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

FATIGUE ( 13 FDA reports)
DIARRHOEA ( 10 FDA reports)
PAIN ( 9 FDA reports)
PYREXIA ( 8 FDA reports)
VOMITING ( 8 FDA reports)
WEIGHT INCREASED ( 8 FDA reports)
CHEST PAIN ( 7 FDA reports)
CHILLS ( 7 FDA reports)
HEADACHE ( 7 FDA reports)
NAUSEA ( 7 FDA reports)
PAIN IN EXTREMITY ( 7 FDA reports)
ASTHENIA ( 6 FDA reports)
DYSPNOEA ( 6 FDA reports)
RASH ( 6 FDA reports)
ABDOMINAL PAIN ( 5 FDA reports)
ABDOMINAL PAIN UPPER ( 5 FDA reports)
ANAEMIA ( 5 FDA reports)
ATRIAL FIBRILLATION ( 5 FDA reports)
CONSTIPATION ( 5 FDA reports)
DECREASED APPETITE ( 5 FDA reports)
DYSPEPSIA ( 5 FDA reports)
DYSPHAGIA ( 5 FDA reports)
FALL ( 5 FDA reports)
HEART RATE INCREASED ( 5 FDA reports)
INSOMNIA ( 5 FDA reports)
MYALGIA ( 5 FDA reports)
PNEUMONIA ( 5 FDA reports)
SOMNOLENCE ( 5 FDA reports)
THROAT IRRITATION ( 5 FDA reports)
BACK PAIN ( 4 FDA reports)
CHEST DISCOMFORT ( 4 FDA reports)
DEPRESSION ( 4 FDA reports)
DIZZINESS ( 4 FDA reports)
DRY MOUTH ( 4 FDA reports)
HERPES ZOSTER ( 4 FDA reports)
LIP DRY ( 4 FDA reports)
MALAISE ( 4 FDA reports)
NECK PAIN ( 4 FDA reports)
RENAL FAILURE ( 4 FDA reports)
SINUSITIS ( 4 FDA reports)
SWELLING FACE ( 4 FDA reports)
VIRAL INFECTION ( 4 FDA reports)
ABASIA ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
BALANCE DISORDER ( 3 FDA reports)
BRADYARRHYTHMIA ( 3 FDA reports)
BURNING SENSATION ( 3 FDA reports)
CANDIDIASIS ( 3 FDA reports)
DIASTOLIC DYSFUNCTION ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
EATING DISORDER ( 3 FDA reports)
ELECTROLYTE IMBALANCE ( 3 FDA reports)
ENTERITIS ( 3 FDA reports)
FEELING ABNORMAL ( 3 FDA reports)
FLATULENCE ( 3 FDA reports)
GAIT DISTURBANCE ( 3 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
HYPOTHYROIDISM ( 3 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 3 FDA reports)
INFUSION SITE ERYTHEMA ( 3 FDA reports)
MIGRAINE ( 3 FDA reports)
MOBILITY DECREASED ( 3 FDA reports)
MUSCULAR WEAKNESS ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
OXYGEN SATURATION DECREASED ( 3 FDA reports)
PANIC ATTACK ( 3 FDA reports)
PULMONARY HYPERTENSION ( 3 FDA reports)
SKIN EXFOLIATION ( 3 FDA reports)
STRESS FRACTURE ( 3 FDA reports)
TENDONITIS ( 3 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
URTICARIA ( 3 FDA reports)
ABDOMINAL DISCOMFORT ( 2 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ACNE ( 2 FDA reports)
ALOPECIA ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
ASCITES ( 2 FDA reports)
ASTHMA EXERCISE INDUCED ( 2 FDA reports)
ATYPICAL FEMUR FRACTURE ( 2 FDA reports)
BACTERAEMIA ( 2 FDA reports)
BILIARY DILATATION ( 2 FDA reports)
BLOOD AMYLASE INCREASED ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 2 FDA reports)
BOWEL SOUNDS ABNORMAL ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
CATARACT ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
COLD SWEAT ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DIVERTICULITIS ( 2 FDA reports)
FAECES DISCOLOURED ( 2 FDA reports)
FEMUR FRACTURE ( 2 FDA reports)
FOOT FRACTURE ( 2 FDA reports)
GASTRIC DISORDER ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
GINGIVAL SWELLING ( 2 FDA reports)
GLOSSODYNIA ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HAEMORRHOIDS ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
IMPAIRED HEALING ( 2 FDA reports)
INFLAMMATION ( 2 FDA reports)
INTESTINAL POLYP ( 2 FDA reports)
JOINT SWELLING ( 2 FDA reports)
LIP SWELLING ( 2 FDA reports)
LIPASE INCREASED ( 2 FDA reports)
LOCAL SWELLING ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
MALABSORPTION ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
MOUTH ULCERATION ( 2 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
NEPHROLITHIASIS ( 2 FDA reports)
NERVE COMPRESSION ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
NIGHTMARE ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
OEDEMA MOUTH ( 2 FDA reports)
ORAL CANDIDIASIS ( 2 FDA reports)
OSTEOARTHRITIS ( 2 FDA reports)
PAIN IN JAW ( 2 FDA reports)
PANCREATIC PSEUDOCYST ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
RESPIRATORY TRACT INFECTION ( 2 FDA reports)
SCOTOMA ( 2 FDA reports)
SKIN FISSURES ( 2 FDA reports)
SKIN HYPERPIGMENTATION ( 2 FDA reports)
SKIN ULCER ( 2 FDA reports)
SLEEP DISORDER ( 2 FDA reports)
STRESS ( 2 FDA reports)
THIRST ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
TREMOR ( 2 FDA reports)
UPPER LIMB FRACTURE ( 2 FDA reports)
URINE OUTPUT DECREASED ( 2 FDA reports)
VAGINAL DISCHARGE ( 2 FDA reports)
VAGINAL INFECTION ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
WHEEZING ( 2 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
AGITATION ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANAL DISCOMFORT ( 1 FDA reports)
ANAL SPHINCTER ATONY ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANTISOCIAL BEHAVIOUR ( 1 FDA reports)
