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

DYSPNOEA ( 163 FDA reports)
PAIN ( 156 FDA reports)
GLAUCOMA ( 134 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 131 FDA reports)
ASTHENIA ( 127 FDA reports)
FALL ( 121 FDA reports)
DIZZINESS ( 111 FDA reports)
FATIGUE ( 101 FDA reports)
ANXIETY ( 100 FDA reports)
OEDEMA PERIPHERAL ( 94 FDA reports)
PNEUMONIA ( 91 FDA reports)
NAUSEA ( 90 FDA reports)
ANAEMIA ( 88 FDA reports)
DEPRESSION ( 87 FDA reports)
DRUG INEFFECTIVE ( 86 FDA reports)
PYREXIA ( 82 FDA reports)
VISION BLURRED ( 81 FDA reports)
WEIGHT DECREASED ( 81 FDA reports)
HEADACHE ( 80 FDA reports)
CEREBROVASCULAR ACCIDENT ( 79 FDA reports)
HYPERTENSION ( 79 FDA reports)
ARTHRALGIA ( 78 FDA reports)
CHEST PAIN ( 77 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 75 FDA reports)
CONSTIPATION ( 75 FDA reports)
OCULAR HYPERAEMIA ( 75 FDA reports)
EYE IRRITATION ( 74 FDA reports)
PAIN IN EXTREMITY ( 72 FDA reports)
VISUAL ACUITY REDUCED ( 71 FDA reports)
VOMITING ( 71 FDA reports)
CONFUSIONAL STATE ( 69 FDA reports)
ATRIAL FIBRILLATION ( 68 FDA reports)
HYPOTENSION ( 66 FDA reports)
MYOCARDIAL INFARCTION ( 66 FDA reports)
URINARY TRACT INFECTION ( 66 FDA reports)
GAIT DISTURBANCE ( 65 FDA reports)
BACK PAIN ( 64 FDA reports)
CATARACT ( 63 FDA reports)
COUGH ( 63 FDA reports)
INSOMNIA ( 62 FDA reports)
HYPOAESTHESIA ( 60 FDA reports)
DIARRHOEA ( 59 FDA reports)
DIABETES MELLITUS ( 57 FDA reports)
OSTEONECROSIS OF JAW ( 57 FDA reports)
EYE PAIN ( 56 FDA reports)
INFLAMMATION ( 54 FDA reports)
ABDOMINAL PAIN ( 53 FDA reports)
CONDITION AGGRAVATED ( 53 FDA reports)
BLINDNESS ( 52 FDA reports)
BLOOD GLUCOSE INCREASED ( 52 FDA reports)
DEATH ( 52 FDA reports)
VISUAL IMPAIRMENT ( 51 FDA reports)
DEHYDRATION ( 50 FDA reports)
DYSPHAGIA ( 50 FDA reports)
MUSCLE SPASMS ( 48 FDA reports)
PANCYTOPENIA ( 48 FDA reports)
PARAESTHESIA ( 48 FDA reports)
CORONARY ARTERY DISEASE ( 47 FDA reports)
ERYTHEMA ( 47 FDA reports)
BLOOD CREATININE INCREASED ( 45 FDA reports)
CELLULITIS ( 45 FDA reports)
SOMNOLENCE ( 45 FDA reports)
SWELLING ( 45 FDA reports)
THROMBOCYTOPENIA ( 45 FDA reports)
INJURY ( 44 FDA reports)
LOSS OF CONSCIOUSNESS ( 44 FDA reports)
PAIN IN JAW ( 43 FDA reports)
PRURITUS ( 43 FDA reports)
CHEST DISCOMFORT ( 42 FDA reports)
MACULAR DEGENERATION ( 42 FDA reports)
PLEURAL EFFUSION ( 42 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 41 FDA reports)
BRONCHITIS ( 41 FDA reports)
EYE DISORDER ( 41 FDA reports)
INFECTION ( 41 FDA reports)
JOINT SWELLING ( 41 FDA reports)
DRY MOUTH ( 40 FDA reports)
FEELING ABNORMAL ( 39 FDA reports)
SKIN DISCOLOURATION ( 39 FDA reports)
HYPERSENSITIVITY ( 38 FDA reports)
RENAL FAILURE ( 38 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 37 FDA reports)
DRY EYE ( 37 FDA reports)
MYALGIA ( 37 FDA reports)
SYNCOPE ( 37 FDA reports)
DEEP VEIN THROMBOSIS ( 36 FDA reports)
HYPERLIPIDAEMIA ( 36 FDA reports)
RENAL CYST ( 36 FDA reports)
WEIGHT INCREASED ( 36 FDA reports)
DYSPEPSIA ( 35 FDA reports)
RENAL FAILURE CHRONIC ( 35 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 34 FDA reports)
CONTUSION ( 34 FDA reports)
MALAISE ( 34 FDA reports)
NASAL CONGESTION ( 34 FDA reports)
BLOOD PRESSURE INCREASED ( 33 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 33 FDA reports)
NEUROPATHY PERIPHERAL ( 33 FDA reports)
RASH ( 33 FDA reports)
RENAL FAILURE ACUTE ( 33 FDA reports)
DECREASED APPETITE ( 32 FDA reports)
MUSCULOSKELETAL PAIN ( 32 FDA reports)
NEOPLASM MALIGNANT ( 32 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 32 FDA reports)
HYPOKALAEMIA ( 31 FDA reports)
MENTAL STATUS CHANGES ( 31 FDA reports)
METASTASES TO BONE ( 31 FDA reports)
OSTEOPENIA ( 31 FDA reports)
ABDOMINAL DISTENSION ( 30 FDA reports)
HYPOTHYROIDISM ( 30 FDA reports)
SEPSIS ( 30 FDA reports)
ATELECTASIS ( 29 FDA reports)
CATARACT OPERATION ( 29 FDA reports)
DEFORMITY ( 29 FDA reports)
EAR PAIN ( 29 FDA reports)
HAEMOGLOBIN DECREASED ( 29 FDA reports)
OSTEOLYSIS ( 29 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 29 FDA reports)
EYE PRURITUS ( 28 FDA reports)
HIP FRACTURE ( 28 FDA reports)
MICTURITION URGENCY ( 28 FDA reports)
MUSCULAR WEAKNESS ( 28 FDA reports)
ABDOMINAL PAIN UPPER ( 27 FDA reports)
DYSPHONIA ( 27 FDA reports)
DYSURIA ( 27 FDA reports)
EPISTAXIS ( 27 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 27 FDA reports)
HYPERHIDROSIS ( 27 FDA reports)
PALPITATIONS ( 27 FDA reports)
ASCITES ( 26 FDA reports)
BRADYCARDIA ( 26 FDA reports)
DRUG HYPERSENSITIVITY ( 26 FDA reports)
DRUG INTERACTION ( 26 FDA reports)
GINGIVAL SWELLING ( 26 FDA reports)
HAEMORRHAGE ( 26 FDA reports)
TACHYCARDIA ( 26 FDA reports)
TREMOR ( 26 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 25 FDA reports)
BONE DISORDER ( 25 FDA reports)
HYPOGLYCAEMIA ( 25 FDA reports)
INJECTION SITE PAIN ( 25 FDA reports)
LEUKOPENIA ( 25 FDA reports)
ANHEDONIA ( 24 FDA reports)
EMOTIONAL DISTRESS ( 24 FDA reports)
HERPES ZOSTER ( 24 FDA reports)
LACRIMATION INCREASED ( 24 FDA reports)
ORTHOSTATIC HYPOTENSION ( 24 FDA reports)
OSTEOARTHRITIS ( 24 FDA reports)
POLLAKIURIA ( 24 FDA reports)
PULMONARY OEDEMA ( 24 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 23 FDA reports)
BLOOD UREA INCREASED ( 23 FDA reports)
BONE MARROW FAILURE ( 23 FDA reports)
BRUXISM ( 23 FDA reports)
CARDIOMEGALY ( 23 FDA reports)
DISABILITY ( 23 FDA reports)
GASTRITIS ( 23 FDA reports)
HYPOXIA ( 23 FDA reports)
LOOSE TOOTH ( 23 FDA reports)
LYMPHADENOPATHY ( 23 FDA reports)
ROTATOR CUFF SYNDROME ( 23 FDA reports)
SKIN ULCER ( 23 FDA reports)
BONE PAIN ( 22 FDA reports)
CARDIAC DISORDER ( 22 FDA reports)
CHILLS ( 22 FDA reports)
FEAR ( 22 FDA reports)
GASTROINTESTINAL DISORDER ( 22 FDA reports)
ARTHRITIS ( 21 FDA reports)
ECONOMIC PROBLEM ( 21 FDA reports)
HEARING IMPAIRED ( 21 FDA reports)
OSTEOMYELITIS ( 21 FDA reports)
OSTEOPOROSIS ( 21 FDA reports)
SINUSITIS ( 21 FDA reports)
TOOTH EXTRACTION ( 21 FDA reports)
URINARY INCONTINENCE ( 21 FDA reports)
ARTERIOSCLEROSIS ( 20 FDA reports)
HIATUS HERNIA ( 20 FDA reports)
MITRAL VALVE INCOMPETENCE ( 20 FDA reports)
SEASONAL ALLERGY ( 20 FDA reports)
SPINAL OSTEOARTHRITIS ( 20 FDA reports)
AMNESIA ( 19 FDA reports)
BALANCE DISORDER ( 19 FDA reports)
BURSITIS ( 19 FDA reports)
DECUBITUS ULCER ( 19 FDA reports)
DYSGEUSIA ( 19 FDA reports)
EXPOSED BONE IN JAW ( 19 FDA reports)
GANGRENE ( 19 FDA reports)
GINGIVAL BLEEDING ( 19 FDA reports)
HEART RATE INCREASED ( 19 FDA reports)
MENTAL DISORDER ( 19 FDA reports)
MULTIPLE FRACTURES ( 19 FDA reports)
RESPIRATORY FAILURE ( 19 FDA reports)
STAPHYLOCOCCAL INFECTION ( 19 FDA reports)
TINNITUS ( 19 FDA reports)
BASAL CELL CARCINOMA ( 18 FDA reports)
BLEPHARITIS ( 18 FDA reports)
BLINDNESS UNILATERAL ( 18 FDA reports)
BLOOD PRESSURE DECREASED ( 18 FDA reports)
CEREBRAL INFARCTION ( 18 FDA reports)
DYSKINESIA ( 18 FDA reports)
FLUSHING ( 18 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 18 FDA reports)
HEPATIC LESION ( 18 FDA reports)
HYPOPHAGIA ( 18 FDA reports)
NECK PAIN ( 18 FDA reports)
OTITIS MEDIA ( 18 FDA reports)
TOOTHACHE ( 18 FDA reports)
URINARY RETENTION ( 18 FDA reports)
ASTHMA ( 17 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 17 FDA reports)
CONVULSION ( 17 FDA reports)
HAEMATURIA ( 17 FDA reports)
HYPONATRAEMIA ( 17 FDA reports)
LUNG INFILTRATION ( 17 FDA reports)
METASTASES TO LIVER ( 17 FDA reports)
PALLOR ( 17 FDA reports)
PULMONARY EMBOLISM ( 17 FDA reports)
THROMBOSIS ( 17 FDA reports)
VISUAL FIELD DEFECT ( 17 FDA reports)
ABNORMAL DREAMS ( 16 FDA reports)
BLOOD POTASSIUM DECREASED ( 16 FDA reports)
DEBRIDEMENT ( 16 FDA reports)
DERMATITIS ( 16 FDA reports)
DIABETIC NEUROPATHY ( 16 FDA reports)
DRUG DEPENDENCE ( 16 FDA reports)
ESCHERICHIA INFECTION ( 16 FDA reports)
GROWTH OF EYELASHES ( 16 FDA reports)
HOT FLUSH ( 16 FDA reports)
HYPERKALAEMIA ( 16 FDA reports)
INCORRECT DOSE ADMINISTERED ( 16 FDA reports)
JOINT EFFUSION ( 16 FDA reports)
MEDIASTINAL MASS ( 16 FDA reports)
SCOLIOSIS ( 16 FDA reports)
SKIN EXFOLIATION ( 16 FDA reports)
UVEITIS ( 16 FDA reports)
WHEEZING ( 16 FDA reports)
ANOREXIA ( 15 FDA reports)
AZOTAEMIA ( 15 FDA reports)
CULTURE URINE POSITIVE ( 15 FDA reports)
FAILURE TO THRIVE ( 15 FDA reports)
HEPATIC CYST ( 15 FDA reports)
HEPATIC STEATOSIS ( 15 FDA reports)
HYPERTHYROIDISM ( 15 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 15 FDA reports)
