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

PYREXIA ( 47 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 35 FDA reports)
PLATELET COUNT DECREASED ( 31 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 28 FDA reports)
MALAISE ( 28 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 23 FDA reports)
ANOREXIA ( 18 FDA reports)
INJECTION SITE NECROSIS ( 14 FDA reports)
INJECTION SITE ULCER ( 14 FDA reports)
CONVULSION ( 13 FDA reports)
LOSS OF CONSCIOUSNESS ( 13 FDA reports)
BACTERIAL INFECTION ( 11 FDA reports)
DIABETES MELLITUS ( 11 FDA reports)
INSOMNIA ( 11 FDA reports)
NEUTROPHIL COUNT DECREASED ( 10 FDA reports)
PERITONSILLITIS ( 10 FDA reports)
DECREASED APPETITE ( 9 FDA reports)
DEPRESSED MOOD ( 9 FDA reports)
ERYTHEMA ( 9 FDA reports)
WEIGHT DECREASED ( 9 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 8 FDA reports)
CEREBRAL HAEMORRHAGE ( 8 FDA reports)
COMPLETED SUICIDE ( 8 FDA reports)
PROSTATE CANCER ( 8 FDA reports)
AMMONIA INCREASED ( 7 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 7 FDA reports)
INJECTION SITE ERYTHEMA ( 7 FDA reports)
CONDITION AGGRAVATED ( 6 FDA reports)
DEAFNESS ( 6 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 6 FDA reports)
INTERSTITIAL LUNG DISEASE ( 6 FDA reports)
NAUSEA ( 6 FDA reports)
RASH ( 6 FDA reports)
RHABDOMYOLYSIS ( 6 FDA reports)
SEPSIS ( 6 FDA reports)
DEPRESSION ( 5 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 5 FDA reports)
INJECTION SITE PAIN ( 5 FDA reports)
MENTAL DISORDER ( 5 FDA reports)
OEDEMA PERIPHERAL ( 5 FDA reports)
PAIN IN EXTREMITY ( 5 FDA reports)
PANCYTOPENIA ( 5 FDA reports)
PNEUMONIA ( 5 FDA reports)
SKIN NECROSIS ( 5 FDA reports)
SKIN ULCER ( 5 FDA reports)
ANXIETY ( 4 FDA reports)
ARTHRALGIA ( 4 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 4 FDA reports)
DIZZINESS ( 4 FDA reports)
EATING DISORDER ( 4 FDA reports)
ENCEPHALOPATHY ( 4 FDA reports)
FACE OEDEMA ( 4 FDA reports)
FALL ( 4 FDA reports)
HEPATITIS FULMINANT ( 4 FDA reports)
INJECTION SITE PRURITUS ( 4 FDA reports)
NASOPHARYNGITIS ( 4 FDA reports)
RESPIRATORY FAILURE ( 4 FDA reports)
RHEUMATOID ARTHRITIS ( 4 FDA reports)
SPEECH DISORDER ( 4 FDA reports)
VOMITING ( 4 FDA reports)
ASCITES ( 3 FDA reports)
AUTOIMMUNE HEPATITIS ( 3 FDA reports)
BACILLUS INFECTION ( 3 FDA reports)
BACK PAIN ( 3 FDA reports)
BLOOD GLUCOSE INCREASED ( 3 FDA reports)
BLOOD PRESSURE DECREASED ( 3 FDA reports)
CROHN'S DISEASE ( 3 FDA reports)
DELIRIUM ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 3 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 3 FDA reports)
ERYTHEMA NODOSUM ( 3 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 3 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 3 FDA reports)
GASTRITIS ( 3 FDA reports)
HALLUCINATION ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
INSULIN RESISTANT DIABETES ( 3 FDA reports)
LIVER DISORDER ( 3 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 3 FDA reports)
PAIN ( 3 FDA reports)
PANCREATITIS ACUTE ( 3 FDA reports)
PARKINSON'S DISEASE ( 3 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
PSORIASIS ( 3 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 3 FDA reports)
RENAL FAILURE ACUTE ( 3 FDA reports)
RENAL IMPAIRMENT ( 3 FDA reports)
RETINAL VEIN OCCLUSION ( 3 FDA reports)
VASCULAR OCCLUSION ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ABNORMAL BEHAVIOUR ( 2 FDA reports)
AFFECT LABILITY ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
BREAST CANCER MALE ( 2 FDA reports)
C-REACTIVE PROTEIN DECREASED ( 2 FDA reports)
CATHETER SITE RASH ( 2 FDA reports)
CEREBRAL INFARCTION ( 2 FDA reports)
COAGULOPATHY ( 2 FDA reports)
COLITIS ISCHAEMIC ( 2 FDA reports)
DEAFNESS NEUROSENSORY ( 2 FDA reports)
DEAFNESS UNILATERAL ( 2 FDA reports)
DELUSION ( 2 FDA reports)
DIABETIC KETOACIDOSIS ( 2 FDA reports)
DIABETIC RETINOPATHY ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
DRUG ERUPTION ( 2 FDA reports)
EMOTIONAL DISORDER ( 2 FDA reports)
EXCITABILITY ( 2 FDA reports)
EYE HAEMORRHAGE ( 2 FDA reports)
GENERALISED OEDEMA ( 2 FDA reports)
GINGIVAL BLEEDING ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HEMIPLEGIA ( 2 FDA reports)
