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

METASTASES TO LIVER ( 7 FDA reports)
BLOOD PRESSURE DECREASED ( 6 FDA reports)
BREAST CANCER FEMALE ( 6 FDA reports)
FATIGUE ( 6 FDA reports)
HYPONATRAEMIA ( 6 FDA reports)
SOMNOLENCE ( 6 FDA reports)
ARTHRALGIA ( 5 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 5 FDA reports)
BREAST CANCER ( 5 FDA reports)
CARDIAC ARREST ( 5 FDA reports)
HEPATIC ENCEPHALOPATHY ( 5 FDA reports)
HYPERKALAEMIA ( 5 FDA reports)
PLEURAL EFFUSION ( 5 FDA reports)
PULMONARY EMBOLISM ( 5 FDA reports)
ASCITES ( 4 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 4 FDA reports)
BLOOD GLUCOSE INCREASED ( 4 FDA reports)
CONFUSIONAL STATE ( 4 FDA reports)
CONVULSION ( 4 FDA reports)
COUGH ( 4 FDA reports)
DRUG INEFFECTIVE ( 4 FDA reports)
DYSPNOEA ( 4 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 4 FDA reports)
HEART RATE INCREASED ( 4 FDA reports)
JOINT SWELLING ( 4 FDA reports)
PANCYTOPENIA ( 4 FDA reports)
TACHYCARDIA ( 4 FDA reports)
WEIGHT DECREASED ( 4 FDA reports)
AMNESIA ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MM INCREASED ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
FALL ( 3 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 3 FDA reports)
HEPATIC FAILURE ( 3 FDA reports)
HEPATOCELLULAR DAMAGE ( 3 FDA reports)
HEPATORENAL SYNDROME ( 3 FDA reports)
HYPERSPLENISM ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
INTERSTITIAL LUNG DISEASE ( 3 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 3 FDA reports)
OXYGEN SATURATION DECREASED ( 3 FDA reports)
PAIN ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
PORTAL HYPERTENSION ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
WEIGHT INCREASED ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ABNORMAL BEHAVIOUR ( 2 FDA reports)
AGGRESSION ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
ANGER ( 2 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
APHASIA ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BODY HEIGHT DECREASED ( 2 FDA reports)
BONE MARROW DISORDER ( 2 FDA reports)
BURNING SENSATION ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 2 FDA reports)
COLLAGEN DISORDER ( 2 FDA reports)
CYSTITIS ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DISTURBANCE IN ATTENTION ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
DYSGRAPHIA ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
DYSSTASIA ( 2 FDA reports)
EUPHORIC MOOD ( 2 FDA reports)
EYE PAIN ( 2 FDA reports)
GINGIVAL BLEEDING ( 2 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 2 FDA reports)
HEPATITIS FULMINANT ( 2 FDA reports)
HYPERPLASIA ( 2 FDA reports)
HYPERPROTEINAEMIA ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
IRRITABILITY ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
MYOPATHY ( 2 FDA reports)
NASAL OEDEMA ( 2 FDA reports)
NIGHTMARE ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
OSTEOARTHRITIS ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PHOTOSENSITIVITY REACTION ( 2 FDA reports)
PROCEDURAL COMPLICATION ( 2 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 2 FDA reports)
RESPIRATORY RATE INCREASED ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
SUSPICIOUSNESS ( 2 FDA reports)
THROMBOCYTHAEMIA ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
TREMOR ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
VOMITING ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ACNE ( 1 FDA reports)
ANAESTHETIC COMPLICATION CARDIAC ( 1 FDA reports)
ANURIA ( 1 FDA reports)
APTYALISM ( 1 FDA reports)
ARTERIAL DISORDER ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ARTHRITIS INFECTIVE ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BREATH SOUNDS DECREASED ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CLOSTRIDIUM COLITIS ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
COLONIC POLYP ( 1 FDA reports)
COLORECTAL CANCER METASTATIC ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
DEATH OF FRIEND ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
EXOSTOSIS ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL HYPERMOTILITY ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GENITAL PRURITUS FEMALE ( 1 FDA reports)
GOUT ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HAPTOGLOBIN DECREASED ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HYPERACUSIS ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
INADEQUATE ANALGESIA ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INTENTIONAL MISUSE ( 1 FDA reports)
INTESTINAL HYPOMOTILITY ( 1 FDA reports)
IRRITABLE BOWEL SYNDROME ( 1 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
LIP DRY ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
LYMPHOEDEMA ( 1 FDA reports)
MASTECTOMY ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
METASTASES TO BONE MARROW ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MUSCLE HAEMORRHAGE ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NASAL DRYNESS ( 1 FDA reports)
NASOPHARYNGEAL DISORDER ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PHLEBITIS ( 1 FDA reports)
PITTING OEDEMA ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
REGRESSIVE BEHAVIOUR ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESUSCITATION ( 1 FDA reports)
RETICULOCYTOSIS ( 1 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SCREAMING ( 1 FDA reports)
SENSATION OF FOREIGN BODY ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN HYPOPIGMENTATION ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SKIN NECROSIS ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
STRESS SYMPTOMS ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
THIRST ( 1 FDA reports)
TONGUE OEDEMA ( 1 FDA reports)
TUMOUR LYSIS SYNDROME ( 1 FDA reports)
UPPER LIMB FRACTURE ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)

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