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

AGGRESSION ( 14 FDA reports)
DRUG INEFFECTIVE ( 12 FDA reports)
ANXIETY ( 11 FDA reports)
DEPRESSION ( 11 FDA reports)
WEIGHT INCREASED ( 11 FDA reports)
ABNORMAL BEHAVIOUR ( 9 FDA reports)
CONVULSION ( 8 FDA reports)
FATIGUE ( 8 FDA reports)
HEART RATE INCREASED ( 8 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 7 FDA reports)
AGITATION ( 6 FDA reports)
DISTURBANCE IN ATTENTION ( 6 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 6 FDA reports)
SOMNOLENCE ( 6 FDA reports)
SUICIDAL IDEATION ( 6 FDA reports)
ASTHENIA ( 5 FDA reports)
COMPLETED SUICIDE ( 5 FDA reports)
HEADACHE ( 5 FDA reports)
HYPERTENSION ( 5 FDA reports)
INSOMNIA ( 5 FDA reports)
MEDICATION ERROR ( 5 FDA reports)
PSYCHOTIC DISORDER ( 5 FDA reports)
TREMOR ( 5 FDA reports)
VOMITING ( 5 FDA reports)
ALOPECIA ( 4 FDA reports)
ANOREXIA ( 4 FDA reports)
CROHN'S DISEASE ( 4 FDA reports)
DIZZINESS ( 4 FDA reports)
DYSPNOEA ( 4 FDA reports)
IRRITABILITY ( 4 FDA reports)
MOOD SWINGS ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
PRESCRIBED OVERDOSE ( 4 FDA reports)
RASH ( 4 FDA reports)
RECTAL HAEMORRHAGE ( 4 FDA reports)
SENSORY DISTURBANCE ( 4 FDA reports)
ABDOMINAL PAIN UPPER ( 3 FDA reports)
ANGER ( 3 FDA reports)
CHEST PAIN ( 3 FDA reports)
COMA ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 3 FDA reports)
DYSARTHRIA ( 3 FDA reports)
DYSPEPSIA ( 3 FDA reports)
DYSTONIA ( 3 FDA reports)
EDUCATIONAL PROBLEM ( 3 FDA reports)
FALL ( 3 FDA reports)
GASTROINTESTINAL DISORDER ( 3 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 3 FDA reports)
GRAND MAL CONVULSION ( 3 FDA reports)
HYPOAESTHESIA ( 3 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 3 FDA reports)
INTESTINAL HAEMORRHAGE ( 3 FDA reports)
MALAISE ( 3 FDA reports)
MULTI-ORGAN DISORDER ( 3 FDA reports)
MYDRIASIS ( 3 FDA reports)
NERVOUSNESS ( 3 FDA reports)
OFF LABEL USE ( 3 FDA reports)
PAIN ( 3 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 3 FDA reports)
SYNCOPE ( 3 FDA reports)
TIC ( 3 FDA reports)
WEIGHT DECREASED ( 3 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 2 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
CAROTIDYNIA ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DENTAL CARIES ( 2 FDA reports)
DEPRESSED MOOD ( 2 FDA reports)
DIFFICULTY IN WALKING ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
DRY EYE ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
DRY SKIN ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
DYSPHORIA ( 2 FDA reports)
EMOTIONAL DISORDER ( 2 FDA reports)
EXCORIATION ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
HYPERCHOLESTEROLAEMIA ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
HYPERPHAGIA ( 2 FDA reports)
HYPERSOMNIA ( 2 FDA reports)
ILL-DEFINED DISORDER ( 2 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
INJECTION SITE REACTION ( 2 FDA reports)
INJURY ( 2 FDA reports)
LIP DRY ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
MANIA ( 2 FDA reports)
MUSCLE TWITCHING ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
MYOCLONUS ( 2 FDA reports)
NASAL CONGESTION ( 2 FDA reports)
NASAL DRYNESS ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
PANIC ATTACK ( 2 FDA reports)
PETECHIAE ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
PHARYNGITIS ( 2 FDA reports)
PHYSICAL ASSAULT ( 2 FDA reports)
POLYTRAUMATISM ( 2 FDA reports)
PRESYNCOPE ( 2 FDA reports)
PRURITUS ANI ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
SCOLIOSIS ( 2 FDA reports)
SINUSITIS ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 2 FDA reports)
THINKING ABNORMAL ( 2 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
ABSCESS LIMB ( 1 FDA reports)
ABSCESS SOFT TISSUE ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACTINIC KERATOSIS ( 1 FDA reports)
ADNEXA UTERI MASS ( 1 FDA reports)
AMPHETAMINES POSITIVE ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANAL FISTULA ( 1 FDA reports)
ANHEDONIA ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BENIGN OVARIAN TUMOUR ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD ALBUMIN INCREASED ( 1 FDA reports)
BLOOD CANNABINOIDS INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BONE LESION ( 1 FDA reports)
BREAST TENDERNESS ( 1 FDA reports)
BROWN-SEQUARD SYNDROME ( 1 FDA reports)
BURNS THIRD DEGREE ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CERVICAL SPINAL STENOSIS ( 1 FDA reports)
CHANGE IN SUSTAINED ATTENTION ( 1 FDA reports)
CHOLESTEATOMA ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CLOSTRIDIUM COLITIS ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COLITIS ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CORNEAL ABRASION ( 1 FDA reports)
CRYING ( 1 FDA reports)
DEAFNESS NEUROSENSORY ( 1 FDA reports)
DEATH ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DISSOCIATION ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DYSAESTHESIA ( 1 FDA reports)
DYSMENORRHOEA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
EAR HAEMORRHAGE ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
