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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 107310544 | 10731054 | 4 | F | 20151007 | 20160830 | 20150122 | 20160906 | EXP | US-PFIZER INC-2015027747 | PFIZER | 40.00 | YR | F | Y | 0.00000 | 20160906 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 107310544 | 10731054 | 1 | PS | LYRICA | PREGABALIN | 1 | Oral | 200 MG, 2X/DAY (ONE IN THE MORNING AND ONE AT 10PM AT NIGHT), (TAKE A CAPSULE BY MOUTH TWICE DAILY) | L49665 | 21446 | 200 | MG | CAPSULE, HARD | BID | |||||
| 107310544 | 10731054 | 2 | SS | LYRICA | PREGABALIN | 1 | 21446 | CAPSULE, HARD | |||||||||||
| 107310544 | 10731054 | 3 | SS | LYRICA | PREGABALIN | 1 | 21446 | CAPSULE, HARD | |||||||||||
| 107310544 | 10731054 | 4 | SS | EFFEXOR XR | VENLAFAXINE HYDROCHLORIDE | 1 | 75 MG AT 4:00 PM AND 150 MG AT BEDTIME | U | 20699 | 225 | MG | PROLONGED-RELEASE CAPSULE | |||||||
| 107310544 | 10731054 | 5 | SS | EFFEXOR XR | VENLAFAXINE HYDROCHLORIDE | 1 | U | 20699 | PROLONGED-RELEASE CAPSULE | ||||||||||
| 107310544 | 10731054 | 6 | SS | EFFEXOR | VENLAFAXINE HYDROCHLORIDE | 1 | 37.5 OR 75MG TWICE A DAY | U | 20699 | TABLET | BID | ||||||||
| 107310544 | 10731054 | 7 | SS | EFFEXOR | VENLAFAXINE HYDROCHLORIDE | 1 | U | 20699 | TABLET | ||||||||||
| 107310544 | 10731054 | 8 | C | CLINDAMYCIN PHOSPHATE. | CLINDAMYCIN PHOSPHATE | 1 | UNK | 0 | |||||||||||
| 107310544 | 10731054 | 9 | C | BACLOFEN. | BACLOFEN | 1 | 10 MG, 2X/DAY | 0 | 10 | MG | BID | ||||||||
| 107310544 | 10731054 | 10 | C | BACLOFEN. | BACLOFEN | 1 | 0 | ||||||||||||
| 107310544 | 10731054 | 11 | C | VIMPAT | LACOSAMIDE | 1 | 50 MG, 3X/DAY | 0 | 50 | MG | TID | ||||||||
| 107310544 | 10731054 | 12 | C | VITAMINS /00067501/ | VITAMINS | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 107310544 | 10731054 | 1 | Seizure |
| 107310544 | 10731054 | 2 | Partial seizures |
| 107310544 | 10731054 | 3 | Ear discomfort |
| 107310544 | 10731054 | 4 | Depressed mood |
| 107310544 | 10731054 | 5 | Crying |
| 107310544 | 10731054 | 6 | Nerve injury |
| 107310544 | 10731054 | 7 | Muscle disorder |
| 107310544 | 10731054 | 9 | Nerve injury |
| 107310544 | 10731054 | 10 | Muscle disorder |
| 107310544 | 10731054 | 11 | Seizure |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 107310544 | 10731054 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 107310544 | 10731054 | Fatigue | |
| 107310544 | 10731054 | Mouth injury | |
| 107310544 | 10731054 | Nausea | |
| 107310544 | 10731054 | Seizure | |
| 107310544 | 10731054 | Skin reaction | |
| 107310544 | 10731054 | Somnolence | |
| 107310544 | 10731054 | 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 |
|---|---|---|---|---|---|---|
| 107310544 | 10731054 | 1 | 2010 | 0 |