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

PYREXIA ( 64 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 43 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 34 FDA reports)
DIARRHOEA ( 30 FDA reports)
PLATELET COUNT DECREASED ( 30 FDA reports)
RHABDOMYOLYSIS ( 30 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 29 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 28 FDA reports)
PRURITUS ( 27 FDA reports)
ERYTHEMA ( 26 FDA reports)
INTERSTITIAL LUNG DISEASE ( 26 FDA reports)
MALAISE ( 25 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 24 FDA reports)
NAUSEA ( 23 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 22 FDA reports)
DYSPNOEA ( 22 FDA reports)
CHILLS ( 21 FDA reports)
DECREASED APPETITE ( 21 FDA reports)
DERMATITIS EXFOLIATIVE ( 21 FDA reports)
PLEURAL EFFUSION ( 21 FDA reports)
VOMITING ( 21 FDA reports)
BACK PAIN ( 19 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 19 FDA reports)
INFLAMMATION ( 19 FDA reports)
RENAL IMPAIRMENT ( 19 FDA reports)
RASH ( 18 FDA reports)
BLOOD GLUCOSE INCREASED ( 17 FDA reports)
LIVER DISORDER ( 17 FDA reports)
PAIN ( 17 FDA reports)
PNEUMONIA ( 17 FDA reports)
ASTHMA ( 16 FDA reports)
LOSS OF CONSCIOUSNESS ( 15 FDA reports)
NASOPHARYNGITIS ( 15 FDA reports)
RENAL FAILURE ACUTE ( 15 FDA reports)
SEPSIS ( 15 FDA reports)
ANAEMIA ( 14 FDA reports)
HEADACHE ( 14 FDA reports)
INFUSION RELATED REACTION ( 14 FDA reports)
RESTLESSNESS ( 14 FDA reports)
STOMATITIS ( 14 FDA reports)
ATRIAL FIBRILLATION ( 13 FDA reports)
BLOOD CREATININE INCREASED ( 13 FDA reports)
CHEST PAIN ( 13 FDA reports)
EOSINOPHIL COUNT INCREASED ( 13 FDA reports)
HALLUCINATION ( 13 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 13 FDA reports)
SEPTIC SHOCK ( 13 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 12 FDA reports)
ASTHENIA ( 12 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 12 FDA reports)
CARDIOMEGALY ( 12 FDA reports)
CONDITION AGGRAVATED ( 12 FDA reports)
FACE OEDEMA ( 12 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 12 FDA reports)
HERPES ZOSTER ( 12 FDA reports)
HYPERTENSION ( 12 FDA reports)
HYPONATRAEMIA ( 12 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 12 FDA reports)
MYALGIA ( 12 FDA reports)
RESPIRATORY FAILURE ( 12 FDA reports)
VENTRICULAR FIBRILLATION ( 12 FDA reports)
ABDOMINAL PAIN ( 11 FDA reports)
CARDIAC FUNCTION TEST ABNORMAL ( 11 FDA reports)
CARDIOMYOPATHY ( 11 FDA reports)
CATHETERISATION CARDIAC ( 11 FDA reports)
CHOLANGITIS ( 11 FDA reports)
DELIRIUM ( 11 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 11 FDA reports)
NEUTROPHIL COUNT DECREASED ( 11 FDA reports)
OROPHARYNGEAL PAIN ( 11 FDA reports)
PERICARDIAL EFFUSION ( 11 FDA reports)
RESPIRATORY DISORDER ( 11 FDA reports)
ABNORMAL BEHAVIOUR ( 10 FDA reports)
ANOREXIA ( 10 FDA reports)
BLOOD PRESSURE INCREASED ( 10 FDA reports)
PANCYTOPENIA ( 10 FDA reports)
SUBILEUS ( 10 FDA reports)
URTICARIA ( 10 FDA reports)
BLOOD BILIRUBIN INCREASED ( 9 FDA reports)
CARDIAC FAILURE ( 9 FDA reports)
DIZZINESS ( 9 FDA reports)
EOSINOPHILIA ( 9 FDA reports)
GASTRIC ULCER ( 9 FDA reports)
PALPITATIONS ( 9 FDA reports)
RASH PUSTULAR ( 9 FDA reports)
RENAL FAILURE ( 9 FDA reports)
