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

DRUG INEFFECTIVE ( 21 FDA reports)
NAUSEA ( 21 FDA reports)
HEADACHE ( 17 FDA reports)
INSOMNIA ( 16 FDA reports)
FATIGUE ( 15 FDA reports)
PRODUCT QUALITY ISSUE ( 14 FDA reports)
ANXIETY ( 13 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 13 FDA reports)
SOMNOLENCE ( 12 FDA reports)
ABNORMAL BEHAVIOUR ( 10 FDA reports)
DEPRESSION ( 10 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 10 FDA reports)
WEIGHT DECREASED ( 10 FDA reports)
DIZZINESS ( 9 FDA reports)
DYSPNOEA ( 9 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 9 FDA reports)
DECREASED APPETITE ( 8 FDA reports)
DRUG EFFECT DECREASED ( 8 FDA reports)
FEELING ABNORMAL ( 8 FDA reports)
IRRITABILITY ( 8 FDA reports)
TREMOR ( 8 FDA reports)
DEHYDRATION ( 7 FDA reports)
HEART RATE INCREASED ( 7 FDA reports)
PYREXIA ( 7 FDA reports)
VOMITING ( 7 FDA reports)
BLOOD PRESSURE INCREASED ( 6 FDA reports)
CHEST PAIN ( 6 FDA reports)
CONFUSIONAL STATE ( 6 FDA reports)
CONVULSION ( 6 FDA reports)
PALPITATIONS ( 6 FDA reports)
TACHYCARDIA ( 6 FDA reports)
ABDOMINAL PAIN UPPER ( 5 FDA reports)
AGGRESSION ( 5 FDA reports)
CHEST DISCOMFORT ( 5 FDA reports)
CONDITION AGGRAVATED ( 5 FDA reports)
DISTURBANCE IN ATTENTION ( 5 FDA reports)
DRUG INTERACTION ( 5 FDA reports)
DRY MOUTH ( 5 FDA reports)
HYPERTENSION ( 5 FDA reports)
MEDICATION ERROR ( 5 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 5 FDA reports)
TIC ( 5 FDA reports)
AGITATION ( 4 FDA reports)
ANGER ( 4 FDA reports)
ANOREXIA ( 4 FDA reports)
COGNITIVE DISORDER ( 4 FDA reports)
CONGENITAL HYPOTHYROIDISM ( 4 FDA reports)
CONSTIPATION ( 4 FDA reports)
CRYING ( 4 FDA reports)
DEVELOPMENTAL COORDINATION DISORDER ( 4 FDA reports)
DIFFICULTY IN WALKING ( 4 FDA reports)
EDUCATIONAL PROBLEM ( 4 FDA reports)
FALL ( 4 FDA reports)
FLUSHING ( 4 FDA reports)
HALLUCINATION, VISUAL ( 4 FDA reports)
HYPERSENSITIVITY ( 4 FDA reports)
MIGRAINE ( 4 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 4 FDA reports)
VISION BLURRED ( 4 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 3 FDA reports)
ASTHENIA ( 3 FDA reports)
CARDIOMEGALY ( 3 FDA reports)
CONGENITAL PYLORIC STENOSIS ( 3 FDA reports)
COORDINATION ABNORMAL ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
DRUG ABUSER ( 3 FDA reports)
DRUG DEPENDENCE ( 3 FDA reports)
HALLUCINATION ( 3 FDA reports)
HYPERHIDROSIS ( 3 FDA reports)
INABILITY TO CRAWL ( 3 FDA reports)
INCORRECT DOSE ADMINISTERED ( 3 FDA reports)
MOOD ALTERED ( 3 FDA reports)
MUSCLE TWITCHING ( 3 FDA reports)
MUSCULAR WEAKNESS ( 3 FDA reports)
MYDRIASIS ( 3 FDA reports)
PAIN ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
PARANOIA ( 3 FDA reports)
PRE-ECLAMPSIA ( 3 FDA reports)
PRESCRIBED OVERDOSE ( 3 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 3 FDA reports)
RESTLESSNESS ( 3 FDA reports)
SPEECH DISORDER ( 3 FDA reports)
STOMACH DISCOMFORT ( 3 FDA reports)
SUICIDAL IDEATION ( 3 FDA reports)
VERTIGO ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ABORTION SPONTANEOUS ( 2 FDA reports)
ACCIDENTAL EXPOSURE ( 2 FDA reports)
ACNE ( 2 FDA reports)
ALOPECIA ( 2 FDA reports)
ANAPHYLACTIC SHOCK ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
CAESAREAN SECTION ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
COMPLETED SUICIDE ( 2 FDA reports)
COUGH ( 2 FDA reports)
DENTAL CARIES ( 2 FDA reports)
DILATATION VENTRICULAR ( 2 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 2 FDA reports)
DIZZINESS POSTURAL ( 2 FDA reports)
DRUG INTOLERANCE ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
DYSTONIA ( 2 FDA reports)
EMOTIONAL DISORDER ( 2 FDA reports)
EPIGASTRIC DISCOMFORT ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
EYE DISORDER ( 2 FDA reports)
FEAR ( 2 FDA reports)
GASTRIC DISORDER ( 2 FDA reports)
HALLUCINATION, AUDITORY ( 2 FDA reports)
HOMICIDAL IDEATION ( 2 FDA reports)
HOSTILITY ( 2 FDA reports)
HYPERSOMNIA ( 2 FDA reports)
HYPERVENTILATION ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
IMPULSIVE BEHAVIOUR ( 2 FDA reports)
INCREASED APPETITE ( 2 FDA reports)
INDUCED LABOUR ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
INFUSION SITE REACTION ( 2 FDA reports)
LIBIDO INCREASED ( 2 FDA reports)
MAJOR DEPRESSION ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
MOBILITY DECREASED ( 2 FDA reports)
MOOD SWINGS ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
NERVOUSNESS ( 2 FDA reports)
PANIC ATTACK ( 2 FDA reports)
PERFORMANCE STATUS DECREASED ( 2 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PRIAPISM ( 2 FDA reports)
PRODUCT MEASURED POTENCY ISSUE ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PULMONARY HYPERTENSION ( 2 FDA reports)
RASH PRURITIC ( 2 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 2 FDA reports)
SPINAL CORD DISORDER ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
SUICIDE ATTEMPT ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
