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

DRUG INEFFECTIVE ( 35 FDA reports)
DEPRESSION ( 30 FDA reports)
INSOMNIA ( 24 FDA reports)
AGGRESSION ( 22 FDA reports)
OEDEMA PERIPHERAL ( 21 FDA reports)
WEIGHT INCREASED ( 21 FDA reports)
ANXIETY ( 20 FDA reports)
FATIGUE ( 16 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 16 FDA reports)
ALOPECIA ( 15 FDA reports)
PSYCHOTIC DISORDER ( 15 FDA reports)
ABNORMAL BEHAVIOUR ( 14 FDA reports)
FALL ( 13 FDA reports)
MANIA ( 13 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 12 FDA reports)
GAIT DISTURBANCE ( 12 FDA reports)
GASTROINTESTINAL DISORDER ( 12 FDA reports)
HEADACHE ( 12 FDA reports)
LOSS OF CONSCIOUSNESS ( 12 FDA reports)
ROAD TRAFFIC ACCIDENT ( 12 FDA reports)
CONVULSION ( 11 FDA reports)
DIZZINESS ( 11 FDA reports)
DRUG EFFECT DECREASED ( 11 FDA reports)
FEELING ABNORMAL ( 11 FDA reports)
SUICIDAL IDEATION ( 11 FDA reports)
TREMOR ( 11 FDA reports)
ASTHENIA ( 10 FDA reports)
CONSTIPATION ( 10 FDA reports)
DYSPNOEA ( 10 FDA reports)
INJURY ( 10 FDA reports)
PAIN ( 10 FDA reports)
CONDITION AGGRAVATED ( 9 FDA reports)
DECREASED APPETITE ( 9 FDA reports)
DIARRHOEA ( 9 FDA reports)
LABORATORY TEST ABNORMAL ( 9 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 9 FDA reports)
SEROTONIN SYNDROME ( 9 FDA reports)
SOMNOLENCE ( 9 FDA reports)
STAPHYLOCOCCAL INFECTION ( 9 FDA reports)
DRUG TOXICITY ( 8 FDA reports)
FOLLICULITIS ( 8 FDA reports)
HALLUCINATIONS, MIXED ( 8 FDA reports)
IRRITABILITY ( 8 FDA reports)
LIMB DISCOMFORT ( 8 FDA reports)
NAUSEA ( 8 FDA reports)
VOMITING ( 8 FDA reports)
ABDOMINAL PAIN UPPER ( 7 FDA reports)
ARTHRALGIA ( 7 FDA reports)
BLOOD GLUCOSE INCREASED ( 7 FDA reports)
CROHN'S DISEASE ( 7 FDA reports)
DISTURBANCE IN ATTENTION ( 7 FDA reports)
DYSPEPSIA ( 7 FDA reports)
FIBULA FRACTURE ( 7 FDA reports)
HEART RATE INCREASED ( 7 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 7 FDA reports)
MYALGIA ( 7 FDA reports)
ABSCESS ( 6 FDA reports)
ANGER ( 6 FDA reports)
BIPOLAR DISORDER ( 6 FDA reports)
CHEST PAIN ( 6 FDA reports)
FUNGAL SKIN INFECTION ( 6 FDA reports)
HAEMATOCRIT DECREASED ( 6 FDA reports)
HYPOAESTHESIA ( 6 FDA reports)
INTENTIONAL DRUG MISUSE ( 6 FDA reports)
INTESTINAL HAEMORRHAGE ( 6 FDA reports)
LIPOHYPERTROPHY ( 6 FDA reports)
MULTI-ORGAN DISORDER ( 6 FDA reports)
RASH ( 6 FDA reports)
RECTAL HAEMORRHAGE ( 6 FDA reports)
RENAL FAILURE ACUTE ( 6 FDA reports)
SKIN BACTERIAL INFECTION ( 6 FDA reports)
SKIN DISCOLOURATION ( 6 FDA reports)
SUICIDE ATTEMPT ( 6 FDA reports)
WEIGHT DECREASED ( 6 FDA reports)
ATELECTASIS ( 5 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 5 FDA reports)
BACK PAIN ( 5 FDA reports)
CARDIOMEGALY ( 5 FDA reports)
CREPITATIONS ( 5 FDA reports)
DEHYDRATION ( 5 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 5 FDA reports)
DIABETIC NEUROPATHY ( 5 FDA reports)
DIABETIC RETINOPATHY ( 5 FDA reports)
FOOT FRACTURE ( 5 FDA reports)
HAEMOGLOBIN DECREASED ( 5 FDA reports)
LYMPHADENOPATHY ( 5 FDA reports)
MALAISE ( 5 FDA reports)
MAMMOPLASTY ( 5 FDA reports)
MEDICATION ERROR ( 5 FDA reports)
MEMORY IMPAIRMENT ( 5 FDA reports)
MUSCLE RIGIDITY ( 5 FDA reports)
NECK PAIN ( 5 FDA reports)
NERVOUSNESS ( 5 FDA reports)
PAIN IN EXTREMITY ( 5 FDA reports)
PALPITATIONS ( 5 FDA reports)
PARAESTHESIA ( 5 FDA reports)
PRODUCT QUALITY ISSUE ( 5 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 5 FDA reports)
