Person who experienced the adverse event (patient)
| Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 8248632 | 8485916 | I | 8248632-7 | 20120319 | 20120331 | EXP | US-MYLANLABS-2012S1006434 | MYLAN PHARMACEUTICALS INC. | YR | F | Y | 94.35 | KG | 20120330 | CN | UNITED STATES |
Drug(s) used by person
| Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 8248632 | 1019282232 | C | AMIODARONE HCL | 1 | X 2 DAYS (DATES UNKNOWN) | ||||||
| 8248632 | 1019282233 | C | ASPIRIN | 1 | ORAL | ||||||
| 8248632 | 1019282238 | C | DILAUDID | 1 | |||||||
| 8248632 | 1019282240 | C | MULTI-VITAMIN | 1 | |||||||
| 8248632 | 1019282241 | C | FOLIC ACID | 1 | |||||||
| 8248632 | 1019282254 | C | SIMVASTATIN | 1 | ORAL | ||||||
| 8248632 | 1019282230 | C | ALDACTONE | 1 | ORAL | ||||||
| 8248632 | 1019282235 | C | CARDIZEM CD | 1 | ORAL | ||||||
| 8248632 | 1019282236 | C | COREG | 1 | ORAL | ||||||
| 8248632 | 1019282243 | C | GLUCOPHAGE | 1 | ORAL | ||||||
| 8248632 | 1019282239 | C | FERROUS SULFATE TAB | 1 | |||||||
| 8248632 | 1019282244 | C | GLYBURIDE | 1 | ORAL | ||||||
| 8248632 | 1019282257 | C | VIOXX | 1 | ORAL | ||||||
| 8248632 | 1019282250 | C | LASIX | 1 | ORAL | ||||||
| 8248632 | 1019282253 | C | PROCAINAMIDE | 1 | ORAL | 250MG TABLET | |||||
| 8248632 | 1019282259 | C | ZOCOR | 1 | ORAL | ||||||
| 8248632 | 1019282260 | C | ZYRTEC | 1 | ORAL | ||||||
| 8248632 | 1019282234 | C | AVANDIA | 1 | ORAL | ||||||
| 8248632 | 1019282246 | C | IRON SULFATETHIAMIN COMPOUND TAB | 1 | ORAL | ||||||
| 8248632 | 1019282247 | C | POTASSIUM CHLORIDE | 1 | ORAL | ||||||
| 8248632 | 1019282242 | C | FOLIC ACID | 1 | ORAL | ||||||
| 8248632 | 1019282251 | C | MAG-OX | 2 | ORAL | ||||||
| 8248632 | 1019282252 | C | PREVACID | 1 | ORAL | ||||||
| 8248632 | 1019282255 | C | SPIRONOLACTONE | 1 | |||||||
| 8248632 | 1019282229 | PS | DIGOXIN | 1 | ORAL | 040282 | |||||
| 8248632 | 1019282237 | C | COUMADIN | 1 | |||||||
| 8248632 | 1019282245 | C | IMDUR | 1 | ORAL | ||||||
| 8248632 | 1019282248 | C | KLOR-CON | 1 | ORAL | ||||||
| 8248632 | 1019282256 | C | VANCOMYCIN | 1 | |||||||
| 8248632 | 1019282258 | C | ASCORBIC ACID | 1 | ORAL | ||||||
| 8248632 | 1019282231 | C | ALLOPURINOL | 1 | |||||||
| 8248632 | 1019282249 | C | LANTUS | 1 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 8248632 | HO |
| 8248632 | DS |
| 8248632 | LT |
| 8248632 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 8248632 | WOUND INFECTION |
| 8248632 | GENERAL PHYSICAL HEALTH DETERIORATION |
| 8248632 | UNRESPONSIVE TO STIMULI |
| 8248632 | SINUS BRADYCARDIA |
| 8248632 | ADVERSE DRUG REACTION |
| 8248632 | LIVER FUNCTION TEST ABNORMAL |
| 8248632 | BREAST HAEMATOMA |
| 8248632 | ABDOMINAL DISTENSION |
| 8248632 | GOUT |
| 8248632 | BUNDLE BRANCH BLOCK |
| 8248632 | ENDOTRACHEAL INTUBATION |
| 8248632 | CORONARY ARTERY DISEASE |
| 8248632 | TOXICITY TO VARIOUS AGENTS |
| 8248632 | UTERINE CANCER |
| 8248632 | EPISTAXIS |
| 8248632 | FALL |
| 8248632 | CONFUSIONAL STATE |
| 8248632 | CEREBRAL HYPOPERFUSION |
| 8248632 | CARDIAC VALVE DISEASE |
| 8248632 | RENAL FAILURE ACUTE |
| 8248632 | HEMIANOPIA HOMONYMOUS |
| 8248632 | FATIGUE |
| 8248632 | FLATULENCE |
| 8248632 | NAUSEA |
| 8248632 | HYPERHIDROSIS |
| 8248632 | SWELLING |
| 8248632 | HYPOTENSION |
| 8248632 | PULMONARY HYPERTENSION |
| 8248632 | ECCHYMOSIS |
| 8248632 | ATRIAL FIBRILLATION |
| 8248632 | SLEEP APNOEA SYNDROME |
| 8248632 | HYPOKINESIA |
| 8248632 | CARDIAC FAILURE CONGESTIVE |
| 8248632 | TACHYCARDIA |
| 8248632 | SHOCK |
| 8248632 | PULMONARY OEDEMA |
| 8248632 | VISUAL IMPAIRMENT |
| 8248632 | VENOUS INSUFFICIENCY |
| 8248632 | CELLULITIS |
| 8248632 | RENAL FAILURE CHRONIC |
| 8248632 | DEHYDRATION |
| 8248632 | LETHARGY |
| 8248632 | URINE ANALYSIS ABNORMAL |
| 8248632 | MYOCARDIAL ISCHAEMIA |
| 8248632 | VENTRICULAR EXTRASYSTOLES |
| 8248632 | WALKING DISABILITY |
| 8248632 | ARRHYTHMIA |
| 8248632 | DIABETES MELLITUS |
| 8248632 | BLOODY DISCHARGE |
| 8248632 | ORTHOSTATIC HYPOTENSION |
| 8248632 | ENCEPHALOPATHY |
| 8248632 | SEPSIS |
| 8248632 | ANAEMIA |
| 8248632 | ANEURYSM |
| 8248632 | PROTEIN TOTAL INCREASED |
| 8248632 | DRUG ADMINISTRATION ERROR |
| 8248632 | DEPRESSED LEVEL OF CONSCIOUSNESS |
| 8248632 | LABORATORY TEST ABNORMAL |
| 8248632 | CEREBROVASCULAR ACCIDENT |
| 8248632 | MECHANICAL VENTILATION |
| 8248632 | CONSTIPATION |
| 8248632 | ASTHENIA |
| 8248632 | PALPITATIONS |
| 8248632 | CORONARY ARTERY INSUFFICIENCY |
| 8248632 | TREMOR |
| 8248632 | ELECTROCARDIOGRAM ABNORMAL |
| 8248632 | ECHOCARDIOGRAM ABNORMAL |
| 8248632 | VENTRICULAR HYPERTROPHY |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 8248632 | 1019282229 | 20011115 | 20080523 |