THROMBOCYTOPENIA ( 9 FDA reports)
TOXIC SKIN ERUPTION ( 9 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 9 FDA reports)
ABDOMINAL SYMPTOM ( 8 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 8 FDA reports)
BILOMA ( 8 FDA reports)
BLOOD UREA INCREASED ( 8 FDA reports)
CHEILITIS ( 8 FDA reports)
CONVULSION ( 8 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 8 FDA reports)
DRUG ERUPTION ( 8 FDA reports)
ECZEMA ( 8 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 8 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 8 FDA reports)
ENTEROCOLITIS ( 8 FDA reports)
GAIT DISTURBANCE ( 8 FDA reports)
GENERALISED ERYTHEMA ( 8 FDA reports)
HAEMOGLOBIN DECREASED ( 8 FDA reports)
HYPOGLYCAEMIA ( 8 FDA reports)
HYPOXIA ( 8 FDA reports)
INFLUENZA ( 8 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 8 FDA reports)
PUSTULAR PSORIASIS ( 8 FDA reports)
RESPIRATORY DISTRESS ( 8 FDA reports)
SKIN EXFOLIATION ( 8 FDA reports)
SPEECH DISORDER ( 8 FDA reports)
STEVENS-JOHNSON SYNDROME ( 8 FDA reports)
SUBCORNEAL PUSTULAR DERMATOSIS ( 8 FDA reports)
BILIARY ANASTOMOSIS ( 7 FDA reports)
CARDIO-RESPIRATORY ARREST ( 7 FDA reports)
CHEST DISCOMFORT ( 7 FDA reports)
CONSTIPATION ( 7 FDA reports)
DEATH ( 7 FDA reports)
DYSARTHRIA ( 7 FDA reports)
ENTEROCOLITIS BACTERIAL ( 7 FDA reports)
EPILEPSY ( 7 FDA reports)
ERYTHEMA MULTIFORME ( 7 FDA reports)
ESCHERICHIA INFECTION ( 7 FDA reports)
FACIAL PALSY ( 7 FDA reports)
FALL ( 7 FDA reports)
FEELING ABNORMAL ( 7 FDA reports)
HAEMATOCRIT DECREASED ( 7 FDA reports)
HEPATIC FAILURE ( 7 FDA reports)
INTESTINAL DILATATION ( 7 FDA reports)
METABOLIC ACIDOSIS ( 7 FDA reports)
PEMPHIGOID ( 7 FDA reports)
POLYMYOSITIS ( 7 FDA reports)
TACHYPNOEA ( 7 FDA reports)
ANGINA PECTORIS ( 6 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 6 FDA reports)
BLOOD CREATININE DECREASED ( 6 FDA reports)
BLOOD LACTATE DEHYDROGENASE DECREASED ( 6 FDA reports)
BLOOD PRESSURE DECREASED ( 6 FDA reports)
BRONCHIAL WALL THICKENING ( 6 FDA reports)
CARDIAC DISORDER ( 6 FDA reports)
CERVIX CARCINOMA STAGE 0 ( 6 FDA reports)
DERMATITIS ACNEIFORM ( 6 FDA reports)
DEVICE RELATED INFECTION ( 6 FDA reports)
DYSPHAGIA ( 6 FDA reports)
DYSSTASIA ( 6 FDA reports)
ENDOTRACHEAL INTUBATION ( 6 FDA reports)
FEELING HOT ( 6 FDA reports)
HAEMATURIA ( 6 FDA reports)
HILAR LYMPHADENOPATHY ( 6 FDA reports)
HYPOALBUMINAEMIA ( 6 FDA reports)
ILEUS ( 6 FDA reports)
LUNG INFILTRATION ( 6 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 6 FDA reports)
MECHANICAL VENTILATION ( 6 FDA reports)
MUSCULOSKELETAL PAIN ( 6 FDA reports)
NECK PAIN ( 6 FDA reports)
NEUTROPHIL COUNT INCREASED ( 6 FDA reports)
NON-CARDIAC CHEST PAIN ( 6 FDA reports)
OEDEMA PERIPHERAL ( 6 FDA reports)
OXYGEN SATURATION DECREASED ( 6 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 6 FDA reports)
SJOGREN'S SYNDROME ( 6 FDA reports)
SKIN IRRITATION ( 6 FDA reports)
SPUTUM RETENTION ( 6 FDA reports)
SYNCOPE ( 6 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 6 FDA reports)
TRACHEOSTOMY ( 6 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 6 FDA reports)
URINE OUTPUT DECREASED ( 6 FDA reports)
ABDOMINAL TENDERNESS ( 5 FDA reports)
ASCITES ( 5 FDA reports)
BLISTER ( 5 FDA reports)
