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

ASTHENIA ( 7 FDA reports)
DIARRHOEA ( 7 FDA reports)
PAIN ( 7 FDA reports)
DYSPNOEA ( 6 FDA reports)
OEDEMA PERIPHERAL ( 6 FDA reports)
MALAISE ( 5 FDA reports)
PYREXIA ( 5 FDA reports)
FATIGUE ( 4 FDA reports)
URINARY TRACT INFECTION ( 4 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 3 FDA reports)
COUGH ( 3 FDA reports)
DEAFNESS ( 3 FDA reports)
DISEASE PROGRESSION ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
FEELING ABNORMAL ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
INFLUENZA LIKE ILLNESS ( 3 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
OSTEONECROSIS ( 3 FDA reports)
RASH ( 3 FDA reports)
TACHYCARDIA ( 3 FDA reports)
ANAEMIA ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CEREBRAL INFARCTION ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DRUG DOSE OMISSION ( 2 FDA reports)
DYSPHONIA ( 2 FDA reports)
EAR PAIN ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
FIBROMYALGIA ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
INJECTION SITE PAIN ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
OROPHARYNGEAL PAIN ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PAIN IN JAW ( 2 FDA reports)
PARKINSONISM ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
SWELLING FACE ( 2 FDA reports)
TOOTH EXTRACTION ( 2 FDA reports)
TREMOR ( 2 FDA reports)
VIRAL INFECTION ( 2 FDA reports)
VISUAL IMPAIRMENT ( 2 FDA reports)
WHEEZING ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ABORTION ( 1 FDA reports)
ABSCESS JAW ( 1 FDA reports)
ACNE ( 1 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
AORTIC VALVE REPAIR ( 1 FDA reports)
APPENDIX DISORDER ( 1 FDA reports)
APPLICATION SITE REACTION ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ASPERGILLOSIS ( 1 FDA reports)
ATROPHY ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BONE CYST ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
BONE FRAGMENTATION ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BRADYKINESIA ( 1 FDA reports)
BRAIN ABSCESS ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)
CALCIPHYLAXIS ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM NECROSIS ( 1 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 1 FDA reports)
CEREBRAL ASPERGILLOSIS ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHORIORETINITIS ( 1 FDA reports)
CLONUS ( 1 FDA reports)
CLUBBING ( 1 FDA reports)
COAGULATION TIME PROLONGED ( 1 FDA reports)
COGWHEEL RIGIDITY ( 1 FDA reports)
COLITIS COLLAGENOUS ( 1 FDA reports)
COLITIS MICROSCOPIC ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CORTISOL FREE URINE DECREASED ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CULTURE WOUND POSITIVE ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
CYSTIC FIBROSIS ( 1 FDA reports)
DENTAL OPERATION ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 1 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 1 FDA reports)
EMBOLIA CUTIS MEDICAMENTOSA ( 1 FDA reports)
ENDOTRACHEAL INTUBATION ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
ESCHAR ( 1 FDA reports)
EXPIRED DRUG ADMINISTERED ( 1 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
GALLBLADDER OPERATION ( 1 FDA reports)
GASTROINTESTINAL TOXICITY ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GINGIVITIS ( 1 FDA reports)
GRANULOMA ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
IMPAIRED SELF-CARE ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INJECTION SITE DISCOLOURATION ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INJECTION SITE HYPERSENSITIVITY ( 1 FDA reports)
INJECTION SITE INFLAMMATION ( 1 FDA reports)
INJECTION SITE MASS ( 1 FDA reports)
INJECTION SITE NECROSIS ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INJECTION SITE SCAB ( 1 FDA reports)
INJECTION SITE SCAR ( 1 FDA reports)
INJECTION SITE URTICARIA ( 1 FDA reports)
INJURY ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LOWER EXTREMITY MASS ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
METHAEMOGLOBINAEMIA ( 1 FDA reports)
MIDDLE EAR EFFUSION ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MUSCLE TIGHTNESS ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
OCCULT BLOOD POSITIVE ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
OSTEONECROSIS OF JAW ( 1 FDA reports)
OSTEOSCLEROSIS ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PNEUMONIA BACTERIAL ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 1 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 1 FDA reports)
QUALITY OF LIFE DECREASED ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
SCAR ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN PLAQUE ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 1 FDA reports)
STRESS CARDIOMYOPATHY ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TOOTH ABSCESS ( 1 FDA reports)
TOOTH DISORDER ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
URINARY CASTS ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VAGINAL ODOUR ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VITREOUS FLOATERS ( 1 FDA reports)
VOMITING ( 1 FDA reports)
VULVOVAGINAL DRYNESS ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 1 FDA reports)

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