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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 107208954 | 10720895 | 4 | F | 20160923 | 20150119 | 20160929 | PER | US-PFIZER INC-2015019290 | PFIZER | 53.00 | YR | F | Y | 0.00000 | 20160929 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 107208954 | 10720895 | 1 | PS | LYRICA | PREGABALIN | 1 | Oral | 200 MG, 3X/DAY (200MG 3X'S/DAY) | U | 21446 | 200 | MG | CAPSULE, HARD | TID | |||||
| 107208954 | 10720895 | 2 | C | VITAMIN D3 | CHOLECALCIFEROL | 1 | UNK | 0 | |||||||||||
| 107208954 | 10720895 | 3 | C | CELEXA | CITALOPRAM HYDROBROMIDE | 1 | UNK | 0 | |||||||||||
| 107208954 | 10720895 | 4 | C | MAGNESIUM MALATE | 2 | UNK | 0 | ||||||||||||
| 107208954 | 10720895 | 5 | C | PROTOPIC | TACROLIMUS | 1 | UNK | 0 | |||||||||||
| 107208954 | 10720895 | 6 | C | URSODIOL. | URSODIOL | 1 | UNK | 0 | |||||||||||
| 107208954 | 10720895 | 7 | C | AMBIEN | ZOLPIDEM TARTRATE | 1 | UNK | 0 | |||||||||||
| 107208954 | 10720895 | 8 | C | OMEGA 3 | OMEGA-3 FATTY ACIDS | 1 | UNK | 0 | |||||||||||
| 107208954 | 10720895 | 9 | C | NYSTATIN. | NYSTATIN | 1 | UNK | 0 | |||||||||||
| 107208954 | 10720895 | 10 | C | TRAMADOL. | TRAMADOL | 1 | UNK | 0 | |||||||||||
| 107208954 | 10720895 | 11 | C | KLONOPIN | CLONAZEPAM | 1 | UNK | 0 | |||||||||||
| 107208954 | 10720895 | 12 | C | VALIUM | DIAZEPAM | 1 | UNK | 0 | |||||||||||
| 107208954 | 10720895 | 13 | C | CALCIUM | CALCIUM | 1 | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 107208954 | 10720895 | 1 | Fibromyalgia |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 107208954 | 10720895 | Diarrhoea | |
| 107208954 | 10720895 | Gastric disorder | |
| 107208954 | 10720895 | Nausea | |
| 107208954 | 10720895 | Oropharyngeal pain | |
| 107208954 | 10720895 | Withdrawal syndrome |
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 |
|---|---|---|---|---|---|---|
| 107208954 | 10720895 | 1 | 201403 | 0 |