BLOOD AMYLASE INCREASED ( 5 FDA reports)
BLOOD POTASSIUM DECREASED ( 5 FDA reports)
CARDIAC OUTPUT DECREASED ( 5 FDA reports)
CARDIOVASCULAR DISORDER ( 5 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 5 FDA reports)
DRUG INTERACTION ( 5 FDA reports)
DYSKINESIA ( 5 FDA reports)
DYSLALIA ( 5 FDA reports)
ENCEPHALITIS ( 5 FDA reports)
GASTROINTESTINAL NECROSIS ( 5 FDA reports)
GENERALISED OEDEMA ( 5 FDA reports)
GRANULOCYTE COUNT DECREASED ( 5 FDA reports)
HAEMOPHILUS INFECTION ( 5 FDA reports)
HYPERHIDROSIS ( 5 FDA reports)
HYPERKALAEMIA ( 5 FDA reports)
HYPOCALCAEMIA ( 5 FDA reports)
HYPOMAGNESAEMIA ( 5 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 5 FDA reports)
INTERVERTEBRAL DISCITIS ( 5 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 5 FDA reports)
LIVER ABSCESS ( 5 FDA reports)
MUSCULAR WEAKNESS ( 5 FDA reports)
OEDEMA ( 5 FDA reports)
OVERDOSE ( 5 FDA reports)
PANCREATIC ENZYMES INCREASED ( 5 FDA reports)
PHOTOSENSITIVITY REACTION ( 5 FDA reports)
PULSE ABSENT ( 5 FDA reports)
RASH GENERALISED ( 5 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 5 FDA reports)
RENAL DISORDER ( 5 FDA reports)
RESPIRATORY ARREST ( 5 FDA reports)
SOMNOLENCE ( 5 FDA reports)
SPONDYLITIS ( 5 FDA reports)
STAPHYLOCOCCAL INFECTION ( 5 FDA reports)
TREMOR ( 5 FDA reports)
URINARY TRACT INFECTION ( 5 FDA reports)
ABORTION SPONTANEOUS ( 4 FDA reports)
ANAPHYLACTIC SHOCK ( 4 FDA reports)
ARRHYTHMIA ( 4 FDA reports)
BLOOD POTASSIUM INCREASED ( 4 FDA reports)
BRUGADA SYNDROME ( 4 FDA reports)
CARDIAC FAILURE ACUTE ( 4 FDA reports)
COGNITIVE DISORDER ( 4 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 4 FDA reports)
COUGH ( 4 FDA reports)
DERMATITIS ( 4 FDA reports)
DIABETES MELLITUS ( 4 FDA reports)
DISEASE PROGRESSION ( 4 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 4 FDA reports)
DYSPNOEA EXERTIONAL ( 4 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 4 FDA reports)
ENANTHEMA ( 4 FDA reports)
EYE DISCHARGE ( 4 FDA reports)
FEBRILE NEUTROPENIA ( 4 FDA reports)
FLUID INTAKE REDUCED ( 4 FDA reports)
FOOD POISONING ( 4 FDA reports)
GINGIVAL BLEEDING ( 4 FDA reports)
GLOMERULONEPHRITIS PROLIFERATIVE ( 4 FDA reports)
HALLUCINATION, AUDITORY ( 4 FDA reports)
HALLUCINATION, VISUAL ( 4 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 4 FDA reports)
HYPOAESTHESIA ( 4 FDA reports)
HYPOKALAEMIA ( 4 FDA reports)
LACUNAR INFARCTION ( 4 FDA reports)
LIMB DISCOMFORT ( 4 FDA reports)
LUNG DISORDER ( 4 FDA reports)
LYMPHADENOPATHY ( 4 FDA reports)
MALNUTRITION ( 4 FDA reports)
MUSCLE SPASMS ( 4 FDA reports)
NON-SMALL CELL LUNG CANCER ( 4 FDA reports)
OLIGURIA ( 4 FDA reports)
PANCREATITIS ACUTE ( 4 FDA reports)
PNEUMONITIS ( 4 FDA reports)
PORIOMANIA ( 4 FDA reports)
PROTEIN URINE PRESENT ( 4 FDA reports)
REFLUX OESOPHAGITIS ( 4 FDA reports)
SKIN LESION ( 4 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 4 FDA reports)
SWELLING ( 4 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 4 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 4 FDA reports)
ABDOMINAL PAIN UPPER ( 3 FDA reports)
ABORTION ( 3 FDA reports)
APLASTIC ANAEMIA ( 3 FDA reports)
ARTERIOSCLEROSIS ( 3 FDA reports)
ASPIRATION ( 3 FDA reports)
