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

RASH ERYTHEMATOUS ( 9 FDA reports)
LEUKOCYTOSIS ( 8 FDA reports)
RASH PUSTULAR ( 8 FDA reports)
PUSTULAR PSORIASIS ( 6 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 5 FDA reports)
NEUTROPHIL COUNT INCREASED ( 5 FDA reports)
TOOTH EXTRACTION ( 5 FDA reports)
POLYARTHRITIS ( 4 FDA reports)
PRURITUS ( 4 FDA reports)
PYREXIA ( 4 FDA reports)
THROMBOCYTHAEMIA ( 4 FDA reports)
ANAEMIA ( 3 FDA reports)
ANHEDONIA ( 3 FDA reports)
ANKYLOSING SPONDYLITIS ( 3 FDA reports)
ANXIETY ( 3 FDA reports)
BACK PAIN ( 3 FDA reports)
BONE DISORDER ( 3 FDA reports)
BREAST CANCER METASTATIC ( 3 FDA reports)
DENTAL CARIES ( 3 FDA reports)
DENTURE WEARER ( 3 FDA reports)
DISABILITY ( 3 FDA reports)
EMPHYSEMA ( 3 FDA reports)
GASTRITIS ( 3 FDA reports)
IMPAIRED HEALING ( 3 FDA reports)
INJURY ( 3 FDA reports)
MASTICATION DISORDER ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
NECK PAIN ( 3 FDA reports)
OSTEOARTHRITIS ( 3 FDA reports)
PAIN ( 3 FDA reports)
PANCYTOPENIA ( 3 FDA reports)
SENSITIVITY OF TEETH ( 3 FDA reports)
TOOTHACHE ( 3 FDA reports)
VOMITING ( 3 FDA reports)
WEIGHT DECREASED ( 3 FDA reports)
ADRENAL ADENOMA ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 2 FDA reports)
ARTERIOSCLEROSIS ( 2 FDA reports)
ATAXIA ( 2 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 2 FDA reports)
AXILLARY MASS ( 2 FDA reports)
BACTERIAL TEST NEGATIVE ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
BONE LESION ( 2 FDA reports)
BONE MARROW FAILURE ( 2 FDA reports)
BRACHIAL PLEXOPATHY ( 2 FDA reports)
CERVICAL SPINAL STENOSIS ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 2 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 2 FDA reports)
COLONIC STENOSIS ( 2 FDA reports)
COMPRESSION FRACTURE ( 2 FDA reports)
DEAFNESS ( 2 FDA reports)
DEATH ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
FACE OEDEMA ( 2 FDA reports)
FASCIITIS ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
GRANULOCYTOPENIA ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HEART RATE IRREGULAR ( 2 FDA reports)
HYPERSOMNIA ( 2 FDA reports)
HYPOTHYROIDISM ( 2 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 2 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 2 FDA reports)
LIP DRY ( 2 FDA reports)
MALNUTRITION ( 2 FDA reports)
METASTASES TO BONE ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
NEOPLASM MALIGNANT ( 2 FDA reports)
NEURALGIA ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
OSTEONECROSIS OF JAW ( 2 FDA reports)
PANCOAST'S TUMOUR ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
PURPURA ( 2 FDA reports)
RASH MACULO-PAPULAR ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
RED BLOOD CELLS URINE ( 2 FDA reports)
RESPIRATORY TRACT INFECTION ( 2 FDA reports)
RIB FRACTURE ( 2 FDA reports)
SPINAL OSTEOARTHRITIS ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
TOOTH ABSCESS ( 2 FDA reports)
TREMOR ( 2 FDA reports)
URINARY INCONTINENCE ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
URINE ANALYSIS ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
WHITE BLOOD CELL COUNT ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BONE DEBRIDEMENT ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CARDIOPULMONARY FAILURE ( 1 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 1 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 1 FDA reports)
CHEILITIS ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
EPIGASTRIC DISCOMFORT ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
FOLLICULITIS ( 1 FDA reports)
GLOSSITIS ( 1 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MICROCYTIC ANAEMIA ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
SALIVARY HYPERSECRETION ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN NECROSIS ( 1 FDA reports)
SUPERINFECTION ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TONGUE DISCOLOURATION ( 1 FDA reports)
TONGUE OEDEMA ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
VASCULAR PURPURA ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)

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