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

FATIGUE ( 16 FDA reports)
OEDEMA PERIPHERAL ( 15 FDA reports)
BACK PAIN ( 12 FDA reports)
DYSPNOEA ( 12 FDA reports)
SWELLING FACE ( 12 FDA reports)
ARTHRALGIA ( 9 FDA reports)
PAIN ( 9 FDA reports)
ASTHENIA ( 8 FDA reports)
ERYTHEMA ( 8 FDA reports)
HYPERHIDROSIS ( 8 FDA reports)
NAUSEA ( 8 FDA reports)
URINARY TRACT INFECTION ( 8 FDA reports)
URINE OUTPUT DECREASED ( 8 FDA reports)
WEIGHT INCREASED ( 8 FDA reports)
BLOOD PRESSURE DECREASED ( 7 FDA reports)
BREAST ENLARGEMENT ( 7 FDA reports)
CARDIAC DISORDER ( 7 FDA reports)
DYSTONIA ( 7 FDA reports)
GAIT DISTURBANCE ( 7 FDA reports)
SKIN DISCOLOURATION ( 7 FDA reports)
WITHDRAWAL SYNDROME ( 7 FDA reports)
ABDOMINAL PAIN ( 6 FDA reports)
ANAEMIA ( 6 FDA reports)
HYPERTENSION ( 6 FDA reports)
BLOOD BILIRUBIN INCREASED ( 5 FDA reports)
BLOOD CHROMOGRANIN A INCREASED ( 5 FDA reports)
BLOOD GLUCOSE INCREASED ( 5 FDA reports)
CONSTIPATION ( 5 FDA reports)
CYSTITIS ( 5 FDA reports)
EYE IRRITATION ( 5 FDA reports)
FLANK PAIN ( 5 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 5 FDA reports)
GASTROENTERITIS VIRAL ( 5 FDA reports)
HAEMOGLOBIN DECREASED ( 5 FDA reports)
HEPATOMEGALY ( 5 FDA reports)
INFLUENZA ( 5 FDA reports)
KIDNEY INFECTION ( 5 FDA reports)
MACULAR DEGENERATION ( 5 FDA reports)
MASS ( 5 FDA reports)
MELANOCYTIC NAEVUS ( 5 FDA reports)
MENISCUS REMOVAL ( 5 FDA reports)
MOLE EXCISION ( 5 FDA reports)
MUSCULOSKELETAL PAIN ( 5 FDA reports)
NECROSIS ( 5 FDA reports)
POLLAKIURIA ( 5 FDA reports)
POLYDIPSIA ( 5 FDA reports)
PYELONEPHRITIS ( 5 FDA reports)
RASH ( 5 FDA reports)
SLEEP DISORDER ( 5 FDA reports)
SYNCOPE ( 5 FDA reports)
TOOTHACHE ( 5 FDA reports)
ABDOMINAL DISTENSION ( 4 FDA reports)
ANGINA PECTORIS ( 4 FDA reports)
CONFUSIONAL STATE ( 4 FDA reports)
DEATH ( 4 FDA reports)
EYE INFECTION ( 4 FDA reports)
FAECES DISCOLOURED ( 4 FDA reports)
HALLUCINATION ( 4 FDA reports)
HYDRONEPHROSIS ( 4 FDA reports)
INCONTINENCE ( 4 FDA reports)
PNEUMONIA ( 4 FDA reports)
PYREXIA ( 4 FDA reports)
RESTLESSNESS ( 4 FDA reports)
VOMITING ( 4 FDA reports)
ABDOMINAL ADHESIONS ( 3 FDA reports)
BLOOD SODIUM DECREASED ( 3 FDA reports)
BLOOD URINE ( 3 FDA reports)
CHOLECYSTITIS ( 3 FDA reports)
COGNITIVE DISORDER ( 3 FDA reports)
DELIRIUM ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
DRY MOUTH ( 3 FDA reports)
DRY SKIN ( 3 FDA reports)
FALL ( 3 FDA reports)
GALLBLADDER OPERATION ( 3 FDA reports)
GASTROINTESTINAL PAIN ( 3 FDA reports)
HYPOPHAGIA ( 3 FDA reports)
INTESTINAL OBSTRUCTION ( 3 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 3 FDA reports)
METASTASES TO LIVER ( 3 FDA reports)
ORAL HERPES ( 3 FDA reports)
PSORIASIS ( 3 FDA reports)
RASH PRURITIC ( 3 FDA reports)
SKIN EXFOLIATION ( 3 FDA reports)
TREMOR ( 3 FDA reports)
TRIPLE VESSEL BYPASS GRAFT ( 3 FDA reports)
WEIGHT DECREASED ( 3 FDA reports)
ADHESION ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
BLADDER OBSTRUCTION ( 2 FDA reports)
CELLULITIS ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CHILLS ( 2 FDA reports)
GALLBLADDER DISORDER ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HEPATIC LESION ( 2 FDA reports)
HIP ARTHROPLASTY ( 2 FDA reports)
HIP FRACTURE ( 2 FDA reports)
HOSPITALISATION ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 2 FDA reports)
INJECTION SITE ERYTHEMA ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
MALNUTRITION ( 2 FDA reports)
NERVE COMPRESSION ( 2 FDA reports)
ORTHOSTATIC HYPOTENSION ( 2 FDA reports)
PALLIATIVE CARE ( 2 FDA reports)
POLYCHONDRITIS ( 2 FDA reports)
RADIAL NERVE INJURY ( 2 FDA reports)
RADIOTHERAPY ( 2 FDA reports)
SCIATICA ( 2 FDA reports)
SJOGREN'S SYNDROME ( 2 FDA reports)
ADRENAL DISORDER ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BLOOD CORTISOL DECREASED ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
CARPAL TUNNEL SYNDROME ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
COUGH ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DERMATITIS CONTACT ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEPATIC NEOPLASM ( 1 FDA reports)
HODGKIN'S DISEASE STAGE III ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE MASS ( 1 FDA reports)
INJECTION SITE OEDEMA ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENISCUS LESION ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MUSCLE CRAMP ( 1 FDA reports)
MUSCLE SPASTICITY ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OSTEITIS ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
STRESS ( 1 FDA reports)
TOOTH INFECTION ( 1 FDA reports)
TYPE 1 DIABETES MELLITUS ( 1 FDA reports)
VAGINAL DISCHARGE ( 1 FDA reports)
WOUND ( 1 FDA reports)

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