BLOOD BILIRUBIN DECREASED ( 3 FDA reports)
BLOOD SODIUM DECREASED ( 3 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 3 FDA reports)
BREAST CANCER RECURRENT ( 3 FDA reports)
CELLULITIS ( 3 FDA reports)
COLORECTAL CANCER ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
DEMENTIA ( 3 FDA reports)
DERMATITIS ATOPIC ( 3 FDA reports)
DIALYSIS ( 3 FDA reports)
DRUG HYPERSENSITIVITY ( 3 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 3 FDA reports)
EPIDERMOLYSIS ( 3 FDA reports)
FEEDING TUBE COMPLICATION ( 3 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 3 FDA reports)
HAEMATEMESIS ( 3 FDA reports)
HAEMOPTYSIS ( 3 FDA reports)
HEPATITIS ( 3 FDA reports)
HEPATOCELLULAR INJURY ( 3 FDA reports)
HUMERUS FRACTURE ( 3 FDA reports)
HYPERSENSITIVITY ( 3 FDA reports)
HYPOAESTHESIA ORAL ( 3 FDA reports)
HYPOGLYCAEMIC COMA ( 3 FDA reports)
HYPOREFLEXIA ( 3 FDA reports)
INFECTION ( 3 FDA reports)
INGUINAL HERNIA ( 3 FDA reports)
JAUNDICE ( 3 FDA reports)
LIPASE INCREASED ( 3 FDA reports)
LUPUS NEPHRITIS ( 3 FDA reports)
LUPUS-LIKE SYNDROME ( 3 FDA reports)
MULTI-ORGAN FAILURE ( 3 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 3 FDA reports)
MUSCLE ATROPHY ( 3 FDA reports)
NEOPLASM ( 3 FDA reports)
NEUROSIS ( 3 FDA reports)
NEUTROPENIC INFECTION ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 3 FDA reports)
PNEUMONIA ASPIRATION ( 3 FDA reports)
PROTEUS INFECTION ( 3 FDA reports)
PSEUDOMONAS INFECTION ( 3 FDA reports)
PSOAS ABSCESS ( 3 FDA reports)
PSYCHIATRIC SYMPTOM ( 3 FDA reports)
PULMONARY HAEMORRHAGE ( 3 FDA reports)
PULMONARY MASS ( 3 FDA reports)
RETINAL HAEMORRHAGE ( 3 FDA reports)
RETINAL VEIN OCCLUSION ( 3 FDA reports)
RETROPERITONEAL ABSCESS ( 3 FDA reports)
RHINORRHOEA ( 3 FDA reports)
SENSORY DISTURBANCE ( 3 FDA reports)
SERUM FERRITIN INCREASED ( 3 FDA reports)
SHOCK ( 3 FDA reports)
SUDDEN DEATH ( 3 FDA reports)
TACHYCARDIA ( 3 FDA reports)
THYROIDITIS ( 3 FDA reports)
TOOTH DISCOLOURATION ( 3 FDA reports)
TOOTH HYPOPLASIA ( 3 FDA reports)
URINARY INCONTINENCE ( 3 FDA reports)
VENTRICULAR TACHYCARDIA ( 3 FDA reports)
VISUAL ACUITY REDUCED ( 3 FDA reports)
WEIGHT DECREASED ( 3 FDA reports)
ABASIA ( 2 FDA reports)
ACID FAST BACILLI INFECTION ( 2 FDA reports)
ACIDOSIS ( 2 FDA reports)
ACUTE CORONARY SYNDROME ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
AGRANULOCYTOSIS ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
ANAPHYLACTOID REACTION ( 2 FDA reports)
ANGIOEDEMA ( 2 FDA reports)
ANGIOSARCOMA ( 2 FDA reports)
ANTI-INSULIN ANTIBODY ( 2 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 2 FDA reports)
ARTHRITIS ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK ( 2 FDA reports)
BACTERIAL INFECTION ( 2 FDA reports)
BASEDOW'S DISEASE ( 2 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 2 FDA reports)
BLOOD PH DECREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 2 FDA reports)
BONE MARROW FAILURE ( 2 FDA reports)
BRAIN STEM HAEMORRHAGE ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
BRONCHOSTENOSIS ( 2 FDA reports)
CANCER PAIN ( 2 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 2 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 2 FDA reports)
CEREBELLAR ATAXIA ( 2 FDA reports)
