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

ARTHRALGIA ( 9 FDA reports)
DEHYDRATION ( 8 FDA reports)
MENTAL STATUS CHANGES ( 8 FDA reports)
ABSCESS ( 7 FDA reports)
ANAEMIA ( 7 FDA reports)
ANXIETY ( 7 FDA reports)
ARRHYTHMIA ( 7 FDA reports)
BACK PAIN ( 7 FDA reports)
BONE DISORDER ( 7 FDA reports)
BRONCHITIS ( 7 FDA reports)
CATARACT ( 7 FDA reports)
CELLULITIS ( 7 FDA reports)
CHOLELITHIASIS ( 7 FDA reports)
COLITIS ( 7 FDA reports)
COMPRESSION FRACTURE ( 7 FDA reports)
CONJUNCTIVITIS ( 7 FDA reports)
DECREASED APPETITE ( 7 FDA reports)
DEFORMITY ( 7 FDA reports)
DIARRHOEA ( 7 FDA reports)
DIPLOPIA ( 7 FDA reports)
DIZZINESS ( 7 FDA reports)
DYSPNOEA EXERTIONAL ( 7 FDA reports)
DYSURIA ( 7 FDA reports)
EATING DISORDER ( 7 FDA reports)
EMOTIONAL DISTRESS ( 7 FDA reports)
ENTHESOPATHY ( 7 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 7 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 7 FDA reports)
GINGIVAL DISORDER ( 7 FDA reports)
HEADACHE ( 7 FDA reports)
HOT FLUSH ( 7 FDA reports)
HYPOKALAEMIA ( 7 FDA reports)
HYPOPHAGIA ( 7 FDA reports)
IMPAIRED HEALING ( 7 FDA reports)
INFECTION ( 7 FDA reports)
IRON DEFICIENCY ANAEMIA ( 7 FDA reports)
JAW DISORDER ( 7 FDA reports)
JOINT EFFUSION ( 7 FDA reports)
KYPHOSIS ( 7 FDA reports)
LYMPH GLAND INFECTION ( 7 FDA reports)
MASS ( 7 FDA reports)
METASTASES TO MENINGES ( 7 FDA reports)
MUSCULAR WEAKNESS ( 7 FDA reports)
OESOPHAGEAL DISORDER ( 7 FDA reports)
ORAL PAIN ( 7 FDA reports)
OSTEOARTHRITIS ( 7 FDA reports)
OSTEOMALACIA ( 7 FDA reports)
OSTEOMYELITIS ( 7 FDA reports)
OSTEONECROSIS OF JAW ( 7 FDA reports)
OSTEOPOROSIS ( 7 FDA reports)
OVARIAN MASS ( 7 FDA reports)
PAIN ( 7 FDA reports)
PAIN IN EXTREMITY ( 7 FDA reports)
PANCYTOPENIA ( 7 FDA reports)
PARAESTHESIA ORAL ( 7 FDA reports)
PERONEAL NERVE PALSY ( 7 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 7 FDA reports)
PYREXIA ( 7 FDA reports)
SCIATICA ( 7 FDA reports)
SEPSIS ( 7 FDA reports)
SPINAL FRACTURE ( 7 FDA reports)
SPINAL OSTEOARTHRITIS ( 7 FDA reports)
STAPHYLOCOCCAL INFECTION ( 7 FDA reports)
SWELLING FACE ( 7 FDA reports)
SYNOVITIS ( 7 FDA reports)
TINEA PEDIS ( 7 FDA reports)
TOOTH FRACTURE ( 7 FDA reports)
URINARY INCONTINENCE ( 7 FDA reports)
URINARY TRACT INFECTION ( 7 FDA reports)
WEIGHT DECREASED ( 7 FDA reports)
ASTHMA ( 6 FDA reports)
CANDIDIASIS ( 6 FDA reports)
HYPERCHOLESTEROLAEMIA ( 6 FDA reports)
LUMBAR RADICULOPATHY ( 6 FDA reports)
MUCOSAL INFLAMMATION ( 6 FDA reports)
PERIODONTITIS ( 6 FDA reports)
BONE FRAGMENTATION ( 5 FDA reports)
HAEMORRHAGE ( 5 FDA reports)
INSOMNIA ( 5 FDA reports)
PRIMARY SEQUESTRUM ( 5 FDA reports)
ATELECTASIS ( 4 FDA reports)
CHEST PAIN ( 4 FDA reports)
LUNG NEOPLASM ( 4 FDA reports)
MULTIPLE DRUG OVERDOSE ( 3 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DIABETIC FOOT ( 2 FDA reports)
FEELING COLD ( 2 FDA reports)
ONYCHOMYCOSIS ( 2 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CUTANEOUS VASCULITIS ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
FALL ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC INFARCTION ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
ORAL MUCOSAL BLISTERING ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PURPURA ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
TENDON DISORDER ( 1 FDA reports)
VARICES OESOPHAGEAL ( 1 FDA reports)
VOMITING ( 1 FDA reports)

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