | IRON | 1 | UNK | 0 | |||||||||||
90320683 | 9032068 | 7 | C | ZOCOR | SIMVASTATIN | 1 | 20 MG, 1X/DAY | 0 | 20 | MG | TABLET | QD | |||||||
90320683 | 9032068 | 8 | C | PRILOSEC | OMEPRAZOLE MAGNESIUM | 1 | 20 MG, 1X/DAY (ONE EVERY MORNING BEFORE SHE EATS) | 0 | 20 | MG | CAPSULE | QD | |||||||
90320683 | 9032068 | 9 | C | DULOXETINE. | DULOXETINE | 1 | 60 MG, AS NEEDED (MORNING EVERY DAY) | 0 | 60 | MG | CAPSULE | ||||||||
90320683 | 9032068 | 10 | C | LISINOPRIL. | LISINOPRIL | 1 | 25 MG, 1X/DAY | 0 | 25 | MG | TABLET | QD | |||||||
90320683 | 9032068 | 11 | C | LORTAB | ACETAMINOPHENHYDROCODONE BITARTRATE | 1 | 1 DF, 2X/DAY | 0 | 1 | DF | TABLET | BID |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
90320683 | 9032068 | 1 | Paraesthesia |
90320683 | 9032068 | 2 | Nerve injury |
90320683 | 9032068 | 5 | Diabetes mellitus |
90320683 | 9032068 | 7 | Blood cholesterol abnormal |
90320683 | 9032068 | 8 | Dyspepsia |
90320683 | 9032068 | 9 | Nerve injury |
90320683 | 9032068 | 10 | Blood pressure abnormal |
90320683 | 9032068 | 11 | Pain |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
90320683 | 9032068 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
90320683 | 9032068 | Abasia | |
90320683 | 9032068 | Balance disorder | |
90320683 | 9032068 | Burning sensation | |
90320683 | 9032068 | Dizziness | |
90320683 | 9032068 | Drug intolerance | |
90320683 | 9032068 | Fall | |
90320683 | 9032068 | Hypoaesthesia | |
90320683 | 9032068 | Mental disorder | |
90320683 | 9032068 | Oedema peripheral | |
90320683 | 9032068 | Sensory loss | |
90320683 | 9032068 | Somnolence | |
90320683 | 9032068 | Speech disorder |
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 |
---|---|---|---|---|---|---|
90320683 | 9032068 | 1 | 2002 | 0 | ||
90320683 | 9032068 | 4 | 2015 | 0 | ||
90320683 | 9032068 | 9 | 2016 | 0 |