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

NAUSEA ( 29 FDA reports)
FALL ( 25 FDA reports)
ANXIETY ( 22 FDA reports)
DIZZINESS ( 21 FDA reports)
FATIGUE ( 21 FDA reports)
CONFUSIONAL STATE ( 19 FDA reports)
AGITATION ( 18 FDA reports)
MALAISE ( 18 FDA reports)
SUICIDAL IDEATION ( 18 FDA reports)
COMA ( 16 FDA reports)
DRUG INEFFECTIVE ( 15 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 15 FDA reports)
DYSPNOEA ( 15 FDA reports)
TREMOR ( 15 FDA reports)
VOMITING ( 15 FDA reports)
ACCIDENTAL OVERDOSE ( 14 FDA reports)
ASTHENIA ( 14 FDA reports)
DRUG INTERACTION ( 14 FDA reports)
CONVULSION ( 13 FDA reports)
OVERDOSE ( 13 FDA reports)
AGGRESSION ( 12 FDA reports)
DEPRESSION ( 12 FDA reports)
DIARRHOEA ( 12 FDA reports)
HYPOTENSION ( 12 FDA reports)
INSOMNIA ( 12 FDA reports)
PAIN ( 12 FDA reports)
PARAESTHESIA ( 12 FDA reports)
ANAEMIA ( 11 FDA reports)
ARTHRALGIA ( 11 FDA reports)
PALPITATIONS ( 11 FDA reports)
WITHDRAWAL SYNDROME ( 11 FDA reports)
DISTURBANCE IN ATTENTION ( 10 FDA reports)
GAIT DISTURBANCE ( 10 FDA reports)
HEADACHE ( 10 FDA reports)
MEMORY IMPAIRMENT ( 10 FDA reports)
NIGHTMARE ( 10 FDA reports)
PAIN IN EXTREMITY ( 10 FDA reports)
AMNESIA ( 9 FDA reports)
BLOOD GLUCOSE INCREASED ( 9 FDA reports)
COMPLETED SUICIDE ( 9 FDA reports)
IRRITABILITY ( 9 FDA reports)
LOSS OF CONSCIOUSNESS ( 9 FDA reports)
PNEUMONIA ( 9 FDA reports)
PYREXIA ( 9 FDA reports)
BRADYCARDIA ( 8 FDA reports)
CHEST PAIN ( 8 FDA reports)
DEHYDRATION ( 8 FDA reports)
HYPERHIDROSIS ( 8 FDA reports)
HYPOAESTHESIA ( 8 FDA reports)
INFLUENZA LIKE ILLNESS ( 8 FDA reports)
PARANOIA ( 8 FDA reports)
PULMONARY OEDEMA ( 8 FDA reports)
BALANCE DISORDER ( 7 FDA reports)
CONDITION AGGRAVATED ( 7 FDA reports)
DEPRESSED MOOD ( 7 FDA reports)
EMOTIONAL DISTRESS ( 7 FDA reports)
ERYTHEMA ( 7 FDA reports)
FEELING ABNORMAL ( 7 FDA reports)
MOOD SWINGS ( 7 FDA reports)
MUSCLE SPASMS ( 7 FDA reports)
MYALGIA ( 7 FDA reports)
OEDEMA PERIPHERAL ( 7 FDA reports)
PANIC ATTACK ( 7 FDA reports)
SOMNOLENCE ( 7 FDA reports)
SUICIDE ATTEMPT ( 7 FDA reports)
TACHYCARDIA ( 7 FDA reports)
ABDOMINAL PAIN UPPER ( 6 FDA reports)
ABNORMAL BEHAVIOUR ( 6 FDA reports)
CARDIO-RESPIRATORY ARREST ( 6 FDA reports)
CONTUSION ( 6 FDA reports)
EPISTAXIS ( 6 FDA reports)
FEAR ( 6 FDA reports)
HALLUCINATION ( 6 FDA reports)
HEPATIC STEATOSIS ( 6 FDA reports)
LETHARGY ( 6 FDA reports)
MOBILITY DECREASED ( 6 FDA reports)
MUSCULOSKELETAL PAIN ( 6 FDA reports)
PANCYTOPENIA ( 6 FDA reports)
SLEEP DISORDER ( 6 FDA reports)
SWOLLEN TONGUE ( 6 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 6 FDA reports)
VISUAL DISTURBANCE ( 6 FDA reports)
WEIGHT DECREASED ( 6 FDA reports)
ANGER ( 5 FDA reports)
CARDIAC ARREST ( 5 FDA reports)
DEATH ( 5 FDA reports)
DRUG TOXICITY ( 5 FDA reports)
DRY MOUTH ( 5 FDA reports)
JOINT SWELLING ( 5 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 5 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 5 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 5 FDA reports)
RASH ( 5 FDA reports)
RASH MACULAR ( 5 FDA reports)
SWELLING ( 5 FDA reports)
TEARFULNESS ( 5 FDA reports)
VISION BLURRED ( 5 FDA reports)
WEIGHT INCREASED ( 5 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
AFFECT LABILITY ( 4 FDA reports)
ANOREXIA ( 4 FDA reports)
ARTHRITIS ( 4 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 4 FDA reports)
AUTOIMMUNE DISORDER ( 4 FDA reports)
BLOOD BILIRUBIN INCREASED ( 4 FDA reports)
CEREBROVASCULAR ACCIDENT ( 4 FDA reports)
CHEST DISCOMFORT ( 4 FDA reports)
COGNITIVE DISORDER ( 4 FDA reports)
CONNECTIVE TISSUE DISORDER ( 4 FDA reports)
CONSTIPATION ( 4 FDA reports)
CRYING ( 4 FDA reports)