EJACULATION DELAYED ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
EXCITABILITY ( 1 FDA reports)
EXPOSED BONE IN JAW ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
EYELID DISORDER ( 1 FDA reports)
FACIAL BONES FRACTURE ( 1 FDA reports)
FAILURE TO THRIVE ( 1 FDA reports)
FEAR ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FEMALE SEXUAL DYSFUNCTION ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
FIGHT IN SCHOOL ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FOOD CRAVING ( 1 FDA reports)
FRACTURED SACRUM ( 1 FDA reports)
FURUNCLE ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GASTRIC POLYPS ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GENITAL HAEMORRHAGE ( 1 FDA reports)
GLYCOSURIA ( 1 FDA reports)
GROIN ABSCESS ( 1 FDA reports)
GROWTH RETARDATION ( 1 FDA reports)
GYNAECOMASTIA ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HAIRY CELL LEUKAEMIA ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HEAD BANGING ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPATIC CYST ( 1 FDA reports)
HEPATIC LESION ( 1 FDA reports)
HEPATIC MASS ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATITIS VIRAL ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HICCUPS ( 1 FDA reports)
HOMICIDAL IDEATION ( 1 FDA reports)
HUNGER ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERKERATOSIS ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 1 FDA reports)
HYPERTROPHY ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
HYSTERECTOMY ( 1 FDA reports)
ILEITIS ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE MASS ( 1 FDA reports)
INJECTION SITE NECROSIS ( 1 FDA reports)
INJECTION SITE URTICARIA ( 1 FDA reports)
INJURY ASPHYXIATION ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
KERATITIS ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIBIDO DECREASED ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LOOSE TOOTH ( 1 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
LYMPHOEDEMA ( 1 FDA reports)
MEDICATION RESIDUE ( 1 FDA reports)
MEDICATION TAMPERING ( 1 FDA reports)
MENSTRUATION IRREGULAR ( 1 FDA reports)
METRORRHAGIA ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NASAL SEPTUM DEVIATION ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NEGATIVISM ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NEURITIS ( 1 FDA reports)
NEURODERMATITIS ( 1 FDA reports)
NEUTROPENIA NEONATAL ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
OBSESSIVE RUMINATION ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OSTEOCHONDROSIS ( 1 FDA reports)
OSTEONECROSIS OF JAW ( 1 FDA reports)
OSTEOPENIA ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
OVARIAN CYST ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PAPILLOMA ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PARONYCHIA ( 1 FDA reports)
PELVIC FRACTURE ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PERIRECTAL ABSCESS ( 1 FDA reports)
PERSONALITY CHANGE ( 1 FDA reports)
PERSONALITY DISORDER ( 1 FDA reports)
PETIT MAL EPILEPSY ( 1 FDA reports)
PHLEBITIS ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PLEURAL FIBROSIS ( 1 FDA reports)
POISONING ( 1 FDA reports)
POOR PERIPHERAL CIRCULATION ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PRODUCT SOLUBILITY ABNORMAL ( 1 FDA reports)
PSYCHIATRIC SYMPTOM ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PULSE PRESSURE INCREASED ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RECTAL POLYP ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL PAIN ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RESTLESS LEGS SYNDROME ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RETINAL DISORDER ( 1 FDA reports)
RHINITIS ALLERGIC ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SCAR ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SELF MUTILATION ( 1 FDA reports)
SENSITIVITY OF TEETH ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
SPINAL FRACTURE ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
SPLENIC LESION ( 1 FDA reports)
SPONDYLOLISTHESIS ( 1 FDA reports)
SPONDYLOLYSIS ( 1 FDA reports)
SUBCUTANEOUS ABSCESS ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SYNOVIAL CYST ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TARDIVE DYSKINESIA ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 1 FDA reports)
TINEA PEDIS ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TONGUE DISCOLOURATION ( 1 FDA reports)
TOOTH DISORDER ( 1 FDA reports)
TOOTH INJURY ( 1 FDA reports)
TOURETTE'S DISORDER ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TUMOUR EXCISION ( 1 FDA reports)
TYPE 1 DIABETES MELLITUS ( 1 FDA reports)
TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
UNINTENDED PREGNANCY ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VAGINAL DISCHARGE ( 1 FDA reports)
VEIN DISORDER ( 1 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
VITAMIN D DECREASED ( 1 FDA reports)
VULVOVAGINITIS ( 1 FDA reports)
WITHDRAWAL SYNDROME ( 1 FDA reports)

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