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

DYSPNOEA ( 271 FDA reports)
PAIN ( 267 FDA reports)
NAUSEA ( 242 FDA reports)
FATIGUE ( 208 FDA reports)
DIZZINESS ( 193 FDA reports)
ANXIETY ( 181 FDA reports)
HEADACHE ( 177 FDA reports)
BACK PAIN ( 162 FDA reports)
ARTHRALGIA ( 141 FDA reports)
FALL ( 140 FDA reports)
ABDOMINAL PAIN ( 138 FDA reports)
VOMITING ( 138 FDA reports)
CHEST PAIN ( 137 FDA reports)
COUGH ( 136 FDA reports)
DEPRESSION ( 131 FDA reports)
OEDEMA PERIPHERAL ( 131 FDA reports)
ASTHENIA ( 124 FDA reports)
DRUG INEFFECTIVE ( 122 FDA reports)
DIARRHOEA ( 121 FDA reports)
PRURITUS ( 120 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 117 FDA reports)
INSOMNIA ( 117 FDA reports)
HYPERTENSION ( 111 FDA reports)
INJURY ( 109 FDA reports)
CONSTIPATION ( 104 FDA reports)
MUSCLE SPASMS ( 102 FDA reports)
ANAEMIA ( 101 FDA reports)
PYREXIA ( 97 FDA reports)
ABDOMINAL PAIN UPPER ( 96 FDA reports)
PAIN IN EXTREMITY ( 95 FDA reports)
WEIGHT DECREASED ( 95 FDA reports)
ASTHMA ( 94 FDA reports)
PNEUMONIA ( 92 FDA reports)
RASH ( 92 FDA reports)
OSTEOARTHRITIS ( 91 FDA reports)
EMOTIONAL DISTRESS ( 90 FDA reports)
PAIN IN JAW ( 88 FDA reports)
SOMNOLENCE ( 85 FDA reports)
CHEST DISCOMFORT ( 84 FDA reports)
OSTEONECROSIS OF JAW ( 83 FDA reports)
ANHEDONIA ( 81 FDA reports)
ATRIAL FIBRILLATION ( 81 FDA reports)
SINUSITIS ( 81 FDA reports)
TREMOR ( 79 FDA reports)
WEIGHT INCREASED ( 77 FDA reports)
DRY MOUTH ( 70 FDA reports)
GAIT DISTURBANCE ( 70 FDA reports)
BONE DISORDER ( 69 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 68 FDA reports)
MITRAL VALVE INCOMPETENCE ( 68 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 67 FDA reports)
MYALGIA ( 67 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 66 FDA reports)
PURULENT DISCHARGE ( 66 FDA reports)
SPINAL OSTEOARTHRITIS ( 66 FDA reports)
SYNCOPE ( 66 FDA reports)
ANAPHYLACTIC REACTION ( 65 FDA reports)
TOOTH DISORDER ( 65 FDA reports)
TOOTH FRACTURE ( 65 FDA reports)
CHOLELITHIASIS ( 63 FDA reports)
NASAL CONGESTION ( 62 FDA reports)
VISION BLURRED ( 61 FDA reports)
HYPOTENSION ( 58 FDA reports)
JOINT SWELLING ( 56 FDA reports)
URINARY TRACT INFECTION ( 56 FDA reports)
CONVULSION ( 55 FDA reports)
HYPOAESTHESIA ( 55 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 55 FDA reports)
HYPERKERATOSIS ( 54 FDA reports)
WHEEZING ( 53 FDA reports)
ATELECTASIS ( 52 FDA reports)
BURSITIS ( 52 FDA reports)
OSTEONECROSIS ( 52 FDA reports)
CEREBROVASCULAR ACCIDENT ( 51 FDA reports)
HYPERSENSITIVITY ( 51 FDA reports)
OSTEOPENIA ( 51 FDA reports)
SWELLING ( 51 FDA reports)
DEFORMITY ( 50 FDA reports)
DYSPHAGIA ( 50 FDA reports)
RENAL FAILURE ACUTE ( 50 FDA reports)
IMPAIRED HEALING ( 49 FDA reports)
TENDONITIS ( 49 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 49 FDA reports)
PALPITATIONS ( 48 FDA reports)
JOINT EFFUSION ( 47 FDA reports)
MALAISE ( 47 FDA reports)
NEUROPATHY PERIPHERAL ( 46 FDA reports)
PARAESTHESIA ( 46 FDA reports)
TOOTH LOSS ( 46 FDA reports)
VERTIGO ( 46 FDA reports)
BALANCE DISORDER ( 45 FDA reports)
CORONARY ARTERY DISEASE ( 45 FDA reports)
DEEP VEIN THROMBOSIS ( 45 FDA reports)
DEHYDRATION ( 45 FDA reports)
MEMORY IMPAIRMENT ( 45 FDA reports)
MYOCARDIAL INFARCTION ( 45 FDA reports)
PANCREATITIS ( 45 FDA reports)
PULMONARY EMBOLISM ( 45 FDA reports)
URTICARIA ( 45 FDA reports)
DIVERTICULUM ( 44 FDA reports)
HYPERHIDROSIS ( 44 FDA reports)
HYPOPHAGIA ( 44 FDA reports)
TOOTH EXTRACTION ( 44 FDA reports)
AMNESIA ( 43 FDA reports)
COLONIC POLYP ( 43 FDA reports)
CYST ( 43 FDA reports)
FEELING ABNORMAL ( 43 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 43 FDA reports)
RHINITIS ALLERGIC ( 42 FDA reports)
ROTATOR CUFF SYNDROME ( 42 FDA reports)
SWELLING FACE ( 42 FDA reports)
ARTHRITIS ( 41 FDA reports)
CATARACT ( 41 FDA reports)
DERMATITIS ( 41 FDA reports)
LOSS OF CONSCIOUSNESS ( 41 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 41 FDA reports)
BLOOD GLUCOSE INCREASED ( 40 FDA reports)
ERYTHEMA ( 40 FDA reports)
INFLAMMATION ( 40 FDA reports)
RHINITIS ( 40 FDA reports)
SPINAL COLUMN STENOSIS ( 40 FDA reports)
ABSCESS ( 39 FDA reports)
BLOOD PRESSURE INCREASED ( 39 FDA reports)
CARDIOMEGALY ( 39 FDA reports)
SCOLIOSIS ( 39 FDA reports)
BRONCHITIS ( 38 FDA reports)
FLUSHING ( 38 FDA reports)
CHILLS ( 37 FDA reports)
DENTAL FISTULA ( 37 FDA reports)
ENDODONTIC PROCEDURE ( 37 FDA reports)
HALLUCINATION ( 37 FDA reports)
MUSCULOSKELETAL PAIN ( 37 FDA reports)
SLEEP DISORDER ( 37 FDA reports)
TINNITUS ( 37 FDA reports)
CONDITION AGGRAVATED ( 36 FDA reports)
DIABETES MELLITUS ( 36 FDA reports)
DYSGEUSIA ( 36 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 36 FDA reports)
MUSCULAR WEAKNESS ( 36 FDA reports)
RENAL CYST ( 36 FDA reports)
RENAL FAILURE ( 36 FDA reports)
SKIN DISORDER ( 36 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 35 FDA reports)
CHOLECYSTITIS CHRONIC ( 35 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 35 FDA reports)
DYSPEPSIA ( 35 FDA reports)
DYSURIA ( 35 FDA reports)
GASTRITIS ( 35 FDA reports)
DRUG INTERACTION ( 34 FDA reports)
ECONOMIC PROBLEM ( 34 FDA reports)
FOOT FRACTURE ( 34 FDA reports)
HAEMORRHOIDS ( 34 FDA reports)
MIGRAINE ( 34 FDA reports)
MOUTH ULCERATION ( 34 FDA reports)
NECK PAIN ( 34 FDA reports)
RETCHING ( 34 FDA reports)
STRESS ( 34 FDA reports)
ACUTE SINUSITIS ( 33 FDA reports)
EMPHYSEMA ( 33 FDA reports)
HYPERLIPIDAEMIA ( 33 FDA reports)
OROPHARYNGEAL PAIN ( 33 FDA reports)
DIVERTICULUM INTESTINAL ( 32 FDA reports)
FOOT DEFORMITY ( 32 FDA reports)
HYPERGLYCAEMIA ( 32 FDA reports)
INFECTION ( 32 FDA reports)
OSTEOPOROSIS ( 32 FDA reports)
TENDERNESS ( 32 FDA reports)
FACIAL PAIN ( 31 FDA reports)
IMPAIRED DRIVING ABILITY ( 31 FDA reports)
OSTEOMYELITIS ( 31 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 31 FDA reports)
VIRAL INFECTION ( 31 FDA reports)
BONE PAIN ( 30 FDA reports)
CARDIAC FAILURE ( 30 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 30 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 30 FDA reports)