PROTEINURIA ( 5 FDA reports)
PROTHROMBIN TIME PROLONGED ( 5 FDA reports)
PULMONARY EMBOLISM ( 5 FDA reports)
RETCHING ( 5 FDA reports)
SINUSITIS ( 5 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 5 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
ANHEDONIA ( 4 FDA reports)
BACTERIAL DISEASE CARRIER ( 4 FDA reports)
BRONCHOPLEURAL FISTULA ( 4 FDA reports)
CEREBROVASCULAR DISORDER ( 4 FDA reports)
CERVICAL CYST ( 4 FDA reports)
CERVICAL SPINAL STENOSIS ( 4 FDA reports)
CHEST TUBE INSERTION ( 4 FDA reports)
COLITIS ( 4 FDA reports)
CYST ( 4 FDA reports)
DEEP VEIN THROMBOSIS ( 4 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 4 FDA reports)
DIABETIC EYE DISEASE ( 4 FDA reports)
DRY SKIN ( 4 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 4 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 4 FDA reports)
EMPHYSEMA ( 4 FDA reports)
EMPYEMA ( 4 FDA reports)
ENDODONTIC PROCEDURE ( 4 FDA reports)
EYE DISCHARGE ( 4 FDA reports)
FAECAL INCONTINENCE ( 4 FDA reports)
FEAR OF DEATH ( 4 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 4 FDA reports)
FOOT DEFORMITY ( 4 FDA reports)
GASTRITIS ( 4 FDA reports)
HAEMATOMA ( 4 FDA reports)
HAEMORRHAGE ( 4 FDA reports)
HALLUCINATION, VISUAL ( 4 FDA reports)
HEAD INJURY ( 4 FDA reports)
HYDROPNEUMOTHORAX ( 4 FDA reports)
HYPERTENSION ( 4 FDA reports)
HYPOTENSION ( 4 FDA reports)
INJURY CORNEAL ( 4 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 4 FDA reports)
LIP DISCOLOURATION ( 4 FDA reports)
LIP DRY ( 4 FDA reports)
MASTICATION DISORDER ( 4 FDA reports)
MENOPAUSE ( 4 FDA reports)
NASOPHARYNGITIS ( 4 FDA reports)
NEUROPATHY PERIPHERAL ( 4 FDA reports)
OEDEMA ( 4 FDA reports)
OSTEOARTHRITIS ( 4 FDA reports)
OSTEONECROSIS ( 4 FDA reports)
OSTEOPENIA ( 4 FDA reports)
OSTEOPOROSIS ( 4 FDA reports)
OSTEORADIONECROSIS ( 4 FDA reports)
OVERDOSE ( 4 FDA reports)
POSTNASAL DRIP ( 4 FDA reports)
RENAL DISORDER ( 4 FDA reports)
RESPIRATORY DEPRESSION ( 4 FDA reports)
RIB FRACTURE ( 4 FDA reports)
ROTATOR CUFF REPAIR ( 4 FDA reports)
ROTATOR CUFF SYNDROME ( 4 FDA reports)
SWELLING FACE ( 4 FDA reports)
THORACOTOMY ( 4 FDA reports)
TIBIA FRACTURE ( 4 FDA reports)
TOOTH DISORDER ( 4 FDA reports)
URINARY INCONTINENCE ( 4 FDA reports)
URINE OUTPUT DECREASED ( 4 FDA reports)
VAGINAL HAEMORRHAGE ( 4 FDA reports)
VISION BLURRED ( 4 FDA reports)
AMNESIA ( 3 FDA reports)
ANAL FISTULA ( 3 FDA reports)
ARTHRITIS ( 3 FDA reports)
BLISTER ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 3 FDA reports)
BLOOD PRESSURE DECREASED ( 3 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 3 FDA reports)
BONE DENSITY DECREASED ( 3 FDA reports)
BREAST FIBROSIS ( 3 FDA reports)
CAROTIDYNIA ( 3 FDA reports)
CHEST DISCOMFORT ( 3 FDA reports)
DEBRIDEMENT ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
DRY EYE ( 3 FDA reports)
DYSGEUSIA ( 3 FDA reports)
DYSTONIA ( 3 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 3 FDA reports)
EPISTAXIS ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
EYE DISORDER ( 3 FDA reports)
FEELING HOT ( 3 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 3 FDA reports)
GENITAL HERPES ( 3 FDA reports)
HAEMORRHOIDS ( 3 FDA reports)
HALLUCINATION ( 3 FDA reports)
ILL-DEFINED DISORDER ( 3 FDA reports)
IMPRISONMENT ( 3 FDA reports)
INFLUENZA LIKE ILLNESS ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 3 FDA reports)
JOINT SWELLING ( 3 FDA reports)