TARDIVE DYSKINESIA ( 2 FDA reports)
THINKING ABNORMAL ( 2 FDA reports)
TINNITUS ( 2 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ALCOHOL PROBLEM ( 1 FDA reports)
ALLERGY TO ANIMAL ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANGIOGRAM ( 1 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 1 FDA reports)
APATHY ( 1 FDA reports)
APPETITE DISORDER ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTERIOSPASM CORONARY ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ATRIAL SEPTAL DEFECT ( 1 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 1 FDA reports)
AUTISM ( 1 FDA reports)
BACK INJURY ( 1 FDA reports)
BANKRUPTCY ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BLEPHAROSPASM ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BONE MARROW DISORDER ( 1 FDA reports)
BUNDLE BRANCH BLOCK ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CARDIAC HYPERTROPHY ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHANGE OF BOWEL HABIT ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CHOLESTEROSIS ( 1 FDA reports)
CONCUSSION ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
DECREASED INTEREST ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DENTAL PLAQUE ( 1 FDA reports)
DEPENDENCE ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DEVELOPMENTAL DELAY ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIABETIC KETOACIDOSIS ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DISSOCIATION ( 1 FDA reports)
DIVORCED ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
EAR INFECTION ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
EATING DISORDER SYMPTOM ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
ELEVATED MOOD ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EYE ALLERGY ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
FEELING HOT AND COLD ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FEELING OF RELAXATION ( 1 FDA reports)
FLAT AFFECT ( 1 FDA reports)
FLIGHT OF IDEAS ( 1 FDA reports)
FRUSTRATION ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GENERALISED ANXIETY DISORDER ( 1 FDA reports)
GINGIVAL RECESSION ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
GRANDIOSITY ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEART RATE ABNORMAL ( 1 FDA reports)
HEAT EXHAUSTION ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOMANIA ( 1 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INJURY ASPHYXIATION ( 1 FDA reports)
INTENTIONAL MISUSE ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
LEARNING DISORDER ( 1 FDA reports)
LEGAL PROBLEM ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LIVEDO RETICULARIS ( 1 FDA reports)
LOSS OF EMPLOYMENT ( 1 FDA reports)
LOSS OF LIBIDO ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
MANIA ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
MITRAL VALVE DISEASE ( 1 FDA reports)
MUCOUS STOOLS ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MUSCLE STRAIN ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
NARCOLEPSY ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 1 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERSONALITY CHANGE ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COUNTERFEIT ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PHYSICAL ASSAULT ( 1 FDA reports)
POSITIVE ROMBERGISM ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PREMATURE LABOUR ( 1 FDA reports)
PRODUCT FORMULATION ISSUE ( 1 FDA reports)
PRODUCT PACKAGING ISSUE ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PYLORIC STENOSIS ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RENAL PAIN ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RHINITIS ALLERGIC ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SALIVARY HYPERSECRETION ( 1 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 1 FDA reports)
SELF MUTILATION ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SLEEP PARALYSIS ( 1 FDA reports)
STRESS ( 1 FDA reports)
STRESS FRACTURE ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUDDEN CARDIAC DEATH ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
SUSPICIOUSNESS ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
TACHYPHRENIA ( 1 FDA reports)
TEARFULNESS ( 1 FDA reports)
TESTICULAR PAIN ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THIRST ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
THYROID DISORDER ( 1 FDA reports)
TIBIA FRACTURE ( 1 FDA reports)
TONGUE BITING ( 1 FDA reports)
TOOTH DISCOLOURATION ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
UNEXPECTED THERAPEUTIC DRUG EFFECT ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
UVEITIS ( 1 FDA reports)
VENTRICLE RUPTURE ( 1 FDA reports)
VICTIM OF CRIME ( 1 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VITAMIN D DECREASED ( 1 FDA reports)
WEIGHT GAIN POOR ( 1 FDA reports)
WOLFF-PARKINSON-WHITE SYNDROME ( 1 FDA reports)
YAWNING ( 1 FDA reports)

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