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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 101602503 | 10160250 | 3 | F | 1999 | 20160718 | 20140508 | 20160801 | EXP | US-PFIZER INC-2013194152 | PFIZER | 57.00 | YR | M | Y | 84.00000 | KG | 20160801 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 101602503 | 10160250 | 1 | PS | TENORMIN | ATENOLOL | 1 | Oral | 50 DAILY IN THE AM AND 25 MG IN THE EVENING AS NEEDED | 73676 | TABLET | |||||||||
| 101602503 | 10160250 | 2 | SS | AMOXICILLIN. | AMOXICILLIN | 1 | Unknown | 3 COURSES OF 500 MG THREE TIMES A DAY | U | 0 | |||||||||
| 101602503 | 10160250 | 3 | SS | AMOXICILLIN. | AMOXICILLIN | 1 | Unknown | 2000 MG, AS NEEDED | U | 0 | 2000 | MG | |||||||
| 101602503 | 10160250 | 4 | SS | ZITHROMAX | AZITHROMYCIN DIHYDRATE | 1 | Unknown | UNK,NON AZ PRODUCT | U | 50670 | |||||||||
| 101602503 | 10160250 | 5 | SS | BRILINTA | TICAGRELOR | 1 | Oral | 90 MG, 2X/DAY | 0 | 90 | MG | TABLET | BID | ||||||
| 101602503 | 10160250 | 6 | SS | BIAXIN | CLARITHROMYCIN | 1 | Unknown | 500 MG, 2X/DAY | Y | 0 | 500 | MG | BID | ||||||
| 101602503 | 10160250 | 7 | SS | LEVAQUIN | LEVOFLOXACIN | 1 | Unknown | UNK | U | 0 | |||||||||
| 101602503 | 10160250 | 8 | C | ASPIRIN. | ASPIRIN | 1 | Unknown | 325 MG, 1X/DAY | 0 | 325 | MG | QD | |||||||
| 101602503 | 10160250 | 9 | C | VIAGRA | SILDENAFIL CITRATE | 1 | Unknown | 25 MG, AS NEEDED | 0 | 25 | MG | ||||||||
| 101602503 | 10160250 | 10 | C | NASOCORT | BUDESONIDE | 1 | Unknown | 1 -2 SPRAYS,AS NEEDED | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 101602503 | 10160250 | 1 | Arrhythmia |
| 101602503 | 10160250 | 2 | Antibiotic prophylaxis |
| 101602503 | 10160250 | 4 | Bronchitis |
| 101602503 | 10160250 | 5 | Acute coronary syndrome |
| 101602503 | 10160250 | 6 | Bronchitis |
| 101602503 | 10160250 | 7 | Bronchitis |
| 101602503 | 10160250 | 8 | Prophylaxis |
| 101602503 | 10160250 | 10 | Multiple allergies |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 101602503 | 10160250 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 101602503 | 10160250 | Abdominal discomfort | |
| 101602503 | 10160250 | Arrhythmia | |
| 101602503 | 10160250 | Blood pressure fluctuation | |
| 101602503 | 10160250 | Body height decreased | |
| 101602503 | 10160250 | Bronchitis | |
| 101602503 | 10160250 | Dyspnoea | |
| 101602503 | 10160250 | Escherichia infection | |
| 101602503 | 10160250 | Flatulence | |
| 101602503 | 10160250 | Intentional product misuse | |
| 101602503 | 10160250 | Lower respiratory tract infection | |
| 101602503 | 10160250 | Myocardial infarction | |
| 101602503 | 10160250 | Pyrexia | |
| 101602503 | 10160250 | Seasonal allergy |
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 |
|---|---|---|---|---|---|---|
| 101602503 | 10160250 | 5 | 2016 | 0 | ||
| 101602503 | 10160250 | 6 | 20130225 | 0 |