MENSTRUATION IRREGULAR ( 3 FDA reports)
MENTAL DISORDER ( 3 FDA reports)
MOOD SWINGS ( 3 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 3 FDA reports)
MUSCLE FLAP OPERATION ( 3 FDA reports)
MUSCULOSKELETAL PAIN ( 3 FDA reports)
NASAL DRYNESS ( 3 FDA reports)
OBSESSIVE THOUGHTS ( 3 FDA reports)
OTITIS EXTERNA ( 3 FDA reports)
PERIRECTAL ABSCESS ( 3 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
POISONING ( 3 FDA reports)
PRODUCT FORMULATION ISSUE ( 3 FDA reports)
PRURITUS ANI ( 3 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
RESTLESSNESS ( 3 FDA reports)
RHABDOMYOLYSIS ( 3 FDA reports)
SEDATION ( 3 FDA reports)
SEROMA ( 3 FDA reports)
SKIN PAPILLOMA ( 3 FDA reports)
SUBSTANCE ABUSE ( 3 FDA reports)
SUNBURN ( 3 FDA reports)
TACHYCARDIA ( 3 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 3 FDA reports)
TINNITUS ( 3 FDA reports)
TOOTHACHE ( 3 FDA reports)
TOURETTE'S DISORDER ( 3 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 3 FDA reports)
VENA CAVA THROMBOSIS ( 3 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ABDOMINOPLASTY ( 2 FDA reports)
AGITATION ( 2 FDA reports)
AKATHISIA ( 2 FDA reports)
AMENORRHOEA ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
APPENDICECTOMY ( 2 FDA reports)
ARTHROSCOPIC SURGERY ( 2 FDA reports)
BACTERIA URINE ( 2 FDA reports)
BILE DUCT STONE ( 2 FDA reports)
BLOOD AMYLASE INCREASED ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CHOLECYSTITIS CHRONIC ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
CHONDROMALACIA ( 2 FDA reports)
COLD SWEAT ( 2 FDA reports)
COMPLETED SUICIDE ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
COORDINATION ABNORMAL ( 2 FDA reports)
CYSTITIS ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DIVERTICULITIS ( 2 FDA reports)
DOPAMINE DYSREGULATION SYNDROME ( 2 FDA reports)
DRUG DIVERSION ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
DRUG INTOLERANCE ( 2 FDA reports)
DRUG LEVEL CHANGED ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
DYSPHEMIA ( 2 FDA reports)
ECONOMIC PROBLEM ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
EDUCATIONAL PROBLEM ( 2 FDA reports)
EMPYEMA DRAINAGE ( 2 FDA reports)
EPENDYMOMA ( 2 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 2 FDA reports)
EYE HAEMORRHAGE ( 2 FDA reports)
EYELID INJURY ( 2 FDA reports)
EYELID PTOSIS ( 2 FDA reports)
FEAR OF DISEASE ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
FOOD CRAVING ( 2 FDA reports)
GALLBLADDER PAIN ( 2 FDA reports)
GASTRITIS EROSIVE ( 2 FDA reports)
GOUT ( 2 FDA reports)
HAEMATOCHEZIA ( 2 FDA reports)
HALLUCINATION, AUDITORY ( 2 FDA reports)
HYPERCOAGULATION ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPERPHAGIA ( 2 FDA reports)
HYPERTHERMIA MALIGNANT ( 2 FDA reports)
HYPOKINESIA ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
ILEITIS ( 2 FDA reports)
IMPAIRED DRIVING ABILITY ( 2 FDA reports)
IMPAIRED WORK ABILITY ( 2 FDA reports)
IMPULSIVE BEHAVIOUR ( 2 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 2 FDA reports)
INNER EAR DISORDER ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
LARGE INTESTINE PERFORATION ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
LUNG INFECTION ( 2 FDA reports)
LUNG NEOPLASM MALIGNANT ( 2 FDA reports)
LUNG OPERATION ( 2 FDA reports)
LYMPHADENITIS ( 2 FDA reports)
MIGRAINE ( 2 FDA reports)
MOVEMENT DISORDER ( 2 FDA reports)
