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ANXIETY ( 35 FDA reports)
DEPRESSION ( 27 FDA reports)
NAUSEA ( 25 FDA reports)
MENTAL IMPAIRMENT ( 17 FDA reports)
ABNORMAL BEHAVIOUR ( 16 FDA reports)
HOMICIDAL IDEATION ( 16 FDA reports)
PAIN ( 16 FDA reports)
HEADACHE ( 15 FDA reports)
SELF-INJURIOUS IDEATION ( 14 FDA reports)
AGGRESSION ( 11 FDA reports)
DIZZINESS ( 11 FDA reports)
DRUG INEFFECTIVE ( 11 FDA reports)
FALL ( 11 FDA reports)
FATIGUE ( 11 FDA reports)
OEDEMA PERIPHERAL ( 11 FDA reports)
SOMNOLENCE ( 11 FDA reports)
VOMITING ( 11 FDA reports)
DRUG DEPENDENCE ( 10 FDA reports)
HYPOAESTHESIA ( 10 FDA reports)
NERVOUSNESS ( 10 FDA reports)
ASTHENIA ( 9 FDA reports)
DRUG INTERACTION ( 9 FDA reports)
DYSPNOEA ( 9 FDA reports)
INTENTIONAL OVERDOSE ( 9 FDA reports)
FEELING ABNORMAL ( 8 FDA reports)
HYPERSOMNIA ( 8 FDA reports)
SUICIDAL IDEATION ( 8 FDA reports)
SUICIDE ATTEMPT ( 8 FDA reports)
WEIGHT INCREASED ( 8 FDA reports)
ABDOMINAL DISTENSION ( 7 FDA reports)
ALOPECIA ( 7 FDA reports)
BURNING SENSATION ( 7 FDA reports)
DIARRHOEA ( 7 FDA reports)
GAIT DISTURBANCE ( 7 FDA reports)
IMPAIRED DRIVING ABILITY ( 7 FDA reports)
MEMORY IMPAIRMENT ( 7 FDA reports)
RASH ( 7 FDA reports)
ABNORMAL DREAMS ( 6 FDA reports)
CONVULSION ( 6 FDA reports)
DRUG DOSE OMISSION ( 6 FDA reports)
DYSARTHRIA ( 6 FDA reports)
INSOMNIA ( 6 FDA reports)
IRRITABILITY ( 6 FDA reports)
LOSS OF CONSCIOUSNESS ( 6 FDA reports)
MALAISE ( 6 FDA reports)
OVERDOSE ( 6 FDA reports)
PAIN IN EXTREMITY ( 6 FDA reports)
PARAESTHESIA ( 6 FDA reports)
ROAD TRAFFIC ACCIDENT ( 6 FDA reports)
STRESS ( 6 FDA reports)
ALCOHOL USE ( 5 FDA reports)
AMNESIA ( 5 FDA reports)
BLOOD MAGNESIUM INCREASED ( 5 FDA reports)
CONSTIPATION ( 5 FDA reports)
COUGH ( 5 FDA reports)
DECREASED APPETITE ( 5 FDA reports)
DEHYDRATION ( 5 FDA reports)
DISTURBANCE IN ATTENTION ( 5 FDA reports)
MEDICATION ERROR ( 5 FDA reports)
MUSCLE SPASMS ( 5 FDA reports)
MUSCLE TWITCHING ( 5 FDA reports)
MUSCULAR WEAKNESS ( 5 FDA reports)
MYALGIA ( 5 FDA reports)
PSYCHOTIC DISORDER ( 5 FDA reports)
SUBSTANCE ABUSE ( 5 FDA reports)
ABASIA ( 4 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
ARTHRALGIA ( 4 FDA reports)
BLISTER ( 4 FDA reports)
CHEST DISCOMFORT ( 4 FDA reports)
CLAUSTROPHOBIA ( 4 FDA reports)
COMPLETED SUICIDE ( 4 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
CYANOSIS ( 4 FDA reports)
DENTAL CARIES ( 4 FDA reports)
DISORIENTATION ( 4 FDA reports)
HYPERTENSION ( 4 FDA reports)
MENTAL DISORDER ( 4 FDA reports)
MOBILITY DECREASED ( 4 FDA reports)
PNEUMONIA ( 4 FDA reports)
RENAL FAILURE ( 4 FDA reports)
RESTLESSNESS ( 4 FDA reports)
SPEECH DISORDER ( 4 FDA reports)
TREATMENT NONCOMPLIANCE ( 4 FDA reports)
VISUAL DISTURBANCE ( 4 FDA reports)
VISUAL IMPAIRMENT ( 4 FDA reports)
ANGER ( 3 FDA reports)
BLOOD PRESSURE ABNORMAL ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
CYSTITIS ( 3 FDA reports)
DEATH ( 3 FDA reports)
DELIRIUM ( 3 FDA reports)
DENTAL NECROSIS ( 3 FDA reports)
FACIAL PALSY ( 3 FDA reports)
FEELING HOT ( 3 FDA reports)
GASTRIC ULCER ( 3 FDA reports)
HALLUCINATION, VISUAL ( 3 FDA reports)
HYPERSENSITIVITY ( 3 FDA reports)
HYPOGLYCAEMIA ( 3 FDA reports)
HYPOPHAGIA ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
IMPAIRED HEALING ( 3 FDA reports)
INABILITY TO CRAWL ( 3 FDA reports)
INCORRECT DOSE ADMINISTERED ( 3 FDA reports)
INFECTION ( 3 FDA reports)
INTENTIONAL SELF-INJURY ( 3 FDA reports)
NECK PAIN ( 3 FDA reports)
NEURALGIA ( 3 FDA reports)
OFF LABEL USE ( 3 FDA reports)
ORAL HERPES ( 3 FDA reports)
PANIC ATTACK ( 3 FDA reports)
SYNCOPE ( 3 FDA reports)