CEREBROVASCULAR DISORDER ( 2 FDA reports)
CHEST X-RAY ABNORMAL ( 2 FDA reports)
CHOLANGITIS ACUTE ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 2 FDA reports)
CONVERSION DISORDER ( 2 FDA reports)
CYSTITIS HAEMORRHAGIC ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DERMATITIS BULLOUS ( 2 FDA reports)
DERMATITIS CONTACT ( 2 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 2 FDA reports)
DISCOMFORT ( 2 FDA reports)
DISSEMINATED TUBERCULOSIS ( 2 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
DRY SKIN ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
ELEVATED MOOD ( 2 FDA reports)
ENCEPHALOPATHY ( 2 FDA reports)
EOSINOPHILIC PNEUMONIA ( 2 FDA reports)
EYE LUXATION ( 2 FDA reports)
EYE MOVEMENT DISORDER ( 2 FDA reports)
EYELID OEDEMA ( 2 FDA reports)
FACIAL PAIN ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
FEELING DRUNK ( 2 FDA reports)
FLANK PAIN ( 2 FDA reports)
GALLBLADDER PERFORATION ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
GASTROINTESTINAL PERFORATION ( 2 FDA reports)
GINGIVAL INFECTION ( 2 FDA reports)
GLAUCOMA ( 2 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 2 FDA reports)
GOITRE ( 2 FDA reports)
GRANULOCYTOPENIA ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
HELICOBACTER INFECTION ( 2 FDA reports)
HYPERCALCAEMIA ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
HYPERLIPIDAEMIA ( 2 FDA reports)
HYPERNATRAEMIA ( 2 FDA reports)
HYPERVENTILATION ( 2 FDA reports)
HYPOPROTEINAEMIA ( 2 FDA reports)
IMMOBILE ( 2 FDA reports)
INCREASED APPETITE ( 2 FDA reports)
INJECTION SITE ERYTHEMA ( 2 FDA reports)
INJECTION SITE INDURATION ( 2 FDA reports)
INJECTION SITE REACTION ( 2 FDA reports)
INJECTION SITE SWELLING ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
IRON BINDING CAPACITY UNSATURATED DECREASED ( 2 FDA reports)
JUVENILE ARTHRITIS ( 2 FDA reports)
LABORATORY TEST ABNORMAL ( 2 FDA reports)
LARGE INTESTINAL ULCER ( 2 FDA reports)
LARGE INTESTINE CARCINOMA ( 2 FDA reports)
LARYNGEAL HAEMORRHAGE ( 2 FDA reports)
LARYNGEAL INFLAMMATION ( 2 FDA reports)
LARYNGOTRACHEO BRONCHITIS ( 2 FDA reports)
LISTERIA SEPSIS ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 2 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 2 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 2 FDA reports)
MELAENA ( 2 FDA reports)
METABOLIC ENCEPHALOPATHY ( 2 FDA reports)
MOUTH ULCERATION ( 2 FDA reports)
MUSCLE RIGIDITY ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME ( 2 FDA reports)
MYOCLONUS ( 2 FDA reports)
NEUROGENIC BLADDER ( 2 FDA reports)
NIGHTMARE ( 2 FDA reports)
ORAL PAIN ( 2 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 2 FDA reports)
PANCREATIC PSEUDOCYST ( 2 FDA reports)
PAROTID GLAND ENLARGEMENT ( 2 FDA reports)
PERICARDIAL DRAINAGE ( 2 FDA reports)
PNEUMATOSIS INTESTINALIS ( 2 FDA reports)
PNEUMOTHORAX ( 2 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 2 FDA reports)
PREGNANCY ( 2 FDA reports)
PROCEDURAL PAIN ( 2 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 2 FDA reports)
PULMONARY FIBROSIS ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
RESPIRATORY TRACT INFECTION ( 2 FDA reports)
SCREAMING ( 2 FDA reports)
SEROTONIN SYNDROME ( 2 FDA reports)
