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

NAUSEA ( 32 FDA reports)
VOMITING ( 27 FDA reports)
INSOMNIA ( 21 FDA reports)
PAIN ( 21 FDA reports)
DEPRESSION ( 20 FDA reports)
DIARRHOEA ( 20 FDA reports)
DRUG DEPENDENCE ( 19 FDA reports)
HEADACHE ( 18 FDA reports)
HYPERHIDROSIS ( 18 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 17 FDA reports)
NERVOUSNESS ( 16 FDA reports)
DRUG INEFFECTIVE ( 15 FDA reports)
IRRITABILITY ( 15 FDA reports)
TREMOR ( 15 FDA reports)
ANXIETY ( 13 FDA reports)
CHOLECYSTITIS CHRONIC ( 13 FDA reports)
ABDOMINAL PAIN ( 11 FDA reports)
SINUSITIS ( 11 FDA reports)
CHOLELITHIASIS ( 10 FDA reports)
EMOTIONAL DISTRESS ( 10 FDA reports)
HYPERTENSION ( 10 FDA reports)
BRONCHITIS ACUTE ( 9 FDA reports)
PYREXIA ( 9 FDA reports)
ASTHENIA ( 8 FDA reports)
CEREBROVASCULAR ACCIDENT ( 8 FDA reports)
DIZZINESS ( 8 FDA reports)
VISION BLURRED ( 8 FDA reports)
DRUG ABUSER ( 7 FDA reports)
DYSPNOEA ( 7 FDA reports)
FLANK PAIN ( 7 FDA reports)
MAJOR DEPRESSION ( 7 FDA reports)
SUICIDAL IDEATION ( 7 FDA reports)
TREATMENT NONCOMPLIANCE ( 7 FDA reports)
VISUAL DISTURBANCE ( 7 FDA reports)
ABDOMINAL HERNIA ( 6 FDA reports)
ABDOMINAL PAIN UPPER ( 6 FDA reports)
CARDIAC DISORDER ( 6 FDA reports)
DEEP VEIN THROMBOSIS ( 6 FDA reports)
HYPOACUSIS ( 6 FDA reports)
INJURY ( 6 FDA reports)
PULMONARY EMBOLISM ( 6 FDA reports)
WEIGHT INCREASED ( 6 FDA reports)
BACK PAIN ( 5 FDA reports)
BRONCHITIS ( 5 FDA reports)
CONTUSION ( 5 FDA reports)
COUGH ( 5 FDA reports)
FATIGUE ( 5 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 5 FDA reports)
HEPATITIS C ( 5 FDA reports)
HYPOTENSION ( 5 FDA reports)
NECK PAIN ( 5 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 5 FDA reports)
PULMONARY HYPERTENSION ( 5 FDA reports)
ROAD TRAFFIC ACCIDENT ( 5 FDA reports)
ADVERSE DRUG REACTION ( 4 FDA reports)
ARTHRALGIA ( 4 FDA reports)
CERVIX CARCINOMA RECURRENT ( 4 FDA reports)
INCREASED TENDENCY TO BRUISE ( 4 FDA reports)
LEGAL PROBLEM ( 4 FDA reports)
LEUKOCYTOSIS ( 4 FDA reports)
MITRAL VALVE PROLAPSE ( 4 FDA reports)
MOBILITY DECREASED ( 4 FDA reports)
MUSCLE CRAMP ( 4 FDA reports)
MUSCLE SPASMS ( 4 FDA reports)
OEDEMA PERIPHERAL ( 4 FDA reports)
OLIGOHYDRAMNIOS ( 4 FDA reports)
PARAESTHESIA ( 4 FDA reports)
PULMONARY CONGESTION ( 4 FDA reports)
RASH ( 4 FDA reports)
SPINAL COLUMN STENOSIS ( 4 FDA reports)
THROMBOCYTOSIS ( 4 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 4 FDA reports)
ANAEMIA ( 3 FDA reports)
ANAPHYLACTIC SHOCK ( 3 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 3 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
CARDIAC MURMUR ( 3 FDA reports)
CARDIOMEGALY ( 3 FDA reports)
CEREBRAL INFARCTION ( 3 FDA reports)
CHEST PAIN ( 3 FDA reports)
CHILLS ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
DERMATITIS EXFOLIATIVE ( 3 FDA reports)
DIASTOLIC DYSFUNCTION ( 3 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
FEAR ( 3 FDA reports)
FEELING ABNORMAL ( 3 FDA reports)
HAEMOCHROMATOSIS ( 3 FDA reports)
HEPATIC STEATOSIS ( 3 FDA reports)
INADEQUATE ANALGESIA ( 3 FDA reports)
INCISIONAL HERNIA ( 3 FDA reports)
INCREASED BRONCHIAL SECRETION ( 3 FDA reports)
PALPITATIONS ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
SINUS ARRHYTHMIA ( 3 FDA reports)
TACHYCARDIA ( 3 FDA reports)
WEIGHT DECREASED ( 3 FDA reports)
ABNORMAL FAECES ( 2 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 2 FDA reports)
ARTHROPATHY ( 2 FDA reports)
ASCITES ( 2 FDA reports)
ATELECTASIS ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST NEONATAL ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
CHOLECYSTITIS ( 2 FDA reports)
CHORIOAMNIONITIS ( 2 FDA reports)
CORONARY ARTERY DISEASE ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DECREASED INTEREST ( 2 FDA reports)
DEMYELINATION ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
EMBOLIC STROKE ( 2 FDA reports)
EXOSTOSIS ( 2 FDA reports)
FALL ( 2 FDA reports)
FEELING HOT AND COLD ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HEPATIC FIBROSIS ( 2 FDA reports)
HEPATOCELLULAR DAMAGE ( 2 FDA reports)
HERNIA ( 2 FDA reports)
HYPERCOAGULATION ( 2 FDA reports)
HYPERLIPIDAEMIA ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
INJECTION SITE PAIN ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
IRON DEFICIENCY ANAEMIA ( 2 FDA reports)
LIPODYSTROPHY ACQUIRED ( 2 FDA reports)
