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

DYSPNOEA ( 5 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 5 FDA reports)
MALAISE ( 5 FDA reports)
PNEUMONIA ( 5 FDA reports)
CHILLS ( 4 FDA reports)
HYPERHIDROSIS ( 4 FDA reports)
PULMONARY EMBOLISM ( 4 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ANXIETY ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ASTHENIA ( 3 FDA reports)
BLOOD BILIRUBIN INCREASED ( 3 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
DRY SKIN ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 3 FDA reports)
ANAEMIA ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CARDIOMEGALY ( 2 FDA reports)
CARDIOVASCULAR DISORDER ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
DYSPNOEA AT REST ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
LIVIDITY ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
PNEUMONITIS ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
RIGHT VENTRICULAR FAILURE ( 2 FDA reports)
SINUS BRADYCARDIA ( 2 FDA reports)
SLEEP DISORDER ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
AGITATED DEPRESSION ( 1 FDA reports)
ALVEOLITIS ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRONCHIAL SECRETION RETENTION ( 1 FDA reports)
BURN OESOPHAGEAL ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DRY THROAT ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
FALL ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HELICOBACTER GASTRITIS ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPERVISCOSITY SYNDROME ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
LEUKOCYTURIA ( 1 FDA reports)
LUNG CYST ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
NASAL DRYNESS ( 1 FDA reports)
NASAL OBSTRUCTION ( 1 FDA reports)
NASAL POLYPS ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
PANCREATITIS CHRONIC ( 1 FDA reports)
PNEUMOCONIOSIS ( 1 FDA reports)
POLYCYTHAEMIA ( 1 FDA reports)
POOR QUALITY SLEEP ( 1 FDA reports)
RELAPSING FEVER ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
SLEEP TALKING ( 1 FDA reports)
SNORING ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPINAL PAIN ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
SUFFOCATION FEELING ( 1 FDA reports)
SURGERY ( 1 FDA reports)
TREMOR ( 1 FDA reports)
UPPER LIMB FRACTURE ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VOMITING ( 1 FDA reports)

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