MUCOUS STOOLS ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 2 FDA reports)
MULTIPLE INJURIES ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
MUSCLE STRAIN ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
NASAL CONGESTION ( 2 FDA reports)
OROPHARYNGEAL PAIN ( 2 FDA reports)
ORTHOSTATIC HYPOTENSION ( 2 FDA reports)
PNEUMOTHORAX ( 2 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
PULMONARY AIR LEAKAGE ( 2 FDA reports)
PULMONARY FIBROSIS ( 2 FDA reports)
RENAL CYST ( 2 FDA reports)
RHINITIS ALLERGIC ( 2 FDA reports)
SEBORRHOEIC DERMATITIS ( 2 FDA reports)
SINUS OPERATION ( 2 FDA reports)
SKIN LACERATION ( 2 FDA reports)
SKIN LESION ( 2 FDA reports)
SLEEP DISORDER ( 2 FDA reports)
STRESS ( 2 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 2 FDA reports)
THIRST ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
THROMBOSIS IN DEVICE ( 2 FDA reports)
TIC ( 2 FDA reports)
TOOTH FRACTURE ( 2 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
VULVOVAGINAL PRURITUS ( 2 FDA reports)
WALKING DISABILITY ( 2 FDA reports)
WOUND HAEMORRHAGE ( 2 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 2 FDA reports)
ABDOMINAL COMPARTMENT SYNDROME ( 1 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ACCIDENT ( 1 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACNE ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
AFFECT LABILITY ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
AMPHETAMINES POSITIVE ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANKLE FRACTURE ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANTIMICROBIAL SUSCEPTIBILITY TEST RESISTANT ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
APNOEA ( 1 FDA reports)
APPENDICITIS ( 1 FDA reports)
APPENDICITIS PERFORATED ( 1 FDA reports)
APPENDIX DISORDER ( 1 FDA reports)
APPLICATION SITE ERYTHEMA ( 1 FDA reports)
APPLICATION SITE PAIN ( 1 FDA reports)
APPLICATION SITE REACTION ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTERIAL STENT INSERTION ( 1 FDA reports)
ARTERIAL THROMBOSIS ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
ASTROCYTOMA ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
ATROPHIC VULVOVAGINITIS ( 1 FDA reports)
AVOIDANT PERSONALITY DISORDER ( 1 FDA reports)
AXILLARY VEIN THROMBOSIS ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BIPOLAR I DISORDER ( 1 FDA reports)
BIPOLAR II DISORDER ( 1 FDA reports)
BITE ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLUE TOE SYNDROME ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BREAST CANCER IN SITU ( 1 FDA reports)
BREAST HYPERPLASIA ( 1 FDA reports)
BREATH ODOUR ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIAC FIBRILLATION ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CATHETER SITE RELATED REACTION ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 1 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHRONIC FATIGUE SYNDROME ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
COAGULATION TIME PROLONGED ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
COLONIC POLYP ( 1 FDA reports)
COMPULSIONS ( 1 FDA reports)
CONCUSSION ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
COUNTERFEIT DRUG ADMINISTERED ( 1 FDA reports)
CRYING ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DERMAL CYST ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DERMATITIS PSORIASIFORM ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIABETIC NEPHROPATHY ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISSOCIATION ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG LEVEL FLUCTUATING ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTIVE SURGERY ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