TOBACCO USER ( 3 FDA reports)
TRANSAMINASES INCREASED ( 3 FDA reports)
TREMOR ( 3 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 3 FDA reports)
WRONG DRUG ADMINISTERED ( 3 FDA reports)
ABORTION INDUCED ( 2 FDA reports)
ACUTE PSYCHOSIS ( 2 FDA reports)
ADVERSE EVENT ( 2 FDA reports)
AGITATION ( 2 FDA reports)
AMENORRHOEA ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
ARTHROPATHY ( 2 FDA reports)
ATAXIA ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD CREATININE ABNORMAL ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BONE PAIN ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 2 FDA reports)
CEREBRAL INFARCTION ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
COAGULOPATHY ( 2 FDA reports)
COLITIS COLLAGENOUS ( 2 FDA reports)
COMA ( 2 FDA reports)
CONCUSSION ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
CROHN'S DISEASE ( 2 FDA reports)
CRYING ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 2 FDA reports)
DRUG ABUSER ( 2 FDA reports)
DRUG DIVERSION ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
DRUG TOLERANCE ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
EXOSTOSIS ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
FRACTURED COCCYX ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
GINGIVAL ERYTHEMA ( 2 FDA reports)
HAEMORRHOIDS ( 2 FDA reports)
HEMIANOPIA HOMONYMOUS ( 2 FDA reports)
HICCUPS ( 2 FDA reports)
HYPERPHAGIA ( 2 FDA reports)
IMPAIRED WORK ABILITY ( 2 FDA reports)
IMPATIENCE ( 2 FDA reports)
INADEQUATE ANALGESIA ( 2 FDA reports)
INCREASED APPETITE ( 2 FDA reports)
INJECTION SITE PAIN ( 2 FDA reports)
INTENTIONAL DRUG MISUSE ( 2 FDA reports)
MENINGIOMA ( 2 FDA reports)
MOOD ALTERED ( 2 FDA reports)
MOUTH ULCERATION ( 2 FDA reports)
NICOTINE DEPENDENCE ( 2 FDA reports)
OBESITY ( 2 FDA reports)
OEDEMA MOUTH ( 2 FDA reports)
ORAL PAIN ( 2 FDA reports)
OSTEOMYELITIS ( 2 FDA reports)
OSTEONECROSIS OF JAW ( 2 FDA reports)
PAIN IN JAW ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 2 FDA reports)
POOR QUALITY SLEEP ( 2 FDA reports)
PRESYNCOPE ( 2 FDA reports)
PRIMARY SEQUESTRUM ( 2 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 2 FDA reports)
PSORIASIS ( 2 FDA reports)
PSYCHIATRIC SYMPTOM ( 2 FDA reports)
PYELONEPHRITIS ( 2 FDA reports)
RADIUS FRACTURE ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
SALIVA ALTERED ( 2 FDA reports)
SCHIZOPHRENIA ( 2 FDA reports)
SCREAMING ( 2 FDA reports)
SECRETION DISCHARGE ( 2 FDA reports)
SEDATION ( 2 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 2 FDA reports)
SKIN LESION ( 2 FDA reports)
SLEEP DISORDER ( 2 FDA reports)
SOMNAMBULISM ( 2 FDA reports)
SWELLING ( 2 FDA reports)
THROAT IRRITATION ( 2 FDA reports)
TOOTH ABSCESS ( 2 FDA reports)
TOOTH FRACTURE ( 2 FDA reports)
TOOTH INFECTION ( 2 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABDOMINAL RIGIDITY ( 1 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
ADNEXA UTERI MASS ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
AMPHETAMINES POSITIVE ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANEURYSM ( 1 FDA reports)
ANKLE FRACTURE ( 1 FDA reports)
ANURIA ( 1 FDA reports)
APATHY ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
APPLICATION SITE ERYTHEMA ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ASPIRATION BRONCHIAL ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
AUDIOGRAM ABNORMAL ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD PROLACTIN INCREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BONE MARROW TRANSPLANT ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRADYCARDIA FOETAL ( 1 FDA reports)
