Please choose an event type to view the corresponding MedsFacts report:

LOSS OF CONSCIOUSNESS ( 11 FDA reports)
BLOOD GLUCOSE INCREASED ( 9 FDA reports)
FALL ( 6 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 5 FDA reports)
HYPOGLYCAEMIA ( 5 FDA reports)
DYSPNOEA ( 4 FDA reports)
FEELING ABNORMAL ( 4 FDA reports)
VOMITING ( 4 FDA reports)
WEIGHT DECREASED ( 4 FDA reports)
ABDOMINAL PAIN UPPER ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
ASTHENIA ( 3 FDA reports)
BEDRIDDEN ( 3 FDA reports)
COMPLEX PARTIAL SEIZURES ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
HEPATIC NECROSIS ( 3 FDA reports)
MYOSITIS ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
PAIN ( 3 FDA reports)
PARAESTHESIA ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
PULMONARY OEDEMA ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
RENAL FAILURE ACUTE ( 3 FDA reports)
RESPIRATORY DISTRESS ( 3 FDA reports)
SPEECH DISORDER ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
ALCOHOL POISONING ( 2 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
BILIARY CIRRHOSIS ( 2 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 2 FDA reports)
BLOOD IRON INCREASED ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
CELLULITIS ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
EPILEPSY ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
GALLBLADDER DISORDER ( 2 FDA reports)
GANGRENE ( 2 FDA reports)
GLUCOSE URINE PRESENT ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HEPATITIS FULMINANT ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
INCISION SITE COMPLICATION ( 2 FDA reports)
INFECTION ( 2 FDA reports)
ISCHAEMIA ( 2 FDA reports)
JOINT SWELLING ( 2 FDA reports)
KETONURIA ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
MEDICATION RESIDUE ( 2 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
NEUTROPHILIA ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
PHARYNGEAL OEDEMA ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
PORTAL HYPERTENSION ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
RHONCHI ( 2 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 2 FDA reports)
SWELLING ( 2 FDA reports)
THINKING ABNORMAL ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
VASCULAR GRAFT ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
ABDOMINAL ADHESIONS ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE HEPATIC FAILURE ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANTI-ERYTHROCYTE ANTIBODY POSITIVE ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APLASIA PURE RED CELL ( 1 FDA reports)
APPARENT LIFE THREATENING EVENT ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BLADDER CYST ( 1 FDA reports)
BLADDER NEOPLASM ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CONVULSIVE THRESHOLD LOWERED ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
COUGH ( 1 FDA reports)
CRYING ( 1 FDA reports)
DEATH ( 1 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DEVICE FAILURE ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DISEASE COMPLICATION ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRUG INTERACTION POTENTIATION ( 1 FDA reports)
DRUG TOLERANCE ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
DYSTHYMIC DISORDER ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
ENTERITIS ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
EXOSTOSIS ( 1 FDA reports)
FAECALOMA ( 1 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPERAMMONAEMIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 1 FDA reports)
INADEQUATE ANALGESIA ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INCREASED TENDENCY TO BRUISE ( 1 FDA reports)
INGROWING NAIL ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
JOINT SPRAIN ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MITRAL VALVE DISEASE ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MULTIPLE ALLERGIES ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NEOPLASM RECURRENCE ( 1 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 1 FDA reports)
NEUROMA ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 1 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OVARIAN CYST ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PHOTOSENSITIVITY ALLERGIC REACTION ( 1 FDA reports)
PLANTAR FASCIITIS ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
POST PROCEDURAL OEDEMA ( 1 FDA reports)
POSTOPERATIVE ADHESION ( 1 FDA reports)
PROTEIN C DECREASED ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PSYCHIATRIC EVALUATION ABNORMAL ( 1 FDA reports)
PSYCHOMOTOR RETARDATION ( 1 FDA reports)
RASH ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
RHINITIS ALLERGIC ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN TIGHTNESS ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
TARSAL TUNNEL SYNDROME ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
TINEA PEDIS ( 1 FDA reports)
TOE AMPUTATION ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TRICUSPID VALVE DISEASE ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URINE OUTPUT INCREASED ( 1 FDA reports)
UROSEPSIS ( 1 FDA reports)
VEIN DISORDER ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VERTIGO ( 1 FDA reports)

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