VISUAL IMPAIRMENT ( 30 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 29 FDA reports)
HYPOKALAEMIA ( 29 FDA reports)
INTENTIONAL DRUG MISUSE ( 29 FDA reports)
SKELETAL INJURY ( 29 FDA reports)
SLEEP APNOEA SYNDROME ( 29 FDA reports)
CONFUSIONAL STATE ( 28 FDA reports)
CONTUSION ( 28 FDA reports)
ECZEMA ( 28 FDA reports)
HAEMORRHAGE ( 28 FDA reports)
LYMPHADENOPATHY ( 28 FDA reports)
MITRAL VALVE PROLAPSE ( 28 FDA reports)
TOOTH INFECTION ( 28 FDA reports)
TOOTHACHE ( 28 FDA reports)
ABDOMINAL DISTENSION ( 27 FDA reports)
AORTIC ANEURYSM ( 27 FDA reports)
EPISTAXIS ( 27 FDA reports)
FLANK PAIN ( 27 FDA reports)
PLEURAL EFFUSION ( 27 FDA reports)
PRODUCT QUALITY ISSUE ( 27 FDA reports)
RHINORRHOEA ( 27 FDA reports)
STOMATITIS ( 27 FDA reports)
BLOOD CALCIUM INCREASED ( 26 FDA reports)
DEATH ( 26 FDA reports)
EAR INFECTION ( 26 FDA reports)
PRIMARY SEQUESTRUM ( 26 FDA reports)
THROMBOSIS ( 26 FDA reports)
CARDIAC DISORDER ( 25 FDA reports)
DEAFNESS ( 25 FDA reports)
DECREASED APPETITE ( 25 FDA reports)
GLAUCOMA ( 25 FDA reports)
HAEMOGLOBIN DECREASED ( 25 FDA reports)
LACERATION ( 25 FDA reports)
MULTIPLE MYELOMA ( 25 FDA reports)
ORAL CAVITY FISTULA ( 25 FDA reports)
OTORRHOEA ( 25 FDA reports)
SUICIDAL IDEATION ( 25 FDA reports)
ABASIA ( 24 FDA reports)
COLITIS ( 24 FDA reports)
DISCOMFORT ( 24 FDA reports)
DYSPHONIA ( 24 FDA reports)
GOITRE ( 24 FDA reports)
HEART RATE IRREGULAR ( 24 FDA reports)
HYPOVOLAEMIA ( 24 FDA reports)
MENISCUS LESION ( 24 FDA reports)
MYOPATHY ( 24 FDA reports)
OEDEMA ( 24 FDA reports)
POLLAKIURIA ( 24 FDA reports)
RADICULOPATHY ( 24 FDA reports)
RESTLESS LEGS SYNDROME ( 24 FDA reports)
THYROID CANCER ( 24 FDA reports)
URINARY INCONTINENCE ( 24 FDA reports)
ABNORMAL DREAMS ( 23 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 23 FDA reports)
DYSPNOEA EXERTIONAL ( 23 FDA reports)
FAECAL INCONTINENCE ( 23 FDA reports)
GINGIVAL DISORDER ( 23 FDA reports)
HEART RATE INCREASED ( 23 FDA reports)
INFLUENZA LIKE ILLNESS ( 23 FDA reports)
LARYNGEAL OEDEMA ( 23 FDA reports)
NASOPHARYNGITIS ( 23 FDA reports)
OPEN WOUND ( 23 FDA reports)
PARAESTHESIA ORAL ( 23 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 23 FDA reports)
PULMONARY FIBROSIS ( 23 FDA reports)
BILE DUCT STENOSIS ( 22 FDA reports)
BRAIN NEOPLASM ( 22 FDA reports)
CARDIOMYOPATHY ( 22 FDA reports)
DEPENDENCE ( 22 FDA reports)
DRUG ABUSE ( 22 FDA reports)
DRY EYE ( 22 FDA reports)
EATING DISORDER ( 22 FDA reports)
FLUID OVERLOAD ( 22 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 22 FDA reports)
HYPOCALCAEMIA ( 22 FDA reports)
HYPOTHYROIDISM ( 22 FDA reports)
LARYNGITIS ( 22 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 22 FDA reports)
MEDICATION ERROR ( 22 FDA reports)
MUSCLE INJURY ( 22 FDA reports)
NASAL TURBINATE HYPERTROPHY ( 22 FDA reports)
NERVOUSNESS ( 22 FDA reports)
OSTEOSCLEROSIS ( 22 FDA reports)
SLEEP TALKING ( 22 FDA reports)
SOMNAMBULISM ( 22 FDA reports)
STOMATITIS NECROTISING ( 22 FDA reports)
TENDON INJURY ( 22 FDA reports)
TONGUE COATED ( 22 FDA reports)
ABDOMINAL DISCOMFORT ( 21 FDA reports)
BREAST CANCER ( 21 FDA reports)
GINGIVAL RECESSION ( 21 FDA reports)
INJECTION SITE PAIN ( 21 FDA reports)
TACHYCARDIA ( 21 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 21 FDA reports)
AGITATION ( 20 FDA reports)
ANGIOPATHY ( 20 FDA reports)
BACTERAEMIA ( 20 FDA reports)
BONE DEBRIDEMENT ( 20 FDA reports)
DEPRESSED MOOD ( 20 FDA reports)
EAR DISORDER ( 20 FDA reports)
EMOTIONAL DISORDER ( 20 FDA reports)
HEPATIC CYST ( 20 FDA reports)
JAW OPERATION ( 20 FDA reports)
LUMBAR SPINE FLATTENING ( 20 FDA reports)
NECK INJURY ( 20 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 20 FDA reports)
RIB FRACTURE ( 20 FDA reports)
SKIN LESION ( 20 FDA reports)
SKIN NEOPLASM EXCISION ( 20 FDA reports)
SWOLLEN TONGUE ( 20 FDA reports)
ADVERSE EVENT ( 19 FDA reports)
ANGER ( 19 FDA reports)
ARRHYTHMIA ( 19 FDA reports)
ARTHROPATHY ( 19 FDA reports)
BONE DENSITY DECREASED ( 19 FDA reports)
BONE EROSION ( 19 FDA reports)
BONE FRAGMENTATION ( 19 FDA reports)
CANDIDIASIS ( 19 FDA reports)
CRYING ( 19 FDA reports)
DRUG HYPERSENSITIVITY ( 19 FDA reports)
ECZEMA ASTEATOTIC ( 19 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 19 FDA reports)
FIBROUS HISTIOCYTOMA ( 19 FDA reports)
GALLBLADDER DISORDER ( 19 FDA reports)
HAEMATURIA ( 19 FDA reports)
HALLUCINATION, AUDITORY ( 19 FDA reports)
HEAD INJURY ( 19 FDA reports)
ICHTHYOSIS ( 19 FDA reports)
KNEE ARTHROPLASTY ( 19 FDA reports)
LIMB INJURY ( 19 FDA reports)
LOOSE TOOTH ( 19 FDA reports)
MALNUTRITION ( 19 FDA reports)
MENTAL STATUS CHANGES ( 19 FDA reports)
ORAL MUCOSA ATROPHY ( 19 FDA reports)
ORTHODONTIC APPLIANCE USER ( 19 FDA reports)
OTITIS MEDIA ( 19 FDA reports)
PNEUMOTHORAX ( 19 FDA reports)
PRODUCTIVE COUGH ( 19 FDA reports)
PRURITUS GENERALISED ( 19 FDA reports)
SEPSIS ( 19 FDA reports)
SERRATIA INFECTION ( 19 FDA reports)
TONGUE DISCOLOURATION ( 19 FDA reports)
UTERINE LEIOMYOMA ( 19 FDA reports)
BACK INJURY ( 18 FDA reports)
BASAL CELL CARCINOMA ( 18 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 18 FDA reports)
CHOLECYSTITIS ( 18 FDA reports)
DYSARTHRIA ( 18 FDA reports)
EYE IRRITATION ( 18 FDA reports)
FUNGAL INFECTION ( 18 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 18 FDA reports)
HAEMATOCRIT DECREASED ( 18 FDA reports)
HIATUS HERNIA ( 18 FDA reports)
INFLUENZA ( 18 FDA reports)
JAW FRACTURE ( 18 FDA reports)
JOINT INJURY ( 18 FDA reports)
MUCOSAL INFLAMMATION ( 18 FDA reports)
PRESYNCOPE ( 18 FDA reports)
RESPIRATORY FAILURE ( 18 FDA reports)
TOOTH ABSCESS ( 18 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 17 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 17 FDA reports)
DIPLOPIA ( 17 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 17 FDA reports)
EXOSTOSIS ( 17 FDA reports)
FIBROMYALGIA ( 17 FDA reports)
FLATULENCE ( 17 FDA reports)
ILL-DEFINED DISORDER ( 17 FDA reports)
INCORRECT DOSE ADMINISTERED ( 17 FDA reports)
LUNG INFECTION ( 17 FDA reports)
NEPHROLITHIASIS ( 17 FDA reports)