BRAIN DAMAGE ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BRONCHITIS CHRONIC ( 1 FDA reports)
BRUXISM ( 1 FDA reports)
CAPSULE PHYSICAL ISSUE ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CELL DEATH ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
DEAFNESS BILATERAL ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DEPERSONALISATION ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DEVICE EXPULSION ( 1 FDA reports)
DIET REFUSAL ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISLOCATION OF VERTEBRA ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
ENDOTRACHEAL INTUBATION ( 1 FDA reports)
ENERGY INCREASED ( 1 FDA reports)
EPIGASTRIC DISCOMFORT ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
EXPIRED DRUG ADMINISTERED ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EXTRUSION OF DEVICE ( 1 FDA reports)
EYE INFECTION ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
FEAR ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
FRUSTRATION ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GAS POISONING ( 1 FDA reports)
GASTROENTERITIS VIRAL ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HAIR TEXTURE ABNORMAL ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERPROLACTINAEMIA ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 1 FDA reports)
INCREASED BRONCHIAL SECRETION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INHIBITORY DRUG INTERACTION ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE NODULE ( 1 FDA reports)
INJURY ( 1 FDA reports)
IUCD COMPLICATION ( 1 FDA reports)
KLEPTOMANIA ( 1 FDA reports)
LAZINESS ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
MANIA ( 1 FDA reports)
MENOPAUSE ( 1 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ( 1 FDA reports)
MULTIPLE INJURIES ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
MUSCLE STRAIN ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 1 FDA reports)
NAIL DISORDER ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
OCULOGYRIC CRISIS ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PARALYTIC LAGOPHTHALMOS ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PARENT-CHILD PROBLEM ( 1 FDA reports)
PAROSMIA ( 1 FDA reports)
PARTNER STRESS ( 1 FDA reports)
PERSONALITY CHANGE ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POLYSUBSTANCE ABUSE ( 1 FDA reports)
POOR PERIPHERAL CIRCULATION ( 1 FDA reports)
PRESCRIBED OVERDOSE ( 1 FDA reports)
PRODUCT ADHESION ISSUE ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PSYCHOPATHIC PERSONALITY ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RADIATION INJURY ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RETINAL DETACHMENT ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
RHONCHI ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SICK SINUS SYNDROME ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SPINAL CORD INJURY ( 1 FDA reports)
SPINAL FUSION SURGERY ( 1 FDA reports)
SPUTUM DISCOLOURED ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
STUPOR ( 1 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 1 FDA reports)
SUFFOCATION FEELING ( 1 FDA reports)
SUICIDAL BEHAVIOUR ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
TARDIVE DYSKINESIA ( 1 FDA reports)
TENDONITIS ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
THYMUS DISORDER ( 1 FDA reports)
TONGUE OEDEMA ( 1 FDA reports)
TOOTH DISORDER ( 1 FDA reports)
TOOTH LOSS ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
TRANCE ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VICTIM OF HOMICIDE ( 1 FDA reports)
WHEEZING ( 1 FDA reports)

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