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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126778401 | 12677840 | 1 | I | 20151208 | 20160816 | 20160823 | 20160823 | EXP | AT-PFIZER INC-2016389633 | PFIZER | 73.00 | YR | F | Y | 57.00000 | KG | 20160823 | CN | AT | AT |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126778401 | 12677840 | 1 | PS | GABAPENTIN. | GABAPENTIN | 1 | UNK | Y | 20882 | FILM-COATED TABLET | |||||||||
| 126778401 | 12677840 | 2 | SS | LYRICA | PREGABALIN | 1 | 75 MG, 2X/DAY | Y | 21446 | 75 | MG | CAPSULE, HARD | BID | ||||||
| 126778401 | 12677840 | 3 | SS | CYMBALTA | DULOXETINE HYDROCHLORIDE | 1 | 30 MG, 1X/DAY | Y | 0 | 30 | MG | QD | |||||||
| 126778401 | 12677840 | 4 | C | TEMESTA | LORAZEPAM | 1 | 2.5 MG, DAILY | 0 | 2.5 | MG | |||||||||
| 126778401 | 12677840 | 5 | C | TEMESTA | LORAZEPAM | 1 | 2 MG, DAILY | 0 | 2 | MG | |||||||||
| 126778401 | 12677840 | 6 | C | NOAX | 2 | 50 MG, 2X/DAY | 0 | 50 | MG | BID | |||||||||
| 126778401 | 12677840 | 7 | C | TRAMAL | TRAMADOL | 1 | 0 | ||||||||||||
| 126778401 | 12677840 | 8 | C | EUTHYROX | LEVOTHYROXINE SODIUM | 1 | 50 UG, UNK | 0 | 50 | UG | |||||||||
| 126778401 | 12677840 | 9 | C | ULCOSAN | 2 | 1-2 DF | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126778401 | 12677840 | 1 | Pain |
| 126778401 | 12677840 | 4 | Sleep disorder |
| 126778401 | 12677840 | 7 | Pain |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126778401 | 12677840 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126778401 | 12677840 | Abdominal pain upper | |
| 126778401 | 12677840 | Arthralgia | |
| 126778401 | 12677840 | Ataxia | |
| 126778401 | 12677840 | Blood pressure fluctuation | |
| 126778401 | 12677840 | Condition aggravated | |
| 126778401 | 12677840 | Cough | |
| 126778401 | 12677840 | Depressed mood | |
| 126778401 | 12677840 | Dizziness | |
| 126778401 | 12677840 | Eructation | |
| 126778401 | 12677840 | Erythema | |
| 126778401 | 12677840 | Fall | |
| 126778401 | 12677840 | Gait disturbance | |
| 126778401 | 12677840 | General physical health deterioration | |
| 126778401 | 12677840 | Headache | |
| 126778401 | 12677840 | Intentional product misuse | |
| 126778401 | 12677840 | Muscular weakness | |
| 126778401 | 12677840 | Nausea | |
| 126778401 | 12677840 | Oedema peripheral | |
| 126778401 | 12677840 | Pain in extremity | |
| 126778401 | 12677840 | Palpitations | |
| 126778401 | 12677840 | Pollakiuria | |
| 126778401 | 12677840 | Polyneuropathy | |
| 126778401 | 12677840 | Reflux laryngitis | |
| 126778401 | 12677840 | Sensory loss | |
| 126778401 | 12677840 | Sleep disorder | |
| 126778401 | 12677840 | Vomiting |
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 |
|---|---|---|---|---|---|---|
| 126778401 | 12677840 | 1 | 201505 | 201602 | 0 | |
| 126778401 | 12677840 | 2 | 201602 | 0 | ||
| 126778401 | 12677840 | 3 | 201602 | 0 |