PHARYNGITIS ( 17 FDA reports)
PURULENCE ( 17 FDA reports)
RESPIRATORY DISTRESS ( 17 FDA reports)
SINUS BRADYCARDIA ( 17 FDA reports)
SURGERY ( 17 FDA reports)
TENDON RUPTURE ( 17 FDA reports)
THROAT IRRITATION ( 17 FDA reports)
TOOTH REPAIR ( 17 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 16 FDA reports)
ANOREXIA ( 16 FDA reports)
BLOOD CREATININE INCREASED ( 16 FDA reports)
CARDIAC MURMUR ( 16 FDA reports)
CELLULITIS ( 16 FDA reports)
CHONDROMALACIA ( 16 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 16 FDA reports)
CORONARY ARTERY OCCLUSION ( 16 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 16 FDA reports)
EXPOSED BONE IN JAW ( 16 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 16 FDA reports)
HYPERPHAGIA ( 16 FDA reports)
LUNG NEOPLASM MALIGNANT ( 16 FDA reports)
MENOPAUSE ( 16 FDA reports)
OESOPHAGEAL MUCOSAL HYPERPLASIA ( 16 FDA reports)
ORAL FIBROMA ( 16 FDA reports)
PANCREATITIS ACUTE ( 16 FDA reports)
PERIODONTAL DISEASE ( 16 FDA reports)
PIGMENTATION DISORDER ( 16 FDA reports)
POSTNASAL DRIP ( 16 FDA reports)
STEM CELL TRANSPLANT ( 16 FDA reports)
THROMBOCYTOPENIA ( 16 FDA reports)
THYROIDECTOMY ( 16 FDA reports)
TIBIA FRACTURE ( 16 FDA reports)
ACTINOMYCOSIS ( 15 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 15 FDA reports)
AZOTAEMIA ( 15 FDA reports)
BARRETT'S OESOPHAGUS ( 15 FDA reports)
BLOOD PRESSURE DECREASED ( 15 FDA reports)
CERVICAL MYELOPATHY ( 15 FDA reports)
CERVICAL SPINAL STENOSIS ( 15 FDA reports)
CHROMATURIA ( 15 FDA reports)
COLON ADENOMA ( 15 FDA reports)
DIVERTICULITIS ( 15 FDA reports)
DYSKINESIA ( 15 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 15 FDA reports)
HEPATIC ENZYME INCREASED ( 15 FDA reports)
HEPATIC STEATOSIS ( 15 FDA reports)
HYPERSOMNIA ( 15 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 15 FDA reports)
INJECTION SITE ERYTHEMA ( 15 FDA reports)
MASTICATION DISORDER ( 15 FDA reports)
MIDDLE INSOMNIA ( 15 FDA reports)
MYOCARDIAL ISCHAEMIA ( 15 FDA reports)
OFF LABEL USE ( 15 FDA reports)
ORTHOSTATIC HYPOTENSION ( 15 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 15 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 15 FDA reports)
PLASMACYTOSIS ( 15 FDA reports)
POLYURIA ( 15 FDA reports)
PULMONARY AIR LEAKAGE ( 15 FDA reports)
PULMONARY GRANULOMA ( 15 FDA reports)
SHOULDER ARTHROPLASTY ( 15 FDA reports)
STAPHYLOCOCCAL INFECTION ( 15 FDA reports)
ULCER ( 15 FDA reports)
ALOPECIA ( 14 FDA reports)
ALVEOLOPLASTY ( 14 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 14 FDA reports)
BACTERIAL DISEASE CARRIER ( 14 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 14 FDA reports)
BONE LESION ( 14 FDA reports)
BRONCHOPLEURAL FISTULA ( 14 FDA reports)
CARDIAC ARREST ( 14 FDA reports)
CEREBROVASCULAR DISORDER ( 14 FDA reports)
CRANIOTOMY ( 14 FDA reports)
DENTAL CARIES ( 14 FDA reports)
DIURETIC THERAPY ( 14 FDA reports)
DRUG EFFECT DECREASED ( 14 FDA reports)
EAR PAIN ( 14 FDA reports)
EMPYEMA ( 14 FDA reports)
EYE DISCHARGE ( 14 FDA reports)
FIBULA FRACTURE ( 14 FDA reports)
FISTULA ( 14 FDA reports)
HYDROPNEUMOTHORAX ( 14 FDA reports)
HYPOGLYCAEMIA ( 14 FDA reports)
INJURY CORNEAL ( 14 FDA reports)
IRRITABLE BOWEL SYNDROME ( 14 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 14 FDA reports)
LIP DISCOLOURATION ( 14 FDA reports)
LUNG DISORDER ( 14 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 14 FDA reports)
NEURALGIA ( 14 FDA reports)
ORAL DISORDER ( 14 FDA reports)
OSTEOCHONDROSIS ( 14 FDA reports)
OSTEORADIONECROSIS ( 14 FDA reports)
PETECHIAE ( 14 FDA reports)
RHEUMATOID ARTHRITIS ( 14 FDA reports)
SINUS OPERATION ( 14 FDA reports)
TACHYPNOEA ( 14 FDA reports)
UNEVALUABLE EVENT ( 14 FDA reports)
VENTRICULAR SEPTAL DEFECT REPAIR ( 14 FDA reports)
WOUND DEHISCENCE ( 14 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 13 FDA reports)
CONGENITAL KNEE DEFORMITY ( 13 FDA reports)
DRUG ERUPTION ( 13 FDA reports)
GASTROENTERITIS ( 13 FDA reports)
GASTROINTESTINAL DISORDER ( 13 FDA reports)
GINGIVAL GRAFT ( 13 FDA reports)
GYNAECOMASTIA ( 13 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 13 FDA reports)
HEPATOMEGALY ( 13 FDA reports)
HIP FRACTURE ( 13 FDA reports)
HYPOAESTHESIA ORAL ( 13 FDA reports)
INTESTINAL MUCOSAL HYPERTROPHY ( 13 FDA reports)
LUNG NEOPLASM ( 13 FDA reports)
MASS ( 13 FDA reports)
METASTASES TO LYMPH NODES ( 13 FDA reports)
MOBILITY DECREASED ( 13 FDA reports)
MULTIPLE INJURIES ( 13 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 13 FDA reports)
NEURITIS ( 13 FDA reports)
OOPHORECTOMY ( 13 FDA reports)
PULMONARY CALCIFICATION ( 13 FDA reports)
ROAD TRAFFIC ACCIDENT ( 13 FDA reports)
SCIATICA ( 13 FDA reports)
SINUS DISORDER ( 13 FDA reports)
URINARY RETENTION ( 13 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 13 FDA reports)
ABORTION SPONTANEOUS ( 12 FDA reports)
ATROPHIC VULVOVAGINITIS ( 12 FDA reports)
BREAST CALCIFICATIONS ( 12 FDA reports)
BRONCHITIS CHRONIC ( 12 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 12 FDA reports)
CATARACT OPERATION ( 12 FDA reports)
CHRONIC SINUSITIS ( 12 FDA reports)
CYANOSIS ( 12 FDA reports)
DECREASED INTEREST ( 12 FDA reports)
DILATATION VENTRICULAR ( 12 FDA reports)
DRY SKIN ( 12 FDA reports)
FEAR ( 12 FDA reports)
HAEMATOCHEZIA ( 12 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 12 FDA reports)
METASTASES TO BONE ( 12 FDA reports)
MYELOPATHY ( 12 FDA reports)
PANCREATITIS CHRONIC ( 12 FDA reports)
PANCYTOPENIA ( 12 FDA reports)
RASH GENERALISED ( 12 FDA reports)
RENAL DISORDER ( 12 FDA reports)
SCHAMBERG'S DISEASE ( 12 FDA reports)
SKIN IRRITATION ( 12 FDA reports)
THROAT TIGHTNESS ( 12 FDA reports)
TREATMENT NONCOMPLIANCE ( 12 FDA reports)
VENOUS INSUFFICIENCY ( 12 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 12 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 12 FDA reports)
WOUND DRAINAGE ( 12 FDA reports)
AGEUSIA ( 11 FDA reports)
BILIARY DYSKINESIA ( 11 FDA reports)
BLINDNESS ( 11 FDA reports)
BODY HEIGHT DECREASED ( 11 FDA reports)
BRUXISM ( 11 FDA reports)
COGNITIVE DISORDER ( 11 FDA reports)