DECREASED APPETITE ( 4 FDA reports)
DYSARTHRIA ( 4 FDA reports)
DYSPEPSIA ( 4 FDA reports)
DYSPHAGIA ( 4 FDA reports)
EMOTIONAL DISORDER ( 4 FDA reports)
HEART RATE IRREGULAR ( 4 FDA reports)
HOMICIDAL IDEATION ( 4 FDA reports)
HYPERSOMNIA ( 4 FDA reports)
HYPERTENSION ( 4 FDA reports)
HYPOXIA ( 4 FDA reports)
INFECTION ( 4 FDA reports)
INFLAMMATION ( 4 FDA reports)
JOINT CREPITATION ( 4 FDA reports)
LACTIC ACIDOSIS ( 4 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 4 FDA reports)
LYMPHADENOPATHY ( 4 FDA reports)
MUSCLE TWITCHING ( 4 FDA reports)
MYOSITIS ( 4 FDA reports)
NERVOUS SYSTEM DISORDER ( 4 FDA reports)
NEUROPATHY ( 4 FDA reports)
NEUTROPENIA ( 4 FDA reports)
NIGHT SWEATS ( 4 FDA reports)
PERSONALITY CHANGE ( 4 FDA reports)
PHOTOSENSITIVITY REACTION ( 4 FDA reports)
PSYCHIATRIC SYMPTOM ( 4 FDA reports)
PULMONARY CONGESTION ( 4 FDA reports)
PULMONARY EMBOLISM ( 4 FDA reports)
SCIATICA ( 4 FDA reports)
SEDATION ( 4 FDA reports)
SINUSITIS ( 4 FDA reports)
STAPHYLOCOCCAL INFECTION ( 4 FDA reports)
THIRST ( 4 FDA reports)
URINARY TRACT INFECTION ( 4 FDA reports)
VASCULITIS ( 4 FDA reports)
ABNORMAL DREAMS ( 3 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 3 FDA reports)
ALOPECIA ( 3 FDA reports)
APHASIA ( 3 FDA reports)
BACK PAIN ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
BURNING SENSATION ( 3 FDA reports)
CELLULITIS ( 3 FDA reports)
CERVICAL POLYP ( 3 FDA reports)
CERVICOBRACHIAL SYNDROME ( 3 FDA reports)
DEAFNESS ( 3 FDA reports)
DELIRIUM ( 3 FDA reports)
DELUSION ( 3 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 3 FDA reports)
DIPLOPIA ( 3 FDA reports)
DISORIENTATION ( 3 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 3 FDA reports)
EAR PAIN ( 3 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 3 FDA reports)
FEELING DRUNK ( 3 FDA reports)
FEELING OF DESPAIR ( 3 FDA reports)
FIBROMYALGIA ( 3 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 3 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 3 FDA reports)
GENERALISED OEDEMA ( 3 FDA reports)
GRAND MAL CONVULSION ( 3 FDA reports)
HAEMOPTYSIS ( 3 FDA reports)
HERNIA OBSTRUCTIVE ( 3 FDA reports)
ILL-DEFINED DISORDER ( 3 FDA reports)
IMPAIRED WORK ABILITY ( 3 FDA reports)
LUPUS-LIKE SYNDROME ( 3 FDA reports)
MENTAL IMPAIRMENT ( 3 FDA reports)
METRORRHAGIA ( 3 FDA reports)
MUSCULOSKELETAL DISORDER ( 3 FDA reports)
OSTEOARTHRITIS ( 3 FDA reports)
OTORRHOEA ( 3 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 3 FDA reports)
POLYNEUROPATHY ( 3 FDA reports)
RAYNAUD'S PHENOMENON ( 3 FDA reports)
RENAL FAILURE ACUTE ( 3 FDA reports)
RHEUMATOID ARTHRITIS ( 3 FDA reports)
SENSORY DISTURBANCE ( 3 FDA reports)
SEPTIC SHOCK ( 3 FDA reports)
SEROTONIN SYNDROME ( 3 FDA reports)
SPEECH DISORDER ( 3 FDA reports)
SPLENOMEGALY ( 3 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 3 FDA reports)
TENDON RUPTURE ( 3 FDA reports)
TENDONITIS ( 3 FDA reports)
UNRESPONSIVE TO STIMULI ( 3 FDA reports)
VIRAL LOAD INCREASED ( 3 FDA reports)
VIRAL PHARYNGITIS ( 3 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 3 FDA reports)
ABASIA ( 2 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ABSCESS ( 2 FDA reports)
ACCIDENTAL EXPOSURE ( 2 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 2 FDA reports)
ACUTE PULMONARY OEDEMA ( 2 FDA reports)
AORTIC VALVE CALCIFICATION ( 2 FDA reports)
AORTIC VALVE STENOSIS ( 2 FDA reports)
APATHY ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
ARTHROPATHY ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
BACILLUS INFECTION ( 2 FDA reports)
BACK DISORDER ( 2 FDA reports)
BIOPSY MUSCLE ABNORMAL ( 2 FDA reports)
BLINDNESS ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD CALCIUM DECREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
BONE PAIN ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
BRUGADA SYNDROME ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CARDIOMEGALY ( 2 FDA reports)
CATARACT ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
CIRCULATORY COLLAPSE ( 2 FDA reports)
COLD SWEAT ( 2 FDA reports)
COLITIS ISCHAEMIC ( 2 FDA reports)
COLONIC OBSTRUCTION ( 2 FDA reports)
COMPRESSION FRACTURE ( 2 FDA reports)
COUGH ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
CYST ( 2 FDA reports)
DEREALISATION ( 2 FDA reports)
DIALYSIS DEVICE COMPLICATION ( 2 FDA reports)
DRUG ABUSER ( 2 FDA reports)
DRUG DEPENDENCE ( 2 FDA reports)
DRUG DOSE OMISSION ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
DYSGRAPHIA ( 2 FDA reports)
DYSPHASIA ( 2 FDA reports)
DYSSTASIA ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 2 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 2 FDA reports)
ERUCTATION ( 2 FDA reports)
FAECAL INCONTINENCE ( 2 FDA reports)
FAECALOMA ( 2 FDA reports)
FEELING COLD ( 2 FDA reports)
FEELING HOT ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
FUNGAL PERITONITIS ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
GRIP STRENGTH DECREASED ( 2 FDA reports)
GROIN PAIN ( 2 FDA reports)
GUILLAIN-BARRE SYNDROME ( 2 FDA reports)
HAEMANGIOMA OF LIVER ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HAEMOPHILUS INFECTION ( 2 FDA reports)
HEPATIC ENZYME ABNORMAL ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HEPATIC NEOPLASM ( 2 FDA reports)
HEPATOMEGALY ( 2 FDA reports)
HOMICIDE ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
HYPERPYREXIA ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
IMMUNOSUPPRESSION ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INFLUENZA ( 2 FDA reports)
INJECTION SITE REACTION ( 2 FDA reports)
INJURY ( 2 FDA reports)
INTENTIONAL SELF-INJURY ( 2 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 2 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 2 FDA reports)
LIBIDO DECREASED ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
MENTAL DISORDER ( 2 FDA reports)
MIGRAINE ( 2 FDA reports)
MOOD ALTERED ( 2 FDA reports)
MOTOR DYSFUNCTION ( 2 FDA reports)
MOVEMENT DISORDER ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ( 2 FDA reports)
MULTIPLE SCLEROSIS ( 2 FDA reports)
MUSCLE INJURY ( 2 FDA reports)
MUSCLE SPASTICITY ( 2 FDA reports)
MUSCLE TIGHTNESS ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
MYOCLONUS ( 2 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 2 FDA reports)
NERVE INJURY ( 2 FDA reports)
NEURALGIA ( 2 FDA reports)
NEUROPSYCHOLOGICAL TEST ABNORMAL ( 2 FDA reports)
OBESITY ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PAIN IN JAW ( 2 FDA reports)
PANIC REACTION ( 2 FDA reports)
PARALYSIS ( 2 FDA reports)
PARAPARESIS ( 2 FDA reports)
PERINEPHRIC COLLECTION ( 2 FDA reports)
PERIPHERAL NERVE LESION ( 2 FDA reports)
PERITONITIS BACTERIAL ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
PNEUMOTHORAX ( 2 FDA reports)
POOR QUALITY SLEEP ( 2 FDA reports)
PROTEIN TOTAL INCREASED ( 2 FDA reports)
RASH PAPULAR ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 2 FDA reports)
RENAL INFARCT ( 2 FDA reports)
RESPIRATORY TRACT INFECTION ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
RHEUMATOID FACTOR INCREASED ( 2 FDA reports)
SELF-INJURIOUS IDEATION ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
SINUS DISORDER ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
SKIN STRIAE ( 2 FDA reports)
SNEEZING ( 2 FDA reports)
SOCIAL PHOBIA ( 2 FDA reports)
SOPOR ( 2 FDA reports)
SPINAL COMPRESSION FRACTURE ( 2 FDA reports)
SPINAL OSTEOARTHRITIS ( 2 FDA reports)
SPLEEN CONGESTION ( 2 FDA reports)
STOMACH DISCOMFORT ( 2 FDA reports)
STREPTOCOCCAL INFECTION ( 2 FDA reports)
STRESS ( 2 FDA reports)
STRESS URINARY INCONTINENCE ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
SURGERY ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 2 FDA reports)
TACHYPNOEA ( 2 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 2 FDA reports)
TENDON DISORDER ( 2 FDA reports)
THINKING ABNORMAL ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
TINNITUS ( 2 FDA reports)
TONGUE DRY ( 2 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 2 FDA reports)
VAGINAL DISCHARGE ( 2 FDA reports)
VARICOSE VEIN ( 2 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
VULVOVAGINAL DISCOMFORT ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
WOUND DEHISCENCE ( 2 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 2 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 2 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABDOMINAL WALL ABSCESS ( 1 FDA reports)
ABDOMINAL WALL INFECTION ( 1 FDA reports)
ACCIDENTAL DEATH ( 1 FDA reports)
ACNE ( 1 FDA reports)
ACTIVATION SYNDROME ( 1 FDA reports)
ADJUSTMENT DISORDER ( 1 FDA reports)
ADRENAL DISORDER ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
AEROMONA INFECTION ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ALCOHOL INTERACTION ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ALLERGY TO CHEMICALS ( 1 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANHEDONIA ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
APPLICATION SITE SCAB ( 1 FDA reports)
APPLICATION SITE SCAR ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ARTERIAL STENOSIS ( 1 FDA reports)
ARTERIAL THROMBOSIS ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ARTHRITIS BACTERIAL ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
AURICULAR SWELLING ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BEZOAR ( 1 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BONE DENSITY DECREASED ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
BONE OPERATION ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
BREAST CANCER IN SITU ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 1 FDA reports)
BUNION OPERATION ( 1 FDA reports)
BURNS SECOND DEGREE ( 1 FDA reports)
BURSA DISORDER ( 1 FDA reports)
BURSITIS ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CARDIAC VALVE VEGETATION ( 1 FDA reports)
CARDIOTOXICITY ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CARDIOVERSION ( 1 FDA reports)
CAROTID ARTERY OCCLUSION ( 1 FDA reports)
CATARACT OPERATION ( 1 FDA reports)
CATARACT SUBCAPSULAR ( 1 FDA reports)
CATHETER PLACEMENT ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CATHETER REMOVAL ( 1 FDA reports)
CATHETER SEPSIS ( 1 FDA reports)
CATHETER SITE PAIN ( 1 FDA reports)
CEREBRAL HAEMATOMA ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHOLANGITIS ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CHOREA ( 1 FDA reports)
CHOROIDAL NEOVASCULARISATION ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 1 FDA reports)
COMPLEX PARTIAL SEIZURES ( 1 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 1 FDA reports)
CONVERSION DISORDER ( 1 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CRANIOSYNOSTOSIS ( 1 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
CSF GLUCOSE ABNORMAL ( 1 FDA reports)
CSF PROTEIN ABNORMAL ( 1 FDA reports)
CSF TEST ABNORMAL ( 1 FDA reports)
CSF WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
CULTURE POSITIVE ( 1 FDA reports)
CYCLOTHYMIC DISORDER ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