ENDOPHTHALMITIS ( 1 FDA reports)
ERYTHEMA OF EYELID ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
ESSENTIAL HYPERTENSION ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
EXTERNAL EAR CELLULITIS ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
FACET JOINT SYNDROME ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FEAR ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FOREIGN BODY ( 1 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 1 FDA reports)
FRUSTRATION ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTROENTERITIS VIRAL ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GENITAL PAIN ( 1 FDA reports)
HAEMATOCRIT INCREASED ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 1 FDA reports)
HAIR GROWTH ABNORMAL ( 1 FDA reports)
HAIR TEXTURE ABNORMAL ( 1 FDA reports)
HEPATIC CYST ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATIC LESION ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HUNGER ( 1 FDA reports)
HYPERNATRAEMIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERTRICHOSIS ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOMANIA ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
ILEAL STENOSIS ( 1 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 1 FDA reports)
IMPATIENCE ( 1 FDA reports)
IMPLANT SITE REACTION ( 1 FDA reports)
IMPULSE-CONTROL DISORDER ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
INFUSION SITE CELLULITIS ( 1 FDA reports)
INGROWING NAIL ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 1 FDA reports)
INSTILLATION SITE IRRITATION ( 1 FDA reports)
INSTILLATION SITE PAIN ( 1 FDA reports)
INTENTIONAL MISUSE ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
INTENTIONAL SELF-INJURY ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
INTESTINAL FISTULA ( 1 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 1 FDA reports)
INTUSSUSCEPTION ( 1 FDA reports)
IRRITABLE BOWEL SYNDROME ( 1 FDA reports)
JOINT INJURY ( 1 FDA reports)
JOINT SPRAIN ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
LARYNGEAL MASS ( 1 FDA reports)
LEARNING DISORDER ( 1 FDA reports)
LEGAL PROBLEM ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LIP BLISTER ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LIPOSUCTION ( 1 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
LUNG CANCER METASTATIC ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
MASS ( 1 FDA reports)
METASTASES TO ADRENALS ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
METASTATIC PAIN ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MOLE EXCISION ( 1 FDA reports)
MONONUCLEOSIS SYNDROME ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MUSCLE TIGHTNESS ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
MYELITIS TRANSVERSE ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NARCOLEPSY ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 1 FDA reports)
NEPHROPATHY ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
NODULE ON EXTREMITY ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OESOPHAGEAL DISORDER ( 1 FDA reports)
OESOPHAGEAL ULCER ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
ONYCHOCLASIS ( 1 FDA reports)
OPEN WOUND ( 1 FDA reports)