DERMATITIS CONTACT ( 11 FDA reports)
DEVICE FAILURE ( 11 FDA reports)
DISTURBANCE IN ATTENTION ( 11 FDA reports)
DYSSTASIA ( 11 FDA reports)
EJECTION FRACTION DECREASED ( 11 FDA reports)
EYELID PTOSIS ( 11 FDA reports)
FEMUR FRACTURE ( 11 FDA reports)
HAEMOPTYSIS ( 11 FDA reports)
HYPONATRAEMIA ( 11 FDA reports)
HYPOXIA ( 11 FDA reports)
JOINT STIFFNESS ( 11 FDA reports)
LETHARGY ( 11 FDA reports)
LIVER DISORDER ( 11 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 11 FDA reports)
NIGHT SWEATS ( 11 FDA reports)
NOCTURIA ( 11 FDA reports)
OCULAR HYPERAEMIA ( 11 FDA reports)
PHARYNGEAL OEDEMA ( 11 FDA reports)
PHYSICAL DISABILITY ( 11 FDA reports)
RECTAL POLYP ( 11 FDA reports)
RENAL IMPAIRMENT ( 11 FDA reports)
STRESS FRACTURE ( 11 FDA reports)
TINEA CRURIS ( 11 FDA reports)
VIITH NERVE PARALYSIS ( 11 FDA reports)
WRIST FRACTURE ( 11 FDA reports)
ACUTE RESPIRATORY FAILURE ( 10 FDA reports)
ANOSMIA ( 10 FDA reports)
ATRIAL SEPTAL DEFECT ( 10 FDA reports)
BACK DISORDER ( 10 FDA reports)
BLOOD IRON DECREASED ( 10 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 10 FDA reports)
BRADYCARDIA ( 10 FDA reports)
BREAST CANCER METASTATIC ( 10 FDA reports)
CARPAL TUNNEL SYNDROME ( 10 FDA reports)
CEREBRAL ATROPHY ( 10 FDA reports)
CIRCULATORY COLLAPSE ( 10 FDA reports)
COLON POLYPECTOMY ( 10 FDA reports)
DRUG TOXICITY ( 10 FDA reports)
FOETAL HEART RATE ABNORMAL ( 10 FDA reports)
GINGIVAL BLEEDING ( 10 FDA reports)
HERPES ZOSTER ( 10 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 10 FDA reports)
INJECTION SITE HAEMATOMA ( 10 FDA reports)
INJECTION SITE HAEMORRHAGE ( 10 FDA reports)
KNEE OPERATION ( 10 FDA reports)
LACRIMATION INCREASED ( 10 FDA reports)
LOW TURNOVER OSTEOPATHY ( 10 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 10 FDA reports)
MAMMOPLASTY ( 10 FDA reports)
OVARIAN DISORDER ( 10 FDA reports)
PLEURAL FIBROSIS ( 10 FDA reports)
PULMONARY HYPERTENSION ( 10 FDA reports)
RASH ERYTHEMATOUS ( 10 FDA reports)
RENAL FAILURE CHRONIC ( 10 FDA reports)
SOFT TISSUE DISORDER ( 10 FDA reports)
STERNOTOMY ( 10 FDA reports)
TARDIVE DYSKINESIA ( 10 FDA reports)
TOBACCO USER ( 10 FDA reports)
VENTRICULAR TACHYCARDIA ( 10 FDA reports)
VISUAL ACUITY REDUCED ( 10 FDA reports)
WITHDRAWAL SYNDROME ( 10 FDA reports)
ANGINA PECTORIS ( 9 FDA reports)
ANGINA UNSTABLE ( 9 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST ( 9 FDA reports)
ARTERIOSCLEROSIS ( 9 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 9 FDA reports)
BLOOD CALCIUM DECREASED ( 9 FDA reports)
BREAST MASS ( 9 FDA reports)
CHOLECYSTITIS ACUTE ( 9 FDA reports)
CONGENITAL HAIR DISORDER ( 9 FDA reports)
CONGENITAL HEART VALVE DISORDER ( 9 FDA reports)
DEBRIDEMENT ( 9 FDA reports)
DEFORMITY THORAX ( 9 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 9 FDA reports)
DILATATION ATRIAL ( 9 FDA reports)
DISABILITY ( 9 FDA reports)
ECCHYMOSIS ( 9 FDA reports)
ENCEPHALOMALACIA ( 9 FDA reports)
FOOD INTOLERANCE ( 9 FDA reports)
GOUT ( 9 FDA reports)
HEARING IMPAIRED ( 9 FDA reports)
HEMIPARESIS ( 9 FDA reports)
HEPATIC FAILURE ( 9 FDA reports)
HISTOPLASMOSIS ( 9 FDA reports)
HYPERBILIRUBINAEMIA ( 9 FDA reports)
JOINT DISLOCATION ( 9 FDA reports)
LABORATORY TEST ABNORMAL ( 9 FDA reports)
LIGAMENT OPERATION ( 9 FDA reports)
LUNG INFILTRATION ( 9 FDA reports)
MACULAR DEGENERATION ( 9 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 9 FDA reports)
MUSCULOSKELETAL DISORDER ( 9 FDA reports)
MYOMECTOMY ( 9 FDA reports)
NEOPLASM MALIGNANT ( 9 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 9 FDA reports)
NERVOUS SYSTEM DISORDER ( 9 FDA reports)
NODULE ( 9 FDA reports)
OBESITY ( 9 FDA reports)
OVERDOSE ( 9 FDA reports)
PATHOLOGICAL GAMBLING ( 9 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 9 FDA reports)
PREGNANCY ( 9 FDA reports)
PROSTATOMEGALY ( 9 FDA reports)
PTERYGIUM COLLI ( 9 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 9 FDA reports)
SPUTUM DISCOLOURED ( 9 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 9 FDA reports)
TURNER'S SYNDROME ( 9 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 9 FDA reports)
ABDOMINAL HERNIA ( 8 FDA reports)
APPETITE DISORDER ( 8 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 8 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 8 FDA reports)
BURNING SENSATION ( 8 FDA reports)
CAROTID ARTERY STENOSIS ( 8 FDA reports)
DISORIENTATION ( 8 FDA reports)
DYSPLASIA ( 8 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 8 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 8 FDA reports)
FIBROSIS ( 8 FDA reports)
FLUID RETENTION ( 8 FDA reports)
GALLBLADDER INJURY ( 8 FDA reports)
GASTRIC ULCER ( 8 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 8 FDA reports)
GLOSSITIS ( 8 FDA reports)
HEART RATE DECREASED ( 8 FDA reports)
HICCUPS ( 8 FDA reports)
INJECTION SITE SWELLING ( 8 FDA reports)
JAUNDICE ( 8 FDA reports)
KYPHOSIS ( 8 FDA reports)
LEUKAEMIA ( 8 FDA reports)
MANIA ( 8 FDA reports)
MENTAL DISORDER ( 8 FDA reports)
MULTIPLE ALLERGIES ( 8 FDA reports)
MUSCLE CRAMP ( 8 FDA reports)
NAIL DISORDER ( 8 FDA reports)
OSTEOLYSIS ( 8 FDA reports)
PATHOLOGICAL FRACTURE ( 8 FDA reports)
PELVIC FRACTURE ( 8 FDA reports)
POLYP ( 8 FDA reports)
POLYPECTOMY ( 8 FDA reports)
PULMONARY CONGESTION ( 8 FDA reports)
PULMONARY OEDEMA ( 8 FDA reports)
RESPIRATORY DISORDER ( 8 FDA reports)
SINUS CONGESTION ( 8 FDA reports)
SKIN DISCOLOURATION ( 8 FDA reports)
SKIN FIBROSIS ( 8 FDA reports)
SPEECH DISORDER ( 8 FDA reports)
SPINAL FRACTURE ( 8 FDA reports)
SPONDYLOLISTHESIS ( 8 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 8 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 8 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 8 FDA reports)
TONGUE ULCERATION ( 8 FDA reports)
TYPE 2 DIABETES MELLITUS ( 8 FDA reports)
UNRESPONSIVE TO STIMULI ( 8 FDA reports)
VAGINAL DISCHARGE ( 8 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 8 FDA reports)
ABDOMINAL PAIN LOWER ( 7 FDA reports)
ABNORMAL BEHAVIOUR ( 7 FDA reports)
ACCIDENTAL OVERDOSE ( 7 FDA reports)
