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HEADACHE ( 66 FDA reports)
BLINDNESS TRANSIENT ( 46 FDA reports)
DYSARTHRIA ( 24 FDA reports)
INFUSION RELATED REACTION ( 24 FDA reports)
APPENDICITIS ( 17 FDA reports)
PYREXIA ( 13 FDA reports)
POLYARTHRITIS ( 10 FDA reports)
MYALGIA ( 8 FDA reports)
DEHYDRATION ( 7 FDA reports)
NAUSEA ( 7 FDA reports)
FEELING ABNORMAL ( 6 FDA reports)
ARTHRALGIA ( 5 FDA reports)
DIZZINESS ( 5 FDA reports)
PAIN ( 5 FDA reports)
HYPOTENSION ( 4 FDA reports)
INFLUENZA LIKE ILLNESS ( 4 FDA reports)
JOINT STIFFNESS ( 4 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 4 FDA reports)
VISUAL ACUITY REDUCED ( 4 FDA reports)
ACUTE PULMONARY OEDEMA ( 3 FDA reports)
BLINDNESS ( 3 FDA reports)
COUGH ( 3 FDA reports)
DIFFICULTY IN WALKING ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
FALL ( 3 FDA reports)
HEPATITIS ACUTE ( 3 FDA reports)
HYPERSENSITIVITY ( 3 FDA reports)
HYPOKALAEMIA ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
MYOCARDIAL INFARCTION ( 3 FDA reports)
OPTIC NEURITIS ( 3 FDA reports)
RASH ( 3 FDA reports)
RASH GENERALISED ( 3 FDA reports)
STOMACH DISCOMFORT ( 3 FDA reports)
VOMITING ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ADRENAL INSUFFICIENCY ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
ARTHRITIS ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
BRONCHOSPASM ( 2 FDA reports)
CANDIDIASIS ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CORONARY ARTERY OCCLUSION ( 2 FDA reports)
CYST ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DERMATITIS ALLERGIC ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DRUG EFFECT DECREASED ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
FACIAL PALSY ( 2 FDA reports)
FEELING HOT ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HOSPITALISATION ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
HYPOTHYROIDISM ( 2 FDA reports)
IMMUNE SYSTEM DISORDER ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
LIVEDO RETICULARIS ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MOVEMENT DISORDER ( 2 FDA reports)
MUSCLE RIGIDITY ( 2 FDA reports)
NEPHRITIS INTERSTITIAL ( 2 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
PNEUMONIA KLEBSIELLA ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
SERUM SICKNESS ( 2 FDA reports)
SKIN INFECTION ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
SUICIDE ATTEMPT ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
5-HYDROXYINDOLACETIC ACID INCREASED ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ALCOHOLISM ( 1 FDA reports)
ANAPLASTIC LARGE CELL LYMPHOMA T- AND NULL-CELL TYPES ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ANTI-HBS ANTIBODY POSITIVE ( 1 FDA reports)
ANTIBODY TEST ABNORMAL ( 1 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
ARTERIAL THROMBOSIS ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ASPHYXIA ( 1 FDA reports)
AUDIOGRAM ABNORMAL ( 1 FDA reports)
AUTOIMMUNE HEPATITIS ( 1 FDA reports)
BACK DISORDER ( 1 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 1 FDA reports)
BASAL CELL CARCINOMA ( 1 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 1 FDA reports)
BILIARY CIRRHOSIS ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CHROMOGRANIN A INCREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD PARATHYROID HORMONE DECREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRAIN DAMAGE ( 1 FDA reports)
BRAIN DEATH ( 1 FDA reports)
BRAIN STEM HAEMORRHAGE ( 1 FDA reports)
BREAST MASS ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CARCINOID SYNDROME ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 1 FDA reports)
CHORIORETINAL DISORDER ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COMA ( 1 FDA reports)
COMPLEMENT FACTOR DECREASED ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
CYTOLOGY ABNORMAL ( 1 FDA reports)
DEAFNESS BILATERAL ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
FAMILY STRESS ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
GALACTORRHOEA ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
GUN SHOT WOUND ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATITIS VIRAL ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HIRSUTISM ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 1 FDA reports)
ILEUS PARALYTIC ( 1 FDA reports)
INAPPROPRIATE AFFECT ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
INTENTIONAL SELF-INJURY ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
LOSS OF LIBIDO ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 1 FDA reports)
NASAL DRYNESS ( 1 FDA reports)
NASAL SINUS DRAINAGE ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OLIGODIPSIA ( 1 FDA reports)
PAINFUL RESPIRATION ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANIC DISORDER ( 1 FDA reports)
PARANEOPLASTIC SYNDROME ( 1 FDA reports)
PEMPHIGOID ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERIPHERAL ISCHAEMIA ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PLANTAR ERYTHEMA ( 1 FDA reports)
PLEURITIC PAIN ( 1 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
POLYSEROSITIS ( 1 FDA reports)
POSTPARTUM HAEMORRHAGE ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PRESCRIBED OVERDOSE ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RETINAL TEAR ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SKIN HAEMORRHAGE ( 1 FDA reports)
SKIN NODULE ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
SPUTUM RETENTION ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STEM CELL TRANSPLANT ( 1 FDA reports)
SUDDEN CARDIAC DEATH ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SUDDEN HEARING LOSS ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 1 FDA reports)
URINARY HESITATION ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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