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

DYSPNOEA ( 88 FDA reports)
DRUG INEFFECTIVE ( 52 FDA reports)
ASTHMA ( 48 FDA reports)
PNEUMONIA ( 45 FDA reports)
NAUSEA ( 41 FDA reports)
FATIGUE ( 40 FDA reports)
THROAT IRRITATION ( 40 FDA reports)
HYPERSENSITIVITY ( 37 FDA reports)
VOMITING ( 34 FDA reports)
PAIN IN EXTREMITY ( 33 FDA reports)
CHEST PAIN ( 32 FDA reports)
DIZZINESS ( 32 FDA reports)
OEDEMA PERIPHERAL ( 32 FDA reports)
ASTHENIA ( 30 FDA reports)
PAIN ( 30 FDA reports)
ANXIETY ( 29 FDA reports)
OROPHARYNGEAL PAIN ( 29 FDA reports)
PYREXIA ( 28 FDA reports)
BACK PAIN ( 27 FDA reports)
WEIGHT DECREASED ( 27 FDA reports)
HEADACHE ( 26 FDA reports)
CHEST DISCOMFORT ( 25 FDA reports)
WHEEZING ( 25 FDA reports)
BRONCHITIS ( 24 FDA reports)
GAIT DISTURBANCE ( 24 FDA reports)
MALAISE ( 24 FDA reports)
DEPRESSION ( 22 FDA reports)
HAEMOGLOBIN DECREASED ( 22 FDA reports)
OEDEMA ( 22 FDA reports)
COUGH ( 21 FDA reports)
DEHYDRATION ( 21 FDA reports)
DIARRHOEA ( 20 FDA reports)
PARAESTHESIA ( 20 FDA reports)
ARTHRALGIA ( 19 FDA reports)
INSOMNIA ( 19 FDA reports)
ATRIAL FIBRILLATION ( 18 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 18 FDA reports)
FALL ( 18 FDA reports)
FEELING ABNORMAL ( 18 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 18 FDA reports)
MYOCARDIAL INFARCTION ( 18 FDA reports)
RESPIRATORY FAILURE ( 18 FDA reports)
ANAEMIA ( 17 FDA reports)
CONDITION AGGRAVATED ( 17 FDA reports)
HYPOTENSION ( 17 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 17 FDA reports)
SKIN HYPERTROPHY ( 17 FDA reports)
CONFUSIONAL STATE ( 16 FDA reports)
LOSS OF CONSCIOUSNESS ( 16 FDA reports)
BLOOD PRESSURE INCREASED ( 15 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 15 FDA reports)
CEREBROVASCULAR ACCIDENT ( 15 FDA reports)
HYPERTENSION ( 15 FDA reports)
SKIN HYPERPIGMENTATION ( 15 FDA reports)
SKIN INDURATION ( 15 FDA reports)
SKIN TIGHTNESS ( 15 FDA reports)
TREMOR ( 15 FDA reports)
URTICARIA ( 15 FDA reports)
CONTUSION ( 14 FDA reports)
PULMONARY EMBOLISM ( 14 FDA reports)
URINARY TRACT INFECTION ( 14 FDA reports)
ABDOMINAL PAIN ( 13 FDA reports)
DEATH ( 13 FDA reports)
DECREASED APPETITE ( 13 FDA reports)
DRUG INTERACTION ( 13 FDA reports)
INCORRECT DOSE ADMINISTERED ( 13 FDA reports)
MYALGIA ( 13 FDA reports)
PRURITUS ( 13 FDA reports)
RASH PAPULAR ( 13 FDA reports)
STRESS ( 13 FDA reports)
WEIGHT INCREASED ( 13 FDA reports)
CONVULSION ( 12 FDA reports)
ERYTHEMA ( 12 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 12 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 12 FDA reports)
PRODUCT QUALITY ISSUE ( 12 FDA reports)
RENAL FAILURE ACUTE ( 12 FDA reports)
SEPSIS ( 12 FDA reports)
ABDOMINAL PAIN UPPER ( 11 FDA reports)
DYSPHAGIA ( 11 FDA reports)
EMOTIONAL DISTRESS ( 11 FDA reports)
HEART RATE INCREASED ( 11 FDA reports)
IRRITABILITY ( 11 FDA reports)
MEDICATION ERROR ( 11 FDA reports)
RENAL IMPAIRMENT ( 11 FDA reports)
TACHYCARDIA ( 11 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 11 FDA reports)
BLOOD CREATININE INCREASED ( 10 FDA reports)
BONE PAIN ( 10 FDA reports)
MITRAL VALVE INCOMPETENCE ( 10 FDA reports)
MUSCLE SPASMS ( 10 FDA reports)
OSTEOPOROSIS ( 10 FDA reports)
SOMNOLENCE ( 10 FDA reports)
SYNCOPE ( 10 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 9 FDA reports)
BLOOD GLUCOSE INCREASED ( 9 FDA reports)
BLOOD PRESSURE DECREASED ( 9 FDA reports)
CHILLS ( 9 FDA reports)
DRY SKIN ( 9 FDA reports)
DYSURIA ( 9 FDA reports)
MUSCLE FATIGUE ( 9 FDA reports)
PERICARDIAL EFFUSION ( 9 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 9 FDA reports)
PULMONARY OEDEMA ( 9 FDA reports)
RASH PRURITIC ( 9 FDA reports)
RECTAL HAEMORRHAGE ( 9 FDA reports)
SKIN PLAQUE ( 9 FDA reports)
ANHEDONIA ( 8 FDA reports)
AREFLEXIA ( 8 FDA reports)
CARDIAC DISORDER ( 8 FDA reports)
CARDIAC FAILURE ( 8 FDA reports)
CONSTIPATION ( 8 FDA reports)
DIABETES MELLITUS ( 8 FDA reports)
DYSPHONIA ( 8 FDA reports)
EXFOLIATIVE RASH ( 8 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 8 FDA reports)
HYPERHIDROSIS ( 8 FDA reports)
HYPERKERATOSIS ( 8 FDA reports)
HYPOKALAEMIA ( 8 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 8 FDA reports)
JOINT STIFFNESS ( 8 FDA reports)
MIGRAINE ( 8 FDA reports)
MUSCULAR WEAKNESS ( 8 FDA reports)
NASOPHARYNGITIS ( 8 FDA reports)
NEUTROPHIL COUNT DECREASED ( 8 FDA reports)
PANCREATITIS ( 8 FDA reports)
RASH ( 8 FDA reports)
SCAR ( 8 FDA reports)
SKIN DISCOLOURATION ( 8 FDA reports)
SKIN EXFOLIATION ( 8 FDA reports)
SUBCUTANEOUS NODULE ( 8 FDA reports)
VERTIGO ( 8 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 8 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 8 FDA reports)
ALOPECIA ( 7 FDA reports)
BLOOD UREA INCREASED ( 7 FDA reports)
CELLULITIS ( 7 FDA reports)
CRYING ( 7 FDA reports)
DRUG EFFECT DECREASED ( 7 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 7 FDA reports)
DUPUYTREN'S CONTRACTURE OPERATION ( 7 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 7 FDA reports)
INFECTION ( 7 FDA reports)
INFLUENZA ( 7 FDA reports)
INFLUENZA LIKE ILLNESS ( 7 FDA reports)
JOINT CONTRACTURE ( 7 FDA reports)
MEMORY IMPAIRMENT ( 7 FDA reports)
MUSCLE CONTRACTURE ( 7 FDA reports)
MUSCLE TWITCHING ( 7 FDA reports)
NEUTROPHIL COUNT INCREASED ( 7 FDA reports)
OSTEOARTHRITIS ( 7 FDA reports)
PAIN OF SKIN ( 7 FDA reports)
POLLAKIURIA ( 7 FDA reports)
PRODUCTIVE COUGH ( 7 FDA reports)
SKIN DISORDER ( 7 FDA reports)
SUICIDAL IDEATION ( 7 FDA reports)
SWELLING FACE ( 7 FDA reports)
VISION BLURRED ( 7 FDA reports)
AMNESIA ( 6 FDA reports)
ATRIAL SEPTAL DEFECT ( 6 FDA reports)
BRONCHOSPASM ( 6 FDA reports)
CARDIAC FUNCTION TEST ( 6 FDA reports)
DEEP VEIN THROMBOSIS ( 6 FDA reports)
DRUG HYPERSENSITIVITY ( 6 FDA reports)
DRY MOUTH ( 6 FDA reports)
DYSARTHRIA ( 6 FDA reports)
EXTRAVASATION ( 6 FDA reports)
EXTREMITY CONTRACTURE ( 6 FDA reports)
FLANK PAIN ( 6 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 6 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 6 FDA reports)
HAEMATURIA ( 6 FDA reports)
HYPONATRAEMIA ( 6 FDA reports)
MASS ( 6 FDA reports)
NASAL CONGESTION ( 6 FDA reports)
OXYGEN SATURATION DECREASED ( 6 FDA reports)
PRODUCT CONTAMINATION ( 6 FDA reports)
PROTHROMBIN TIME PROLONGED ( 6 FDA reports)
PULMONARY HYPERTENSION ( 6 FDA reports)
RENAL FAILURE ( 6 FDA reports)
RESPIRATORY DISTRESS ( 6 FDA reports)
SKIN LESION ( 6 FDA reports)
SWOLLEN TONGUE ( 6 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 6 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 6 FDA reports)
TYPE 2 DIABETES MELLITUS ( 6 FDA reports)
VENTRICULAR TACHYCARDIA ( 6 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 6 FDA reports)
VIRAL INFECTION ( 6 FDA reports)
ABNORMAL BEHAVIOUR ( 5 FDA reports)
AGITATION ( 5 FDA reports)
ANOREXIA ( 5 FDA reports)
BURNING SENSATION ( 5 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 5 FDA reports)
CARDIOMEGALY ( 5 FDA reports)
CEREBELLAR INFARCTION ( 5 FDA reports)
DRUG TOXICITY ( 5 FDA reports)
DYSGEUSIA ( 5 FDA reports)
ECONOMIC PROBLEM ( 5 FDA reports)
ESCHERICHIA TEST POSITIVE ( 5 FDA reports)
FLUID OVERLOAD ( 5 FDA reports)
FOOT FRACTURE ( 5 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 5 FDA reports)
GLOSSODYNIA ( 5 FDA reports)
HAEMATOCRIT DECREASED ( 5 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 5 FDA reports)
HYPERTHERMIA MALIGNANT ( 5 FDA reports)
INJECTION SITE PAIN ( 5 FDA reports)
JOINT SWELLING ( 5 FDA reports)
LIVER DISORDER ( 5 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 5 FDA reports)
MULTIPLE INJURIES ( 5 FDA reports)
MUSCULOSKELETAL PAIN ( 5 FDA reports)
NECK PAIN ( 5 FDA reports)
PHARYNGEAL OEDEMA ( 5 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 5 FDA reports)
PLEURAL EFFUSION ( 5 FDA reports)
POISONING ( 5 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 5 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 5 FDA reports)
PULMONARY CONGESTION ( 5 FDA reports)
RESPIRATORY RATE INCREASED ( 5 FDA reports)
RHINORRHOEA ( 5 FDA reports)
SNORING ( 5 FDA reports)
SPEECH DISORDER ( 5 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 5 FDA reports)
APHAGIA ( 4 FDA reports)
ARRHYTHMIA ( 4 FDA reports)
BLISTER ( 4 FDA reports)
BLOOD CALCIUM DECREASED ( 4 FDA reports)
BLOOD POTASSIUM DECREASED ( 4 FDA reports)
BONE LESION ( 4 FDA reports)
BRADYCARDIA ( 4 FDA reports)
BRAIN INJURY ( 4 FDA reports)
BURKHOLDERIA CEPACIA INFECTION ( 4 FDA reports)
CARDIAC ARREST ( 4 FDA reports)
CARDIOGENIC SHOCK ( 4 FDA reports)
CEREBRAL HAEMORRHAGE ( 4 FDA reports)
CHOLELITHIASIS ( 4 FDA reports)
COLD SWEAT ( 4 FDA reports)
COMPRESSION FRACTURE ( 4 FDA reports)
CONGENITAL ANOMALY ( 4 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 4 FDA reports)
DILATATION ATRIAL ( 4 FDA reports)
DISEASE PROGRESSION ( 4 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 4 FDA reports)
DISTURBANCE IN ATTENTION ( 4 FDA reports)
DRUG DOSE OMISSION ( 4 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 4 FDA reports)
DRY EYE ( 4 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 4 FDA reports)
EPISTAXIS ( 4 FDA reports)
H1N1 INFLUENZA ( 4 FDA reports)
HYPERKALAEMIA ( 4 FDA reports)
HYPOAESTHESIA ( 4 FDA reports)
INFUSION RELATED REACTION ( 4 FDA reports)
INJURY ( 4 FDA reports)
INTERSTITIAL LUNG DISEASE ( 4 FDA reports)
LACERATION ( 4 FDA reports)
LACTIC ACIDOSIS ( 4 FDA reports)
LETHARGY ( 4 FDA reports)
LUNG INFILTRATION ( 4 FDA reports)
MENTAL DISORDER ( 4 FDA reports)
MENTAL IMPAIRMENT ( 4 FDA reports)
METABOLIC ACIDOSIS ( 4 FDA reports)
MOBILITY DECREASED ( 4 FDA reports)
MYOCARDIAL ISCHAEMIA ( 4 FDA reports)
NEPHROLITHIASIS ( 4 FDA reports)
NEURODEVELOPMENTAL DISORDER ( 4 FDA reports)
NEUTROPENIA ( 4 FDA reports)
NIGHT SWEATS ( 4 FDA reports)
OFF LABEL USE ( 4 FDA reports)
OSTEOMYELITIS ( 4 FDA reports)
PALLOR ( 4 FDA reports)
PALPITATIONS ( 4 FDA reports)
PEAU D'ORANGE ( 4 FDA reports)
PRESYNCOPE ( 4 FDA reports)
PSORIASIS ( 4 FDA reports)
PUPIL FIXED ( 4 FDA reports)
RESTLESS LEGS SYNDROME ( 4 FDA reports)
RESTLESSNESS ( 4 FDA reports)
SINUS TACHYCARDIA ( 4 FDA reports)
SINUSITIS ( 4 FDA reports)
SLEEP APNOEA SYNDROME ( 4 FDA reports)
SPLENOMEGALY ( 4 FDA reports)
STOMATITIS ( 4 FDA reports)
SWELLING ( 4 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 4 FDA reports)
THROMBOSIS ( 4 FDA reports)
TONGUE DISORDER ( 4 FDA reports)
TOOTH LOSS ( 4 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 4 FDA reports)
TREATMENT NONCOMPLIANCE ( 4 FDA reports)
TRICUSPID VALVE DISEASE ( 4 FDA reports)
UNRESPONSIVE TO STIMULI ( 4 FDA reports)
VITAMIN D DEFICIENCY ( 4 FDA reports)
WITHDRAWAL SYNDROME ( 4 FDA reports)
ABDOMINAL DISCOMFORT ( 3 FDA reports)
ADENOIDAL HYPERTROPHY ( 3 FDA reports)
ADRENAL SUPPRESSION ( 3 FDA reports)
ANGER ( 3 FDA reports)
ANGIOEDEMA ( 3 FDA reports)
AORTIC VALVE INCOMPETENCE ( 3 FDA reports)
ARTHRITIS ( 3 FDA reports)
ATELECTASIS ( 3 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 3 FDA reports)
AUTISM ( 3 FDA reports)
BALANCE DISORDER ( 3 FDA reports)
BLOOD GLUCOSE DECREASED ( 3 FDA reports)
BREATH SOUNDS ABNORMAL ( 3 FDA reports)
BRONCHIAL SECRETION RETENTION ( 3 FDA reports)
CALCULUS URETERIC ( 3 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 3 FDA reports)
CARDIOMYOPATHY ( 3 FDA reports)
COAGULOPATHY ( 3 FDA reports)
COMA SCALE ABNORMAL ( 3 FDA reports)
CONJUNCTIVITIS ( 3 FDA reports)
COORDINATION ABNORMAL ( 3 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 3 FDA reports)
CROUP INFECTIOUS ( 3 FDA reports)
DEFAECATION URGENCY ( 3 FDA reports)
DELIRIUM ( 3 FDA reports)
DENTAL CARIES ( 3 FDA reports)
DIVERTICULITIS ( 3 FDA reports)
DRUG ABUSE ( 3 FDA reports)
DRUG INTOLERANCE ( 3 FDA reports)
DRY THROAT ( 3 FDA reports)
DYSPEPSIA ( 3 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 3 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 3 FDA reports)
ESSENTIAL HYPERTENSION ( 3 FDA reports)
EXPOSURE TO TOXIC AGENT ( 3 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 3 FDA reports)
FACIAL ASYMMETRY ( 3 FDA reports)
FACIAL PARESIS ( 3 FDA reports)
FLUID RETENTION ( 3 FDA reports)
FLUSHING ( 3 FDA reports)
FORCEPS DELIVERY ( 3 FDA reports)
GANGRENE ( 3 FDA reports)
GASTRITIS EROSIVE ( 3 FDA reports)
GASTROENTERITIS VIRAL ( 3 FDA reports)
HAEMOPTYSIS ( 3 FDA reports)
HAEMORRHAGE ( 3 FDA reports)
HALLUCINATION ( 3 FDA reports)
HEAD INJURY ( 3 FDA reports)
HEART RATE ABNORMAL ( 3 FDA reports)
HEART RATE IRREGULAR ( 3 FDA reports)
HERPES ZOSTER ( 3 FDA reports)
HIP FRACTURE ( 3 FDA reports)
HYPERCALCAEMIA ( 3 FDA reports)
HYPERGLYCAEMIA ( 3 FDA reports)
HYPERTONIA ( 3 FDA reports)
HYPERVENTILATION ( 3 FDA reports)
HYPERVISCOSITY SYNDROME ( 3 FDA reports)
HYPOPHAGIA ( 3 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 3 FDA reports)
ISCHAEMIA ( 3 FDA reports)
JAUNDICE ( 3 FDA reports)
KIDNEY INFECTION ( 3 FDA reports)
LARYNGEAL STENOSIS ( 3 FDA reports)
LARYNGOTRACHEO BRONCHITIS ( 3 FDA reports)
LIMB ASYMMETRY ( 3 FDA reports)
LOBAR PNEUMONIA ( 3 FDA reports)
LOCALISED INFECTION ( 3 FDA reports)
LUNG INFECTION ( 3 FDA reports)
LUNG NEOPLASM ( 3 FDA reports)
MENSTRUATION IRREGULAR ( 3 FDA reports)
MICTURITION URGENCY ( 3 FDA reports)
MUSCLE RIGIDITY ( 3 FDA reports)
MUSCLE STRAIN ( 3 FDA reports)
NEOPLASM MALIGNANT ( 3 FDA reports)
NERVOUSNESS ( 3 FDA reports)
NEUROPATHY PERIPHERAL ( 3 FDA reports)
NON-SMALL CELL LUNG CANCER ( 3 FDA reports)
ORAL PAIN ( 3 FDA reports)
OTITIS MEDIA CHRONIC ( 3 FDA reports)
OVERDOSE ( 3 FDA reports)
PANCREATIC ABSCESS ( 3 FDA reports)
PETECHIAE ( 3 FDA reports)
PLATELET COUNT INCREASED ( 3 FDA reports)
PLEURISY ( 3 FDA reports)
PNEUMONITIS ( 3 FDA reports)
POOR QUALITY SLEEP ( 3 FDA reports)
PROTEIN URINE ( 3 FDA reports)
PULMONARY ARTERY STENOSIS ( 3 FDA reports)
PULMONARY FIBROSIS ( 3 FDA reports)
PULMONARY INFARCTION ( 3 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 3 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 3 FDA reports)
QRS AXIS ABNORMAL ( 3 FDA reports)
RESPIRATORY DISORDER ( 3 FDA reports)
RESPIRATORY TRACT INFECTION ( 3 FDA reports)
RHEUMATOID ARTHRITIS ( 3 FDA reports)
RHINITIS ( 3 FDA reports)
SCAB ( 3 FDA reports)
SECRETION DISCHARGE ( 3 FDA reports)
SERUM SICKNESS ( 3 FDA reports)
SKIN BURNING SENSATION ( 3 FDA reports)
SKIN CANCER ( 3 FDA reports)
SLEEP DISORDER ( 3 FDA reports)
SPINAL COMPRESSION FRACTURE ( 3 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 3 FDA reports)
TEMPERATURE INTOLERANCE ( 3 FDA reports)
THERAPEUTIC PRODUCT CONTAMINATION ( 3 FDA reports)
THROAT TIGHTNESS ( 3 FDA reports)
TOOTH ABSCESS ( 3 FDA reports)
TOOTH FRACTURE ( 3 FDA reports)
TOOTH INFECTION ( 3 FDA reports)
TRISMUS ( 3 FDA reports)
UNEVALUABLE EVENT ( 3 FDA reports)
VACUUM EXTRACTOR DELIVERY ( 3 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 3 FDA reports)
VIITH NERVE PARALYSIS ( 3 FDA reports)
VIRAL PHARYNGITIS ( 3 FDA reports)
VISUAL FIELD DEFECT ( 3 FDA reports)
ABASIA ( 2 FDA reports)
ABDOMINAL ADHESIONS ( 2 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ABDOMINAL HERNIA ( 2 FDA reports)
ABSCESS ( 2 FDA reports)
ACUTE RESPIRATORY FAILURE ( 2 FDA reports)
AGEUSIA ( 2 FDA reports)
AGGRESSION ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
ANAPHYLACTIC SHOCK ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
AORTIC STENOSIS ( 2 FDA reports)
APHONIA ( 2 FDA reports)
APNOEA ( 2 FDA reports)
BABINSKI REFLEX TEST ( 2 FDA reports)
BIPOLAR I DISORDER ( 2 FDA reports)
BLINDNESS ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BLOOD CORTISOL DECREASED ( 2 FDA reports)
BLOOD PH DECREASED ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 2 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ( 2 FDA reports)
BRAIN DEATH ( 2 FDA reports)
BRONCHIECTASIS ( 2 FDA reports)
BRONCHITIS CHEMICAL ( 2 FDA reports)
BRONCHITIS CHRONIC ( 2 FDA reports)
BRONCHOPNEUMONIA ( 2 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 2 FDA reports)
BURN OESOPHAGEAL ( 2 FDA reports)
CANDIDIASIS ( 2 FDA reports)
CAROTID BRUIT ( 2 FDA reports)
CHOLECYSTITIS ( 2 FDA reports)
CHOLECYSTITIS CHRONIC ( 2 FDA reports)
COMA ( 2 FDA reports)
COMPLETED SUICIDE ( 2 FDA reports)
CONDUCTION DISORDER ( 2 FDA reports)
CORONARY ARTERY OCCLUSION ( 2 FDA reports)
CREATININE URINE INCREASED ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
CYSTITIS HAEMORRHAGIC ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DEVICE MISUSE ( 2 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 2 FDA reports)
DIPLOPIA ( 2 FDA reports)
DISABILITY ( 2 FDA reports)
DISCOMFORT ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DRUG ABUSER ( 2 FDA reports)
DRUG DEPENDENCE ( 2 FDA reports)
DYSGRAPHIA ( 2 FDA reports)
DYSPNOEA EXERTIONAL ( 2 FDA reports)
EAR INFECTION ( 2 FDA reports)
EJECTION FRACTION DECREASED ( 2 FDA reports)
EMOTIONAL DISORDER ( 2 FDA reports)
EPILEPSY ( 2 FDA reports)
ERUCTATION ( 2 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 2 FDA reports)
EXERCISE TOLERANCE DECREASED ( 2 FDA reports)
EYE DISORDER ( 2 FDA reports)
EYE MOVEMENT DISORDER ( 2 FDA reports)
FAECAL INCONTINENCE ( 2 FDA reports)
FEAR ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
FEELING COLD ( 2 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 2 FDA reports)
FEMUR FRACTURE ( 2 FDA reports)
FIBROMYALGIA ( 2 FDA reports)
FIBROSIS ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 2 FDA reports)
FOOD ALLERGY ( 2 FDA reports)
FOOD POISONING ( 2 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 2 FDA reports)
GALLBLADDER DISORDER ( 2 FDA reports)
GASTRIC DISORDER ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
GASTRITIS ATROPHIC ( 2 FDA reports)
GASTROENTERITIS ROTAVIRUS ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HAEMODYNAMIC INSTABILITY ( 2 FDA reports)
HAEMOPHILUS INFECTION ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HIP DYSPLASIA ( 2 FDA reports)
HIRSUTISM ( 2 FDA reports)
HYDROCELE ( 2 FDA reports)
HYPERCHOLESTEROLAEMIA ( 2 FDA reports)
HYPERPHAGIA ( 2 FDA reports)
HYPERTENSIVE CRISIS ( 2 FDA reports)
HYPOAESTHESIA ORAL ( 2 FDA reports)
HYPOTONIA ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
ILL-DEFINED DISORDER ( 2 FDA reports)
INAPPROPRIATE AFFECT ( 2 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 2 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 2 FDA reports)
INJECTION SITE ERYTHEMA ( 2 FDA reports)
INJECTION SITE HAEMATOMA ( 2 FDA reports)
INJECTION SITE REACTION ( 2 FDA reports)
INTESTINAL OBSTRUCTION ( 2 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 2 FDA reports)
JOINT INJURY ( 2 FDA reports)
JOINT LOCK ( 2 FDA reports)
LATENT TUBERCULOSIS ( 2 FDA reports)
LEARNING DISORDER ( 2 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA METASTATIC ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
LYMPHOPENIA ( 2 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 2 FDA reports)
MENINGITIS ( 2 FDA reports)
MENISCUS LESION ( 2 FDA reports)
MENTAL STATUS CHANGES ( 2 FDA reports)
METAL POISONING ( 2 FDA reports)
MOOD SWINGS ( 2 FDA reports)
MUCOUS MEMBRANE DISORDER ( 2 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 2 FDA reports)
NASAL DISCOMFORT ( 2 FDA reports)
NASAL DRYNESS ( 2 FDA reports)
NASAL OBSTRUCTION ( 2 FDA reports)
NASAL ODOUR ( 2 FDA reports)
NASAL POLYPS ( 2 FDA reports)
NEOPLASM ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
NODAL ARRHYTHMIA ( 2 FDA reports)
OPEN WOUND ( 2 FDA reports)
ORAL CANDIDIASIS ( 2 FDA reports)
ORAL INTAKE REDUCED ( 2 FDA reports)
OROPHARYNGEAL PLAQUE ( 2 FDA reports)
OSTEOPENIA ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PANIC ATTACK ( 2 FDA reports)
PHOTOSENSITIVITY REACTION ( 2 FDA reports)
PO2 DECREASED ( 2 FDA reports)
POLYARTERITIS NODOSA ( 2 FDA reports)
POLYNEUROPATHY ( 2 FDA reports)
RADIUS FRACTURE ( 2 FDA reports)
RASH ERYTHEMATOUS ( 2 FDA reports)
RASH MACULAR ( 2 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 2 FDA reports)
REFLUX OESOPHAGITIS ( 2 FDA reports)
RESPIRATORY TRACT IRRITATION ( 2 FDA reports)
SENSORY DISTURBANCE ( 2 FDA reports)
SICK SINUS SYNDROME ( 2 FDA reports)
SINUS ARRHYTHMIA ( 2 FDA reports)
SINUS BRADYCARDIA ( 2 FDA reports)
SKIN ATROPHY ( 2 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 2 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 2 FDA reports)
SOFT TISSUE MASS ( 2 FDA reports)
SPINAL PAIN ( 2 FDA reports)
SQUAMOUS CELL CARCINOMA ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
SUFFOCATION FEELING ( 2 FDA reports)
SUICIDE ATTEMPT ( 2 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
SYNOVIAL CYST ( 2 FDA reports)
TEARFULNESS ( 2 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
THYROID DISORDER ( 2 FDA reports)
TOOTH DISORDER ( 2 FDA reports)
TOOTH EROSION ( 2 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 2 FDA reports)
URINE OUTPUT DECREASED ( 2 FDA reports)
UTERINE PERFORATION ( 2 FDA reports)
VAGINAL HAEMORRHAGE ( 2 FDA reports)
VENTRICULAR FIBRILLATION ( 2 FDA reports)
VISUAL DISTURBANCE ( 2 FDA reports)
VISUAL IMPAIRMENT ( 2 FDA reports)
WEIGHT FLUCTUATION ( 2 FDA reports)
WRIST FRACTURE ( 2 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
ABSCESS LIMB ( 1 FDA reports)
ACNE ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
ADENOIDECTOMY ( 1 FDA reports)
ADENOVIRUS INFECTION ( 1 FDA reports)
ADVERSE REACTION ( 1 FDA reports)
AFFECT LABILITY ( 1 FDA reports)
ALCOHOL POISONING ( 1 FDA reports)
ALCOHOL PROBLEM ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANION GAP INCREASED ( 1 FDA reports)
ANKYLOSING SPONDYLITIS ( 1 FDA reports)
ANOSMIA ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
AORTIC VALVE CALCIFICATION ( 1 FDA reports)
APPARENT DEATH ( 1 FDA reports)
APPETITE DISORDER ( 1 FDA reports)
APPLICATION SITE URTICARIA ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ASOCIAL BEHAVIOUR ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ASPERGILLOSIS ( 1 FDA reports)
ASPHYXIA ( 1 FDA reports)
ASPIRATION BIOPSY ( 1 FDA reports)
ASPIRATION PLEURAL CAVITY ABNORMAL ( 1 FDA reports)
ASTHMATIC CRISIS ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
BILIARY COLIC ( 1 FDA reports)
BILIARY DRAINAGE ( 1 FDA reports)
BILIARY DYSKINESIA ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
BLEPHARITIS ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD MERCURY ABNORMAL ( 1 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD PROLACTIN INCREASED ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BONE DENSITY DECREASED ( 1 FDA reports)
BONE LOSS ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BRAIN STEM INFARCTION ( 1 FDA reports)
BRAIN STEM ISCHAEMIA ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BREAST CANCER STAGE I ( 1 FDA reports)
BREATH SOUNDS ABSENT ( 1 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 1 FDA reports)
BRONCHIAL IRRITATION ( 1 FDA reports)
BRONCHIAL OBSTRUCTION ( 1 FDA reports)
BRONCHITIS ACUTE ( 1 FDA reports)
BRONCHOSPASM PARADOXICAL ( 1 FDA reports)
CARBON DIOXIDE INCREASED ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CARDIAC OPERATION ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 1 FDA reports)
CARDIOTOXICITY ( 1 FDA reports)
CARDIOVERSION ( 1 FDA reports)
CARPAL TUNNEL SYNDROME ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CATARACT DIABETIC ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBRAL DISORDER ( 1 FDA reports)
CHAPPED LIPS ( 1 FDA reports)
CHEMICAL POISONING ( 1 FDA reports)
CHILDHOOD DEPRESSION ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
CHOLECYSTITIS ACUTE ( 1 FDA reports)
CHOLESTEROSIS ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 1 FDA reports)
CLAUSTROPHOBIA ( 1 FDA reports)
CLAVICLE FRACTURE ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
COARCTATION OF THE AORTA ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
COLON ADENOMA ( 1 FDA reports)
COLONIC FISTULA ( 1 FDA reports)
COLOSTOMY ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
CONGENITAL CARDIOVASCULAR ANOMALY ( 1 FDA reports)
CORNEAL DISORDER ( 1 FDA reports)
CORNEAL PERFORATION ( 1 FDA reports)
CORNEAL REFLEX DECREASED ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
CREATINE URINE INCREASED ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
CYST ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
CYSTOID MACULAR OEDEMA ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DEVELOPMENTAL DELAY ( 1 FDA reports)
DEVICE BREAKAGE ( 1 FDA reports)
DEVICE DISLOCATION ( 1 FDA reports)
DEVICE FAILURE ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DIABETIC NEUROPATHY ( 1 FDA reports)
DIASTOLIC DYSFUNCTION ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DISINHIBITION ( 1 FDA reports)
DISLOCATION OF VERTEBRA ( 1 FDA reports)
DIVORCED ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG EFFECT DELAYED ( 1 FDA reports)
DRUG EFFECT INCREASED ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG LABEL CONFUSION ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
EDUCATIONAL PROBLEM ( 1 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
ENAMEL ANOMALY ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
ENTEROVESICAL FISTULA ( 1 FDA reports)
ERYTHEMA INFECTIOSUM ( 1 FDA reports)
EXCITABILITY ( 1 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
EYELID FUNCTION DISORDER ( 1 FDA reports)
FACE INJURY ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FAECALOMA ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FALLOT'S TETRALOGY ( 1 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 1 FDA reports)
FAT NECROSIS ( 1 FDA reports)
FEBRILE CONVULSION ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FLOPPY IRIS SYNDROME ( 1 FDA reports)
FOETAL MACROSOMIA ( 1 FDA reports)
FOOD AVERSION ( 1 FDA reports)
FOREARM FRACTURE ( 1 FDA reports)
FUNGAL SKIN INFECTION ( 1 FDA reports)
GALLBLADDER OPERATION ( 1 FDA reports)
GASTRIC INFECTION ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTRITIS HAEMORRHAGIC ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GASTROENTERITIS EOSINOPHILIC ( 1 FDA reports)
GENERALISED ANXIETY DISORDER ( 1 FDA reports)
GINGIVAL DISORDER ( 1 FDA reports)
GINGIVAL PAIN ( 1 FDA reports)
GOITRE ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HAIR COLOUR CHANGES ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HEART INJURY ( 1 FDA reports)
HEART SOUNDS ABNORMAL ( 1 FDA reports)
HEART VALVE INCOMPETENCE ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC INFECTION ( 1 FDA reports)
HEPATIC LESION ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATITIS B ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATOBLASTOMA ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HISTOPLASMOSIS ( 1 FDA reports)
HOMICIDAL IDEATION ( 1 FDA reports)
HOUSE DUST ALLERGY ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERTONIC BLADDER ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
HYPOPLASTIC LEFT HEART SYNDROME ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
ILEUS ( 1 FDA reports)
ILEUS PARALYTIC ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 1 FDA reports)
INCORRECT DRUG DOSAGE FORM ADMINISTERED ( 1 FDA reports)
INCORRECT STORAGE OF DRUG ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
INJECTION SITE INDURATION ( 1 FDA reports)
INJECTION SITE PALLOR ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTERVERTEBRAL DISCITIS ( 1 FDA reports)
INTESTINAL HAEMORRHAGE ( 1 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 1 FDA reports)
INTRACRANIAL HYPOTENSION ( 1 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 1 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 1 FDA reports)
JOINT DISLOCATION ( 1 FDA reports)
JOINT EFFUSION ( 1 FDA reports)
KYPHOSIS ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LACTATION DISORDER ( 1 FDA reports)
LARYNGITIS ( 1 FDA reports)
LEARNING DISABILITY ( 1 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LEUKOPLAKIA ORAL ( 1 FDA reports)
LIBIDO DECREASED ( 1 FDA reports)
LIGAMENT SPRAIN ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LIP DISCOLOURATION ( 1 FDA reports)
LIPOMA ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
MACULAR DEGENERATION ( 1 FDA reports)
MALABSORPTION ( 1 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 1 FDA reports)
MALIGNANT GLIOMA ( 1 FDA reports)
MALIGNANT MELANOMA IN SITU ( 1 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 1 FDA reports)
MARITAL PROBLEM ( 1 FDA reports)
MECONIUM IN AMNIOTIC FLUID ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MENINGORRHAGIA ( 1 FDA reports)
MENOPAUSAL SYMPTOMS ( 1 FDA reports)
MENOPAUSE ( 1 FDA reports)
MENTAL RETARDATION SEVERITY UNSPECIFIED ( 1 FDA reports)
MESANGIOPROLIFERATIVE GLOMERULONEPHRITIS ( 1 FDA reports)
METABOLIC ENCEPHALOPATHY ( 1 FDA reports)
METASTASES TO LYMPH NODES ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
MITRAL VALVE CALCIFICATION ( 1 FDA reports)
MITRAL VALVE REPAIR ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MULTIPLE ALLERGIES ( 1 FDA reports)
MUSCLE MASS ( 1 FDA reports)
MUSCLE RUPTURE ( 1 FDA reports)
MUSCLE SPASTICITY ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
MYASTHENIA GRAVIS ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NAIL DISORDER ( 1 FDA reports)
NASAL NEOPLASM ( 1 FDA reports)
NECK INJURY ( 1 FDA reports)
NEGATIVE THOUGHTS ( 1 FDA reports)
NERVE COMPRESSION ( 1 FDA reports)
NERVE INJURY ( 1 FDA reports)
NEUROGENIC BLADDER ( 1 FDA reports)
NEUTROPHILIA ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
NODAL RHYTHM ( 1 FDA reports)
NOSOCOMIAL INFECTION ( 1 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OESOPHAGEAL PAIN ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
OESOPHAGITIS ULCERATIVE ( 1 FDA reports)
OPPOSITIONAL DEFIANT DISORDER ( 1 FDA reports)
ORAL DISCOMFORT ( 1 FDA reports)
ORAL MUCOSAL BLISTERING ( 1 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 1 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
OTITIS EXTERNA ( 1 FDA reports)
OTITIS MEDIA ( 1 FDA reports)