ADVERSE DRUG REACTION ( 7 FDA reports)
AMAUROSIS FUGAX ( 7 FDA reports)
ANGIOMYOLIPOMA ( 7 FDA reports)
ASCITES ( 7 FDA reports)
ATAXIA ( 7 FDA reports)
BIOPSY ( 7 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 7 FDA reports)
CARDIO-RESPIRATORY ARREST ( 7 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 7 FDA reports)
CHEILITIS ( 7 FDA reports)
CHRONIC HEPATIC FAILURE ( 7 FDA reports)
CORONARY ARTERY STENOSIS ( 7 FDA reports)
CYSTITIS ( 7 FDA reports)
DELIRIUM ( 7 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 7 FDA reports)
DISEASE PROGRESSION ( 7 FDA reports)
EAR DISCOMFORT ( 7 FDA reports)
FACIAL BONES FRACTURE ( 7 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 7 FDA reports)
GASTRIC DISORDER ( 7 FDA reports)
GINGIVAL PAIN ( 7 FDA reports)
GINGIVAL SWELLING ( 7 FDA reports)
GINGIVAL ULCERATION ( 7 FDA reports)
GRAND MAL CONVULSION ( 7 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 7 FDA reports)
HEPATIC PAIN ( 7 FDA reports)
HEPATITIS ( 7 FDA reports)
HOT FLUSH ( 7 FDA reports)
HYPOACUSIS ( 7 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 7 FDA reports)
INGUINAL HERNIA ( 7 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 7 FDA reports)
INTERSTITIAL LUNG DISEASE ( 7 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 7 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 7 FDA reports)
LEUKOPLAKIA ( 7 FDA reports)
LIGAMENT SPRAIN ( 7 FDA reports)
MACULOPATHY ( 7 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 7 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 7 FDA reports)
ORAL CANDIDIASIS ( 7 FDA reports)
PLATELET COUNT DECREASED ( 7 FDA reports)
PSYCHIATRIC SYMPTOM ( 7 FDA reports)
RECTAL HAEMORRHAGE ( 7 FDA reports)
RESORPTION BONE INCREASED ( 7 FDA reports)
SCOTOMA ( 7 FDA reports)
SINUS TACHYCARDIA ( 7 FDA reports)
SKIN INDURATION ( 7 FDA reports)
SPLENOMEGALY ( 7 FDA reports)
SUBDURAL HAEMATOMA ( 7 FDA reports)
THORACOTOMY ( 7 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 7 FDA reports)
VARICOSE VEIN ( 7 FDA reports)
VENTRICULAR FIBRILLATION ( 7 FDA reports)
VITAMIN D DEFICIENCY ( 7 FDA reports)
ABDOMINOPLASTY ( 6 FDA reports)
ALLODYNIA ( 6 FDA reports)
ANAPHYLACTIC SHOCK ( 6 FDA reports)
AORTIC VALVE INCOMPETENCE ( 6 FDA reports)
AUTOIMMUNE DISORDER ( 6 FDA reports)
BACTERIAL INFECTION ( 6 FDA reports)
BLINDNESS TRANSIENT ( 6 FDA reports)
BONE LOSS ( 6 FDA reports)
BREAST PAIN ( 6 FDA reports)
CANCER PAIN ( 6 FDA reports)
CARCINOID TUMOUR OF THE STOMACH ( 6 FDA reports)
CERUMEN IMPACTION ( 6 FDA reports)
CHEST TUBE INSERTION ( 6 FDA reports)
COAGULOPATHY ( 6 FDA reports)
COLON CANCER ( 6 FDA reports)
DENTAL IMPLANTATION ( 6 FDA reports)
DEPRESSIVE SYMPTOM ( 6 FDA reports)
DEVICE BREAKAGE ( 6 FDA reports)
DEVICE RELATED INFECTION ( 6 FDA reports)
DRUG ADMINISTRATION ERROR ( 6 FDA reports)
DRUG DOSE OMISSION ( 6 FDA reports)
DRY THROAT ( 6 FDA reports)
DYSAESTHESIA ( 6 FDA reports)
DYSTONIA ( 6 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 6 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 6 FDA reports)
EYE NAEVUS ( 6 FDA reports)
EYE PAIN ( 6 FDA reports)
FAECES DISCOLOURED ( 6 FDA reports)
FEELING HOT ( 6 FDA reports)
FRACTURE NONUNION ( 6 FDA reports)
GASTRIC BYPASS ( 6 FDA reports)
GENERAL SYMPTOM ( 6 FDA reports)
GROIN PAIN ( 6 FDA reports)
HEPATIC LESION ( 6 FDA reports)
HEPATORENAL SYNDROME ( 6 FDA reports)
HERNIA ( 6 FDA reports)
HYPERAESTHESIA ( 6 FDA reports)
HYPERCHOLESTEROLAEMIA ( 6 FDA reports)
HYPERTHERMIA ( 6 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 6 FDA reports)
INCREASED APPETITE ( 6 FDA reports)
INTERCOSTAL NEURALGIA ( 6 FDA reports)
INTESTINAL OBSTRUCTION ( 6 FDA reports)
INTESTINAL PERFORATION ( 6 FDA reports)
INTRA-UTERINE DEATH ( 6 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 6 FDA reports)
IRIS ADHESIONS ( 6 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 6 FDA reports)
LEFT ATRIAL DILATATION ( 6 FDA reports)
LUMBAR SPINAL STENOSIS ( 6 FDA reports)
METABOLIC ACIDOSIS ( 6 FDA reports)
METASTASES TO LIVER ( 6 FDA reports)
MOOD ALTERED ( 6 FDA reports)
MUSCLE TIGHTNESS ( 6 FDA reports)
MYOCLONUS ( 6 FDA reports)
NARCOLEPSY ( 6 FDA reports)
NASAL DISCOMFORT ( 6 FDA reports)
NERVE COMPRESSION ( 6 FDA reports)
NEUROLOGICAL SYMPTOM ( 6 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 6 FDA reports)
ONYCHOMADESIS ( 6 FDA reports)
OSTECTOMY ( 6 FDA reports)
OXYGEN SATURATION DECREASED ( 6 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 6 FDA reports)
PANIC ATTACK ( 6 FDA reports)
PHOTOPSIA ( 6 FDA reports)
PLANTAR FASCIITIS ( 6 FDA reports)
PLATELET COUNT INCREASED ( 6 FDA reports)
PLEURITIC PAIN ( 6 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 6 FDA reports)
PRODUCT TASTE ABNORMAL ( 6 FDA reports)
RASH MACULO-PAPULAR ( 6 FDA reports)
RESPIRATORY TRACT INFECTION ( 6 FDA reports)
SENSITIVITY OF TEETH ( 6 FDA reports)
SKIN FISSURES ( 6 FDA reports)
SKIN LACERATION ( 6 FDA reports)
SNEEZING ( 6 FDA reports)
STOMACH DISCOMFORT ( 6 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 6 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 6 FDA reports)
TENOSYNOVITIS ( 6 FDA reports)
TENSION ( 6 FDA reports)
THYROID DISORDER ( 6 FDA reports)
URETHRAL STENOSIS ( 6 FDA reports)
UROSEPSIS ( 6 FDA reports)
ADRENAL INSUFFICIENCY ( 5 FDA reports)
AKATHISIA ( 5 FDA reports)
ALLERGY TO ARTHROPOD STING ( 5 FDA reports)
ANKLE FRACTURE ( 5 FDA reports)
AORTIC VALVE STENOSIS ( 5 FDA reports)
APHAGIA ( 5 FDA reports)
ARTHROSCOPIC SURGERY ( 5 FDA reports)
ASPIRATION ( 5 FDA reports)
ASTERIXIS ( 5 FDA reports)
AXILLARY MASS ( 5 FDA reports)
BENIGN NEOPLASM OF ADRENAL GLAND ( 5 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 5 FDA reports)
BLADDER DISORDER ( 5 FDA reports)
BLOOD ALBUMIN DECREASED ( 5 FDA reports)
BLOOD BILIRUBIN INCREASED ( 5 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 5 FDA reports)
BLOOD UREA ABNORMAL ( 5 FDA reports)
BODY DYSMORPHIC DISORDER ( 5 FDA reports)
BREAST ENLARGEMENT ( 5 FDA reports)
BREATH SOUNDS ABNORMAL ( 5 FDA reports)
BRONCHOSPASM ( 5 FDA reports)
BUTTERFLY RASH ( 5 FDA reports)
DENTURE WEARER ( 5 FDA reports)
DIASTOLIC DYSFUNCTION ( 5 FDA reports)
DIFFICULTY IN WALKING ( 5 FDA reports)
DYSKINESIA OESOPHAGEAL ( 5 FDA reports)
DYSLIPIDAEMIA ( 5 FDA reports)
DYSMENORRHOEA ( 5 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 5 FDA reports)
EMPYEMA DRAINAGE ( 5 FDA reports)
ENCEPHALOPATHY ( 5 FDA reports)
ERYTHEMA NODOSUM ( 5 FDA reports)
ESSENTIAL HYPERTENSION ( 5 FDA reports)
EXPIRED DRUG ADMINISTERED ( 5 FDA reports)
EYE INFECTION ( 5 FDA reports)
EYE OPERATION ( 5 FDA reports)
FACET JOINT SYNDROME ( 5 FDA reports)
FEELING JITTERY ( 5 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 5 FDA reports)
FRACTURE ( 5 FDA reports)
FRACTURE DELAYED UNION ( 5 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 5 FDA reports)
GINGIVAL CYST ( 5 FDA reports)
GINGIVAL ERYTHEMA ( 5 FDA reports)
HAEMANGIOMA ( 5 FDA reports)
HAEMATEMESIS ( 5 FDA reports)
HEART INJURY ( 5 FDA reports)
HIP SURGERY ( 5 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 5 FDA reports)
IMMUNE SYSTEM DISORDER ( 5 FDA reports)
INCOHERENT ( 5 FDA reports)
INFUSION SITE PRURITUS ( 5 FDA reports)
INITIAL INSOMNIA ( 5 FDA reports)
INTERMITTENT CLAUDICATION ( 5 FDA reports)
IODINE ALLERGY ( 5 FDA reports)
IRRITABILITY ( 5 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 5 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 5 FDA reports)
LEUKOCYTOSIS ( 5 FDA reports)
LIVER TRANSPLANT ( 5 FDA reports)
LOOSE STOOLS ( 5 FDA reports)
LUNG OPERATION ( 5 FDA reports)
MENORRHAGIA ( 5 FDA reports)
METASTASES TO SPINE ( 5 FDA reports)
MOOD SWINGS ( 5 FDA reports)
MUSCLE FLAP OPERATION ( 5 FDA reports)
NEUTROPHIL COUNT ( 5 FDA reports)
OCULAR ICTERUS ( 5 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 5 FDA reports)
ORAL DISCOMFORT ( 5 FDA reports)
OSTEOMYELITIS CHRONIC ( 5 FDA reports)
PAIN OF SKIN ( 5 FDA reports)
PERIODONTITIS ( 5 FDA reports)
PHOTOSENSITIVITY REACTION ( 5 FDA reports)
POST PROCEDURAL INFECTION ( 5 FDA reports)
PROSTATE CANCER ( 5 FDA reports)
PSORIASIS ( 5 FDA reports)
PULPITIS DENTAL ( 5 FDA reports)
RADICAL MASTECTOMY ( 5 FDA reports)
RENAL INJURY ( 5 FDA reports)
RESPIRATORY RATE INCREASED ( 5 FDA reports)
RESTLESSNESS ( 5 FDA reports)
ROTATOR CUFF REPAIR ( 5 FDA reports)
SCAR ( 5 FDA reports)
SEBORRHOEIC KERATOSIS ( 5 FDA reports)
SENSATION OF FOREIGN BODY ( 5 FDA reports)
SEPTIC SHOCK ( 5 FDA reports)
SKIN DEGENERATIVE DISORDER ( 5 FDA reports)
SKIN ULCER ( 5 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 5 FDA reports)
SPINAL COMPRESSION FRACTURE ( 5 FDA reports)
SPINAL FUSION SURGERY ( 5 FDA reports)
SPONDYLOARTHROPATHY ( 5 FDA reports)
SUBCUTANEOUS NODULE ( 5 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 5 FDA reports)
TOOTH DEPOSIT ( 5 FDA reports)
URINARY TRACT DISORDER ( 5 FDA reports)
URINE FLOW DECREASED ( 5 FDA reports)
VULVAL DISORDER ( 5 FDA reports)
WRIST SURGERY ( 5 FDA reports)
ABSCESS DRAINAGE ( 4 FDA reports)
ABSCESS MANAGEMENT ( 4 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 4 FDA reports)
ALLERGY TO CHEMICALS ( 4 FDA reports)
AMENORRHOEA ( 4 FDA reports)
ANEURYSM ( 4 FDA reports)
ANTIMICROBIAL SUSCEPTIBILITY TEST RESISTANT ( 4 FDA reports)
APHASIA ( 4 FDA reports)
APNOEA ( 4 FDA reports)
ASTHENOPIA ( 4 FDA reports)
ATRIAL FLUTTER ( 4 FDA reports)
BIOPSY LIVER ( 4 FDA reports)
BLADDER CATHETERISATION ( 4 FDA reports)
BLISTER ( 4 FDA reports)
BLOOD GLUCOSE DECREASED ( 4 FDA reports)
BLOOD POTASSIUM DECREASED ( 4 FDA reports)
BLOOD POTASSIUM INCREASED ( 4 FDA reports)
BLOOD SODIUM DECREASED ( 4 FDA reports)
BLOOD TEST ABNORMAL ( 4 FDA reports)
BLOOD UREA INCREASED ( 4 FDA reports)
BONE GRAFT ( 4 FDA reports)
BONE OPERATION ( 4 FDA reports)
BREAST CANCER FEMALE ( 4 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 4 FDA reports)
CARDIAC PACEMAKER REVISION ( 4 FDA reports)
CARDIOVASCULAR DISORDER ( 4 FDA reports)
CAROTID BRUIT ( 4 FDA reports)
CATHETER RELATED COMPLICATION ( 4 FDA reports)
CEREBELLAR HAEMORRHAGE ( 4 FDA reports)
CEREBELLAR SYNDROME ( 4 FDA reports)
CEREBRAL INFARCTION ( 4 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 4 FDA reports)
CHRONIC FATIGUE SYNDROME ( 4 FDA reports)
CLOSTRIDIAL INFECTION ( 4 FDA reports)
CLOSTRIDIUM COLITIS ( 4 FDA reports)
COLONOSCOPY ( 4 FDA reports)
COMPRESSION FRACTURE ( 4 FDA reports)
COORDINATION ABNORMAL ( 4 FDA reports)
CRANIECTOMY ( 4 FDA reports)
CROHN'S DISEASE ( 4 FDA reports)
DISEASE RECURRENCE ( 4 FDA reports)
DIZZINESS POSTURAL ( 4 FDA reports)
DRUG DEPENDENCE ( 4 FDA reports)
DRUG INTOLERANCE ( 4 FDA reports)
DYSGRAPHIA ( 4 FDA reports)
DYSPLASTIC NAEVUS ( 4 FDA reports)
EAR IRRIGATION ( 4 FDA reports)
ENTEROCOCCAL SEPSIS ( 4 FDA reports)
EPIGASTRIC DISCOMFORT ( 4 FDA reports)
ERECTILE DYSFUNCTION ( 4 FDA reports)
EROSIVE OESOPHAGITIS ( 4 FDA reports)
ERUCTATION ( 4 FDA reports)
EXCORIATION ( 4 FDA reports)
EXERCISE TOLERANCE DECREASED ( 4 FDA reports)
EYE DISORDER ( 4 FDA reports)
EYE PRURITUS ( 4 FDA reports)
FACE INJURY ( 4 FDA reports)
FAMILY STRESS ( 4 FDA reports)
FEELING COLD ( 4 FDA reports)
GASTROINTESTINAL PAIN ( 4 FDA reports)
GLOSSODYNIA ( 4 FDA reports)
HAEMODYNAMIC INSTABILITY ( 4 FDA reports)
HAIR DISORDER ( 4 FDA reports)
HALLUCINATION, VISUAL ( 4 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 4 FDA reports)
HEPATIC MASS ( 4 FDA reports)
HEPATOCELLULAR DAMAGE ( 4 FDA reports)
HOSPITALISATION ( 4 FDA reports)
HYDROCELE ( 4 FDA reports)
INADEQUATE ANALGESIA ( 4 FDA reports)
INFUSION RELATED REACTION ( 4 FDA reports)
INJECTION SITE REACTION ( 4 FDA reports)
INJECTION SITE URTICARIA ( 4 FDA reports)
JOINT SPRAIN ( 4 FDA reports)
LIP SWELLING ( 4 FDA reports)
LIPIDS INCREASED ( 4 FDA reports)
LOSS OF EMPLOYMENT ( 4 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 4 FDA reports)
LYMPHOEDEMA ( 4 FDA reports)
MELANOCYTIC NAEVUS ( 4 FDA reports)
MUCOUS MEMBRANE DISORDER ( 4 FDA reports)
MULTI-ORGAN FAILURE ( 4 FDA reports)
NASAL SINUS DRAINAGE ( 4 FDA reports)
NEPHROPATHY ( 4 FDA reports)
