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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124935704 | 12493570 | 4 | F | 201510 | 20160826 | 20160623 | 20160901 | EXP | US-PFIZER INC-2016310321 | PFIZER | 53.00 | YR | F | Y | 54.00000 | KG | 20160901 | PH | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124935704 | 12493570 | 1 | PS | LYRICA | PREGABALIN | 1 | 50 MG, 3X/DAY | M49795 | 21446 | 50 | MG | CAPSULE, HARD | TID | ||||||
| 124935704 | 12493570 | 2 | SS | LYRICA | PREGABALIN | 1 | 75 MG, 3X/DAY | 21446 | 75 | MG | CAPSULE, HARD | TID | |||||||
| 124935704 | 12493570 | 3 | SS | SYNTHROID | LEVOTHYROXINE SODIUM | 1 | 137 UG, 1X/DAY | 1048419 | 0 | 137 | UG | QD | |||||||
| 124935704 | 12493570 | 4 | SS | PREDNISONE. | PREDNISONE | 1 | UNK | N | 0 | ||||||||||
| 124935704 | 12493570 | 5 | SS | BONIVA | IBANDRONATE SODIUM | 1 | UNK | N | 0 | ||||||||||
| 124935704 | 12493570 | 6 | C | TOPAMAX | TOPIRAMATE | 1 | 200 MG, 2X/DAY | 0 | 200 | MG | BID | ||||||||
| 124935704 | 12493570 | 7 | C | TOPAMAX | TOPIRAMATE | 1 | 0 | ||||||||||||
| 124935704 | 12493570 | 8 | C | IMITREX | SUMATRIPTAN SUCCINATE | 1 | Nasal | ONLY TOOK IT WHEN SHE FELT SHE WAS GOING TO LOSE HER VISION | 0 | NASAL SPRAY | |||||||||
| 124935704 | 12493570 | 9 | C | VITAMIN D | CHOLECALCIFEROL | 1 | 5000 IU, 3 TIMES A WEEK | 0 | 50000 | IU | |||||||||
| 124935704 | 12493570 | 10 | C | REQUIP | ROPINIROLE HYDROCHLORIDE | 1 | 2 MG, ONCE AT NIGHT | 0 | 2 | MG | TABLET | QD | |||||||
| 124935704 | 12493570 | 11 | C | PROPRANOLOL | PROPRANOLOLPROPRANOLOL HYDROCHLORIDE | 1 | 40 MG, 1X/DAY | 0 | 40 | MG | QD | ||||||||
| 124935704 | 12493570 | 12 | C | PROPRANOLOL | PROPRANOLOLPROPRANOLOL HYDROCHLORIDE | 1 | 0 | ||||||||||||
| 124935704 | 12493570 | 13 | C | CYMBALTA | DULOXETINE HYDROCHLORIDE | 1 | 60 MG IN MORNING AND 30 MG ONE TIME AT NIGHT | 0 | BID | ||||||||||
| 124935704 | 12493570 | 14 | C | CYMBALTA | DULOXETINE HYDROCHLORIDE | 1 | 0 | ||||||||||||
| 124935704 | 12493570 | 15 | C | CLONAZEPAM. | CLONAZEPAM | 1 | 1 MG, AT NIGHT | 0 | 1 | MG | QD | ||||||||
| 124935704 | 12493570 | 16 | C | CLONAZEPAM. | CLONAZEPAM | 1 | 0 | ||||||||||||
| 124935704 | 12493570 | 17 | C | HYDROCODONE | HYDROCODONE | 1 | 7.5/325, 2 TIMES A DAY AT NIGHT | 0 | BID | ||||||||||
| 124935704 | 12493570 | 18 | C | AMITRIPTYLINE | AMITRIPTYLINE | 1 | 100 MG, 1X/DAY | 0 | 100 | MG | QD | ||||||||
| 124935704 | 12493570 | 19 | C | AMITRIPTYLINE | AMITRIPTYLINE | 1 | 0 | ||||||||||||
| 124935704 | 12493570 | 20 | C | AMITRIPTYLINE | AMITRIPTYLINE | 1 | 0 | ||||||||||||
| 124935704 | 12493570 | 21 | C | BACLOFEN. | BACLOFEN | 1 | 20 MG, UNK | 0 | 20 | MG | |||||||||
| 124935704 | 12493570 | 22 | C | PROLIA | DENOSUMAB | 1 | ONCE EVERY 6 MONTHS | 0 | INJECTION |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 124935704 | 12493570 | 1 | Fibromyalgia |
| 124935704 | 12493570 | 2 | Nerve injury |
| 124935704 | 12493570 | 3 | Hypothyroidism |
| 124935704 | 12493570 | 4 | Osteitis |
| 124935704 | 12493570 | 5 | Bone disorder |
| 124935704 | 12493570 | 6 | Migraine |
| 124935704 | 12493570 | 7 | Blindness |
| 124935704 | 12493570 | 8 | Blindness |
| 124935704 | 12493570 | 10 | Restless legs syndrome |
| 124935704 | 12493570 | 11 | Blood pressure abnormal |
| 124935704 | 12493570 | 12 | Headache |
| 124935704 | 12493570 | 13 | Muscle spasms |
| 124935704 | 12493570 | 14 | Depression |
| 124935704 | 12493570 | 15 | Insomnia |
| 124935704 | 12493570 | 16 | Dyskinesia |
| 124935704 | 12493570 | 17 | Pain |
| 124935704 | 12493570 | 18 | Anxiety |
| 124935704 | 12493570 | 19 | Depression |
| 124935704 | 12493570 | 20 | Insomnia |
| 124935704 | 12493570 | 21 | Muscle relaxant therapy |
| 124935704 | 12493570 | 22 | Bone disorder |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 124935704 | 12493570 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 124935704 | 12493570 | Activities of daily living impaired | |
| 124935704 | 12493570 | Body height decreased | |
| 124935704 | 12493570 | Complex regional pain syndrome | |
| 124935704 | 12493570 | Drug dose omission | |
| 124935704 | 12493570 | Drug effect incomplete | |
| 124935704 | 12493570 | Fall | |
| 124935704 | 12493570 | Fatigue | |
| 124935704 | 12493570 | Foot fracture | |
| 124935704 | 12493570 | Hand fracture | |
| 124935704 | 12493570 | Impaired work ability | |
| 124935704 | 12493570 | Osteitis | |
| 124935704 | 12493570 | Rotator cuff syndrome | |
| 124935704 | 12493570 | Upper limb fracture | |
| 124935704 | 12493570 | Varicose vein | |
| 124935704 | 12493570 | Weight decreased |
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 |
|---|---|---|---|---|---|---|
| 124935704 | 12493570 | 22 | 201605 | 0 |