HEPATIC NECROSIS ( 2 FDA reports)
HOARSENESS ( 2 FDA reports)
HYPERAMYLASAEMIA ( 2 FDA reports)
HYPERPHAGIA ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPOALBUMINAEMIA ( 2 FDA reports)
IMMUNODEFICIENCY ( 2 FDA reports)
INJECTION SITE DESQUAMATION ( 2 FDA reports)
INTESTINAL OBSTRUCTION ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
MENIERE'S DISEASE ( 2 FDA reports)
MENINGITIS ( 2 FDA reports)
METABOLIC ENCEPHALOPATHY ( 2 FDA reports)
MYASTHENIA GRAVIS ( 2 FDA reports)
MYDRIASIS ( 2 FDA reports)
ORAL INTAKE REDUCED ( 2 FDA reports)
PERSECUTORY DELUSION ( 2 FDA reports)
PNEUMONIA BACTERIAL ( 2 FDA reports)
PROTEINURIA ( 2 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
RETINAL HAEMORRHAGE ( 2 FDA reports)
SCAR ( 2 FDA reports)
SCLERODERMA ( 2 FDA reports)
SKIN WARM ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
STRESS INCONTINENCE ( 2 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 2 FDA reports)
SUICIDAL IDEATION ( 2 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 2 FDA reports)
THALAMUS HAEMORRHAGE ( 2 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
THYROIDITIS CHRONIC ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
ANTI-GAD ANTIBODY POSITIVE ( 1 FDA reports)
ANTIBODY TEST ABNORMAL ( 1 FDA reports)
ANURIA ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
AUTOIMMUNE DISORDER ( 1 FDA reports)
AUTOPHONY ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 1 FDA reports)
BRAIN STEM HAEMORRHAGE ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CATHETER SITE INFECTION ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
DEPILATION ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIET REFUSAL ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DIVERTICULUM INTESTINAL ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 1 FDA reports)
ENTEROBACTER INFECTION ( 1 FDA reports)
ENTEROBACTER PNEUMONIA ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
FAMILY STRESS ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HYALURONIC ACID INCREASED ( 1 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
IMPLANT SITE INFECTION ( 1 FDA reports)
INDURATION ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INJECTION SITE INFLAMMATION ( 1 FDA reports)
INJECTION SITE SCAR ( 1 FDA reports)
INJECTION SITE WARMTH ( 1 FDA reports)
INJURY ASPHYXIATION ( 1 FDA reports)
INTESTINAL ISCHAEMIA ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
KETONURIA ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LIP EROSION ( 1 FDA reports)
LOGORRHOEA ( 1 FDA reports)
MACULAR OEDEMA ( 1 FDA reports)
MANIA ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENOMETRORRHAGIA ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST POSITIVE ( 1 FDA reports)
MOYAMOYA DISEASE ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NASOPHARYNGEAL DISORDER ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NEUROSIS ( 1 FDA reports)
NYSTAGMUS ( 1 FDA reports)
OPTIC DISC HAEMORRHAGE ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
PLATELET COUNT ABNORMAL ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 1 FDA reports)
PSYCHIATRIC SYMPTOM ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY MASS ( 1 FDA reports)
PULMONARY MYCOSIS ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RECTAL CANCER ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RETINAL VASCULAR DISORDER ( 1 FDA reports)
RETINAL VEIN THROMBOSIS ( 1 FDA reports)
RETINOPATHY ( 1 FDA reports)
SCREAMING ( 1 FDA reports)
SICK SINUS SYNDROME ( 1 FDA reports)
SKIN HYPERTROPHY ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
SUDDEN HEARING LOSS ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SYSTEMIC SCLEROSIS ( 1 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TONIC CONVULSION ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TREMOR ( 1 FDA reports)
URINE AMYLASE INCREASED ( 1 FDA reports)
URINE KETONE BODY PRESENT ( 1 FDA reports)
VENTRICULAR ARRHYTHMIA ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VIRAEMIA ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VIRAL TEST POSITIVE ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use