NEURODERMATITIS ( 4 FDA reports)
NIGHTMARE ( 4 FDA reports)
NODULE ON EXTREMITY ( 4 FDA reports)
NON-SMALL CELL LUNG CANCER ( 4 FDA reports)
OCCULT BLOOD POSITIVE ( 4 FDA reports)
OESOPHAGEAL PAIN ( 4 FDA reports)
ORAL PAIN ( 4 FDA reports)
PALLOR ( 4 FDA reports)
PANIC DISORDER ( 4 FDA reports)
PARKINSON'S DISEASE ( 4 FDA reports)
PARKINSONIAN GAIT ( 4 FDA reports)
PAROSMIA ( 4 FDA reports)
PEPTIC ULCER ( 4 FDA reports)
PERICARDIAL EFFUSION ( 4 FDA reports)
PRODUCT CONTAMINATION ( 4 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 4 FDA reports)
PROSTATECTOMY ( 4 FDA reports)
QUALITY OF LIFE DECREASED ( 4 FDA reports)
RALES ( 4 FDA reports)
RASH PAPULAR ( 4 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 4 FDA reports)
RENAL ARTERY STENOSIS ( 4 FDA reports)
RESPIRATORY ARREST ( 4 FDA reports)
RESPIRATORY TRACT CONGESTION ( 4 FDA reports)
RHABDOMYOLYSIS ( 4 FDA reports)
SCREAMING ( 4 FDA reports)
SHOCK ( 4 FDA reports)
SICK SINUS SYNDROME ( 4 FDA reports)
SKIN WRINKLING ( 4 FDA reports)
STENT PLACEMENT ( 4 FDA reports)
SUICIDAL BEHAVIOUR ( 4 FDA reports)
SUICIDE ATTEMPT ( 4 FDA reports)
SUTURE RELATED COMPLICATION ( 4 FDA reports)
TENSION HEADACHE ( 4 FDA reports)
THYROID NEOPLASM ( 4 FDA reports)
TOBACCO WITHDRAWAL SYMPTOMS ( 4 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 4 FDA reports)
VASCULAR INJURY ( 4 FDA reports)
VENOUS THROMBOSIS ( 4 FDA reports)
VENTRICULAR HYPERTROPHY ( 4 FDA reports)
VISUAL FIELD DEFECT ( 4 FDA reports)
VITILIGO ( 4 FDA reports)
VITREOUS FLOATERS ( 4 FDA reports)
WALKING AID USER ( 4 FDA reports)
WOUND ( 4 FDA reports)
ACNE ( 3 FDA reports)
ACTINIC KERATOSIS ( 3 FDA reports)
ACUTE PRERENAL FAILURE ( 3 FDA reports)
ADHESION ( 3 FDA reports)
ADJUSTMENT DISORDER ( 3 FDA reports)
ADNEXA UTERI CYST ( 3 FDA reports)
AGGRESSION ( 3 FDA reports)
ANGIOEDEMA ( 3 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 3 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 3 FDA reports)
ANTITHROMBIN III INCREASED ( 3 FDA reports)
APPENDICITIS ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 3 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 3 FDA reports)
BILE DUCT OBSTRUCTION ( 3 FDA reports)
BILIARY DILATATION ( 3 FDA reports)
BIPOLAR DISORDER ( 3 FDA reports)
BITE ( 3 FDA reports)
BLOOD BICARBONATE DECREASED ( 3 FDA reports)
BLOOD BLISTER ( 3 FDA reports)
BLOOD CHLORIDE DECREASED ( 3 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 3 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 3 FDA reports)
BLOOD URINE PRESENT ( 3 FDA reports)
BONE NEOPLASM ( 3 FDA reports)
BRAIN MASS ( 3 FDA reports)
BUNION ( 3 FDA reports)
CARDIAC FLUTTER ( 3 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 3 FDA reports)
CHEMICAL PERITONITIS ( 3 FDA reports)
CHOKING SENSATION ( 3 FDA reports)
CHOLECYSTECTOMY ( 3 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 3 FDA reports)
COLITIS ISCHAEMIC ( 3 FDA reports)
COLON CANCER STAGE III ( 3 FDA reports)
COLOSTOMY ( 3 FDA reports)
COMA ( 3 FDA reports)
COMPLETED SUICIDE ( 3 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 3 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 3 FDA reports)
CORNEAL DEGENERATION ( 3 FDA reports)
COSTOCHONDRITIS ( 3 FDA reports)
CUSHINGOID ( 3 FDA reports)
DEAFNESS NEUROSENSORY ( 3 FDA reports)
DECUBITUS ULCER ( 3 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 3 FDA reports)
DERMAL CYST ( 3 FDA reports)
DEVICE MISUSE ( 3 FDA reports)
DROOLING ( 3 FDA reports)
DUODENITIS ( 3 FDA reports)
DYSPNOEA EXACERBATED ( 3 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 3 FDA reports)
ESCHERICHIA BACTERAEMIA ( 3 FDA reports)
ESCHERICHIA INFECTION ( 3 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 3 FDA reports)
EYE SWELLING ( 3 FDA reports)
FACE OEDEMA ( 3 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 3 FDA reports)
FEEDING DISORDER ( 3 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 3 FDA reports)
FORMICATION ( 3 FDA reports)
GAIT SPASTIC ( 3 FDA reports)
GALLBLADDER PAIN ( 3 FDA reports)
GENERALISED OEDEMA ( 3 FDA reports)
GUILLAIN-BARRE SYNDROME ( 3 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 3 FDA reports)
HAEMORRHOID OPERATION ( 3 FDA reports)
HANGOVER ( 3 FDA reports)
HEPATIC VEIN THROMBOSIS ( 3 FDA reports)
HEPATITIS ACUTE ( 3 FDA reports)
HERNIA REPAIR ( 3 FDA reports)
HIP ARTHROPLASTY ( 3 FDA reports)
HOUSE DUST ALLERGY ( 3 FDA reports)
HYDRONEPHROSIS ( 3 FDA reports)
HYPERKALAEMIA ( 3 FDA reports)
HYPERNATRAEMIA ( 3 FDA reports)
HYPERTENSIVE HEART DISEASE ( 3 FDA reports)
HYPOAESTHESIA FACIAL ( 3 FDA reports)
HYPOKINESIA ( 3 FDA reports)
HYPOTHERMIA ( 3 FDA reports)
HYPOTONIA ( 3 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 3 FDA reports)
INCISIONAL HERNIA ( 3 FDA reports)
INCONTINENCE ( 3 FDA reports)
INJECTION SITE DISCOMFORT ( 3 FDA reports)
INJECTION SITE RASH ( 3 FDA reports)
INTENTIONAL OVERDOSE ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 3 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 3 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 3 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 3 FDA reports)
INTESTINAL INFARCTION ( 3 FDA reports)
INTESTINAL ISCHAEMIA ( 3 FDA reports)
INTRAMEDULLARY ROD INSERTION ( 3 FDA reports)
KIDNEY INFECTION ( 3 FDA reports)
LACUNAR INFARCTION ( 3 FDA reports)
LIBIDO DECREASED ( 3 FDA reports)
LICHEN PLANUS ( 3 FDA reports)
LIMB DISCOMFORT ( 3 FDA reports)
LIPASE INCREASED ( 3 FDA reports)
LOCAL SWELLING ( 3 FDA reports)
LOGORRHOEA ( 3 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 3 FDA reports)
MACULAR HOLE ( 3 FDA reports)
MACULAR OEDEMA ( 3 FDA reports)
MENIERE'S DISEASE ( 3 FDA reports)
METASTATIC NEOPLASM ( 3 FDA reports)
METRORRHAGIA ( 3 FDA reports)
MOANING ( 3 FDA reports)
MOVEMENT DISORDER ( 3 FDA reports)
MUSCLE RIGIDITY ( 3 FDA reports)
MUSCLE SPASTICITY ( 3 FDA reports)
MUSCLE TWITCHING ( 3 FDA reports)
NASAL POLYPS ( 3 FDA reports)
NEUROPATHY ( 3 FDA reports)
NEUTROPHIL COUNT INCREASED ( 3 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 3 FDA reports)