LIPOSUCTION ( 2 FDA reports)
LUNG INFILTRATION ( 2 FDA reports)
MENTAL DISORDER ( 2 FDA reports)
MITRAL VALVE INCOMPETENCE ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
NIGHT SWEATS ( 2 FDA reports)
NOCTURIA ( 2 FDA reports)
NOCTURNAL DYSPNOEA ( 2 FDA reports)
OBESITY ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PANIC ATTACK ( 2 FDA reports)
PARONYCHIA ( 2 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 2 FDA reports)
PLACENTAL DISORDER ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
PNEUMOTHORAX ( 2 FDA reports)
PULMONARY HAEMORRHAGE ( 2 FDA reports)
PULMONARY INFARCTION ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
RENAL VEIN THROMBOSIS ( 2 FDA reports)
RIGHT ATRIAL DILATATION ( 2 FDA reports)
SEXUAL DYSFUNCTION ( 2 FDA reports)
SINUS DISORDER ( 2 FDA reports)
SINUS POLYP ( 2 FDA reports)
SKIN LESION ( 2 FDA reports)
SPINAL OSTEOARTHRITIS ( 2 FDA reports)
SPONDYLOSIS ( 2 FDA reports)
TENDERNESS ( 2 FDA reports)
THYROID NEOPLASM ( 2 FDA reports)
VERTIGO POSITIONAL ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ACCELERATED IDIOVENTRICULAR RHYTHM ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ALCOHOLISM ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 1 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 1 FDA reports)
APGAR SCORE LOW ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BILIARY DYSKINESIA ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD CREATINE ABNORMAL ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BRONCHIOLITIS ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 1 FDA reports)
CEREBRAL DISORDER ( 1 FDA reports)
CERVIX CARCINOMA ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHOLECYSTITIS ACUTE ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
CYST ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DIARRHOEA INFECTIOUS ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
DYSTROPHIC CALCIFICATION ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
EXERCISE TOLERANCE DECREASED ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FAT INTOLERANCE ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FOLLICULAR THYROID CANCER ( 1 FDA reports)
FOOD INTOLERANCE ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GALLBLADDER INJURY ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROINTESTINAL DISORDER POSTOPERATIVE ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 1 FDA reports)
GOITRE ( 1 FDA reports)
HAEMATOCRIT INCREASED ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERTENSIVE EMERGENCY ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOAESTHESIA FACIAL ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
INJECTION SITE JOINT PAIN ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
JOINT STIFFNESS ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
KIDNEY MALFORMATION ( 1 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
LIP OEDEMA ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOW CARDIAC OUTPUT SYNDROME ( 1 FDA reports)
LOWER LIMB DEFORMITY ( 1 FDA reports)
LOWER LIMB FRACTURE ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MARITAL PROBLEM ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MULTI-ORGAN DISORDER ( 1 FDA reports)
MULTIPLE FRACTURES ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PAROSMIA ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
POISONING ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROSTATIC DISORDER ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PSYCHOLOGICAL TRAUMA ( 1 FDA reports)
QRS AXIS ABNORMAL ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RASH VESICULAR ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 1 FDA reports)
SARCOIDOSIS ( 1 FDA reports)
SKIN CHAPPED ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN IRRITATION ( 1 FDA reports)
SKIN WARM ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
SURGERY ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
TOE OPERATION ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
UNEQUAL LEG LENGTH ACQUIRED ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VENTRICULAR DYSKINESIA ( 1 FDA reports)
VENTRICULAR FAILURE ( 1 FDA reports)
VICTIM OF CRIME ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WITHDRAWAL SYNDROME ( 1 FDA reports)

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