JAW DISORDER ( 15 FDA reports)
LUNG NEOPLASM ( 15 FDA reports)
LYMPHOMA ( 15 FDA reports)
OVERDOSE ( 15 FDA reports)
PERIPHERAL COLDNESS ( 15 FDA reports)
PHOTOPHOBIA ( 15 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 15 FDA reports)
PULMONARY HYPERTENSION ( 15 FDA reports)
SKIN CANCER ( 15 FDA reports)
SNORING ( 15 FDA reports)
SWELLING FACE ( 15 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 15 FDA reports)
UNEVALUABLE EVENT ( 15 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 14 FDA reports)
APNOEA ( 14 FDA reports)
ARRHYTHMIA ( 14 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 14 FDA reports)
BONE FISSURE ( 14 FDA reports)
COLPOCELE ( 14 FDA reports)
DISORIENTATION ( 14 FDA reports)
ECTROPION ( 14 FDA reports)
EMPHYSEMA ( 14 FDA reports)
FACIAL BONES FRACTURE ( 14 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 14 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 14 FDA reports)
GOUT ( 14 FDA reports)
HAEMATOCHEZIA ( 14 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 14 FDA reports)
KIDNEY SMALL ( 14 FDA reports)
LARYNGITIS ( 14 FDA reports)
MITRAL VALVE CALCIFICATION ( 14 FDA reports)
NEURALGIA ( 14 FDA reports)
NOCTURIA ( 14 FDA reports)
OESOPHAGEAL FOOD IMPACTION ( 14 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 14 FDA reports)
OSTEOMA ( 14 FDA reports)
OSTEONECROSIS ( 14 FDA reports)
POST PROCEDURAL COMPLICATION ( 14 FDA reports)
PRIMARY SEQUESTRUM ( 14 FDA reports)
PROTEIN URINE ( 14 FDA reports)
PURULENT DISCHARGE ( 14 FDA reports)
STRESS ( 14 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 14 FDA reports)
TREATMENT NONCOMPLIANCE ( 14 FDA reports)
VAGINAL PROLAPSE ( 14 FDA reports)
BACTERAEMIA ( 13 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 13 FDA reports)
CHOLELITHIASIS ( 13 FDA reports)
CYSTOSCOPY ( 13 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 13 FDA reports)
DIPLOPIA ( 13 FDA reports)
EYELID OEDEMA ( 13 FDA reports)
GINGIVAL PAIN ( 13 FDA reports)
HYPERGLYCAEMIA ( 13 FDA reports)
INJECTION SITE HAEMORRHAGE ( 13 FDA reports)
INTRAOCULAR PRESSURE TEST ABNORMAL ( 13 FDA reports)
MEMORY IMPAIRMENT ( 13 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 13 FDA reports)
OROPHARYNGEAL PAIN ( 13 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 13 FDA reports)
POOR PERIPHERAL CIRCULATION ( 13 FDA reports)
SPINAL CORD COMPRESSION ( 13 FDA reports)
SPLENOMEGALY ( 13 FDA reports)
STRESS URINARY INCONTINENCE ( 13 FDA reports)
VERTIGO ( 13 FDA reports)
WOUND SECRETION ( 13 FDA reports)
ABDOMINAL DISCOMFORT ( 12 FDA reports)
ABSCESS DRAINAGE ( 12 FDA reports)
AORTIC VALVE INCOMPETENCE ( 12 FDA reports)
BACTERIAL INFECTION ( 12 FDA reports)
BLOOD GLUCOSE DECREASED ( 12 FDA reports)
CARDIAC ARREST ( 12 FDA reports)
CARDIOMYOPATHY ( 12 FDA reports)
DENTAL CARIES ( 12 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 12 FDA reports)
HAEMATOCRIT DECREASED ( 12 FDA reports)
HEART RATE DECREASED ( 12 FDA reports)
HEART RATE IRREGULAR ( 12 FDA reports)
HEMIPARESIS ( 12 FDA reports)
INFECTED SKIN ULCER ( 12 FDA reports)
IRON DEFICIENCY ANAEMIA ( 12 FDA reports)
LETHARGY ( 12 FDA reports)
NEPHROLITHIASIS ( 12 FDA reports)
NON-CARDIAC CHEST PAIN ( 12 FDA reports)
OEDEMA ( 12 FDA reports)
OSTEORADIONECROSIS ( 12 FDA reports)
PHYSICAL DISABILITY ( 12 FDA reports)
POST HERPETIC NEURALGIA ( 12 FDA reports)
PRURITUS GENERALISED ( 12 FDA reports)
SCIATICA ( 12 FDA reports)
SPINAL COLUMN INJURY ( 12 FDA reports)
SUICIDAL IDEATION ( 12 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 12 FDA reports)
URTICARIA ( 12 FDA reports)
VISUAL DISTURBANCE ( 12 FDA reports)
ABASIA ( 11 FDA reports)
ABDOMINAL HERNIA ( 11 FDA reports)
ABSCESS ( 11 FDA reports)
ACUTE RESPIRATORY FAILURE ( 11 FDA reports)
ANKLE FRACTURE ( 11 FDA reports)
AORTIC ANEURYSM ( 11 FDA reports)
BONE LESION ( 11 FDA reports)
BRONCHITIS ACUTE ( 11 FDA reports)
BURNING SENSATION ( 11 FDA reports)
DIABETIC RETINOPATHY ( 11 FDA reports)
DISEASE PROGRESSION ( 11 FDA reports)
DYSARTHRIA ( 11 FDA reports)
EXCORIATION ( 11 FDA reports)
EYE INFLAMMATION ( 11 FDA reports)
FLUID RETENTION ( 11 FDA reports)
HAND FRACTURE ( 11 FDA reports)
HEPATIC ENZYME INCREASED ( 11 FDA reports)
INTRAOCULAR LENS IMPLANT ( 11 FDA reports)
JOINT SPRAIN ( 11 FDA reports)
LEUKAEMIA ( 11 FDA reports)
NEUROPATHIC ULCER ( 11 FDA reports)
NIGHTMARE ( 11 FDA reports)
ONYCHOMYCOSIS ( 11 FDA reports)
ORAL DISCOMFORT ( 11 FDA reports)
ORTHOSIS USER ( 11 FDA reports)
PATHOLOGICAL FRACTURE ( 11 FDA reports)
PROSTATE CANCER ( 11 FDA reports)
RETINAL SCAR ( 11 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 11 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 11 FDA reports)
ANGINA PECTORIS ( 10 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 10 FDA reports)
BEREAVEMENT REACTION ( 10 FDA reports)
BLOOD SODIUM DECREASED ( 10 FDA reports)
BODY HEIGHT DECREASED ( 10 FDA reports)
CARDIAC MURMUR ( 10 FDA reports)
CAROTID ARTERY STENOSIS ( 10 FDA reports)
CONJUNCTIVAL OEDEMA ( 10 FDA reports)
CORNEAL OPERATION ( 10 FDA reports)
DEPRESSED MOOD ( 10 FDA reports)
EYE DISCHARGE ( 10 FDA reports)
EYE HAEMORRHAGE ( 10 FDA reports)
EYE SWELLING ( 10 FDA reports)
FEELING HOT ( 10 FDA reports)
FISTULA ( 10 FDA reports)
GASTRIC DISORDER ( 10 FDA reports)
GINGIVAL INFECTION ( 10 FDA reports)
HAEMATOMA ( 10 FDA reports)
HALLUCINATION ( 10 FDA reports)
HYDROPNEUMOTHORAX ( 10 FDA reports)
HYPERCALCAEMIA ( 10 FDA reports)
INADEQUATE ANALGESIA ( 10 FDA reports)
INJECTION SITE ERYTHEMA ( 10 FDA reports)
INTESTINAL OBSTRUCTION ( 10 FDA reports)
INTRAOCULAR PRESSURE FLUCTUATION ( 10 FDA reports)
MULTIPLE SCLEROSIS ( 10 FDA reports)
NASOPHARYNGITIS ( 10 FDA reports)
OSTEOMYELITIS CHRONIC ( 10 FDA reports)
PANCREATITIS ( 10 FDA reports)
PANCREATITIS CHRONIC ( 10 FDA reports)
PNEUMONITIS ( 10 FDA reports)
PROSTATITIS ( 10 FDA reports)
RESPIRATORY ARREST ( 10 FDA reports)
RESPIRATORY DISTRESS ( 10 FDA reports)
SLEEP APNOEA SYNDROME ( 10 FDA reports)
STOMACH DISCOMFORT ( 10 FDA reports)
THYROID CANCER ( 10 FDA reports)
TYPE 2 DIABETES MELLITUS ( 10 FDA reports)
VITREOUS FLOATERS ( 10 FDA reports)
VITREOUS HAEMORRHAGE ( 10 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 10 FDA reports)
ABNORMAL SENSATION IN EYE ( 9 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 9 FDA reports)
AORTIC DILATATION ( 9 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 9 FDA reports)
BLADDER NECK OPERATION ( 9 FDA reports)
BLEPHAROPLASTY ( 9 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 9 FDA reports)
CARBOHYDRATE ANTIGEN 27.29 INCREASED ( 9 FDA reports)
CEREBRAL ATROPHY ( 9 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 9 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 9 FDA reports)
CYSTOPEXY ( 9 FDA reports)
DYSLIPIDAEMIA ( 9 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 9 FDA reports)
HEAD INJURY ( 9 FDA reports)
HEMIPLEGIA ( 9 FDA reports)
HYPERCHOLESTEROLAEMIA ( 9 FDA reports)
INDURATION ( 9 FDA reports)
INFLUENZA LIKE ILLNESS ( 9 FDA reports)
INJECTION SITE BRUISING ( 9 FDA reports)
IRIS ADHESIONS ( 9 FDA reports)
IRITIS ( 9 FDA reports)
JAW FRACTURE ( 9 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 9 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 9 FDA reports)
MACROCYTOSIS ( 9 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 9 FDA reports)
METASTASES TO LUNG ( 9 FDA reports)
MULTI-ORGAN FAILURE ( 9 FDA reports)
MULTIPLE MYELOMA ( 9 FDA reports)
MUSCLE STRAIN ( 9 FDA reports)
OPEN ANGLE GLAUCOMA ( 9 FDA reports)
OPEN REDUCTION OF FRACTURE ( 9 FDA reports)
PERIODONTITIS ( 9 FDA reports)
PERIORBITAL OEDEMA ( 9 FDA reports)
PLATELET COUNT DECREASED ( 9 FDA reports)
RENAL DISORDER ( 9 FDA reports)
RHINITIS ALLERGIC ( 9 FDA reports)
ROAD TRAFFIC ACCIDENT ( 9 FDA reports)
SPINAL COMPRESSION FRACTURE ( 9 FDA reports)
TOOTH DISORDER ( 9 FDA reports)
UNRESPONSIVE TO STIMULI ( 9 FDA reports)
URINE FLOW DECREASED ( 9 FDA reports)
VENTRICULAR TACHYCARDIA ( 9 FDA reports)
ABNORMAL BEHAVIOUR ( 8 FDA reports)
ALOPECIA ( 8 FDA reports)
ASPIRATION ( 8 FDA reports)
BLOOD BILIRUBIN INCREASED ( 8 FDA reports)
CARDIAC FAILURE ( 8 FDA reports)
CORONARY ARTERY OCCLUSION ( 8 FDA reports)
DRUG ADMINISTRATION ERROR ( 8 FDA reports)
EAR HAEMORRHAGE ( 8 FDA reports)
ECCHYMOSIS ( 8 FDA reports)
FEBRILE NEUTROPENIA ( 8 FDA reports)
FLATULENCE ( 8 FDA reports)
ILL-DEFINED DISORDER ( 8 FDA reports)
LEUKOCYTOSIS ( 8 FDA reports)
MACULOPATHY ( 8 FDA reports)
MASTOIDITIS ( 8 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 8 FDA reports)
OESOPHAGEAL STENOSIS ( 8 FDA reports)
OESOPHAGITIS ( 8 FDA reports)
POLYP COLORECTAL ( 8 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 8 FDA reports)
RENAL INJURY ( 8 FDA reports)
RENAL TUBULAR NECROSIS ( 8 FDA reports)
RETCHING ( 8 FDA reports)
RETINAL DETACHMENT ( 8 FDA reports)
RHABDOMYOLYSIS ( 8 FDA reports)
RHINORRHOEA ( 8 FDA reports)
SINUS TACHYCARDIA ( 8 FDA reports)
SUICIDAL BEHAVIOUR ( 8 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 8 FDA reports)
TOOTH FRACTURE ( 8 FDA reports)
ULCERATIVE KERATITIS ( 8 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 8 FDA reports)
ACCIDENTAL EXPOSURE ( 7 FDA reports)
ADVERSE DRUG REACTION ( 7 FDA reports)
AGRANULOCYTOSIS ( 7 FDA reports)
AORTIC DISORDER ( 7 FDA reports)
AORTIC VALVE SCLEROSIS ( 7 FDA reports)
APHASIA ( 7 FDA reports)
CEREBRAL HAEMORRHAGE ( 7 FDA reports)
DRUG DISPENSING ERROR ( 7 FDA reports)
DRUG DOSE OMISSION ( 7 FDA reports)
DRUG EFFECT DECREASED ( 7 FDA reports)
EAR DISCOMFORT ( 7 FDA reports)
EJECTION FRACTION DECREASED ( 7 FDA reports)
EYE OEDEMA ( 7 FDA reports)
FACIAL PAIN ( 7 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 7 FDA reports)
HUMERUS FRACTURE ( 7 FDA reports)
HYPOAESTHESIA ORAL ( 7 FDA reports)
IMPAIRED HEALING ( 7 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 7 FDA reports)
INCREASED APPETITE ( 7 FDA reports)
INFUSION RELATED REACTION ( 7 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 7 FDA reports)
ISCHAEMIC STROKE ( 7 FDA reports)
JAW OPERATION ( 7 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 7 FDA reports)
MASS ( 7 FDA reports)
MEDICATION ERROR ( 7 FDA reports)
MULTIPLE INJURIES ( 7 FDA reports)
MUSCLE ATROPHY ( 7 FDA reports)
MUSCLE TIGHTNESS ( 7 FDA reports)
MYOPATHY ( 7 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 7 FDA reports)
OPEN WOUND ( 7 FDA reports)
PATELLA FRACTURE ( 7 FDA reports)
RENAL IMPAIRMENT ( 7 FDA reports)
RESPIRATORY DISORDER ( 7 FDA reports)
SEBORRHOEIC DERMATITIS ( 7 FDA reports)
SINUS POLYP ( 7 FDA reports)
SKIN INDURATION ( 7 FDA reports)
SKIN LACERATION ( 7 FDA reports)
SOCIAL PROBLEM ( 7 FDA reports)
SPEECH DISORDER ( 7 FDA reports)
STEVENS-JOHNSON SYNDROME ( 7 FDA reports)
SUDDEN DEATH ( 7 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 7 FDA reports)
THYROID DISORDER ( 7 FDA reports)
THYROID HORMONE REPLACEMENT THERAPY ( 7 FDA reports)
THYROID NEOPLASM ( 7 FDA reports)
UMBILICAL HERNIA ( 7 FDA reports)
VASCULAR CALCIFICATION ( 7 FDA reports)
VOCAL CORD PARALYSIS ( 7 FDA reports)
ADRENAL INSUFFICIENCY ( 6 FDA reports)
ADVERSE EVENT ( 6 FDA reports)
ANAPHYLACTIC REACTION ( 6 FDA reports)
ANGER ( 6 FDA reports)
ATRIAL FLUTTER ( 6 FDA reports)
ATRIOVENTRICULAR BLOCK ( 6 FDA reports)
BACK DISORDER ( 6 FDA reports)
BONE MARROW TRANSPLANT ( 6 FDA reports)
BRAIN MASS ( 6 FDA reports)
BREAST CANCER ( 6 FDA reports)
CARDIAC VALVE DISEASE ( 6 FDA reports)
CARDIO-RESPIRATORY ARREST ( 6 FDA reports)
CARDIOGENIC SHOCK ( 6 FDA reports)
CAROTID ARTERY OCCLUSION ( 6 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 6 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 6 FDA reports)
CHOKING ( 6 FDA reports)
COAGULOPATHY ( 6 FDA reports)
CONJUNCTIVITIS ( 6 FDA reports)
CYST ( 6 FDA reports)
DEAFNESS ( 6 FDA reports)
DRUG PRESCRIBING ERROR ( 6 FDA reports)
DRY SKIN ( 6 FDA reports)
DYSSTASIA ( 6 FDA reports)
EMOTIONAL DISORDER ( 6 FDA reports)
ENDARTERECTOMY ( 6 FDA reports)
ERECTILE DYSFUNCTION ( 6 FDA reports)
EYELID DISORDER ( 6 FDA reports)
EYELID MARGIN CRUSTING ( 6 FDA reports)
FIBROMYALGIA ( 6 FDA reports)
GLOSSITIS ( 6 FDA reports)
GLOSSODYNIA ( 6 FDA reports)
HYPOTONIA ( 6 FDA reports)
ILEUS ( 6 FDA reports)
IMMUNE SYSTEM DISORDER ( 6 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 6 FDA reports)
INFLUENZA ( 6 FDA reports)
IRRITABILITY ( 6 FDA reports)
JOINT STIFFNESS ( 6 FDA reports)
KNEE ARTHROPLASTY ( 6 FDA reports)
LACERATION ( 6 FDA reports)
LENTIGO ( 6 FDA reports)
LOBAR PNEUMONIA ( 6 FDA reports)
LOCALISED INFECTION ( 6 FDA reports)
LUNG DISORDER ( 6 FDA reports)
LUNG INFECTION ( 6 FDA reports)
MACULAR HOLE ( 6 FDA reports)
MACULAR OEDEMA ( 6 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 6 FDA reports)
MALNUTRITION ( 6 FDA reports)
MENTAL IMPAIRMENT ( 6 FDA reports)
MYOCARDIAL ISCHAEMIA ( 6 FDA reports)
NERVOUSNESS ( 6 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 6 FDA reports)
ORAL INFECTION ( 6 FDA reports)
PETECHIAE ( 6 FDA reports)
PHOTOPSIA ( 6 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 6 FDA reports)
PULMONARY FIBROSIS ( 6 FDA reports)
RESTLESS LEGS SYNDROME ( 6 FDA reports)
RESUSCITATION ( 6 FDA reports)
RIB FRACTURE ( 6 FDA reports)
SCOTOMA ( 6 FDA reports)
SKIN HYPERPIGMENTATION ( 6 FDA reports)
SKIN NEOPLASM EXCISION ( 6 FDA reports)
SKIN PLAQUE ( 6 FDA reports)
SKIN TIGHTNESS ( 6 FDA reports)
SOFT TISSUE MASS ( 6 FDA reports)
SPINAL COLUMN STENOSIS ( 6 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 6 FDA reports)
SURGERY ( 6 FDA reports)
SWOLLEN TONGUE ( 6 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 6 FDA reports)
THROAT IRRITATION ( 6 FDA reports)
TOOTH LOSS ( 6 FDA reports)
TROPONIN INCREASED ( 6 FDA reports)
VENTRICULAR HYPERTROPHY ( 6 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 6 FDA reports)
ACUTE PRERENAL FAILURE ( 5 FDA reports)
ADRENAL ADENOMA ( 5 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 5 FDA reports)
ANGIOPATHY ( 5 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 5 FDA reports)
APPENDICITIS ( 5 FDA reports)
BLINDNESS TRANSIENT ( 5 FDA reports)
BLISTER ( 5 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 5 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 5 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 5 FDA reports)
BONE DENSITY DECREASED ( 5 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 5 FDA reports)
BREAST PAIN ( 5 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 5 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 5 FDA reports)
CHEST X-RAY ABNORMAL ( 5 FDA reports)
CHROMATURIA ( 5 FDA reports)
COMA ( 5 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 5 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 5 FDA reports)
COR PULMONALE ( 5 FDA reports)
CORNEAL THINNING ( 5 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 5 FDA reports)
DECREASED INTEREST ( 5 FDA reports)
DIFFICULTY IN WALKING ( 5 FDA reports)
DILATATION VENTRICULAR ( 5 FDA reports)
DISEASE RECURRENCE ( 5 FDA reports)
DIVERTICULUM INTESTINAL ( 5 FDA reports)
DRUG INTOLERANCE ( 5 FDA reports)
DRUG TOXICITY ( 5 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 5 FDA reports)
EROSIVE DUODENITIS ( 5 FDA reports)
EROSIVE OESOPHAGITIS ( 5 FDA reports)
EXTRASYSTOLES ( 5 FDA reports)
EYE OPERATION ( 5 FDA reports)
EYE REDNESS ( 5 FDA reports)
FAECAL INCONTINENCE ( 5 FDA reports)
FAECES DISCOLOURED ( 5 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 5 FDA reports)
FUNGAL INFECTION ( 5 FDA reports)
GALLBLADDER DISORDER ( 5 FDA reports)
GASTRIC POLYPS ( 5 FDA reports)
GLAUCOMA SURGERY ( 5 FDA reports)
HAEMANGIOMA OF LIVER ( 5 FDA reports)
HAEMATOCRIT INCREASED ( 5 FDA reports)
HAEMOPTYSIS ( 5 FDA reports)
HEPATOMEGALY ( 5 FDA reports)
HYPERKERATOSIS ( 5 FDA reports)
HYPHAEMA ( 5 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 5 FDA reports)
HYPOPNOEA ( 5 FDA reports)
HYPOVOLAEMIA ( 5 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 5 FDA reports)
INFUSION SITE PAIN ( 5 FDA reports)
INTERSTITIAL LUNG DISEASE ( 5 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 5 FDA reports)
LIBIDO DECREASED ( 5 FDA reports)
MENISCUS LESION ( 5 FDA reports)
METABOLIC ACIDOSIS ( 5 FDA reports)
MIDDLE INSOMNIA ( 5 FDA reports)
MUSCULOSKELETAL DISORDER ( 5 FDA reports)
NAIL HYPERTROPHY ( 5 FDA reports)
NASAL DISCOMFORT ( 5 FDA reports)
NERVE INJURY ( 5 FDA reports)
NEUTROPENIA ( 5 FDA reports)
NO THERAPEUTIC RESPONSE ( 5 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 5 FDA reports)
OEDEMA MOUTH ( 5 FDA reports)
OPEN FRACTURE ( 5 FDA reports)
OPTIC ATROPHY ( 5 FDA reports)
OXYGEN SATURATION DECREASED ( 5 FDA reports)
PANIC DISORDER WITH AGORAPHOBIA ( 5 FDA reports)
PARANOIA ( 5 FDA reports)
PARONYCHIA ( 5 FDA reports)
PERICARDITIS ( 5 FDA reports)
PNEUMONIA ASPIRATION ( 5 FDA reports)
PNEUMOTHORAX ( 5 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 5 FDA reports)
PSORIASIS ( 5 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 5 FDA reports)
RESTLESSNESS ( 5 FDA reports)
RETINAL EXUDATES ( 5 FDA reports)
RETINAL HAEMORRHAGE ( 5 FDA reports)
RETINAL TEAR ( 5 FDA reports)
RETINAL VEIN OCCLUSION ( 5 FDA reports)
RHEUMATOID ARTHRITIS ( 5 FDA reports)
RIGHT VENTRICULAR FAILURE ( 5 FDA reports)
SCAB ( 5 FDA reports)
SEBORRHOEIC KERATOSIS ( 5 FDA reports)
SEPSIS SYNDROME ( 5 FDA reports)
SICK SINUS SYNDROME ( 5 FDA reports)
SKIN HAEMORRHAGE ( 5 FDA reports)
SKIN WARM ( 5 FDA reports)
SQUAMOUS CELL CARCINOMA ( 5 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 5 FDA reports)
SUBCUTANEOUS ABSCESS ( 5 FDA reports)
THROAT TIGHTNESS ( 5 FDA reports)
TRICHIASIS ( 5 FDA reports)
ULCER ( 5 FDA reports)
UPPER LIMB FRACTURE ( 5 FDA reports)
WRONG DRUG ADMINISTERED ( 5 FDA reports)
ACTINIC KERATOSIS ( 4 FDA reports)
AMAUROSIS FUGAX ( 4 FDA reports)
ANGIOEDEMA ( 4 FDA reports)
AORTIC STENOSIS ( 4 FDA reports)
APLASIA PURE RED CELL ( 4 FDA reports)
ASTHENOPIA ( 4 FDA reports)
ASTIGMATISM ( 4 FDA reports)
ATROPHIC VULVOVAGINITIS ( 4 FDA reports)
BEDRIDDEN ( 4 FDA reports)
BENIGN NEOPLASM OF ADRENAL GLAND ( 4 FDA reports)
BLOOD CALCIUM INCREASED ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 4 FDA reports)
BLOOD URIC ACID INCREASED ( 4 FDA reports)
BRONCHOSPASM ( 4 FDA reports)
CARDIOVERSION ( 4 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 4 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 4 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 4 FDA reports)
CHOLECYSTECTOMY ( 4 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 4 FDA reports)
COGNITIVE DISORDER ( 4 FDA reports)
CONGENITAL ATRIAL SEPTAL DEFECT ( 4 FDA reports)
CORONARY ARTERY STENOSIS ( 4 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 4 FDA reports)
DEMENTIA ( 4 FDA reports)
DENTAL OPERATION ( 4 FDA reports)
DEVICE RELATED INFECTION ( 4 FDA reports)
DIASTOLIC DYSFUNCTION ( 4 FDA reports)
DIVERTICULITIS ( 4 FDA reports)
DRUG LEVEL INCREASED ( 4 FDA reports)
DUODENITIS ( 4 FDA reports)
DYSPNOEA EXERTIONAL ( 4 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 4 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 4 FDA reports)
ELECTROLYTE IMBALANCE ( 4 FDA reports)
ERUCTATION ( 4 FDA reports)
ERYTHEMA OF EYELID ( 4 FDA reports)
EYE LASER SURGERY ( 4 FDA reports)
EYE MOVEMENT DISORDER ( 4 FDA reports)
FACIAL PALSY ( 4 FDA reports)
FAMILY STRESS ( 4 FDA reports)
GASTROINTESTINAL PAIN ( 4 FDA reports)
GASTROINTESTINAL ULCER ( 4 FDA reports)
HAEMORRHAGIC ANAEMIA ( 4 FDA reports)
HAEMORRHOIDS ( 4 FDA reports)
HEART INJURY ( 4 FDA reports)
HEPATIC FAILURE ( 4 FDA reports)
HEPATIC PAIN ( 4 FDA reports)
HEREDITARY ANGIOEDEMA ( 4 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 4 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 4 FDA reports)
HYPERPLASIA ( 4 FDA reports)
HYPERTHERMIA ( 4 FDA reports)
HYPOAESTHESIA FACIAL ( 4 FDA reports)
HYPOALBUMINAEMIA ( 4 FDA reports)
IMPAIRED DRIVING ABILITY ( 4 FDA reports)
INCONTINENCE ( 4 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 4 FDA reports)
ISCHAEMIA ( 4 FDA reports)
KERATITIS HERPETIC ( 4 FDA reports)
LABILE BLOOD PRESSURE ( 4 FDA reports)
LIMB DISCOMFORT ( 4 FDA reports)
LIVER DISORDER ( 4 FDA reports)
LOSS OF LIBIDO ( 4 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 4 FDA reports)
LUNG NEOPLASM MALIGNANT ( 4 FDA reports)
LUPUS PNEUMONITIS ( 4 FDA reports)
LYMPHOPENIA ( 4 FDA reports)
MEDICAL DEVICE COMPLICATION ( 4 FDA reports)
MELAENA ( 4 FDA reports)
METASTATIC LYMPHOMA ( 4 FDA reports)
MOUTH ULCERATION ( 4 FDA reports)
MULTIPLE ALLERGIES ( 4 FDA reports)
MYOSITIS ( 4 FDA reports)
NEOPLASM PROGRESSION ( 4 FDA reports)
NERVOUS SYSTEM DISORDER ( 4 FDA reports)
NODAL RHYTHM ( 4 FDA reports)
OCULAR DISCOMFORT ( 4 FDA reports)
OFF LABEL USE ( 4 FDA reports)
ORTHOPNOEA ( 4 FDA reports)
PARKINSON'S DISEASE ( 4 FDA reports)
PARKINSONISM ( 4 FDA reports)
PERICARDITIS LUPUS ( 4 FDA reports)
PERITONITIS ( 4 FDA reports)
PHARYNGEAL DISORDER ( 4 FDA reports)
PHARYNGEAL OEDEMA ( 4 FDA reports)
PHLEBITIS ( 4 FDA reports)
PHOTOSENSITIVITY REACTION ( 4 FDA reports)
PROCTALGIA ( 4 FDA reports)
PROTHROMBIN TIME PROLONGED ( 4 FDA reports)
PULPITIS DENTAL ( 4 FDA reports)
PYELONEPHRITIS ( 4 FDA reports)
RASH ERYTHEMATOUS ( 4 FDA reports)
RASH GENERALISED ( 4 FDA reports)
RASH MACULAR ( 4 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 4 FDA reports)
REFLUX OESOPHAGITIS ( 4 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 4 FDA reports)
RHEUMATOID FACTOR INCREASED ( 4 FDA reports)
SCAR ( 4 FDA reports)
SCLERAL DISORDER ( 4 FDA reports)
SEDATION ( 4 FDA reports)
SENSATION OF FOREIGN BODY ( 4 FDA reports)
SINUS BRADYCARDIA ( 4 FDA reports)
SKELETAL INJURY ( 4 FDA reports)
SKIN LESION ( 4 FDA reports)
SKIN TOXICITY ( 4 FDA reports)
SPINAL FRACTURE ( 4 FDA reports)
TONGUE ULCERATION ( 4 FDA reports)
TONSILLITIS ( 4 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 4 FDA reports)
URINE OUTPUT DECREASED ( 4 FDA reports)
VASCULITIS ( 4 FDA reports)
VENTRICULAR DYSFUNCTION ( 4 FDA reports)
VITREOUS DETACHMENT ( 4 FDA reports)
WEIGHT LOSS POOR ( 4 FDA reports)
WITHDRAWAL SYNDROME ( 4 FDA reports)
ABSCESS LIMB ( 3 FDA reports)
AGEUSIA ( 3 FDA reports)
ANGINA UNSTABLE ( 3 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 3 FDA reports)
ANOSMIA ( 3 FDA reports)
ANTERIOR CHAMBER DISORDER ( 3 FDA reports)
APHAGIA ( 3 FDA reports)
APLASTIC ANAEMIA ( 3 FDA reports)
ARTHROPATHY ( 3 FDA reports)
ARTHROPOD BITE ( 3 FDA reports)
ATAXIA ( 3 FDA reports)
ATRIAL TACHYCARDIA ( 3 FDA reports)
BACTERIAL SEPSIS ( 3 FDA reports)
BIOPSY SKIN ( 3 FDA reports)
BLOOD CHLORIDE DECREASED ( 3 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 3 FDA reports)
BLOOD CREATINE INCREASED ( 3 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 3 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 3 FDA reports)
BODY MASS INDEX INCREASED ( 3 FDA reports)
BODY TEMPERATURE INCREASED ( 3 FDA reports)
BONE DEBRIDEMENT ( 3 FDA reports)
BREAST CANCER FEMALE ( 3 FDA reports)
BREAST CANCER METASTATIC ( 3 FDA reports)
BREAST TENDERNESS ( 3 FDA reports)
C-REACTIVE PROTEIN ABNORMAL ( 3 FDA reports)
CARCINOID TUMOUR OF THE STOMACH ( 3 FDA reports)
CARDIAC PACEMAKER INSERTION ( 3 FDA reports)
CAROTID ARTERY ATHEROMA ( 3 FDA reports)
CATHETER RELATED COMPLICATION ( 3 FDA reports)
CEREBROVASCULAR DISORDER ( 3 FDA reports)
CHROMATOPSIA ( 3 FDA reports)
CLUMSINESS ( 3 FDA reports)
COLITIS ( 3 FDA reports)
COLON CANCER ( 3 FDA reports)
COLONIC POLYP ( 3 FDA reports)
CONGENITAL MUSCULOSKELETAL ANOMALY ( 3 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 3 FDA reports)
CORNEAL INFILTRATES ( 3 FDA reports)
CORNEAL OPACITY ( 3 FDA reports)
CORNEAL THICKENING ( 3 FDA reports)
CORNEAL ULCER ( 3 FDA reports)
CYANOPSIA ( 3 FDA reports)
DANDRUFF ( 3 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 3 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 3 FDA reports)
DERMATITIS EXFOLIATIVE ( 3 FDA reports)
DEVICE MALFUNCTION ( 3 FDA reports)
DIALYSIS ( 3 FDA reports)
DILATATION ATRIAL ( 3 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 3 FDA reports)
DISTURBANCE IN ATTENTION ( 3 FDA reports)
DRUG WITHDRAWAL HEADACHE ( 3 FDA reports)
DRY THROAT ( 3 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 3 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 3 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 3 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ABNORMAL ( 3 FDA reports)
ERYSIPELAS ( 3 FDA reports)
EXOSTOSIS ( 3 FDA reports)
EYE ALLERGY ( 3 FDA reports)
EYE INFECTION ( 3 FDA reports)
EYELASH DISCOLOURATION ( 3 FDA reports)
EYELID PTOSIS ( 3 FDA reports)
FACE OEDEMA ( 3 FDA reports)
FEELING COLD ( 3 FDA reports)
FEELING JITTERY ( 3 FDA reports)
FOOT AMPUTATION ( 3 FDA reports)
FULL BLOOD COUNT DECREASED ( 3 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 3 FDA reports)
GENERAL NUTRITION DISORDER ( 3 FDA reports)
GRAND MAL CONVULSION ( 3 FDA reports)
GRANULOCYTE COUNT INCREASED ( 3 FDA reports)
GROIN PAIN ( 3 FDA reports)
HAEMATEMESIS ( 3 FDA reports)
HAIR DISORDER ( 3 FDA reports)
HELICOBACTER INFECTION ( 3 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 3 FDA reports)
HICCUPS ( 3 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 3 FDA reports)
HYPERCAPNIA ( 3 FDA reports)
HYPERSOMNIA ( 3 FDA reports)
HYPOREFLEXIA ( 3 FDA reports)
HYPOTHERMIA ( 3 FDA reports)
HYPOVENTILATION ( 3 FDA reports)
HYSTERECTOMY ( 3 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 3 FDA reports)
INCOHERENT ( 3 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 3 FDA reports)
INFECTED CYST ( 3 FDA reports)
INJECTION SITE RASH ( 3 FDA reports)
INTESTINAL PERFORATION ( 3 FDA reports)
IRIDOCYCLITIS ( 3 FDA reports)
JAUNDICE ( 3 FDA reports)
JOINT INJURY ( 3 FDA reports)
KIDNEY INFECTION ( 3 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 3 FDA reports)
LIMB INJURY ( 3 FDA reports)
LIP SWELLING ( 3 FDA reports)
LIVER INJURY ( 3 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 3 FDA reports)
MELANOCYTIC NAEVUS ( 3 FDA reports)
MESENTERIC ARTERY STENOSIS ( 3 FDA reports)
METABOLIC DISORDER ( 3 FDA reports)
METABOLIC ENCEPHALOPATHY ( 3 FDA reports)
METASTASES TO LYMPH NODES ( 3 FDA reports)
MIGRAINE ( 3 FDA reports)
MOVEMENT DISORDER ( 3 FDA reports)
MUSCLE DISORDER ( 3 FDA reports)
MUSCULAR DYSTROPHY ( 3 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 3 FDA reports)
MYDRIASIS ( 3 FDA reports)
MYELOPATHY ( 3 FDA reports)
NASAL OPERATION ( 3 FDA reports)
NO ADVERSE EVENT ( 3 FDA reports)
OBSTRUCTION ( 3 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 3 FDA reports)
OPTIC NERVE INJURY ( 3 FDA reports)
ORAL PAIN ( 3 FDA reports)
PANIC ATTACK ( 3 FDA reports)
PARAESTHESIA ORAL ( 3 FDA reports)
PELVIC MASS ( 3 FDA reports)
PERIORBITAL HAEMATOMA ( 3 FDA reports)
PERNICIOUS ANAEMIA ( 3 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 3 FDA reports)
PNEUMONIA HAEMOPHILUS ( 3 FDA reports)
POLYPECTOMY ( 3 FDA reports)
PRESYNCOPE ( 3 FDA reports)
PROSTATIC DISORDER ( 3 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 3 FDA reports)
PSYCHOTIC DISORDER ( 3 FDA reports)
PULMONARY HILUM MASS ( 3 FDA reports)
RENAL TRANSPLANT ( 3 FDA reports)
RESPIRATORY TRACT CONGESTION ( 3 FDA reports)
RETINAL ANEURYSM ( 3 FDA reports)
RETINAL INJURY ( 3 FDA reports)
RHEUMATOID FACTOR NEGATIVE ( 3 FDA reports)
SKIN PAPILLOMA ( 3 FDA reports)
SPINAL DISORDER ( 3 FDA reports)
SPUTUM DISCOLOURED ( 3 FDA reports)
SUNBURN ( 3 FDA reports)
TALIPES ( 3 FDA reports)
THERAPEUTIC PRODUCT CONTAMINATION ( 3 FDA reports)
THINKING ABNORMAL ( 3 FDA reports)
THIRST ( 3 FDA reports)
TOXIC ANTERIOR SEGMENT SYNDROME ( 3 FDA reports)
TRANSPLANT FAILURE ( 3 FDA reports)
TRANSPLANT REJECTION ( 3 FDA reports)
TYPE 1 DIABETES MELLITUS ( 3 FDA reports)
UROBILINOGEN URINE INCREASED ( 3 FDA reports)
UROSEPSIS ( 3 FDA reports)
WALKING AID USER ( 3 FDA reports)
WOUND DEBRIDEMENT ( 3 FDA reports)
WOUND INFECTION ( 3 FDA reports)
ACIDOSIS ( 2 FDA reports)
ACNE ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 2 FDA reports)
ACUTE ABDOMEN ( 2 FDA reports)
AFFECT LABILITY ( 2 FDA reports)
AFFECTIVE DISORDER ( 2 FDA reports)
AGGRESSION ( 2 FDA reports)
AGITATION ( 2 FDA reports)
AMMONIA INCREASED ( 2 FDA reports)
AMYOTROPHY ( 2 FDA reports)
ANAPHYLACTIC SHOCK ( 2 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 2 FDA reports)
APNOEIC ATTACK ( 2 FDA reports)
APPLICATION SITE BURN ( 2 FDA reports)
APPLICATION SITE ERYTHEMA ( 2 FDA reports)
APPLICATION SITE SCAB ( 2 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 2 FDA reports)
ATHEROSCLEROSIS ( 2 FDA reports)
ATRIAL SEPTAL DEFECT ( 2 FDA reports)
ATRIAL THROMBOSIS ( 2 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 2 FDA reports)
BACTERIURIA ( 2 FDA reports)
BLADDER CANCER ( 2 FDA reports)
BLADDER DISORDER ( 2 FDA reports)
BLEPHAROSPASM ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
BLOOD CALCIUM DECREASED ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 2 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 2 FDA reports)
BLOOD URINE PRESENT ( 2 FDA reports)
BONE NEOPLASM MALIGNANT ( 2 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 2 FDA reports)
BRADYARRHYTHMIA ( 2 FDA reports)
BRONCHOPNEUMONIA ( 2 FDA reports)
BUNION OPERATION ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CARBON DIOXIDE DECREASED ( 2 FDA reports)
CARDIAC OPERATION ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
CARDIOVASCULAR DISORDER ( 2 FDA reports)
CATARACT OPERATION COMPLICATION ( 2 FDA reports)
CATHETER RELATED INFECTION ( 2 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 2 FDA reports)
CEREBRAL DISORDER ( 2 FDA reports)
CEREBRAL ISCHAEMIA ( 2 FDA reports)
CERUMEN IMPACTION ( 2 FDA reports)
CHALAZION ( 2 FDA reports)
CHOLANGITIS ( 2 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 2 FDA reports)
CHONDROMALACIA ( 2 FDA reports)
CHRONIC SINUSITIS ( 2 FDA reports)
CILIARY BODY DISORDER ( 2 FDA reports)
CONDUCTION DISORDER ( 2 FDA reports)
CONGENITAL CENTRAL NERVOUS SYSTEM ANOMALY ( 2 FDA reports)
CONGENITAL FOOT MALFORMATION ( 2 FDA reports)
CONGENITAL HAND MALFORMATION ( 2 FDA reports)
CONGENITAL MUSCLE ABSENCE ( 2 FDA reports)
CONJUNCTIVAL DISORDER ( 2 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 2 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 2 FDA reports)
COORDINATION ABNORMAL ( 2 FDA reports)
CORNEAL DECOMPENSATION ( 2 FDA reports)
CORNEAL OEDEMA ( 2 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 2 FDA reports)
CORONARY ARTERY BYPASS ( 2 FDA reports)
CYST REMOVAL ( 2 FDA reports)
DEAFNESS NEUROSENSORY ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DELLEN ( 2 FDA reports)
DEPERSONALISATION ( 2 FDA reports)
DERMATITIS CONTACT ( 2 FDA reports)
DEVICE FAILURE ( 2 FDA reports)
DIABETIC COMPLICATION ( 2 FDA reports)
DIABETIC GASTROPARESIS ( 2 FDA reports)
DIABETIC RETINAL OEDEMA ( 2 FDA reports)
DISCOMFORT ( 2 FDA reports)
DIVERTICULUM ( 2 FDA reports)
DIZZINESS POSTURAL ( 2 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 2 FDA reports)
DROOLING ( 2 FDA reports)
DUODENAL ULCER ( 2 FDA reports)
DYSAESTHESIA ( 2 FDA reports)
DYSAESTHESIA PHARYNX ( 2 FDA reports)
DYSPLASIA ( 2 FDA reports)
ECZEMA NUMMULAR ( 2 FDA reports)
ENCEPHALITIS ( 2 FDA reports)
ENCEPHALOMALACIA ( 2 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 2 FDA reports)
ESSENTIAL HYPERTENSION ( 2 FDA reports)
EXCITABILITY ( 2 FDA reports)
EXERCISE TOLERANCE DECREASED ( 2 FDA reports)
EXPIRED DRUG ADMINISTERED ( 2 FDA reports)
EYE PENETRATION ( 2 FDA reports)
EYELASH THICKENING ( 2 FDA reports)
EYELID EXFOLIATION ( 2 FDA reports)
EYELID IRRITATION ( 2 FDA reports)
EYELIDS PRURITUS ( 2 FDA reports)
FLAT AFFECT ( 2 FDA reports)
FLUID OVERLOAD ( 2 FDA reports)
FOOD INTOLERANCE ( 2 FDA reports)
FORMICATION ( 2 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 2 FDA reports)
GASTRIC ULCER ( 2 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 2 FDA reports)
GASTRIC VARICES ( 2 FDA reports)
GASTROENTERITIS ( 2 FDA reports)
GASTROSTOMY CLOSURE ( 2 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 2 FDA reports)
GENERALISED OEDEMA ( 2 FDA reports)
GOITRE ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HAEMOLYTIC ANAEMIA ( 2 FDA reports)
HAIR GROWTH ABNORMAL ( 2 FDA reports)
HAND DEFORMITY ( 2 FDA reports)
HEART DISEASE CONGENITAL ( 2 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 2 FDA reports)
HERPES SIMPLEX OPHTHALMIC ( 2 FDA reports)
HIP ARTHROPLASTY ( 2 FDA reports)
HIP DYSPLASIA ( 2 FDA reports)
HYPERPARATHYROIDISM ( 2 FDA reports)
HYPERTENSIVE HEART DISEASE ( 2 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 2 FDA reports)
HYPOVITAMINOSIS ( 2 FDA reports)
IMMOBILE ( 2 FDA reports)
IMPAIRED FASTING GLUCOSE ( 2 FDA reports)
INCORRECT STORAGE OF DRUG ( 2 FDA reports)
INCREASED TENDENCY TO BRUISE ( 2 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 2 FDA reports)
INGUINAL HERNIA ( 2 FDA reports)
INJECTION SITE IRRITATION ( 2 FDA reports)
INJECTION SITE OEDEMA ( 2 FDA reports)
INJECTION SITE PRURITUS ( 2 FDA reports)
INJECTION SITE SWELLING ( 2 FDA reports)
INJECTION SITE WARMTH ( 2 FDA reports)
INJURY ASPHYXIATION ( 2 FDA reports)
INJURY CORNEAL ( 2 FDA reports)
INTESTINAL OPERATION ( 2 FDA reports)
INTRACARDIAC THROMBUS ( 2 FDA reports)
IRIS DISORDER ( 2 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 2 FDA reports)
JOINT DISLOCATION ( 2 FDA reports)
KERATITIS ( 2 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 2 FDA reports)
KERATORHEXIS ( 2 FDA reports)
KYPHOSIS ( 2 FDA reports)
LABORATORY TEST ABNORMAL ( 2 FDA reports)
LACUNAR INFARCTION ( 2 FDA reports)
LENS IMPLANT ( 2 FDA reports)
LIGAMENT RUPTURE ( 2 FDA reports)
LIPASE INCREASED ( 2 FDA reports)
LISTLESS ( 2 FDA reports)
LUMBAR SPINAL STENOSIS ( 2 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 2 FDA reports)
LYMPHOEDEMA ( 2 FDA reports)
MACULAR CYST ( 2 FDA reports)
MALIGNANT HYPERTENSION ( 2 FDA reports)
MANDIBULECTOMY ( 2 FDA reports)
MEDIASTINAL DISORDER ( 2 FDA reports)
MEDICATION RESIDUE ( 2 FDA reports)
MENOPAUSE ( 2 FDA reports)
MESENTERIC OCCLUSION ( 2 FDA reports)
METASTASES TO SPINE ( 2 FDA reports)
MICTURITION DISORDER ( 2 FDA reports)
MIOSIS ( 2 FDA reports)
MOBILITY DECREASED ( 2 FDA reports)
MOOD ALTERED ( 2 FDA reports)
MUSCLE CRAMP ( 2 FDA reports)
MUSCLE FATIGUE ( 2 FDA reports)
MUSCLE TWITCHING ( 2 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME ( 2 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 2 FDA reports)
NAIL INFECTION ( 2 FDA reports)
NASAL DISORDER ( 2 FDA reports)
NEOVASCULARISATION ( 2 FDA reports)
NEPHRITIS ALLERGIC ( 2 FDA reports)
NEUROPATHY ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
NIGHT SWEATS ( 2 FDA reports)
NITRITE URINE PRESENT ( 2 FDA reports)
OCULAR HYPERTENSION ( 2 FDA reports)
OCULAR VASCULAR DISORDER ( 2 FDA reports)
OESOPHAGEAL SPASM ( 2 FDA reports)
OESOPHAGITIS ULCERATIVE ( 2 FDA reports)
OPTIC NERVE DISORDER ( 2 FDA reports)
ORAL CANDIDIASIS ( 2 FDA reports)
ORAL DISORDER ( 2 FDA reports)
ORAL DYSAESTHESIA ( 2 FDA reports)
OSTEOMYELITIS DRAINAGE ( 2 FDA reports)
PAIN OF SKIN ( 2 FDA reports)
PANCREATIC CARCINOMA ( 2 FDA reports)
PANCREATITIS ACUTE ( 2 FDA reports)
PAPILLOEDEMA ( 2 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 2 FDA reports)
PERICARDIAL EFFUSION ( 2 FDA reports)
PERIPHERAL ISCHAEMIA ( 2 FDA reports)
PERITONITIS BACTERIAL ( 2 FDA reports)
PHARYNGEAL HYPOAESTHESIA ( 2 FDA reports)
PLASMACYTOMA ( 2 FDA reports)
PLEURITIC PAIN ( 2 FDA reports)
PNEUMONIA KLEBSIELLA ( 2 FDA reports)
POLYMENORRHOEA ( 2 FDA reports)
POLYNEUROPATHY ( 2 FDA reports)
POSTICTAL STATE ( 2 FDA reports)
POSTNASAL DRIP ( 2 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 2 FDA reports)
PROCEDURAL PAIN ( 2 FDA reports)
PRODUCT CONTAINER SEAL ISSUE ( 2 FDA reports)
PRODUCT QUALITY ISSUE ( 2 FDA reports)
PRODUCT TAMPERING ( 2 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
PROTEIN TOTAL DECREASED ( 2 FDA reports)
PROTEIN URINE PRESENT ( 2 FDA reports)
PROTEINURIA ( 2 FDA reports)
PSEUDOPHAKIA ( 2 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 2 FDA reports)
PULMONARY MASS ( 2 FDA reports)
PULMONARY TOXICITY ( 2 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 2 FDA reports)
PULSE ABSENT ( 2 FDA reports)
PULSE PRESSURE DECREASED ( 2 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 2 FDA reports)
PURULENCE ( 2 FDA reports)
PYODERMA ( 2 FDA reports)
RADIOTHERAPY ( 2 FDA reports)
RADIUS FRACTURE ( 2 FDA reports)
RALES ( 2 FDA reports)
RASH MORBILLIFORM ( 2 FDA reports)
RASH PRURITIC ( 2 FDA reports)
RASH SCALY ( 2 FDA reports)
REGURGITATION ( 2 FDA reports)
RENAL ARTERY STENOSIS ( 2 FDA reports)
RESPIRATORY RATE INCREASED ( 2 FDA reports)
RETINAL DEGENERATION ( 2 FDA reports)
RETINAL DISORDER ( 2 FDA reports)
RETINAL ISCHAEMIA ( 2 FDA reports)
RETINITIS ( 2 FDA reports)
RETROPERITONEAL HAEMATOMA ( 2 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 2 FDA reports)
REVERSIBLE ISCHAEMIC NEUROLOGICAL DEFICIT ( 2 FDA reports)
RHINALGIA ( 2 FDA reports)
SARCOIDOSIS ( 2 FDA reports)
SCLERAL HYPERAEMIA ( 2 FDA reports)
SECRETION DISCHARGE ( 2 FDA reports)
SELF-MEDICATION ( 2 FDA reports)
SENILE DEMENTIA ( 2 FDA reports)
SERUM FERRITIN INCREASED ( 2 FDA reports)
SEXUAL DYSFUNCTION ( 2 FDA reports)
SHOCK HAEMORRHAGIC ( 2 FDA reports)
SINUS CONGESTION ( 2 FDA reports)
SKIN CHAPPED ( 2 FDA reports)
SKIN FISSURES ( 2 FDA reports)
SKIN HYPERTROPHY ( 2 FDA reports)
SKIN INFECTION ( 2 FDA reports)
SKIN ODOUR ABNORMAL ( 2 FDA reports)
SKIN REACTION ( 2 FDA reports)
SLEEP ATTACKS ( 2 FDA reports)
SNEEZING ( 2 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 2 FDA reports)
SPLENIC INFARCTION ( 2 FDA reports)
SPONDYLOARTHROPATHY ( 2 FDA reports)
SPONDYLOLISTHESIS ( 2 FDA reports)
SPONDYLOLISTHESIS ACQUIRED ( 2 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 2 FDA reports)
STENT OCCLUSION ( 2 FDA reports)
SYNOVIAL RUPTURE ( 2 FDA reports)
TARDIVE DYSKINESIA ( 2 FDA reports)
TENDERNESS ( 2 FDA reports)
TENDON INJURY ( 2 FDA reports)
TENOSYNOVITIS ( 2 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
THROMBOCYTHAEMIA ( 2 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 2 FDA reports)
TIBIA FRACTURE ( 2 FDA reports)
TONGUE DISORDER ( 2 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 2 FDA reports)
TOXIC SKIN ERUPTION ( 2 FDA reports)
TRABECULECTOMY ( 2 FDA reports)
TRANSAMINASES INCREASED ( 2 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 2 FDA reports)
UMBILICAL HERNIA REPAIR ( 2 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
VASCULAR OCCLUSION ( 2 FDA reports)
VENA CAVA THROMBOSIS ( 2 FDA reports)
VENTRICULAR HYPOKINESIA ( 2 FDA reports)
VISUAL FIELD TESTS ABNORMAL ( 2 FDA reports)
VITAMIN B12 DEFICIENCY ( 2 FDA reports)
VOCAL CORD DISORDER ( 2 FDA reports)
XEROSIS ( 2 FDA reports)
ABDOMINAL MASS ( 1 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABDOMINAL REBOUND TENDERNESS ( 1 FDA reports)
ACCIDENT ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ADACTYLY ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 1 FDA reports)
ALLERGIC OEDEMA ( 1 FDA reports)
ANAEMIA MACROCYTIC ( 1 FDA reports)
ANEURYSM ( 1 FDA reports)
ANGIOGRAM ABNORMAL ( 1 FDA reports)
ANION GAP DECREASED ( 1 FDA reports)
ANISOMETROPIA ( 1 FDA reports)
ANOXIC ENCEPHALOPATHY ( 1 FDA reports)
ANTIBODY TEST POSITIVE ( 1 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 1 FDA reports)
AORTIC ATHEROSCLEROSIS ( 1 FDA reports)
AORTIC VALVE CALCIFICATION ( 1 FDA reports)
APATHY ( 1 FDA reports)
APHAKIA ( 1 FDA reports)
APPETITE DISORDER ( 1 FDA reports)
APPLICATION SITE IRRITATION ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ARTERIAL DISORDER ( 1 FDA reports)
ARTERIAL INSUFFICIENCY ( 1 FDA reports)
ARTERIOSCLEROTIC RETINOPATHY ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 1 FDA reports)
AUTOIMMUNE DISORDER ( 1 FDA reports)
AUTONOMIC NEUROPATHY ( 1 FDA reports)
BACK INJURY ( 1 FDA reports)
BACTERIA URINE NO ORGANISM OBSERVED ( 1 FDA reports)
BARRETT'S OESOPHAGUS ( 1 FDA reports)
BASEDOW'S DISEASE ( 1 FDA reports)
BENIGN COLONIC NEOPLASM ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BIOPSY BREAST ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BITE ( 1 FDA reports)
BLADDER DILATATION ( 1 FDA reports)
BLADDER OPERATION ( 1 FDA reports)
BLADDER PAIN ( 1 FDA reports)
BLADDER SPASM ( 1 FDA reports)
BLOOD BICARBONATE INCREASED ( 1 FDA reports)
BLOOD CALCIUM ABNORMAL ( 1 FDA reports)
BLOOD CHLORIDE INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 1 FDA reports)
BLOOD COPPER DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD ELECTROLYTES INCREASED ( 1 FDA reports)
BLOOD GASES ABNORMAL ( 1 FDA reports)
BLOOD IRON ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD MAGNESIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ( 1 FDA reports)
BLOOD TEST ABNORMAL ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 1 FDA reports)
BLUE TOE SYNDROME ( 1 FDA reports)
BONE LOSS ( 1 FDA reports)
BONE NEOPLASM ( 1 FDA reports)
BRADYPHRENIA ( 1 FDA reports)
BRADYPNOEA ( 1 FDA reports)
BRAIN INJURY ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BRAIN SCAN ABNORMAL ( 1 FDA reports)
BREAST CALCIFICATIONS ( 1 FDA reports)
BREAST CANCER RECURRENT ( 1 FDA reports)
BREAST CYST ( 1 FDA reports)
BREAST HYPERPLASIA ( 1 FDA reports)
BREAST SWELLING ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
BREECH PRESENTATION ( 1 FDA reports)
BRONCHIAL DISORDER ( 1 FDA reports)
BRONCHIECTASIS ( 1 FDA reports)
BRONCHITIS CHRONIC ( 1 FDA reports)
BRONCHOPLEURAL FISTULA ( 1 FDA reports)
BUNDLE BRANCH BLOCK ( 1 FDA reports)
BUNION ( 1 FDA reports)
BURSAL OPERATION ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CANDIDURIA ( 1 FDA reports)
CAPILLARY LEAK SYNDROME ( 1 FDA reports)
CARBON DIOXIDE INCREASED ( 1 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 1 FDA reports)
CARDIAC DEATH ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
CARDIAC FIBRILLATION ( 1 FDA reports)
CARDIAC FLUTTER ( 1 FDA reports)
CARDIAC VALVE VEGETATION ( 1 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 1 FDA reports)
CARDIO-RESPIRATORY DISTRESS ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 1 FDA reports)
CAROTID ARTERY DISEASE ( 1 FDA reports)
CARPAL TUNNEL SYNDROME ( 1 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 1 FDA reports)
CEREBELLAR ARTERY OCCLUSION ( 1 FDA reports)
CEREBELLAR HAEMORRHAGE ( 1 FDA reports)
CEREBRAL HYPOPERFUSION ( 1 FDA reports)
CERVICAL SPINAL STENOSIS ( 1 FDA reports)
CHOREA ( 1 FDA reports)
CHOROIDITIS ( 1 FDA reports)
CHRONIC GRANULOMATOUS DISEASE ( 1 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 1 FDA reports)
CILIARY HYPERAEMIA ( 1 FDA reports)
CLUBBING ( 1 FDA reports)
COELIAC ARTERY STENOSIS ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COLOSTOMY ( 1 FDA reports)
COLOUR BLINDNESS ( 1 FDA reports)
COMPRESSION FRACTURE ( 1 FDA reports)
CONCUSSION ( 1 FDA reports)
CONDUCTIVE DEAFNESS ( 1 FDA reports)
CONGENITAL ANOMALY ( 1 FDA reports)
CONJUNCTIVAL IRRITATION ( 1 FDA reports)
CONJUNCTIVAL PRIMARY ACQUIRED MELANOSIS ( 1 FDA reports)
CONJUNCTIVAL SCAR ( 1 FDA reports)
CONNECTIVE TISSUE DISORDER ( 1 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 1 FDA reports)
COOMBS TEST POSITIVE ( 1 FDA reports)
CORNEAL ABRASION ( 1 FDA reports)
CORNEAL DEGENERATION ( 1 FDA reports)
CORNEAL DEPOSITS ( 1 FDA reports)
CORNEAL DISORDER ( 1 FDA reports)
CORNEAL EPITHELIUM DISORDER ( 1 FDA reports)
CORNEAL SCAR ( 1 FDA reports)
CORNEAL TRANSPLANT ( 1 FDA reports)
CORONARY ANGIOPLASTY ( 1 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 1 FDA reports)
CORONARY ARTERY THROMBOSIS ( 1 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
CYSTITIS HAEMORRHAGIC ( 1 FDA reports)
CYSTOCELE ( 1 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 1 FDA reports)
DARK CIRCLES UNDER EYES ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DERMATITIS PSORIASIFORM ( 1 FDA reports)
DETOXIFICATION ( 1 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 1 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 1 FDA reports)
DIABETIC BLINDNESS ( 1 FDA reports)
DIABETIC GASTROPATHY ( 1 FDA reports)
DIABETIC KETOACIDOSIS ( 1 FDA reports)
DIABETIC MICROANGIOPATHY ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DIET REFUSAL ( 1 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 1 FDA reports)
DISEASE COMPLICATION ( 1 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 1 FDA reports)
DIVERTICULUM GASTRIC ( 1 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DRUG TOLERANCE ( 1 FDA reports)
DUODENAL PERFORATION ( 1 FDA reports)
DYSACUSIS ( 1 FDA reports)
DYSMORPHISM ( 1 FDA reports)
DYSPNOEA AT REST ( 1 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 1 FDA reports)
DYSSOMNIA ( 1 FDA reports)
EAR DISORDER ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
ECHOLALIA ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
EFFUSION ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ENDOPHTHALMITIS ( 1 FDA reports)
ENDOSCOPY ABNORMAL ( 1 FDA reports)
ENERGY INCREASED ( 1 FDA reports)
ENOPHTHALMOS ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
ENTROPION ( 1 FDA reports)
ENZYME ABNORMALITY ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
EPIGASTRIC DISCOMFORT ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
ERECTION INCREASED ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
ESCHERICHIA TEST POSITIVE ( 1 FDA reports)
ESSENTIAL TREMOR ( 1 FDA reports)
EXTRAOCULAR MUSCLE PARESIS ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EXTREMITY NECROSIS ( 1 FDA reports)
EXTRINSIC VASCULAR COMPRESSION ( 1 FDA reports)
EYE BURNS ( 1 FDA reports)
EYE COMPLICATION ASSOCIATED WITH DEVICE ( 1 FDA reports)
EYE INFECTION BACTERIAL ( 1 FDA reports)
EYE INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
EYE INJURY ( 1 FDA reports)
EYE NAEVUS ( 1 FDA reports)
EYE OPERATION COMPLICATION ( 1 FDA reports)
EYELID CYST ( 1 FDA reports)
EYELID RETRACTION ( 1 FDA reports)
FAECES HARD ( 1 FDA reports)
FAILURE OF IMPLANT ( 1 FDA reports)
FEEDING TUBE COMPLICATION ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
FEMORAL NECK FRACTURE ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FIBULA FRACTURE ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FOOD ALLERGY ( 1 FDA reports)
FOOD INTERACTION ( 1 FDA reports)
FOOT FRACTURE ( 1 FDA reports)
FOREIGN BODY ASPIRATION ( 1 FDA reports)
FOREIGN BODY IN EYE ( 1 FDA reports)
FOREIGN BODY TRAUMA ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
GALLBLADDER OPERATION ( 1 FDA reports)
GASTRECTOMY ( 1 FDA reports)
GASTRIC PH DECREASED ( 1 FDA reports)
GASTRITIS BACTERIAL ( 1 FDA reports)
GASTRO-JEJUNOSTOMY ( 1 FDA reports)
GASTROENTERITIS VIRAL ( 1 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
GASTROINTESTINAL FUNGAL INFECTION ( 1 FDA reports)
GASTROINTESTINAL PERFORATION ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GESTATIONAL DIABETES ( 1 FDA reports)
GLARE ( 1 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 1 FDA reports)
GLOBULINS DECREASED ( 1 FDA reports)
GLYCOSURIA ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
GRUNTING ( 1 FDA reports)
HAEMARTHROSIS ( 1 FDA reports)
HAEMOCHROMATOSIS ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 1 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 1 FDA reports)
HEART RATE ABNORMAL ( 1 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATIC TRAUMA ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HEPATOJUGULAR REFLUX ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HERNIA ( 1 FDA reports)
HERPES OPHTHALMIC ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HOARSENESS ( 1 FDA reports)
HOMOCYSTINAEMIA ( 1 FDA reports)
HORDEOLUM ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HYDROCEPHALUS ( 1 FDA reports)
HYPERAEMIA ( 1 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERCHLORHYDRIA ( 1 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 1 FDA reports)
HYPERKINESIA ( 1 FDA reports)
HYPERMETROPIA ( 1 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 1 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
HYPOPYON ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INFUSION SITE EXTRAVASATION ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INJECTION SITE INDURATION ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INJECTION SITE URTICARIA ( 1 FDA reports)
INNER EAR DISORDER ( 1 FDA reports)
INSTILLATION SITE PAIN ( 1 FDA reports)
INSTILLATION SITE REACTION ( 1 FDA reports)
INSULIN-REQUIRING TYPE II DIABETES MELLITUS ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 1 FDA reports)
INTESTINAL MASS ( 1 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 1 FDA reports)
INTRACRANIAL INJURY ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
INTRAMEDULLARY ROD INSERTION ( 1 FDA reports)
INTRAOCULAR MELANOMA ( 1 FDA reports)
INVESTIGATION ( 1 FDA reports)
IRIDECTOMY ( 1 FDA reports)
IRIDOCELE ( 1 FDA reports)
IRIS NEOVASCULARISATION ( 1 FDA reports)
IRON DEFICIENCY ( 1 FDA reports)
IRRITABLE BOWEL SYNDROME ( 1 FDA reports)
JOINT CONTRACTURE ( 1 FDA reports)
JOINT WARMTH ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
LABORATORY TEST INTERFERENCE ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LACTOSE INTOLERANCE ( 1 FDA reports)
LEFT ATRIAL DILATATION ( 1 FDA reports)
LEG AMPUTATION ( 1 FDA reports)
LENTICULAR OPACITIES ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LICHENOID KERATOSIS ( 1 FDA reports)
LIGAMENT LAXITY ( 1 FDA reports)
LIMB MALFORMATION ( 1 FDA reports)
LIP NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 1 FDA reports)
LIQUID PRODUCT PHYSICAL ISSUE ( 1 FDA reports)
LIVER TRANSPLANT ( 1 FDA reports)
LOSS OF EMPLOYMENT ( 1 FDA reports)
LOWER LIMB FRACTURE ( 1 FDA reports)
LUMBOSACRAL PLEXUS LESION ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
LUNG NEOPLASM SURGERY ( 1 FDA reports)
LYMPHADENITIS ( 1 FDA reports)
MADAROSIS ( 1 FDA reports)
MAJOR DEPRESSION ( 1 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 1 FDA reports)
MANIA ( 1 FDA reports)
MASS EXCISION ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MECHANICAL COMPLICATION OF IMPLANT ( 1 FDA reports)
MENINGEAL NEOPLASM ( 1 FDA reports)
MENINGIOMA ( 1 FDA reports)
MENINGITIS VIRAL ( 1 FDA reports)
MICROANGIOPATHY ( 1 FDA reports)
MICROPHTHALMOS ( 1 FDA reports)
MICROSTOMIA ( 1 FDA reports)
MIDDLE EAR EFFUSION ( 1 FDA reports)
MITRAL VALVE REPLACEMENT ( 1 FDA reports)
MIXED HEPATOCELLULAR-CHOLESTATIC INJURY ( 1 FDA reports)
MONOCYTE COUNT INCREASED ( 1 FDA reports)
MONONUCLEOSIS SYNDROME ( 1 FDA reports)
MONOPARESIS ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
MORGANELLA INFECTION ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
MULTIPLE SYSTEM ATROPHY ( 1 FDA reports)
MUSCLE SPASTICITY ( 1 FDA reports)
MYASTHENIA GRAVIS ( 1 FDA reports)
MYCOSIS FUNGOIDES ( 1 FDA reports)
MYOPIA ( 1 FDA reports)
NASAL OBSTRUCTION ( 1 FDA reports)
NASAL OEDEMA ( 1 FDA reports)
NASAL SEPTUM DEVIATION ( 1 FDA reports)
NECK DEFORMITY ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NEPHROGENIC ANAEMIA ( 1 FDA reports)
NEURODERMATITIS ( 1 FDA reports)
NEUROGENIC BLADDER ( 1 FDA reports)
NEUROMA ( 1 FDA reports)
NIGHT BLINDNESS ( 1 FDA reports)
NO ADVERSE EFFECT ( 1 FDA reports)
NONSPECIFIC REACTION ( 1 FDA reports)
NYSTAGMUS ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OCULAR NEOPLASM ( 1 FDA reports)
ODYNOPHAGIA ( 1 FDA reports)
OESOPHAGEAL HYPOMOTILITY ( 1 FDA reports)
OLFACTORY NERVE DISORDER ( 1 FDA reports)
ONYCHOMADESIS ( 1 FDA reports)
OPHTHALMOLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
OPTIC NEURITIS ( 1 FDA reports)
OPTIC NEUROPATHY ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
ORAL SOFT TISSUE DISORDER ( 1 FDA reports)
OSTEOMYELITIS ACUTE ( 1 FDA reports)
OSTEOSARCOMA METASTATIC ( 1 FDA reports)
OTITIS EXTERNA ( 1 FDA reports)
OTITIS MEDIA CHRONIC ( 1 FDA reports)
OVARIAN EPITHELIAL CANCER STAGE IV ( 1 FDA reports)
PAIN EXACERBATED ( 1 FDA reports)
PAINFUL DEFAECATION ( 1 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PANIC DISORDER ( 1 FDA reports)
PARAESTHESIA CIRCUMORAL ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 1 FDA reports)
PARANOID PERSONALITY DISORDER ( 1 FDA reports)
PARAPARESIS ( 1 FDA reports)
PARATHYROID TUMOUR ( 1 FDA reports)
PARATHYROID TUMOUR BENIGN ( 1 FDA reports)
PAROSMIA ( 1 FDA reports)
PARTNER STRESS ( 1 FDA reports)
PATHOLOGICAL GAMBLING ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PELVIC PAIN ( 1 FDA reports)
PEMPHIGOID ( 1 FDA reports)
PERFORMANCE STATUS DECREASED ( 1 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
PERIPHERAL NERVE OPERATION ( 1 FDA reports)
PERIPHERAL T-CELL LYMPHOMA UNSPECIFIED ( 1 FDA reports)
PERITONEAL FLUID ANALYSIS ABNORMAL ( 1 FDA reports)
PERITONEAL HAEMATOMA ( 1 FDA reports)
PERITONEAL HAEMORRHAGE ( 1 FDA reports)
PERSONALITY CHANGE ( 1 FDA reports)
PERTUSSIS ( 1 FDA reports)
PHLEBOLITH ( 1 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 1 FDA reports)
PLEURAL FIBROSIS ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
PNEUMOCONIOSIS ( 1 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 1 FDA reports)
PNEUMOMEDIASTINUM ( 1 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 1 FDA reports)
POLYDIPSIA ( 1 FDA reports)
POLYP ( 1 FDA reports)
POLYTRAUMATISM ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
POOR QUALITY SLEEP ( 1 FDA reports)
POST CONCUSSION SYNDROME ( 1 FDA reports)
POST PROCEDURAL CELLULITIS ( 1 FDA reports)
POST PROCEDURAL HAEMATOMA ( 1 FDA reports)
POST PROCEDURAL PAIN ( 1 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 1 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
PREMENSTRUAL SYNDROME ( 1 FDA reports)
PRESBYOPIA ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PRODUCT ADHESION ISSUE ( 1 FDA reports)
PRODUCT CONTAINER ISSUE ( 1 FDA reports)
PRODUCT PACKAGING ISSUE ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PSYCHOLOGICAL TRAUMA ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 1 FDA reports)
PULMONARY GRANULOMA ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
PULMONARY VALVE DISEASE ( 1 FDA reports)
PUNCTATE KERATITIS ( 1 FDA reports)
PURPURA ( 1 FDA reports)
PYELONEPHRITIS ACUTE ( 1 FDA reports)
QUADRIPLEGIA ( 1 FDA reports)
RADIATION THYROIDITIS ( 1 FDA reports)
RADICULITIS ( 1 FDA reports)
RADICULITIS LUMBOSACRAL ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
RAYNAUD'S PHENOMENON ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RECTOCELE ( 1 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
RED BLOOD CELL MACROCYTES PRESENT ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 1 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 1 FDA reports)
RESPIRATORY RATE DECREASED ( 1 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 1 FDA reports)
RETINAL ARTERY OCCLUSION ( 1 FDA reports)
RETINAL CYST ( 1 FDA reports)
RETINAL DEPIGMENTATION ( 1 FDA reports)
RETINAL OEDEMA ( 1 FDA reports)
RETINAL VASCULAR OCCLUSION ( 1 FDA reports)
RETINOPATHY ( 1 FDA reports)
RHONCHI ( 1 FDA reports)
RIGHT ATRIAL DILATATION ( 1 FDA reports)
ROSACEA ( 1 FDA reports)
ROTATOR CUFF REPAIR ( 1 FDA reports)
SALIVARY HYPERSECRETION ( 1 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 1 FDA reports)
SCROTAL HAEMATOMA ( 1 FDA reports)
SEBACEOUS GLAND DISORDER ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SERUM SICKNESS ( 1 FDA reports)
SHOULDER PAIN ( 1 FDA reports)
SICKLE CELL ANAEMIA ( 1 FDA reports)
SICKLE CELL TRAIT ( 1 FDA reports)
SIGHT DISABILITY ( 1 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 1 FDA reports)
SILICOSIS ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SINUS OPERATION ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SKIN DESQUAMATION ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN FIBROSIS ( 1 FDA reports)
SKIN IRRITATION ( 1 FDA reports)
SKIN SWELLING ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SLUGGISHNESS ( 1 FDA reports)
SMALL BOWEL ANGIOEDEMA ( 1 FDA reports)
SMALL FOR DATES BABY ( 1 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 1 FDA reports)
SPINAL LAMINECTOMY ( 1 FDA reports)
SPLENECTOMY ( 1 FDA reports)
SPONDYLITIS ( 1 FDA reports)
SPONDYLOLYSIS ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STAPHYLOMA ( 1 FDA reports)
STASIS DERMATITIS ( 1 FDA reports)
STENT PLACEMENT ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
STRESS SYMPTOMS ( 1 FDA reports)
STRIDOR ( 1 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SUDDEN CARDIAC DEATH ( 1 FDA reports)
SUPERINFECTION ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
SYNCOPE VASOVAGAL ( 1 FDA reports)
TENDON PAIN ( 1 FDA reports)
TENDON RUPTURE ( 1 FDA reports)
TENSION ( 1 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 1 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 1 FDA reports)
TONGUE BITING ( 1 FDA reports)
TONGUE DISCOLOURATION ( 1 FDA reports)
TONGUE INJURY ( 1 FDA reports)
TOOTH ABSCESS ( 1 FDA reports)
TOOTH INFECTION ( 1 FDA reports)
TOOTH REPAIR ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TOXIC SHOCK SYNDROME ( 1 FDA reports)
TRACHEOBRONCHITIS ( 1 FDA reports)
TRANSIENT ACANTHOLYTIC DERMATOSIS ( 1 FDA reports)
TRIGEMINAL NEURALGIA ( 1 FDA reports)
TRISMUS ( 1 FDA reports)
TUNNEL VISION ( 1 FDA reports)
URETERAL STENT INSERTION ( 1 FDA reports)
URETHRAL DISORDER ( 1 FDA reports)
URINARY TRACT DISORDER ( 1 FDA reports)
URINE ANALYSIS ABNORMAL ( 1 FDA reports)
URINE BILIRUBIN INCREASED ( 1 FDA reports)
URINE COLOUR ABNORMAL ( 1 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 1 FDA reports)
URINE OUTPUT INCREASED ( 1 FDA reports)
UTERINE HAEMORRHAGE ( 1 FDA reports)
UTERINE LEIOMYOMA ( 1 FDA reports)
VARICOSE VEIN ( 1 FDA reports)
VASCULAR BYPASS GRAFT ( 1 FDA reports)
VASCULAR PSEUDOANEURYSM ( 1 FDA reports)
VASCULAR PURPURA ( 1 FDA reports)
VASCULAR RUPTURE ( 1 FDA reports)
VASCULITIC RASH ( 1 FDA reports)
VEIN DISORDER ( 1 FDA reports)
VENOUS INSUFFICIENCY ( 1 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 1 FDA reports)
VENTRICULAR ARRHYTHMIA ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 1 FDA reports)
VERTIGO POSITIONAL ( 1 FDA reports)
VESTIBULAR DISORDER ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VISUAL ACUITY TESTS ABNORMAL ( 1 FDA reports)
VITAMIN D DECREASED ( 1 FDA reports)
VITILIGO ( 1 FDA reports)
VITREOUS DEGENERATION ( 1 FDA reports)
VOLUME BLOOD DECREASED ( 1 FDA reports)
VOMITING PROJECTILE ( 1 FDA reports)
WHIPLASH INJURY ( 1 FDA reports)
WOUND COMPLICATION ( 1 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
WRIST FRACTURE ( 1 FDA reports)
WRONG DEVICE USED ( 1 FDA reports)
X-RAY LIMB ABNORMAL ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use