OVARIAN CANCER ( 1 FDA reports)
OVARIAN CANCER RECURRENT ( 1 FDA reports)
OXYGEN CONSUMPTION DECREASED ( 1 FDA reports)
OXYGEN CONSUMPTION INCREASED ( 1 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PANIC DISORDER ( 1 FDA reports)
PAROSMIA ( 1 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PELVIC PAIN ( 1 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PERIPHERAL EMBOLISM ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PHARYNGEAL ULCERATION ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PLEURAL HAEMORRHAGE ( 1 FDA reports)
PLEURITIC PAIN ( 1 FDA reports)
PNEUMOTHORAX TRAUMATIC ( 1 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 1 FDA reports)
POPLITEAL PULSE DECREASED ( 1 FDA reports)
POST CONCUSSION SYNDROME ( 1 FDA reports)
POST LUMBAR PUNCTURE SYNDROME ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
POST PROCEDURAL SEPSIS ( 1 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 1 FDA reports)
POSTPARTUM HAEMORRHAGE ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
PROCTOCOLECTOMY ( 1 FDA reports)
PRODUCT TASTE ABNORMAL ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PSORIATIC ARTHROPATHY ( 1 FDA reports)
PSYCHIATRIC SYMPTOM ( 1 FDA reports)
PULMONARY ARTERIOPATHY ( 1 FDA reports)
PULMONARY ARTERY STENOSIS CONGENITAL ( 1 FDA reports)
PULMONARY MASS ( 1 FDA reports)
PULMONARY SARCOIDOSIS ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
PULSE PRESSURE DECREASED ( 1 FDA reports)
PURPURA ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
RALES ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE DECREASED ( 1 FDA reports)
RENAL ARTERY STENOSIS ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL TRANSPLANT ( 1 FDA reports)
RESIDUAL URINE ( 1 FDA reports)
RESPIRATORY ACIDOSIS ( 1 FDA reports)
RESPIRATORY ALKALOSIS ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESUSCITATION ( 1 FDA reports)
RETCHING ( 1 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
RHINITIS ALLERGIC ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SACROILIITIS ( 1 FDA reports)
SARCOIDOSIS ( 1 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 1 FDA reports)
SCHIZOPHRENIA ( 1 FDA reports)
SELF-INJURIOUS IDEATION ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SIALOADENITIS ( 1 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SINUS HEADACHE ( 1 FDA reports)
SKIN HAEMORRHAGE ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SLEEP WALKING ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SPIDER VEIN ( 1 FDA reports)
SPINAL CORD COMPRESSION ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
SPUTUM INCREASED ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STATUS ASTHMATICUS ( 1 FDA reports)
STENT PLACEMENT ( 1 FDA reports)
STRESS CARDIOMYOPATHY ( 1 FDA reports)
STRIDOR ( 1 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
SWEAT GLAND DISORDER ( 1 FDA reports)
TARDIVE DYSKINESIA ( 1 FDA reports)
TELANGIECTASIA ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
TESTICULAR SWELLING ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
THIRST ( 1 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 1 FDA reports)
THYROID NEOPLASM ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TOBACCO ABUSE ( 1 FDA reports)
TOOTH DEPOSIT ( 1 FDA reports)
TOOTH REPAIR ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TUMOUR PAIN ( 1 FDA reports)
TUNNEL VISION ( 1 FDA reports)
TYPE 1 DIABETES MELLITUS ( 1 FDA reports)
ULCER ( 1 FDA reports)
ULNA FRACTURE ( 1 FDA reports)
UNDERDOSE ( 1 FDA reports)
UPPER LIMB FRACTURE ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINE AMYLASE INCREASED ( 1 FDA reports)
URINE ANALYSIS ABNORMAL ( 1 FDA reports)
URINE CALCIUM INCREASED ( 1 FDA reports)
URINE ODOUR ABNORMAL ( 1 FDA reports)
UROGRAM ABNORMAL ( 1 FDA reports)
UROSEPSIS ( 1 FDA reports)
VENA CAVA THROMBOSIS ( 1 FDA reports)
VENOUS INSUFFICIENCY ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VENTRICULAR HYPOPLASIA ( 1 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VITAMIN D DECREASED ( 1 FDA reports)
VITREOUS HAEMORRHAGE ( 1 FDA reports)
VOCAL CORD DISORDER ( 1 FDA reports)
WALKING AID USER ( 1 FDA reports)
WOUND ( 1 FDA reports)
WOUND SECRETION ( 1 FDA reports)

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