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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 1075310510 | 10753105 | 10 | F | 2012 | 20160914 | 20150130 | 20160920 | EXP | US-PFIZER INC-2015034899 | PFIZER | 66.00 | YR | F | Y | 49.00000 | KG | 20160920 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 1075310510 | 10753105 | 1 | PS | LYRICA | PREGABALIN | 1 | Oral | 100 MG, 2X/DAY | MO1165 | 21446 | 100 | MG | CAPSULE, HARD | BID | |||||
| 1075310510 | 10753105 | 2 | SS | LYRICA | PREGABALIN | 1 | Oral | 100 MG, 1X/DAY | 21446 | 100 | MG | CAPSULE, HARD | QD | ||||||
| 1075310510 | 10753105 | 3 | SS | LYRICA | PREGABALIN | 1 | Oral | 100 MG, 2X/DAY | 21446 | 100 | MG | CAPSULE, HARD | BID | ||||||
| 1075310510 | 10753105 | 4 | SS | LYRICA | PREGABALIN | 1 | 21446 | CAPSULE, HARD | |||||||||||
| 1075310510 | 10753105 | 5 | SS | NORCO | ACETAMINOPHENHYDROCODONE BITARTRATE | 1 | 10/325 BID WHEN NECESSARY | U | 0 | ||||||||||
| 1075310510 | 10753105 | 6 | C | LASIX | FUROSEMIDE | 1 | UNK | 0 | |||||||||||
| 1075310510 | 10753105 | 7 | C | PRAZOLAC | 2 | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 1075310510 | 10753105 | 1 | Neuralgia |
| 1075310510 | 10753105 | 2 | Spinal cord disorder |
| 1075310510 | 10753105 | 3 | Neuropathy peripheral |
| 1075310510 | 10753105 | 4 | Fibromyalgia |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 1075310510 | 10753105 | OT |
| 1075310510 | 10753105 | HO |
| 1075310510 | 10753105 | DS |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 1075310510 | 10753105 | Balance disorder | |
| 1075310510 | 10753105 | Body height decreased | |
| 1075310510 | 10753105 | Bone pain | |
| 1075310510 | 10753105 | Burning sensation | |
| 1075310510 | 10753105 | Coma | |
| 1075310510 | 10753105 | Discomfort | |
| 1075310510 | 10753105 | Feeling of body temperature change | |
| 1075310510 | 10753105 | Hypoaesthesia | |
| 1075310510 | 10753105 | Insomnia | |
| 1075310510 | 10753105 | Intentional product use issue | |
| 1075310510 | 10753105 | Lumbar vertebral fracture | |
| 1075310510 | 10753105 | Pain | |
| 1075310510 | 10753105 | Spinal disorder | |
| 1075310510 | 10753105 | Staphylococcal infection | |
| 1075310510 | 10753105 | Weight fluctuation | |
| 1075310510 | 10753105 | Wrist fracture |
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 |
|---|---|---|---|---|---|---|
| 1075310510 | 10753105 | 1 | 200805 | 0 | ||
| 1075310510 | 10753105 | 2 | 2008 | 0 | ||
| 1075310510 | 10753105 | 3 | 2008 | 0 |