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

ASTHENIA ( 6 FDA reports)
FATIGUE ( 6 FDA reports)
HEADACHE ( 5 FDA reports)
PAIN IN JAW ( 5 FDA reports)
SWELLING FACE ( 5 FDA reports)
BRONCHITIS ( 4 FDA reports)
FIBROSIS ( 4 FDA reports)
HYPOAESTHESIA ( 4 FDA reports)
IMPAIRED HEALING ( 4 FDA reports)
INFECTION ( 4 FDA reports)
INFLAMMATION ( 4 FDA reports)
JAW DISORDER ( 4 FDA reports)
LIVEDO RETICULARIS ( 4 FDA reports)
MALAISE ( 4 FDA reports)
MASS ( 4 FDA reports)
NEURALGIA ( 4 FDA reports)
OSTEITIS ( 4 FDA reports)
OSTEOMYELITIS ( 4 FDA reports)
PAIN IN EXTREMITY ( 4 FDA reports)
PRODUCTIVE COUGH ( 4 FDA reports)
SPINAL FRACTURE ( 4 FDA reports)
SWELLING ( 4 FDA reports)
TOOTHACHE ( 4 FDA reports)
ABDOMINAL DISTENSION ( 3 FDA reports)
ALOPECIA ( 3 FDA reports)
ALVEOLAR OSTEITIS ( 3 FDA reports)
ANAEMIA ( 3 FDA reports)
BLOOD BILIRUBIN INCREASED ( 3 FDA reports)
BONE DISORDER ( 3 FDA reports)
CACHEXIA ( 3 FDA reports)
CONSTIPATION ( 3 FDA reports)
DENTAL TREATMENT ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
DYSGEUSIA ( 3 FDA reports)
DYSPEPSIA ( 3 FDA reports)
ENDODONTIC PROCEDURE ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 3 FDA reports)
HEPATOMEGALY ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
JAUNDICE ( 3 FDA reports)
LETHARGY ( 3 FDA reports)
LYMPHOPENIA ( 3 FDA reports)
MOOD SWINGS ( 3 FDA reports)
NEUROPATHY ( 3 FDA reports)
NEUROPATHY PERIPHERAL ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
ORAL SOFT TISSUE DISORDER ( 3 FDA reports)
OSTEOMYELITIS DRAINAGE ( 3 FDA reports)
OSTEONECROSIS ( 3 FDA reports)
PAIN ( 3 FDA reports)
PALLOR ( 3 FDA reports)
PALPITATIONS ( 3 FDA reports)
PLASMODIUM FALCIPARUM INFECTION ( 3 FDA reports)
POLLAKIURIA ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
RENAL IMPAIRMENT ( 3 FDA reports)
SEPSIS ( 3 FDA reports)
SKIN WARM ( 3 FDA reports)
TOOTH EXTRACTION ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
VISION BLURRED ( 3 FDA reports)
VITREOUS FLOATERS ( 3 FDA reports)
WOUND DRAINAGE ( 3 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 2 FDA reports)
GLAUCOMA ( 2 FDA reports)
HYPOAESTHESIA FACIAL ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 2 FDA reports)
APNOEA ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BRAIN ABSCESS ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
CAPILLARY LEAK SYNDROME ( 1 FDA reports)
CARDIAC DEATH ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CELLULITIS ORBITAL ( 1 FDA reports)
CEREBRAL FUNGAL INFECTION ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DIABETES INSIPIDUS ( 1 FDA reports)
DRY SOCKET ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GLIOSIS ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MUSCLE INJURY ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYCOBACTERIUM TUBERCULOSIS COMPLEX TEST NEGATIVE ( 1 FDA reports)
NEUTROPENIC INFECTION ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
OPPORTUNISTIC INFECTION ( 1 FDA reports)
ORAL DISORDER ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OSTEONECROSIS OF JAW ( 1 FDA reports)
PLASMACYTOMA ( 1 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
URINE OUTPUT INCREASED ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
VITH NERVE PARALYSIS ( 1 FDA reports)

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