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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125864641 | 12586464 | 1 | I | 2014 | 20160627 | 20160725 | 20160725 | PER | US-PFIZER INC-2016320502 | PFIZER | 79.00 | YR | F | Y | 0.00000 | 20160725 | OT | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125864641 | 12586464 | 1 | PS | CELEBREX | CELECOXIB | 1 | Oral | 200MG TABLETS, TAKE ON TABLET BY MOUTH 12 HOURS APART | 20998 | 200 | MG | CAPSULE, HARD | BID | ||||||
| 125864641 | 12586464 | 2 | SS | CELEBREX | CELECOXIB | 1 | 20998 | CAPSULE, HARD | |||||||||||
| 125864641 | 12586464 | 3 | C | NOVOLIN R | INSULIN HUMAN | 1 | SLIDING SCALE IN THE EVENING IF NEEDED | 0 | |||||||||||
| 125864641 | 12586464 | 4 | C | LEVEMIR | INSULIN DETEMIR | 1 | 100UNITS INJECTED IN THE MORNING | 0 | 100 | IU | |||||||||
| 125864641 | 12586464 | 5 | C | ALLOPURINOL. | ALLOPURINOL | 1 | Oral | 100 MG, 1X/DAY | 0 | 100 | MG | QD | |||||||
| 125864641 | 12586464 | 6 | C | LOVASTATIN. | LOVASTATIN | 1 | Oral | 40MG TABLET BY MOUTH ONCE A DAY IN THE EVEVEING | 0 | 40 | MG | TABLET | QD | ||||||
| 125864641 | 12586464 | 7 | C | METOPROLOL. | METOPROLOL | 1 | 25MG TABLET, HALF TABLET IN THE MORNING AND IN THE EVENING | 0 | 25 | MG | TABLET | ||||||||
| 125864641 | 12586464 | 8 | C | OMEPRAZOLE. | OMEPRAZOLE | 1 | 20MG TABLET IN THE MORNING BEFORE SHE EATS | 0 | 20 | MG | TABLET | ||||||||
| 125864641 | 12586464 | 9 | C | IPROTROPIUM BROMIDE/ALBUTEROL | 2 | [IPRATROPIUM BROMIDE]/[ALBUTEROL] BREATHING TREAMENT TWICE A DAY | 0 | BID | |||||||||||
| 125864641 | 12586464 | 10 | C | BABY ASPIRIN | ASPIRIN | 1 | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125864641 | 12586464 | 1 | Back pain |
| 125864641 | 12586464 | 2 | Pain in extremity |
| 125864641 | 12586464 | 3 | Diabetes mellitus |
| 125864641 | 12586464 | 4 | Diabetes mellitus |
| 125864641 | 12586464 | 5 | Gout |
| 125864641 | 12586464 | 6 | Blood cholesterol abnormal |
| 125864641 | 12586464 | 7 | Angina pectoris |
| 125864641 | 12586464 | 8 | Gastric disorder |
| 125864641 | 12586464 | 9 | Asthma |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125864641 | 12586464 | Accommodation disorder | |
| 125864641 | 12586464 | Fall | |
| 125864641 | 12586464 | Hypoaesthesia | |
| 125864641 | 12586464 | Sensory loss |
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 |
|---|---|---|---|---|---|---|
| 125864641 | 12586464 | 1 | 2014 | 0 |