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

PAIN ( 8 FDA reports)
HEADACHE ( 7 FDA reports)
PYREXIA ( 6 FDA reports)
SWELLING ( 6 FDA reports)
VIRAL INFECTION ( 6 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
ASTHENIA ( 5 FDA reports)
FATIGUE ( 5 FDA reports)
GAIT DISTURBANCE ( 5 FDA reports)
MALAISE ( 5 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 5 FDA reports)
TOOTH INFECTION ( 5 FDA reports)
APHTHOUS STOMATITIS ( 4 FDA reports)
BLOOD BILIRUBIN INCREASED ( 4 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 4 FDA reports)
COUGH ( 4 FDA reports)
DIARRHOEA INFECTIOUS ( 4 FDA reports)
EATING DISORDER ( 4 FDA reports)
GASTROENTERITIS NOROVIRUS ( 4 FDA reports)
HEAD INJURY ( 4 FDA reports)
HEARING IMPAIRED ( 4 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 4 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 4 FDA reports)
MYALGIA ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
OSTEOPOROSIS ( 4 FDA reports)
PAIN IN EXTREMITY ( 4 FDA reports)
PHARYNGITIS ( 4 FDA reports)
STOMATITIS ( 4 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 4 FDA reports)
ABNORMAL DREAMS ( 3 FDA reports)
ANXIETY ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
BLOOD GLUCOSE INCREASED ( 3 FDA reports)
CHEST DISCOMFORT ( 3 FDA reports)
CONSTIPATION ( 3 FDA reports)
CROHN'S DISEASE ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
FIBROMYALGIA ( 3 FDA reports)
HEART RATE DECREASED ( 3 FDA reports)
MEMORY IMPAIRMENT ( 3 FDA reports)
MUSCLE SPASMS ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
POLLAKIURIA ( 3 FDA reports)
ACNE ( 2 FDA reports)
AGGRESSION ( 2 FDA reports)
ALCOHOL INTERACTION ( 2 FDA reports)
ALCOHOL POISONING ( 2 FDA reports)
ALOPECIA ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BODY HEIGHT DECREASED ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
CARBON DIOXIDE DECREASED ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CARDIAC FLUTTER ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
CHROMATURIA ( 2 FDA reports)
CONJUNCTIVITIS ( 2 FDA reports)
CORONARY ARTERY BYPASS ( 2 FDA reports)
CRYING ( 2 FDA reports)
DERMATITIS ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DISSOCIATION ( 2 FDA reports)
DISTURBANCE IN ATTENTION ( 2 FDA reports)
DROOLING ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
DRY SKIN ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
EMOTIONAL DISORDER ( 2 FDA reports)
ERUCTATION ( 2 FDA reports)
EUPHORIC MOOD ( 2 FDA reports)
EYE PAIN ( 2 FDA reports)
FALL ( 2 FDA reports)
FEAR ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
GASTROINTESTINAL PAIN ( 2 FDA reports)
GENERALISED ANXIETY DISORDER ( 2 FDA reports)
GINGIVAL BLEEDING ( 2 FDA reports)
GINGIVITIS ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HOT FLUSH ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
ILL-DEFINED DISORDER ( 2 FDA reports)
IMMUNE SYSTEM DISORDER ( 2 FDA reports)
IMPAIRED DRIVING ABILITY ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
INTESTINAL OBSTRUCTION ( 2 FDA reports)
IRRITABILITY ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
LIBIDO DECREASED ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 2 FDA reports)
MEAN CELL VOLUME INCREASED ( 2 FDA reports)
MENSTRUAL DISORDER ( 2 FDA reports)
MENTAL IMPAIRMENT ( 2 FDA reports)
MIGRAINE ( 2 FDA reports)
MOOD SWINGS ( 2 FDA reports)
MOTOR DYSFUNCTION ( 2 FDA reports)
MUSCLE TWITCHING ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
ORAL PUSTULE ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
PANIC ATTACK ( 2 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 2 FDA reports)
PHOTOSENSITIVITY REACTION ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PSYCHIATRIC SYMPTOM ( 2 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 2 FDA reports)
PSYCHOTIC DISORDER ( 2 FDA reports)
RESTLESS LEGS SYNDROME ( 2 FDA reports)
RHINORRHOEA ( 2 FDA reports)
SCHIZOPHRENIA ( 2 FDA reports)
SEROTONIN SYNDROME ( 2 FDA reports)
SKIN LESION ( 2 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 2 FDA reports)
STENT-GRAFT MALFUNCTION ( 2 FDA reports)
SUICIDAL IDEATION ( 2 FDA reports)
THINKING ABNORMAL ( 2 FDA reports)
THIRST ( 2 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 2 FDA reports)
TUNNEL VISION ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
VISUAL FIELD DEFECT ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ANHEDONIA ( 1 FDA reports)
APHONIA ( 1 FDA reports)
ARTERIOSPASM CORONARY ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 1 FDA reports)
CHANGE OF BOWEL HABIT ( 1 FDA reports)
CHOLECYSTITIS CHRONIC ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DEVICE MALFUNCTION ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FOREIGN BODY ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
INJURY ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NERVE INJURY ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
ORGAN FAILURE ( 1 FDA reports)
PENILE PAIN ( 1 FDA reports)
POISONING ( 1 FDA reports)
POLYDIPSIA ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
RASH ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
TOBACCO USER ( 1 FDA reports)
TRI-IODOTHYRONINE INCREASED ( 1 FDA reports)
VOMITING ( 1 FDA reports)

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