AORTIC DISORDER ( 1 FDA reports)
APPENDIX DISORDER ( 1 FDA reports)
APPETITE DISORDER ( 1 FDA reports)
APPLICATION SITE BURN ( 1 FDA reports)
APPLICATION SITE DISCOLOURATION ( 1 FDA reports)
APPLICATION SITE INFECTION ( 1 FDA reports)
APPLICATION SITE VESICLES ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ARTERITIS ( 1 FDA reports)
ARTHRITIS INFECTIVE ( 1 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 1 FDA reports)
ASOCIAL BEHAVIOUR ( 1 FDA reports)
AUTOIMMUNE THYROIDITIS ( 1 FDA reports)
BASAL CELL CARCINOMA ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BLADDER CANCER RECURRENT ( 1 FDA reports)
BLADDER PROLAPSE ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD TEST ABNORMAL ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BREAST CANCER METASTATIC ( 1 FDA reports)
BREAST DISORDER ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
BRONCHIECTASIS ( 1 FDA reports)
BURSA CALCIFICATION ( 1 FDA reports)
BURSITIS ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CARDIAC VALVE DISEASE ( 1 FDA reports)
CARPAL TUNNEL SYNDROME ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CHRONIC TONSILLITIS ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 1 FDA reports)
COCCYDYNIA ( 1 FDA reports)
COELIAC DISEASE ( 1 FDA reports)
COLOUR BLINDNESS ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
CORONARY ARTERY BYPASS ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
COSTOCHONDRITIS ( 1 FDA reports)
COUGH ( 1 FDA reports)
CRYING ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
CYSTITIS NONINFECTIVE ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DERMATITIS CONTACT ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
EAR INFECTION ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
EXPIRED DRUG ADMINISTERED ( 1 FDA reports)
EXPOSURE TO COMMUNICABLE DISEASE ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
FACIAL BONES FRACTURE ( 1 FDA reports)
FACIAL PAIN ( 1 FDA reports)
FEAR ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
FOREIGN BODY ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 1 FDA reports)
GINGIVAL DISCOLOURATION ( 1 FDA reports)
GRAVITATIONAL OEDEMA ( 1 FDA reports)
GROWTH ACCELERATED ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HUMAN BITE ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYSTERECTOMY ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INCREASED APPETITE ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INFUSION SITE PAIN ( 1 FDA reports)
INFUSION SITE PRURITUS ( 1 FDA reports)
INFUSION SITE SWELLING ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JOINT EFFUSION ( 1 FDA reports)
KERATITIS ( 1 FDA reports)
KYPHOSIS ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LOWER LIMB FRACTURE ( 1 FDA reports)
LUMBAR SPINAL STENOSIS ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LYME DISEASE ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MANIA ( 1 FDA reports)
MENISCUS LESION ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
METASTASES TO LYMPH NODES ( 1 FDA reports)
METASTATIC NEOPLASM ( 1 FDA reports)
MITRAL VALVE PROLAPSE ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NEUROPATHIC PAIN ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
OBSTRUCTIVE UROPATHY ( 1 FDA reports)
OCCULT BLOOD POSITIVE ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
ORAL HERPES ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OVARIAN CANCER ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 1 FDA reports)
PAROTID GLAND ENLARGEMENT ( 1 FDA reports)
PERICARDIAL RUB ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
POLYARTHRITIS ( 1 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 1 FDA reports)
POST HERPETIC NEURALGIA ( 1 FDA reports)
PREMENSTRUAL SYNDROME ( 1 FDA reports)
PROCTALGIA ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL PAIN ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RETINAL DETACHMENT ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
ROTATOR CUFF SYNDROME ( 1 FDA reports)
SALMONELLOSIS ( 1 FDA reports)
SCAR ( 1 FDA reports)
SCREAMING ( 1 FDA reports)
SKIN DEPIGMENTATION ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SLUGGISHNESS ( 1 FDA reports)
SPINAL CORD NEOPLASM ( 1 FDA reports)
SPLENIC CYST ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SYNOVIAL CYST ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TENDON CALCIFICATION ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TOOTH FRACTURE ( 1 FDA reports)
TOOTH INFECTION ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 1 FDA reports)
URINE COLOUR ABNORMAL ( 1 FDA reports)
VAGINAL ODOUR ( 1 FDA reports)
VASCULAR CALCIFICATION ( 1 FDA reports)
VEIN DISORDER ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VITREOUS HAEMORRHAGE ( 1 FDA reports)
WALKING AID USER ( 1 FDA reports)

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