DAYDREAMING ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
DECREASED INTEREST ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
DEFORMITY ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DEPENDENCE ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DERMATOMYOSITIS ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DIVERTICULUM INTESTINAL ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DUODENITIS ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSPAREUNIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 1 FDA reports)
EAR DISCOMFORT ( 1 FDA reports)
EAR DISORDER ( 1 FDA reports)
EARLY MORNING AWAKENING ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
ERYTHEMA NODOSUM ( 1 FDA reports)
ESSENTIAL TREMOR ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
EXOSTOSIS ( 1 FDA reports)
EXPIRED DRUG ADMINISTERED ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EXTRAVASATION ( 1 FDA reports)
EXTRAVASATION BLOOD ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
EYELID PTOSIS ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FACIAL PARESIS ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FEMORAL NECK FRACTURE ( 1 FDA reports)
FISTULA ( 1 FDA reports)
FLASHBACK ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FOLLICLE CENTRE LYMPHOMA, FOLLICULAR GRADE I, II, III ( 1 FDA reports)
FOOT FRACTURE ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTRITIS EROSIVE ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GENITAL PAIN ( 1 FDA reports)
GINGIVAL PAIN ( 1 FDA reports)
GINGIVAL RECESSION ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GRANULOCYTE COUNT INCREASED ( 1 FDA reports)
HAEMANGIOMA ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATOSPERMIA ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
HANGOVER ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEAD TITUBATION ( 1 FDA reports)
HEARING AID USER ( 1 FDA reports)
HEART RATE ABNORMAL ( 1 FDA reports)
HEART VALVE INCOMPETENCE ( 1 FDA reports)
HELICOBACTER GASTRITIS ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC CONGESTION ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATITIS C VIRUS ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HERNIA ( 1 FDA reports)
HERPES ZOSTER DISSEMINATED ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERMETROPIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
HYPERTONIC BLADDER ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOPHOSPHATAEMIA ( 1 FDA reports)
HYPOPLASTIC LEFT HEART SYNDROME ( 1 FDA reports)
HYPOVENTILATION ( 1 FDA reports)
IMPAIRED DRIVING ABILITY ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
IMPRISONMENT ( 1 FDA reports)
INADEQUATE ANALGESIA ( 1 FDA reports)
INAPPROPRIATE AFFECT ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INGUINAL HERNIA ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE NODULE ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 1 FDA reports)
INTUBATION ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JAW DISORDER ( 1 FDA reports)
JOINT INJURY ( 1 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 1 FDA reports)
JOINT SPRAIN ( 1 FDA reports)
JOINT STIFFNESS ( 1 FDA reports)
JOINT WARMTH ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LIMB DEFORMITY ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LOSS OF CONTROL OF LEGS ( 1 FDA reports)
LOSS OF EMPLOYMENT ( 1 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
MACULAR DEGENERATION ( 1 FDA reports)
MANIA ( 1 FDA reports)
MECONIUM STAIN ( 1 FDA reports)
MENINGITIS ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
MICTURITION DISORDER ( 1 FDA reports)
MIDDLE EAR DISORDER ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MITRAL VALVE CALCIFICATION ( 1 FDA reports)
