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

BACK PAIN ( 6 FDA reports)
RESPIRATORY FAILURE ( 6 FDA reports)
ACUTE VESTIBULAR SYNDROME ( 5 FDA reports)
DYSPNOEA ( 5 FDA reports)
NEUROSIS ( 5 FDA reports)
PYREXIA ( 5 FDA reports)
TOXIC ENCEPHALOPATHY ( 5 FDA reports)
TOXIC NEUROPATHY ( 5 FDA reports)
CARDIAC FAILURE ( 4 FDA reports)
CONSTIPATION ( 4 FDA reports)
DIARRHOEA ( 4 FDA reports)
ERYTHEMA ( 4 FDA reports)
HYPOXIA ( 4 FDA reports)
INFLAMMATION ( 4 FDA reports)
RASH ( 4 FDA reports)
TREMOR ( 4 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
ARRHYTHMIA ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 3 FDA reports)
BRADYKINESIA ( 3 FDA reports)
CARDIOPULMONARY FAILURE ( 3 FDA reports)
CEREBRAL HAEMORRHAGE ( 3 FDA reports)
CHILLS ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
DRY SKIN ( 3 FDA reports)
DYSKINESIA ( 3 FDA reports)
DYSTONIA ( 3 FDA reports)
FIBROMYALGIA ( 3 FDA reports)
FORMICATION ( 3 FDA reports)
HYPERCAPNIA ( 3 FDA reports)
HYPOAESTHESIA ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
INFECTIVE SPONDYLITIS ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
MYELITIS ( 3 FDA reports)
NAIL DISORDER ( 3 FDA reports)
NECK PAIN ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
OSTEOARTHRITIS ( 3 FDA reports)
PAIN ( 3 FDA reports)
PNEUMONIA ASPIRATION ( 3 FDA reports)
RHABDOMYOLYSIS ( 3 FDA reports)
SEPSIS ( 3 FDA reports)
SICK SINUS SYNDROME ( 3 FDA reports)
SINUS POLYP ( 3 FDA reports)
SKIN EXFOLIATION ( 3 FDA reports)
TACHYCARDIA ( 3 FDA reports)
THROMBOCYTOPENIA ( 3 FDA reports)
VOMITING ( 3 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 2 FDA reports)
ARTHROPATHY ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BONE PAIN ( 2 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
CYST ( 2 FDA reports)
DIFFICULTY IN WALKING ( 2 FDA reports)
DIPLEGIA ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
IMPAIRED DRIVING ABILITY ( 2 FDA reports)
JOINT STIFFNESS ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
MULTIPLE SCLEROSIS ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PERIARTHRITIS ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
POLLAKIURIA ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
SCIATICA ( 2 FDA reports)
SENSORY DISTURBANCE ( 2 FDA reports)
SHOCK ( 2 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 2 FDA reports)
URINARY INCONTINENCE ( 2 FDA reports)
URINE OUTPUT DECREASED ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL OPERATION ( 1 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 1 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
APLASTIC ANAEMIA ( 1 FDA reports)
APRAXIA ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK THIRD DEGREE ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD BICARBONATE INCREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CANDIDA SEPSIS ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 1 FDA reports)
CHRONIC SINUSITIS ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COMPRESSION FRACTURE ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
FALL ( 1 FDA reports)
FEELING HOT AND COLD ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GLUTAMATE DEHYDROGENASE INCREASED ( 1 FDA reports)
GRIP STRENGTH DECREASED ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOGEUSIA ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOSMIA ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INFANTILE APNOEIC ATTACK ( 1 FDA reports)
INJURY ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LUNG ABSCESS ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
MALAISE ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NASAL POLYPS ( 1 FDA reports)
NASAL SEPTUM DEVIATION ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PCO2 INCREASED ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PNEUMONIA KLEBSIELLA ( 1 FDA reports)
PO2 INCREASED ( 1 FDA reports)
POLYP ( 1 FDA reports)
POOR PERIPHERAL CIRCULATION ( 1 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 1 FDA reports)
POSTURE ABNORMAL ( 1 FDA reports)
PROCTITIS HAEMORRHAGIC ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PURPURA ( 1 FDA reports)
PYOTHORAX ( 1 FDA reports)
QRS AXIS ABNORMAL ( 1 FDA reports)
RALES ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
REFLEXES ABNORMAL ( 1 FDA reports)
REPERFUSION INJURY ( 1 FDA reports)
RESPIRATORY GAS EXCHANGE DISORDER ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SEPTOPLASTY ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN NECROSIS ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SUPERINFECTION LUNG ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TENDON RUPTURE ( 1 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
WOUND DEHISCENCE ( 1 FDA reports)

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