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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 102707406 | 10270740 | 6 | F | 20160617 | 20140701 | 20160705 | PER | US-PFIZER INC-2014174791 | PFIZER | 59.00 | YR | F | Y | 0.00000 | 20160705 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 102707406 | 10270740 | 1 | PS | LYRICA | PREGABALIN | 1 | Oral | 150 MG, 2X/DAY | U | 21446 | 150 | MG | CAPSULE, HARD | BID | |||||
| 102707406 | 10270740 | 2 | SS | LYRICA | PREGABALIN | 1 | U | 21446 | CAPSULE, HARD | ||||||||||
| 102707406 | 10270740 | 3 | SS | LYRICA | PREGABALIN | 1 | U | 21446 | CAPSULE, HARD | ||||||||||
| 102707406 | 10270740 | 4 | C | PEPCID | FAMOTIDINE | 1 | UNK | 0 | |||||||||||
| 102707406 | 10270740 | 5 | C | PRILOSEC | OMEPRAZOLE MAGNESIUM | 1 | UNK | 0 | |||||||||||
| 102707406 | 10270740 | 6 | C | METFORMIN | METFORMIN HYDROCHLORIDE | 1 | UNK | 0 | |||||||||||
| 102707406 | 10270740 | 7 | C | LOVASTATIN. | LOVASTATIN | 1 | UNK | 0 | |||||||||||
| 102707406 | 10270740 | 8 | C | REGLAN | METOCLOPRAMIDE HYDROCHLORIDE | 1 | UNK | 0 | |||||||||||
| 102707406 | 10270740 | 9 | C | HYDROCHLOROTHIAZIDE. | HYDROCHLOROTHIAZIDE | 1 | UNK | 0 | |||||||||||
| 102707406 | 10270740 | 10 | C | FAMOTIDINE. | FAMOTIDINE | 1 | UNK | 0 | |||||||||||
| 102707406 | 10270740 | 11 | C | LOSARTAN. | LOSARTAN | 1 | UNK | 0 | |||||||||||
| 102707406 | 10270740 | 12 | C | AMITRIPTYLINE | AMITRIPTYLINE | 1 | UNK | 0 | |||||||||||
| 102707406 | 10270740 | 13 | C | NORCO | ACETAMINOPHENHYDROCODONE BITARTRATE | 1 | UNK | 0 | |||||||||||
| 102707406 | 10270740 | 14 | C | VERAPAMIL | VERAPAMIL HYDROCHLORIDE | 1 | 0 | ||||||||||||
| 102707406 | 10270740 | 15 | C | FLEXERIL | CYCLOBENZAPRINE HYDROCHLORIDE | 1 | UNK | 0 | |||||||||||
| 102707406 | 10270740 | 16 | C | KLONOPIN | CLONAZEPAM | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 102707406 | 10270740 | 1 | Myalgia |
| 102707406 | 10270740 | 2 | Myositis |
| 102707406 | 10270740 | 3 | Fibromyalgia |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 102707406 | 10270740 | Drug hypersensitivity | |
| 102707406 | 10270740 | Rash | |
| 102707406 | 10270740 | Withdrawal syndrome |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |