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

DYSPNOEA ( 99 FDA reports)
ASTHMA ( 60 FDA reports)
DRUG INEFFECTIVE ( 54 FDA reports)
COUGH ( 43 FDA reports)
PNEUMONIA ( 42 FDA reports)
NAUSEA ( 39 FDA reports)
DIZZINESS ( 38 FDA reports)
CHEST PAIN ( 36 FDA reports)
DYSPHONIA ( 36 FDA reports)
HEADACHE ( 35 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 33 FDA reports)
PRODUCT QUALITY ISSUE ( 31 FDA reports)
PAIN ( 30 FDA reports)
FATIGUE ( 26 FDA reports)
CONDITION AGGRAVATED ( 25 FDA reports)
VOMITING ( 25 FDA reports)
ARTHRALGIA ( 24 FDA reports)
ASTHENIA ( 23 FDA reports)
MYALGIA ( 23 FDA reports)
MYOCARDIAL INFARCTION ( 23 FDA reports)
BACK PAIN ( 21 FDA reports)
DEPRESSION ( 21 FDA reports)
TREMOR ( 21 FDA reports)
WEIGHT INCREASED ( 21 FDA reports)
CHEST DISCOMFORT ( 20 FDA reports)
DIARRHOEA ( 20 FDA reports)
MUSCLE SPASMS ( 20 FDA reports)
PAIN IN EXTREMITY ( 20 FDA reports)
CANDIDIASIS ( 19 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 18 FDA reports)
HYPERTENSION ( 18 FDA reports)
PALPITATIONS ( 18 FDA reports)
CEREBROVASCULAR ACCIDENT ( 17 FDA reports)
HEART RATE INCREASED ( 17 FDA reports)
OEDEMA PERIPHERAL ( 17 FDA reports)
PRURITUS ( 17 FDA reports)
RASH ( 17 FDA reports)
VISION BLURRED ( 17 FDA reports)
WEIGHT DECREASED ( 17 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 16 FDA reports)
FEELING ABNORMAL ( 16 FDA reports)
BRONCHITIS ( 15 FDA reports)
HYPERSENSITIVITY ( 15 FDA reports)
LOSS OF CONSCIOUSNESS ( 15 FDA reports)
OROPHARYNGEAL PAIN ( 15 FDA reports)
URTICARIA ( 15 FDA reports)
APHONIA ( 14 FDA reports)
BLOOD PRESSURE INCREASED ( 14 FDA reports)
HYPOAESTHESIA ( 14 FDA reports)
EPISTAXIS ( 13 FDA reports)
FALL ( 13 FDA reports)
HYPERHIDROSIS ( 13 FDA reports)
MALAISE ( 13 FDA reports)
PARAESTHESIA ( 13 FDA reports)
CONVULSION ( 12 FDA reports)
DRY MOUTH ( 12 FDA reports)
DYSGEUSIA ( 12 FDA reports)
HAEMOPTYSIS ( 12 FDA reports)
HYPOTENSION ( 12 FDA reports)
INSOMNIA ( 12 FDA reports)
PULMONARY EMBOLISM ( 12 FDA reports)
PYREXIA ( 12 FDA reports)
URINARY TRACT INFECTION ( 12 FDA reports)
WHEEZING ( 12 FDA reports)
CATARACT ( 11 FDA reports)
CHILLS ( 11 FDA reports)
DEHYDRATION ( 11 FDA reports)
MUSCULAR WEAKNESS ( 11 FDA reports)
SOMNOLENCE ( 11 FDA reports)
ABDOMINAL PAIN ( 10 FDA reports)
ANAEMIA ( 10 FDA reports)
ANXIETY ( 10 FDA reports)
ATRIAL FIBRILLATION ( 10 FDA reports)
BLOOD GLUCOSE INCREASED ( 10 FDA reports)
DEATH ( 10 FDA reports)
LUNG DISORDER ( 10 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 10 FDA reports)
CORONARY ARTERY DISEASE ( 9 FDA reports)
DEEP VEIN THROMBOSIS ( 9 FDA reports)
NECK PAIN ( 9 FDA reports)
OSTEOPOROSIS ( 9 FDA reports)
ABDOMINAL PAIN UPPER ( 8 FDA reports)
ARRHYTHMIA ( 8 FDA reports)
BONE PAIN ( 8 FDA reports)
CARDIAC ARREST ( 8 FDA reports)
CONSTIPATION ( 8 FDA reports)
DEVICE FAILURE ( 8 FDA reports)
DYSPHAGIA ( 8 FDA reports)
INFECTION ( 8 FDA reports)
LARYNGITIS ( 8 FDA reports)
OVERDOSE ( 8 FDA reports)
RESPIRATORY DISORDER ( 8 FDA reports)
SLEEP DISORDER ( 8 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 8 FDA reports)
VISUAL ACUITY REDUCED ( 8 FDA reports)
ABDOMINAL DISTENSION ( 7 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 7 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 7 FDA reports)
ANGINA PECTORIS ( 7 FDA reports)
BRONCHOSPASM ( 7 FDA reports)
CARDIAC FAILURE ( 7 FDA reports)
DRUG HYPERSENSITIVITY ( 7 FDA reports)
DYSPEPSIA ( 7 FDA reports)
FLUID RETENTION ( 7 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 7 FDA reports)
HEART RATE IRREGULAR ( 7 FDA reports)
HYPOGLYCAEMIA ( 7 FDA reports)
MEDICATION ERROR ( 7 FDA reports)
NERVOUSNESS ( 7 FDA reports)
ORAL CANDIDIASIS ( 7 FDA reports)
PLEURAL EFFUSION ( 7 FDA reports)
PRODUCTIVE COUGH ( 7 FDA reports)
PULMONARY CONGESTION ( 7 FDA reports)
RENAL FAILURE ( 7 FDA reports)
RESPIRATORY ARREST ( 7 FDA reports)
RESPIRATORY FAILURE ( 7 FDA reports)
RHINORRHOEA ( 7 FDA reports)
SINUSITIS ( 7 FDA reports)
SKIN DISCOLOURATION ( 7 FDA reports)