MITRAL VALVE DISEASE ( 1 FDA reports)
MULTIPLE INJURIES ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCLE CONTRACTURE ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MUSCLE STRAIN ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
NASAL OEDEMA ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NECROTISING RETINITIS ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NERVE ROOT COMPRESSION ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEURALGIC AMYOTROPHY ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NODAL MARGINAL ZONE B-CELL LYMPHOMA ( 1 FDA reports)
NYSTAGMUS ( 1 FDA reports)
OCCULT BLOOD POSITIVE ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
OESOPHAGEAL CARCINOMA ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
OPTIC NEURITIS ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
OSTEOPENIA ( 1 FDA reports)
OTOSCLEROSIS ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PELVIC FRACTURE ( 1 FDA reports)
PERONEAL NERVE PALSY ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PLATELET DISORDER ( 1 FDA reports)
PLATELET TRANSFUSION ( 1 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
POISONING ( 1 FDA reports)
POOR PERIPHERAL CIRCULATION ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 1 FDA reports)
PROGRESSIVE SUPRANUCLEAR PALSY ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PSEUDOMONAL SEPSIS ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
RADICULOPATHY ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
RESTLESS LEGS SYNDROME ( 1 FDA reports)
RESUSCITATION ( 1 FDA reports)
RETINAL DETACHMENT ( 1 FDA reports)
RETINAL INFARCTION ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
SARCOIDOSIS ( 1 FDA reports)
SCLERAL DISORDER ( 1 FDA reports)
SCROTAL DISORDER ( 1 FDA reports)
SCROTAL OEDEMA ( 1 FDA reports)
SEXUAL DYSFUNCTION ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SINUS ARRHYTHMIA ( 1 FDA reports)
SINUS CONGESTION ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SKIN ODOUR ABNORMAL ( 1 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
SPINAL X-RAY ABNORMAL ( 1 FDA reports)
SPLEEN DISORDER ( 1 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
STRABISMUS ( 1 FDA reports)
STREPTOCOCCAL SEPSIS ( 1 FDA reports)
STUPOR ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUBCUTANEOUS ABSCESS ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SYNOVIAL FLUID ANALYSIS ABNORMAL ( 1 FDA reports)
SYNOVITIS ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
THYROID DISORDER ( 1 FDA reports)
THYROID NEOPLASM ( 1 FDA reports)
TONGUE OEDEMA ( 1 FDA reports)
TONGUE ULCERATION ( 1 FDA reports)
TOOTH ABSCESS ( 1 FDA reports)
TOOTH DISORDER ( 1 FDA reports)
TOOTH EXTRACTION ( 1 FDA reports)
TOOTH IMPACTED ( 1 FDA reports)
TOOTH INFECTION ( 1 FDA reports)
TOOTH MALFORMATION ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TRANSFUSION ( 1 FDA reports)
TRICHOTILLOMANIA ( 1 FDA reports)
ULCER ( 1 FDA reports)
UMBILICAL HERNIA ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
UROSEPSIS ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VASCULAR OCCLUSION ( 1 FDA reports)
VENOUS ANGIOMA OF BRAIN ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VERBAL ABUSE ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VIBRATION TEST ABNORMAL ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VITREOUS FLOATERS ( 1 FDA reports)
WALKING AID USER ( 1 FDA reports)
WEANING FAILURE ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WOUND DECOMPOSITION ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)

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