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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125481411 | 12548141 | 1 | I | 20160613 | 20160712 | 20160712 | PER | US-PFIZER INC-2016299768 | PFIZER | 77.00 | YR | F | Y | 80.74000 | KG | 20160712 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125481411 | 12548141 | 1 | PS | LIPITOR | ATORVASTATIN CALCIUM | 1 | Oral | 10 MG, ALTERNATE DAY (EVERY OTHER DAY) | N | 20702 | 10 | MG | FILM-COATED TABLET | QOD | |||||
125481411 | 12548141 | 2 | C | OXAZEPAM. | OXAZEPAM | 1 | Oral | 10 MG, 2X/DAY (TWICE A DAY AS NEEDED) | 0 | 10 | MG | CAPSULE | BID | ||||||
125481411 | 12548141 | 3 | C | PROZAC | FLUOXETINE HYDROCHLORIDE | 1 | Oral | UNK , 1X/DAY | 0 | CAPSULE | QD | ||||||||
125481411 | 12548141 | 4 | C | ATENOLOL. | ATENOLOL | 1 | Oral | 100 MG, DAILY (100MG TABLET BY MOUTH EVERY MORNING) | 0 | 100 | MG | TABLET | |||||||
125481411 | 12548141 | 5 | C | AMLODIPINE | AMLODIPINE BESYLATE | 1 | Oral | 5 MG, 1X/DAY | 0 | 5 | MG | TABLET | QD |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125481411 | 12548141 | 1 | Blood cholesterol abnormal |
125481411 | 12548141 | 2 | Anxiety |
125481411 | 12548141 | 3 | Antidepressant therapy |
125481411 | 12548141 | 4 | Hypertension |
125481411 | 12548141 | 5 | Hypertension |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125481411 | 12548141 | Contusion | |
125481411 | 12548141 | Erythema | |
125481411 | 12548141 | Gait disturbance | |
125481411 | 12548141 | Joint swelling | |
125481411 | 12548141 | Musculoskeletal stiffness | |
125481411 | 12548141 | Pain in extremity | |
125481411 | 12548141 | Paraesthesia | |
125481411 | 12548141 | Peripheral swelling | |
125481411 | 12548141 | Product use issue |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |