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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 103508962 | 10350896 | 2 | F | 201407 | 20160630 | 20140730 | 20160712 | PER | US-PFIZER INC-2014209723 | PFIZER | 58.00 | YR | F | Y | 48.98000 | KG | 20160712 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 103508962 | 10350896 | 1 | PS | LYRICA | PREGABALIN | 1 | Oral | 150 MG, 2X/DAY | 21446 | 150 | MG | CAPSULE, HARD | BID | ||||||
| 103508962 | 10350896 | 2 | SS | LYRICA | PREGABALIN | 1 | 75 MG, 2X/DAY | 21446 | 75 | MG | CAPSULE, HARD | BID | |||||||
| 103508962 | 10350896 | 3 | SS | LYRICA | PREGABALIN | 1 | 75 MG, 4X/DAY | 21446 | 75 | MG | CAPSULE, HARD | QID | |||||||
| 103508962 | 10350896 | 4 | C | SYNTHROID | LEVOTHYROXINE SODIUM | 1 | 88 MG, DAILY | 0 | 88 | MG | |||||||||
| 103508962 | 10350896 | 5 | C | CHANTIX | VARENICLINE TARTRATE | 1 | Oral | 1 MG, 1X/DAY | 0 | 1 | MG | TABLET | QD | ||||||
| 103508962 | 10350896 | 6 | C | BUSPIRONE HCL | BUSPIRONE HYDROCHLORIDE | 1 | Oral | 10 MG, 2X/DAY | 0 | 10 | MG | TABLET | BID | ||||||
| 103508962 | 10350896 | 7 | C | TRIPLE ANTIBIOTIC | BACITRACIN ZINCNEOMYCINNEOMYCIN SULFATEPOLYMYXIN B SULFATE | 1 | Topical | UNK, 1X/DAY | 0 | OINTMENT | QD | ||||||||
| 103508962 | 10350896 | 8 | C | LOVASTATIN. | LOVASTATIN | 1 | Oral | 20 MG, 1X/DAY (1 TABLET WITH A MEAL) | 0 | 20 | MG | TABLET | QD | ||||||
| 103508962 | 10350896 | 9 | C | OMEPRAZOLE. | OMEPRAZOLE | 1 | Oral | 40 MG, 1X/DAY (2 CAPSULE ORALLY) | 0 | 40 | MG | CAPSULE | QD | ||||||
| 103508962 | 10350896 | 10 | C | MUPIROCIN. | MUPIROCIN | 1 | Topical | 2 %, 3X/DAY (APPLICATION TO AFFECTED AREA ON LEFT LEG EXTERNALLY THREE TIMES A DAY) | 0 | 2 | PCT | OINTMENT | TID | ||||||
| 103508962 | 10350896 | 11 | C | CYCLOBENZAPRINE HCL | CYCLOBENZAPRINE HYDROCHLORIDE | 1 | Oral | 10 MG, AS NEEDED (1 TABLET ORALLY BID PRN) | 0 | 10 | MG | TABLET | |||||||
| 103508962 | 10350896 | 12 | C | BACTRIM DS | SULFAMETHOXAZOLETRIMETHOPRIM | 1 | Oral | 2 DF, 2X/DAY (SULFAMETHOXAZOLE:800 MG, TRIMETHOPRIM:160MG) | 0 | 2 | DF | TABLET | BID | ||||||
| 103508962 | 10350896 | 13 | C | GOODYS | ACETAMINOPHENASPIRINCAFFEINE | 1 | Oral | UNK (ACETYLSALICYLIC ACID: 260 MG, CAFFEINE: 16.25MG, PARACETAMOL: 130 MG) | 0 | TABLET | |||||||||
| 103508962 | 10350896 | 14 | C | RANITIDINE HCL | RANITIDINE HYDROCHLORIDE | 1 | Oral | 300 MG, 1X/DAY (1 CAPSULE AT BEDTIME) | 0 | 300 | MG | CAPSULE | QD | ||||||
| 103508962 | 10350896 | 15 | C | PRILOSEC | OMEPRAZOLE MAGNESIUM | 1 | Oral | 20 MG, 1X/DAY | 0 | 20 | MG | CAPSULE | QD | ||||||
| 103508962 | 10350896 | 16 | C | TRAMADOL HCL | TRAMADOL HYDROCHLORIDE | 1 | Oral | 50 MG, AS NEEDED (1 TABLET AS NEEDED ORALLY Q 12 HRS) | 0 | 50 | MG | TABLET | |||||||
| 103508962 | 10350896 | 17 | C | FERROUS SULFATE. | FERROUS SULFATE | 1 | Oral | 325 MG, 1X/DAY | 0 | 325 | MG | TABLET | QD | ||||||
| 103508962 | 10350896 | 18 | C | LEVOTHYROXINE SODIUM. | LEVOTHYROXINE SODIUM | 1 | Oral | 88 UG, 1X/DAY (1 TABLET EVERY MORNING ON AN EMPTY STOMACH ORALLY ONCE A DAY) | 0 | 88 | UG | TABLET | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 103508962 | 10350896 | 1 | Fibromyalgia |
| 103508962 | 10350896 | 4 | Thyroid disorder |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 103508962 | 10350896 | Depression | |
| 103508962 | 10350896 | Malaise | |
| 103508962 | 10350896 | Pain | |
| 103508962 | 10350896 | 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 |
|---|---|---|---|---|---|---|
| 103508962 | 10350896 | 2 | 2014 | 2014 | 0 | |
| 103508962 | 10350896 | 3 | 2014 | 201407 | 0 | |
| 103508962 | 10350896 | 10 | 20160627 | 0 | ||
| 103508962 | 10350896 | 12 | 20160627 | 0 |