SHOCK HAEMORRHAGIC ( 2 FDA reports)
SMALLPOX ( 2 FDA reports)
SNORING ( 2 FDA reports)
SPINAL CORD INJURY ( 2 FDA reports)
STATUS ASTHMATICUS ( 2 FDA reports)
STUPOR ( 2 FDA reports)
SURGERY ( 2 FDA reports)
SYNCOPE VASOVAGAL ( 2 FDA reports)
THALAMUS HAEMORRHAGE ( 2 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 2 FDA reports)
THIRST ( 2 FDA reports)
TRANSAMINASES INCREASED ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
VASCULITIS ( 2 FDA reports)
VIRAL INFECTION ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
VISUAL IMPAIRMENT ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ACARODERMATITIS ( 1 FDA reports)
ACINETOBACTER INFECTION ( 1 FDA reports)
ACUTE ABDOMEN ( 1 FDA reports)
AFFECT LABILITY ( 1 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANAESTHETIC COMPLICATION ( 1 FDA reports)
ANAPLASTIC LARGE CELL LYMPHOMA T- AND NULL-CELL TYPES ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ANTI-INSULIN ANTIBODY POSITIVE ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
APHASIA ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ARTHRITIS BACTERIAL ( 1 FDA reports)
ATHEROSCLEROSIS OBLITERANS ( 1 FDA reports)
AUTOIMMUNE DISORDER ( 1 FDA reports)
AUTOIMMUNE HEPATITIS ( 1 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 1 FDA reports)
BACTERIA STOOL IDENTIFIED ( 1 FDA reports)
BAND NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BILE DUCT CANCER ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CHOLINESTERASE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE BB INCREASED ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BRADYARRHYTHMIA ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRAIN STEM INFARCTION ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CALCIUM METABOLISM DISORDER ( 1 FDA reports)
CANDIDA SEROLOGY POSITIVE ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIAC NEOPLASM MALIGNANT ( 1 FDA reports)
CELL MARKER INCREASED ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CERVIX CARCINOMA ( 1 FDA reports)
CHILLBLAINS ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
COMA SCALE ABNORMAL ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
CORONARY ARTERY THROMBOSIS ( 1 FDA reports)
CRYPTOCOCCOSIS ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DERMATOMYOSITIS ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 1 FDA reports)
ENDOSCOPY ABNORMAL ( 1 FDA reports)
ENTERITIS ( 1 FDA reports)
EOSINOPHILIC MYOCARDITIS ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
FEBRILE CONVULSION ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FOOD INTERACTION ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GASTRIC POLYPS ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GASTROSTOMY ( 1 FDA reports)
GENITAL HAEMORRHAGE ( 1 FDA reports)
GINGIVITIS ( 1 FDA reports)
GOUT ( 1 FDA reports)
GRIP STRENGTH DECREASED ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAIR COLOUR CHANGES ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HOMICIDE ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 1 FDA reports)
HYPERAMMONAEMIA ( 1 FDA reports)
HYPERCOAGULATION ( 1 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 1 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
ILLUSION ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTRA-UTERINE DEATH ( 1 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
ISCHAEMIC HEPATITIS ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
KERATOCONUS ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LOGORRHOEA ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
LUMBAR SPINAL STENOSIS ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 1 FDA reports)
LYMPHOCYTIC INFILTRATION ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
MESENTERIC PANNICULITIS ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
METASTATIC NEOPLASM ( 1 FDA reports)
MONOCYTE COUNT DECREASED ( 1 FDA reports)
MUSCLE CONTRACTURE ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYELITIS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 1 FDA reports)
MYOGLOBIN URINE PRESENT ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEPHRITIS ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 1 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 1 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IIIB ( 1 FDA reports)
OCCUPATIONAL PHYSICAL PROBLEM ( 1 FDA reports)
OCULOMUCOCUTANEOUS SYNDROME ( 1 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PAPULE ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PCO2 INCREASED ( 1 FDA reports)
PELVIC ABSCESS ( 1 FDA reports)
PERIANAL ERYTHEMA ( 1 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PHOSPHORUS METABOLISM DISORDER ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
PLATELET COUNT ABNORMAL ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
PNEUMONIA CHLAMYDIAL ( 1 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 1 FDA reports)
PO2 INCREASED ( 1 FDA reports)
POOR PERIPHERAL CIRCULATION ( 1 FDA reports)
POSTOPERATIVE CONSTIPATION ( 1 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PROTEIN TOTAL INCREASED ( 1 FDA reports)
PRURIGO ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PULMONARY TUBERCULOSIS ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
PYELONEPHRITIS ACUTE ( 1 FDA reports)
PYLORIC STENOSIS ( 1 FDA reports)
PYLORUS DILATATION ( 1 FDA reports)
PYROMANIA ( 1 FDA reports)
RADIATION PNEUMONITIS ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RHINITIS ALLERGIC ( 1 FDA reports)
SACRAL PAIN ( 1 FDA reports)
SALIVARY GLAND PAIN ( 1 FDA reports)
SCLERODERMA ( 1 FDA reports)
SCRATCH ( 1 FDA reports)
SEBORRHOEIC DERMATITIS ( 1 FDA reports)
SECONDARY ADRENOCORTICAL INSUFFICIENCY ( 1 FDA reports)
SHOULDER PAIN ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SMALL INTESTINAL PERFORATION ( 1 FDA reports)
SPLENECTOMY ( 1 FDA reports)
STRESS ( 1 FDA reports)
SUBCUTANEOUS ABSCESS ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
TENDON DISORDER ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TONIC CONVULSION ( 1 FDA reports)
TOXIC ENCEPHALOPATHY ( 1 FDA reports)
TYPE 1 DIABETES MELLITUS ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VITREOUS HAEMORRHAGE ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHITE BLOOD CELL DISORDER ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)
ZINC SULPHATE TURBIDITY INCREASED ( 1 FDA reports)

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