OPPOSITIONAL DEFIANT DISORDER ( 1 FDA reports)
ORAL DISORDER ( 1 FDA reports)
ORAL PRURITUS ( 1 FDA reports)
OSTEOMA ( 1 FDA reports)
OTITIS MEDIA ( 1 FDA reports)
PAIN OF SKIN ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PARAESTHESIA OF GENITAL FEMALE ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PARTIAL SEIZURES ( 1 FDA reports)
PECTUS EXCAVATUM ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PERITONITIS BACTERIAL ( 1 FDA reports)
PERONEAL NERVE PALSY ( 1 FDA reports)
PERSONALITY CHANGE ( 1 FDA reports)
PHARYNGEAL HYPOAESTHESIA ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POLYDIPSIA ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
POST CONCUSSION SYNDROME ( 1 FDA reports)
POST PROCEDURAL DRAINAGE ( 1 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 1 FDA reports)
POTENTIATING DRUG INTERACTION ( 1 FDA reports)
PRECANCEROUS CELLS PRESENT ( 1 FDA reports)
PREMATURE EJACULATION ( 1 FDA reports)
PREMATURE LABOUR ( 1 FDA reports)
PRESCRIBED OVERDOSE ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PROCTALGIA ( 1 FDA reports)
PROCTITIS ( 1 FDA reports)
PROCTITIS ULCERATIVE ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
PUPIL FIXED ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RAYNAUD'S PHENOMENON ( 1 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 1 FDA reports)
RECTAL ABSCESS ( 1 FDA reports)
REFLEXES ABNORMAL ( 1 FDA reports)
RELAPSING-REMITTING MULTIPLE SCLEROSIS ( 1 FDA reports)
RESPIRATORY GAS EXCHANGE DISORDER ( 1 FDA reports)
SCAB ( 1 FDA reports)
SCAR ( 1 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 1 FDA reports)
SCRATCH ( 1 FDA reports)
SECRETION DISCHARGE ( 1 FDA reports)
SELF ESTEEM INFLATED ( 1 FDA reports)
SELF-INJURIOUS IDEATION ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SEXUAL ASSAULT VICTIM ( 1 FDA reports)
SEXUAL DYSFUNCTION ( 1 FDA reports)
SINUS HEADACHE ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN HYPERTROPHY ( 1 FDA reports)
SKIN SWELLING ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 1 FDA reports)
SMEAR CERVIX ABNORMAL ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
SPINAL DEFORMITY ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
STARING ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
STRESS FRACTURE ( 1 FDA reports)
STRESS URINARY INCONTINENCE ( 1 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 1 FDA reports)
SUBCUTANEOUS ABSCESS ( 1 FDA reports)
SUDDEN ONSET OF SLEEP ( 1 FDA reports)
SUICIDAL BEHAVIOUR ( 1 FDA reports)
SWELLING ( 1 FDA reports)
TACHYPHRENIA ( 1 FDA reports)
TEMPERATURE REGULATION DISORDER ( 1 FDA reports)
TENDON DISORDER ( 1 FDA reports)
TENDON RUPTURE ( 1 FDA reports)
TENDONITIS ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
THORACIC OUTLET SYNDROME ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TOBACCO USER ( 1 FDA reports)
TOOTH LOSS ( 1 FDA reports)
TYPE 1 DIABETES MELLITUS ( 1 FDA reports)
TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 1 FDA reports)
VAGAL NERVE STIMULATOR IMPLANTATION ( 1 FDA reports)
VAGINAL DISCHARGE ( 1 FDA reports)
VASCULAR ANOMALY ( 1 FDA reports)
VENOUS THROMBOSIS ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
WALKING AID USER ( 1 FDA reports)
WEIGHT BEARING DIFFICULTY ( 1 FDA reports)
WEIGHT GAIN POOR ( 1 FDA reports)
WOUND INFECTION FUNGAL ( 1 FDA reports)

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