SLEEP APNOEA SYNDROME ( 7 FDA reports)
SWELLING FACE ( 7 FDA reports)
AGGRESSION ( 6 FDA reports)
ALOPECIA ( 6 FDA reports)
ANGINA UNSTABLE ( 6 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 6 FDA reports)
CONFUSIONAL STATE ( 6 FDA reports)
DENTAL CARIES ( 6 FDA reports)
DIABETES MELLITUS ( 6 FDA reports)
DRY THROAT ( 6 FDA reports)
EAR PAIN ( 6 FDA reports)
EYE PAIN ( 6 FDA reports)
HYPERGLYCAEMIA ( 6 FDA reports)
ILL-DEFINED DISORDER ( 6 FDA reports)
IMPAIRED HEALING ( 6 FDA reports)
OEDEMA ( 6 FDA reports)
OSTEONECROSIS ( 6 FDA reports)
OXYGEN SATURATION DECREASED ( 6 FDA reports)
SPEECH DISORDER ( 6 FDA reports)
STOMATITIS ( 6 FDA reports)
SUICIDAL IDEATION ( 6 FDA reports)
THROAT IRRITATION ( 6 FDA reports)
VIRAL INFECTION ( 6 FDA reports)
ADVERSE EVENT ( 5 FDA reports)
AGITATION ( 5 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 5 FDA reports)
BLOOD PRESSURE DECREASED ( 5 FDA reports)
BURNING SENSATION ( 5 FDA reports)
CARDIAC DISORDER ( 5 FDA reports)
CELLULITIS ( 5 FDA reports)
CORONARY ARTERY OCCLUSION ( 5 FDA reports)
DRUG EFFECT DECREASED ( 5 FDA reports)
DRUG INTERACTION ( 5 FDA reports)
EMPHYSEMA ( 5 FDA reports)
FISTULA ( 5 FDA reports)
GAIT DISTURBANCE ( 5 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 5 FDA reports)
HOARSENESS ( 5 FDA reports)
IMPAIRED WORK ABILITY ( 5 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 5 FDA reports)
LUNG INFECTION ( 5 FDA reports)
MUSCLE CRAMP ( 5 FDA reports)
PANIC ATTACK ( 5 FDA reports)
PLEURITIC PAIN ( 5 FDA reports)
PRURITUS GENERALISED ( 5 FDA reports)
PULMONARY HYPERTENSION ( 5 FDA reports)
RENAL FAILURE ACUTE ( 5 FDA reports)
RESPIRATORY DISTRESS ( 5 FDA reports)
SINUS TACHYCARDIA ( 5 FDA reports)
SKIN LACERATION ( 5 FDA reports)
SWELLING ( 5 FDA reports)
SYNCOPE ( 5 FDA reports)
THROAT TIGHTNESS ( 5 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 5 FDA reports)
ABDOMINAL DISCOMFORT ( 4 FDA reports)
ABNORMAL BEHAVIOUR ( 4 FDA reports)
ACCIDENTAL OVERDOSE ( 4 FDA reports)
ADRENAL INSUFFICIENCY ( 4 FDA reports)
APHASIA ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
BACTERIAL INFECTION ( 4 FDA reports)
BALANCE DISORDER ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 4 FDA reports)
BLOOD POTASSIUM DECREASED ( 4 FDA reports)
CARDIO-RESPIRATORY ARREST ( 4 FDA reports)
CONTUSION ( 4 FDA reports)
DELIRIUM ( 4 FDA reports)
DEVICE MALFUNCTION ( 4 FDA reports)
DIASTOLIC DYSFUNCTION ( 4 FDA reports)
DRY EYE ( 4 FDA reports)
DRY SKIN ( 4 FDA reports)
DYSPNOEA EXERTIONAL ( 4 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 4 FDA reports)
FEELING HOT ( 4 FDA reports)
FOOT FRACTURE ( 4 FDA reports)
GASTRITIS ( 4 FDA reports)
GOUT ( 4 FDA reports)
HAEMATOCRIT DECREASED ( 4 FDA reports)
HEPATIC STEATOSIS ( 4 FDA reports)
HYPOAESTHESIA ORAL ( 4 FDA reports)
INCORRECT DOSE ADMINISTERED ( 4 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 4 FDA reports)
JOINT STIFFNESS ( 4 FDA reports)
MACULAR DEGENERATION ( 4 FDA reports)
MEMORY IMPAIRMENT ( 4 FDA reports)
MIGRAINE ( 4 FDA reports)
ORAL DISCOMFORT ( 4 FDA reports)
PANCREATITIS ( 4 FDA reports)
PHARYNGEAL OEDEMA ( 4 FDA reports)
PLATELET COUNT DECREASED ( 4 FDA reports)
POLLAKIURIA ( 4 FDA reports)
PRESYNCOPE ( 4 FDA reports)
PULMONARY OEDEMA ( 4 FDA reports)
RESPIRATORY TRACT INFECTION ( 4 FDA reports)
SEPSIS ( 4 FDA reports)
SINUS CONGESTION ( 4 FDA reports)
SPINAL COLUMN STENOSIS ( 4 FDA reports)
SPUTUM DISCOLOURED ( 4 FDA reports)
TACHYCARDIA ( 4 FDA reports)
THROMBOCYTOPENIA ( 4 FDA reports)
THROMBOSIS ( 4 FDA reports)
TOOTH DISORDER ( 4 FDA reports)
TYPE 2 DIABETES MELLITUS ( 4 FDA reports)
URINARY INCONTINENCE ( 4 FDA reports)
VENTRICULAR FIBRILLATION ( 4 FDA reports)
VERTIGO ( 4 FDA reports)
ABNORMAL DREAMS ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ANAPHYLACTIC REACTION ( 3 FDA reports)
ANGER ( 3 FDA reports)
ANOSMIA ( 3 FDA reports)
ARTHROPATHY ( 3 FDA reports)
BLADDER DISORDER ( 3 FDA reports)
BLINDNESS ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 3 FDA reports)
BRADYCARDIA ( 3 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 3 FDA reports)
CARDIOMEGALY ( 3 FDA reports)
CEREBRAL INFARCTION ( 3 FDA reports)
CHOKING ( 3 FDA reports)
COMA ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
DISEASE PROGRESSION ( 3 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 3 FDA reports)
DYSURIA ( 3 FDA reports)
EJECTION FRACTION DECREASED ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
EXPIRED DRUG ADMINISTERED ( 3 FDA reports)
EYE PRURITUS ( 3 FDA reports)
EYE SWELLING ( 3 FDA reports)
FEAR ( 3 FDA reports)
FLUSHING ( 3 FDA reports)
GASTROINTESTINAL PAIN ( 3 FDA reports)
GINGIVAL BLEEDING ( 3 FDA reports)
GLAUCOMA ( 3 FDA reports)
HAEMATURIA ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
HAEMORRHAGE ( 3 FDA reports)
INCONTINENCE ( 3 FDA reports)
INJURY ( 3 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 3 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 3 FDA reports)
INTRACARDIAC THROMBUS ( 3 FDA reports)
JOINT INJURY ( 3 FDA reports)
JOINT SPRAIN ( 3 FDA reports)
LETHARGY ( 3 FDA reports)
LIMB DISCOMFORT ( 3 FDA reports)
MIDDLE INSOMNIA ( 3 FDA reports)
MOOD ALTERED ( 3 FDA reports)
MOOD SWINGS ( 3 FDA reports)
MOUTH ULCERATION ( 3 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 3 FDA reports)
NASAL CONGESTION ( 3 FDA reports)
NICOTINE DEPENDENCE ( 3 FDA reports)
NO THERAPEUTIC RESPONSE ( 3 FDA reports)
ORAL FUNGAL INFECTION ( 3 FDA reports)
OSTEOARTHRITIS ( 3 FDA reports)
PEAK EXPIRATORY FLOW RATE DECREASED ( 3 FDA reports)
PERICARDIAL EFFUSION ( 3 FDA reports)
PERSONALITY CHANGE ( 3 FDA reports)
PNEUMONITIS ( 3 FDA reports)
PRODUCT TASTE ABNORMAL ( 3 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 3 FDA reports)
RASH GENERALISED ( 3 FDA reports)
SENSATION OF HEAVINESS ( 3 FDA reports)
SINUS HEADACHE ( 3 FDA reports)
SNEEZING ( 3 FDA reports)
SURGERY ( 3 FDA reports)
TOOTH LOSS ( 3 FDA reports)
TROPONIN INCREASED ( 3 FDA reports)
UNRESPONSIVE TO STIMULI ( 3 FDA reports)
URINARY RETENTION ( 3 FDA reports)
VENTRICULAR HYPERTROPHY ( 3 FDA reports)
VISUAL IMPAIRMENT ( 3 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 3 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 3 FDA reports)
ABDOMINAL WALL ABSCESS ( 2 FDA reports)
ABSCESS ( 2 FDA reports)
ABSCESS DRAINAGE ( 2 FDA reports)
ACUTE RESPIRATORY FAILURE ( 2 FDA reports)
ACUTE SINUSITIS ( 2 FDA reports)
ADRENAL DISORDER ( 2 FDA reports)
AFFECTIVE DISORDER ( 2 FDA reports)
AGEUSIA ( 2 FDA reports)
AMENORRHOEA ( 2 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 2 FDA reports)
ANOXIC ENCEPHALOPATHY ( 2 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 2 FDA reports)
APPLICATION SITE ERYTHEMA ( 2 FDA reports)
APPLICATION SITE PRURITUS ( 2 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
ASCITES ( 2 FDA reports)
ATELECTASIS ( 2 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 2 FDA reports)
BLINDNESS UNILATERAL ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD PRESSURE ABNORMAL ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
BONE DISORDER ( 2 FDA reports)
BRONCHIAL HYPERACTIVITY ( 2 FDA reports)
CARDIAC HYPERTROPHY ( 2 FDA reports)
CARDIAC VALVE DISEASE ( 2 FDA reports)
CARDIOMYOPATHY ( 2 FDA reports)
CATHETER REMOVAL ( 2 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 2 FDA reports)
CIRCULATORY COLLAPSE ( 2 FDA reports)
COLITIS ( 2 FDA reports)
COMPULSIVE SHOPPING ( 2 FDA reports)
CONJUNCTIVITIS ( 2 FDA reports)
COR PULMONALE ( 2 FDA reports)
CORNEAL ABRASION ( 2 FDA reports)
CRYING ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 2 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 2 FDA reports)
DIPLOPIA ( 2 FDA reports)
DRUG ABUSER ( 2 FDA reports)
DRUG DEPENDENCE ( 2 FDA reports)
DRUG ERUPTION ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 2 FDA reports)
DYSGRAPHIA ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
EAR DISORDER ( 2 FDA reports)
EAR INFECTION ( 2 FDA reports)
EMOTIONAL DISTRESS ( 2 FDA reports)
EOSINOPHILIA ( 2 FDA reports)
EYE HAEMORRHAGE ( 2 FDA reports)
FAECES DISCOLOURED ( 2 FDA reports)
FEELING JITTERY ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
FOOD ALLERGY ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
GASTROENTERITIS VIRAL ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
GASTROOESOPHAGITIS ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HAEMATOCHEZIA ( 2 FDA reports)
HEARING IMPAIRED ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HEPATIC FIBROSIS ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HERPES ZOSTER ( 2 FDA reports)
HIP FRACTURE ( 2 FDA reports)
HYDROCEPHALUS ( 2 FDA reports)
HYPERADRENALISM ( 2 FDA reports)
HYPERCHOLESTEROLAEMIA ( 2 FDA reports)
HYPERLIPIDAEMIA ( 2 FDA reports)
HYPERSOMNIA ( 2 FDA reports)
HYPERTENSIVE HEART DISEASE ( 2 FDA reports)
HYPERTHYROIDISM ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
INCREASED TENDENCY TO BRUISE ( 2 FDA reports)
INFLAMMATION ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
INJECTION SITE HAEMORRHAGE ( 2 FDA reports)
INJECTION SITE IRRITATION ( 2 FDA reports)
INJECTION SITE PRURITUS ( 2 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 2 FDA reports)
INTRACRANIAL ANEURYSM ( 2 FDA reports)
IRRITABILITY ( 2 FDA reports)
JAUNDICE NEONATAL ( 2 FDA reports)
JOINT SWELLING ( 2 FDA reports)
LABYRINTHITIS ( 2 FDA reports)
LACRIMATION INCREASED ( 2 FDA reports)
LACUNAR INFARCTION ( 2 FDA reports)
LEG AMPUTATION ( 2 FDA reports)
LIMB INJURY ( 2 FDA reports)
LOBAR PNEUMONIA ( 2 FDA reports)
LOCAL SWELLING ( 2 FDA reports)
LOCALISED INFECTION ( 2 FDA reports)
LUNG INFILTRATION ( 2 FDA reports)
LUNG NEOPLASM MALIGNANT ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
MAJOR DEPRESSION ( 2 FDA reports)
MEDICAL DEVICE COMPLICATION ( 2 FDA reports)
MEDICAL DEVICE IMPLANTATION ( 2 FDA reports)
MENORRHAGIA ( 2 FDA reports)
MENSTRUATION IRREGULAR ( 2 FDA reports)
MENTAL DISORDER ( 2 FDA reports)
MICTURITION URGENCY ( 2 FDA reports)
MITRAL VALVE INCOMPETENCE ( 2 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 2 FDA reports)
NASAL POLYPS ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
NEPHROLITHIASIS ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
NIGHTMARE ( 2 FDA reports)
NOCARDIOSIS ( 2 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 2 FDA reports)
OBESITY ( 2 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 2 FDA reports)
OCULAR HYPERAEMIA ( 2 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 2 FDA reports)
OESOPHAGEAL STENOSIS ( 2 FDA reports)
OESOPHAGITIS ( 2 FDA reports)
ORAL PAIN ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PHARYNGITIS ( 2 FDA reports)
PHOTOPSIA ( 2 FDA reports)
PNEUMONIA BACTERIAL ( 2 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 2 FDA reports)
POLYP ( 2 FDA reports)
POOR QUALITY SLEEP ( 2 FDA reports)
PRODUCT PHYSICAL ISSUE ( 2 FDA reports)
PROTEINURIA ( 2 FDA reports)
PSYCHIATRIC SYMPTOM ( 2 FDA reports)
PULMONARY MASS ( 2 FDA reports)
PYELONEPHRITIS ( 2 FDA reports)
PYELONEPHRITIS CHRONIC ( 2 FDA reports)
RASH MACULAR ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
RENAL FAILURE CHRONIC ( 2 FDA reports)
RETCHING ( 2 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
RHEUMATOID ARTHRITIS ( 2 FDA reports)
RHINITIS ( 2 FDA reports)
ROAD TRAFFIC ACCIDENT ( 2 FDA reports)
ROTATOR CUFF SYNDROME ( 2 FDA reports)
SARCOIDOSIS ( 2 FDA reports)
SENSATION OF FOREIGN BODY ( 2 FDA reports)
SINUS BRADYCARDIA ( 2 FDA reports)
SINUS DISORDER ( 2 FDA reports)
SINUS OPERATION ( 2 FDA reports)
SKIN HAEMORRHAGE ( 2 FDA reports)
SKIN IRRITATION ( 2 FDA reports)
SPINAL HAEMATOMA ( 2 FDA reports)
SPINAL OSTEOARTHRITIS ( 2 FDA reports)
SPUTUM RETENTION ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
STRESS ( 2 FDA reports)
STRESS INCONTINENCE ( 2 FDA reports)
SUBDURAL HAEMATOMA ( 2 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
SWOLLEN TONGUE ( 2 FDA reports)
SYNCOPE VASOVAGAL ( 2 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 2 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 2 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
TINNITUS ( 2 FDA reports)
TOBACCO USER ( 2 FDA reports)
TONIC CONVULSION ( 2 FDA reports)
TOOTH FRACTURE ( 2 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 2 FDA reports)
ULCER ( 2 FDA reports)
UNEMPLOYMENT ( 2 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
WOUND SECRETION ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABDOMINAL SEPSIS ( 1 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
ABNORMAL CLOTTING FACTOR ( 1 FDA reports)
ABNORMAL SENSATION IN EYE ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACNE ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 1 FDA reports)
ADENOCARCINOMA ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
AGONAL DEATH STRUGGLE ( 1 FDA reports)
AGORAPHOBIA ( 1 FDA reports)
ALCOHOL ABUSE ( 1 FDA reports)
ALCOHOLISM ( 1 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
AMPHETAMINES POSITIVE ( 1 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 1 FDA reports)
ANAL CANCER ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANURIA ( 1 FDA reports)
ANXIETY DISORDER ( 1 FDA reports)
AORTIC CALCIFICATION ( 1 FDA reports)
AORTIC DILATATION ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
AORTIC VALVE STENOSIS ( 1 FDA reports)
APNOEA ( 1 FDA reports)
APPENDICECTOMY ( 1 FDA reports)
APPENDICITIS ( 1 FDA reports)
APPENDICITIS PERFORATED ( 1 FDA reports)
APPLICATION SITE IRRITATION ( 1 FDA reports)
APPLICATION SITE PAIN ( 1 FDA reports)
APPLICATION SITE REACTION ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ASTHENOPIA ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
ATRIAL TACHYCARDIA ( 1 FDA reports)
ATRIAL THROMBOSIS ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
BACK INJURY ( 1 FDA reports)
BARRETT'S OESOPHAGUS ( 1 FDA reports)
BENIGN NEOPLASM ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
BLADDER CANCER ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BLOODY DISCHARGE ( 1 FDA reports)
BONE DENSITY DECREASED ( 1 FDA reports)
BRAIN DEATH ( 1 FDA reports)
BREAST CELLULITIS ( 1 FDA reports)
BREAST DISCHARGE ( 1 FDA reports)
BREAST SWELLING ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
BRONCHIAL INFECTION ( 1 FDA reports)
BRONCHIAL OBSTRUCTION ( 1 FDA reports)
BRONCHIAL SECRETION RETENTION ( 1 FDA reports)
BRONCHITIS ACUTE ( 1 FDA reports)
BRONCHITIS BACTERIAL ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ALLERGIC ( 1 FDA reports)
BUNION ( 1 FDA reports)
BUTTOCK PAIN ( 1 FDA reports)
CALCULUS URINARY ( 1 FDA reports)
CARDIAC ABLATION ( 1 FDA reports)
CARDIAC FIBRILLATION ( 1 FDA reports)
CARDIAC FLUTTER ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 1 FDA reports)
CARDIAC TAMPONADE ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CARPAL TUNNEL SYNDROME ( 1 FDA reports)
CATARACT NUCLEAR ( 1 FDA reports)
CATARACT SUBCAPSULAR ( 1 FDA reports)
CATHETERISATION CARDIAC ( 1 FDA reports)
CENTRAL OBESITY ( 1 FDA reports)
CEREBELLAR ATROPHY ( 1 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 1 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CHAPPED LIPS ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
CHOLECYSTITIS ACUTE ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CHRONIC FATIGUE SYNDROME ( 1 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 1 FDA reports)
CHRONIC SINUSITIS ( 1 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COCCYDYNIA ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COLLAPSE OF LUNG ( 1 FDA reports)
COMPARTMENT SYNDROME ( 1 FDA reports)
COMPLEX PARTIAL SEIZURES ( 1 FDA reports)
CONNECTIVE TISSUE DISORDER ( 1 FDA reports)
CONVERSION DISORDER ( 1 FDA reports)
COOMBS POSITIVE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CORONARY ARTERY BYPASS ( 1 FDA reports)
CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
CUSHING'S SYNDROME ( 1 FDA reports)
CYST ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DEVELOPMENTAL DELAY ( 1 FDA reports)
DEVICE BREAKAGE ( 1 FDA reports)
DIABETIC NEUROPATHY ( 1 FDA reports)
DIAPHRAGMATIC DISORDER ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISLOCATION OF VERTEBRA ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG EFFECT DELAYED ( 1 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 1 FDA reports)
DYSPHASIA ( 1 FDA reports)
DYSPHEMIA ( 1 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 1 FDA reports)
EAR DISCOMFORT ( 1 FDA reports)
EAR PRURITUS ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
ENAMEL ANOMALY ( 1 FDA reports)
ENZYME ABNORMALITY ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
EOSINOPHILIC MYOCARDITIS ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
EROSIVE OESOPHAGITIS ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
EXFOLIATIVE RASH ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EXTREMITY NECROSIS ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE INFECTION ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
EYE PENETRATION ( 1 FDA reports)
EYELID PTOSIS ( 1 FDA reports)
FACE INJURY ( 1 FDA reports)
FACIAL PARESIS ( 1 FDA reports)
FAILURE TO THRIVE ( 1 FDA reports)
FALLOT'S TETRALOGY ( 1 FDA reports)
FEAR OF FALLING ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FEELING OF DESPAIR ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
FOETAL HEART RATE ABNORMAL ( 1 FDA reports)
FORMICATION ( 1 FDA reports)
FRUSTRATION ( 1 FDA reports)
FUNGAL OESOPHAGITIS ( 1 FDA reports)
FURUNCLE ( 1 FDA reports)
GALLBLADDER POLYP ( 1 FDA reports)
GASTRIC POLYPS ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTROINTESTINAL FUNGAL INFECTION ( 1 FDA reports)
GASTROINTESTINAL INFECTION ( 1 FDA reports)
GASTROINTESTINAL NECROSIS ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GENERALISED ANXIETY DISORDER ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GINGIVAL DISCOLOURATION ( 1 FDA reports)
GINGIVAL DISORDER ( 1 FDA reports)
GINGIVAL ERYTHEMA ( 1 FDA reports)
GINGIVAL PAIN ( 1 FDA reports)
GINGIVAL SWELLING ( 1 FDA reports)
GLOSSITIS ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
GLYCOSURIA ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEART INJURY ( 1 FDA reports)
HEART RATE ( 1 FDA reports)
HEART RATE ABNORMAL ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEART VALVE INSUFFICIENCY ( 1 FDA reports)
HELICOBACTER INFECTION ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HERNIA REPAIR ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HYPOAESTHESIA FACIAL ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
HYPOVENTILATION ( 1 FDA reports)
HYPOVOLAEMIC SHOCK ( 1 FDA reports)
IMMOBILE ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
IMPAIRED DRIVING ABILITY ( 1 FDA reports)
IMPLANT SITE REACTION ( 1 FDA reports)
INADEQUATE ANALGESIA ( 1 FDA reports)
INCISIONAL HERNIA ( 1 FDA reports)
INCISIONAL HERNIA REPAIR ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INCREASED APPETITE ( 1 FDA reports)
INCREASED BRONCHIAL SECRETION ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INGROWING NAIL ( 1 FDA reports)
INHALATION THERAPY ( 1 FDA reports)
INJECTION SITE BRUISING ( 1 FDA reports)
INJECTION SITE INFLAMMATION ( 1 FDA reports)
INJECTION SITE NODULE ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 1 FDA reports)
INTESTINAL ISCHAEMIA ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
INTESTINAL PERFORATION ( 1 FDA reports)
INTESTINAL RESECTION ( 1 FDA reports)
IRRITABLE BOWEL SYNDROME ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
JAW FRACTURE ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LAPAROTOMY ( 1 FDA reports)
LEARNING DISORDER ( 1 FDA reports)
LEIOMYOSARCOMA ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LEUKOPLAKIA ( 1 FDA reports)
LIBIDO DECREASED ( 1 FDA reports)
LIP DISORDER ( 1 FDA reports)
LIP DRY ( 1 FDA reports)
LIPIDS INCREASED ( 1 FDA reports)
LIPOMA ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LOWER LIMB FRACTURE ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
LUNG CANCER METASTATIC ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
LYMPHOEDEMA ( 1 FDA reports)
MACULAR HOLE ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MASTOIDITIS ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 1 FDA reports)
MEDIASTINAL HAEMORRHAGE ( 1 FDA reports)
MEDICAL DEVICE REMOVAL ( 1 FDA reports)
MENIERE'S DISEASE ( 1 FDA reports)
MENINGIOMA ( 1 FDA reports)
MENINGITIS ( 1 FDA reports)
MENSTRUAL DISORDER ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
METABOLIC SYNDROME ( 1 FDA reports)
MICROCEPHALY ( 1 FDA reports)
MIGRAINE WITH AURA ( 1 FDA reports)
MITRAL VALVE PROLAPSE ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUCOSAL DRYNESS ( 1 FDA reports)
MUCOSAL HAEMORRHAGE ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MULTI-ORGAN DISORDER ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MULTIPLE ALLERGIES ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ( 1 FDA reports)
MULTIPLE INJURIES ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
MUSCLE FATIGUE ( 1 FDA reports)
MUSCLE HAEMORRHAGE ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NASAL DISCOMFORT ( 1 FDA reports)
NASAL SINUS DRAINAGE ( 1 FDA reports)
NASAL ULCER ( 1 FDA reports)
NASOPHARYNGEAL DISORDER ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NEPHROCALCINOSIS ( 1 FDA reports)
NEPHROSCLEROSIS ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NEUROENDOCRINE CARCINOMA ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NO ADVERSE DRUG EFFECT ( 1 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
NORMAL DELIVERY ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
ODYNOPHAGIA ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
OESOPHAGEAL ACHALASIA ( 1 FDA reports)
OESOPHAGEAL ADENOCARCINOMA STAGE IV ( 1 FDA reports)
OESOPHAGEAL DISORDER ( 1 FDA reports)
OESOPHAGEAL INFECTION ( 1 FDA reports)
OESOPHAGEAL MASS ( 1 FDA reports)
OESOPHAGEAL PAIN ( 1 FDA reports)
OESOPHAGITIS ULCERATIVE ( 1 FDA reports)
ONYCHOMADESIS ( 1 FDA reports)
ONYCHOMYCOSIS ( 1 FDA reports)
OPEN ANGLE GLAUCOMA ( 1 FDA reports)
OPERATIVE HAEMORRHAGE ( 1 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 1 FDA reports)
ORAL MUCOSAL BLISTERING ( 1 FDA reports)
ORAL PRURITUS ( 1 FDA reports)
ORAL TORUS ( 1 FDA reports)
ORBITAL OEDEMA ( 1 FDA reports)
ORF ( 1 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 1 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
OSTEOMYELITIS CHRONIC ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PANCREATIC ATROPHY ( 1 FDA reports)
PANCREATIC CYST ( 1 FDA reports)
PANCREATIC DUCT DILATATION ( 1 FDA reports)
PANCREATIC INSUFFICIENCY ( 1 FDA reports)
PANCREATITIS CHRONIC ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PANIC DISORDER ( 1 FDA reports)
PANIC REACTION ( 1 FDA reports)
PANNICULITIS ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 1 FDA reports)
PATHOLOGICAL FRACTURE ( 1 FDA reports)
PELVIC FRACTURE ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PERIORBITAL OEDEMA ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 1 FDA reports)
PHARYNX DISCOMFORT ( 1 FDA reports)
PICKWICKIAN SYNDROME ( 1 FDA reports)
PIGMENT DISPERSION SYNDROME ( 1 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 1 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 1 FDA reports)
POISONING ( 1 FDA reports)
POLYMYALGIA RHEUMATICA ( 1 FDA reports)
POLYP COLORECTAL ( 1 FDA reports)
PORTAL HYPERTENSION ( 1 FDA reports)
PORTAL HYPERTENSIVE GASTROPATHY ( 1 FDA reports)
POST CHOLECYSTECTOMY SYNDROME ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 1 FDA reports)
POSTNASAL DRIP ( 1 FDA reports)
POSTOPERATIVE ADHESION ( 1 FDA reports)
POSTOPERATIVE INFECTION ( 1 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 1 FDA reports)
PRESCRIBED OVERDOSE ( 1 FDA reports)
PRODUCT CONTAMINATION ( 1 FDA reports)
PRODUCT FORMULATION ISSUE ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 1 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 1 FDA reports)
PULMONARY ARTERY ATRESIA ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY GRANULOMA ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
PULMONARY INTERSTITIAL EMPHYSEMA SYNDROME ( 1 FDA reports)
PULMONARY MYCOSIS ( 1 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 1 FDA reports)
PUNCTATE KERATITIS ( 1 FDA reports)
PUSTULAR PSORIASIS ( 1 FDA reports)
QUADRIPLEGIA ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
REBOUND EFFECT ( 1 FDA reports)
RECTOCELE ( 1 FDA reports)
RED BLOOD CELL ABNORMALITY ( 1 FDA reports)
RED MAN SYNDROME ( 1 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RENAL PAIN ( 1 FDA reports)
RENAL TRANSPLANT ( 1 FDA reports)
RESORPTION BONE INCREASED ( 1 FDA reports)
RESPIRATION ABNORMAL ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESPIRATORY TRACT IRRITATION ( 1 FDA reports)
RETINAL ARTERY OCCLUSION ( 1 FDA reports)
RETINAL DISORDER ( 1 FDA reports)
RETINAL OPERATION ( 1 FDA reports)
RETINOPATHY ( 1 FDA reports)
RHINALGIA ( 1 FDA reports)
RHINITIS ALLERGIC ( 1 FDA reports)
RHONCHI ( 1 FDA reports)
RICKETS ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
SALIVARY HYPERSECRETION ( 1 FDA reports)
SCIATICA ( 1 FDA reports)
SEBORRHOEIC KERATOSIS ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SENSITIVITY OF TEETH ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SHOULDER PAIN ( 1 FDA reports)
SIMPLE PARTIAL SEIZURES ( 1 FDA reports)
SINUS ARREST ( 1 FDA reports)
SKIN ATROPHY ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SKIN NECROSIS ( 1 FDA reports)
SKIN PAPILLOMA ( 1 FDA reports)
SKIN TOXICITY ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SLUGGISHNESS ( 1 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 1 FDA reports)
SMALL INTESTINAL RESECTION ( 1 FDA reports)
SMOKER ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
SPASMODIC DYSPHONIA ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
SPINAL CORPECTOMY ( 1 FDA reports)
SPUTUM PURULENT ( 1 FDA reports)
STENT OCCLUSION ( 1 FDA reports)
STENT PLACEMENT ( 1 FDA reports)
STILLBIRTH ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
STOOL ANALYSIS ABNORMAL ( 1 FDA reports)
SUBDURAL HAEMORRHAGE ( 1 FDA reports)
SUDDEN CARDIAC DEATH ( 1 FDA reports)
SUICIDAL BEHAVIOUR ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
SYPHILIS ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
TENDON RUPTURE ( 1 FDA reports)
TENSION ( 1 FDA reports)
THERAPEUTIC REACTION TIME DECREASED ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 1 FDA reports)
THIRST ( 1 FDA reports)
THOUGHT BLOCKING ( 1 FDA reports)
THROMBOCYTHAEMIA ( 1 FDA reports)
THROMBOPHLEBITIS ( 1 FDA reports)
THYROID CANCER ( 1 FDA reports)
THYROID DISORDER ( 1 FDA reports)
THYROID NEOPLASM ( 1 FDA reports)
THYROXINE FREE INCREASED ( 1 FDA reports)
TONGUE DISCOLOURATION ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TONGUE ULCERATION ( 1 FDA reports)
TOOTH INFECTION ( 1 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TRICHORRHEXIS ( 1 FDA reports)
TRISMUS ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
TYPE 1 DIABETES MELLITUS ( 1 FDA reports)
ULCER HAEMORRHAGE ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
UPPER LIMB FRACTURE ( 1 FDA reports)
URINARY TRACT DISORDER ( 1 FDA reports)
URINE FLOW DECREASED ( 1 FDA reports)
UROSEPSIS ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)
UTERINE CANCER ( 1 FDA reports)
VASCULAR GRAFT OCCLUSION ( 1 FDA reports)
VASCULAR INJURY ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VASCULITIS NECROTISING ( 1 FDA reports)
VASODILATATION ( 1 FDA reports)
VENOUS INSUFFICIENCY ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VISUAL FIELD DEFECT ( 1 FDA reports)
VITAMIN D DECREASED ( 1 FDA reports)
VITAMIN D DEFICIENCY ( 1 FDA reports)
VITREOUS FLOATERS ( 1 FDA reports)
VITREOUS HAEMORRHAGE ( 1 FDA reports)
VOCAL CORD DISORDER ( 1 FDA reports)
VOCAL CORD NEOPLASM ( 1 FDA reports)
VOCAL CORD THICKENING ( 1 FDA reports)
WALKING AID USER ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL DISORDER ( 1 FDA reports)
WOUND DRAINAGE ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)
ZINC DEFICIENCY ( 1 FDA reports)

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