NO THERAPEUTIC RESPONSE ( 3 FDA reports)
OESOPHAGEAL DISORDER ( 3 FDA reports)
OESOPHAGEAL SPASM ( 3 FDA reports)
OESOPHAGITIS ( 3 FDA reports)
OPEN REDUCTION OF FRACTURE ( 3 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 3 FDA reports)
ORAL SURGERY ( 3 FDA reports)
ORGAN FAILURE ( 3 FDA reports)
ORGANIC ERECTILE DYSFUNCTION ( 3 FDA reports)
OROPHARYNGEAL BLISTERING ( 3 FDA reports)
PARATHYROID DISORDER ( 3 FDA reports)
PARATHYROID TUMOUR BENIGN ( 3 FDA reports)
PEAK EXPIRATORY FLOW RATE DECREASED ( 3 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 3 FDA reports)
PERITONITIS ( 3 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 3 FDA reports)
POLYCYTHAEMIA ( 3 FDA reports)
POLYDIPSIA ( 3 FDA reports)
POLYMYOSITIS ( 3 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 3 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 3 FDA reports)
POSTOPERATIVE ILEUS ( 3 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 3 FDA reports)
PRESCRIBED OVERDOSE ( 3 FDA reports)
PROCTITIS HERPES ( 3 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 3 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 3 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 3 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 3 FDA reports)
PULSE ABSENT ( 3 FDA reports)
PYELONEPHRITIS ( 3 FDA reports)
RESIDUAL URINE ( 3 FDA reports)
RESUSCITATION ( 3 FDA reports)
RETINAL DETACHMENT ( 3 FDA reports)
RHINALGIA ( 3 FDA reports)
SCAB ( 3 FDA reports)
SCAPULA FRACTURE ( 3 FDA reports)
SCROTAL OEDEMA ( 3 FDA reports)
SELF-MEDICATION ( 3 FDA reports)
SEQUESTRECTOMY ( 3 FDA reports)
SINUS HEADACHE ( 3 FDA reports)
SKIN BURNING SENSATION ( 3 FDA reports)
SKIN EXFOLIATION ( 3 FDA reports)
SKIN TIGHTNESS ( 3 FDA reports)
SNORING ( 3 FDA reports)
SPINAL DISORDER ( 3 FDA reports)
STEVENS-JOHNSON SYNDROME ( 3 FDA reports)
STRIDOR ( 3 FDA reports)
SUDDEN ONSET OF SLEEP ( 3 FDA reports)
SYNCOPE VASOVAGAL ( 3 FDA reports)
SYNOVIAL CYST ( 3 FDA reports)
SYNOVITIS ( 3 FDA reports)
TENDON PAIN ( 3 FDA reports)
THERAPY NON-RESPONDER ( 3 FDA reports)
TRANSAMINASES INCREASED ( 3 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 3 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 3 FDA reports)
UMBILICAL HERNIA ( 3 FDA reports)
UPPER AIRWAY RESISTANCE SYNDROME ( 3 FDA reports)
URINE ANALYSIS ABNORMAL ( 3 FDA reports)
VAGINAL DYSPLASIA ( 3 FDA reports)
VAGINAL MYCOSIS ( 3 FDA reports)
VENTRICULAR DYSFUNCTION ( 3 FDA reports)
VIRAL LOAD INCREASED ( 3 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 3 FDA reports)
VULVOVAGINAL PRURITUS ( 3 FDA reports)
ABDOMINAL RIGIDITY ( 2 FDA reports)
ABDOMINAL TENDERNESS ( 2 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 2 FDA reports)
ABNORMAL CLOTTING FACTOR ( 2 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 2 FDA reports)
ABNORMAL SENSATION IN EYE ( 2 FDA reports)
ACCIDENT ( 2 FDA reports)
ACROCHORDON ( 2 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 2 FDA reports)
ACUTE STRESS DISORDER ( 2 FDA reports)
ADDISON'S DISEASE ( 2 FDA reports)
ADENOIDECTOMY ( 2 FDA reports)
ALCOHOL ABUSE ( 2 FDA reports)
ALCOHOLISM ( 2 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 2 FDA reports)
ALVEOLITIS ALLERGIC ( 2 FDA reports)
ANAEMIA POSTOPERATIVE ( 2 FDA reports)
ANAL SPHINCTEROTOMY ( 2 FDA reports)
ANAPHYLACTOID REACTION ( 2 FDA reports)
ANASTOMOTIC STENOSIS ( 2 FDA reports)
ANXIETY DISORDER ( 2 FDA reports)
AORTIC DISSECTION ( 2 FDA reports)
AORTIC OCCLUSION ( 2 FDA reports)
AORTIC VALVE SCLEROSIS ( 2 FDA reports)
APATHY ( 2 FDA reports)
APHONIA ( 2 FDA reports)
APPENDIX DISORDER ( 2 FDA reports)
APPLICATION SITE ERYTHEMA ( 2 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
ARTERIOSPASM CORONARY ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 2 FDA reports)
ATROPHY ( 2 FDA reports)
B-CELL LYMPHOMA ( 2 FDA reports)
BACTERIAL TEST POSITIVE ( 2 FDA reports)
BEDRIDDEN ( 2 FDA reports)
BETA-2 GLYCOPROTEIN ANTIBODY POSITIVE ( 2 FDA reports)
BILIARY TRACT DISORDER ( 2 FDA reports)
BLADDER CANCER ( 2 FDA reports)
BLADDER REPAIR ( 2 FDA reports)
BLOOD DISORDER ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 2 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 2 FDA reports)
BREAST CYST ( 2 FDA reports)
BREAST DISORDER ( 2 FDA reports)
BRONCHIECTASIS ( 2 FDA reports)
BRONCHIOLITIS ( 2 FDA reports)
CARBON DIOXIDE INCREASED ( 2 FDA reports)
CARDIAC FAILURE CHRONIC ( 2 FDA reports)
CARDIAC VALVE DISEASE ( 2 FDA reports)
CAUDA EQUINA SYNDROME ( 2 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 2 FDA reports)
CEREBRAL ISCHAEMIA ( 2 FDA reports)
CHEST X-RAY ABNORMAL ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
CHOLESTEROSIS ( 2 FDA reports)
CHOREA ( 2 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 2 FDA reports)
CLAVICLE FRACTURE ( 2 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 2 FDA reports)
COAGULATION FACTOR VIII LEVEL INCREASED ( 2 FDA reports)
COLD SWEAT ( 2 FDA reports)
COLECTOMY PARTIAL ( 2 FDA reports)
COLLAPSE OF LUNG ( 2 FDA reports)
COLONOSCOPY ABNORMAL ( 2 FDA reports)
COMPLEX PARTIAL SEIZURES ( 2 FDA reports)
CONCUSSION ( 2 FDA reports)
CONJUNCTIVITIS ( 2 FDA reports)
CONNECTIVE TISSUE DISORDER ( 2 FDA reports)
CORNEAL ABRASION ( 2 FDA reports)
CORONARY ARTERY BYPASS ( 2 FDA reports)
CORONARY ARTERY THROMBOSIS ( 2 FDA reports)
CUBITAL TUNNEL SYNDROME ( 2 FDA reports)
DEFICIENCY ANAEMIA ( 2 FDA reports)
DEVICE MALFUNCTION ( 2 FDA reports)
DIABETIC NEUROPATHY ( 2 FDA reports)
DIABETIC RETINOPATHY ( 2 FDA reports)
DIALYSIS ( 2 FDA reports)
DRUG ABUSER ( 2 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 2 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
DRUG PRESCRIBING ERROR ( 2 FDA reports)
DUPUYTREN'S CONTRACTURE ( 2 FDA reports)
DYSTHYMIC DISORDER ( 2 FDA reports)
EAR CONGESTION ( 2 FDA reports)
ECTROPION OF CERVIX ( 2 FDA reports)
EDUCATIONAL PROBLEM ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 2 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
ENDOMETRIAL CANCER ( 2 FDA reports)
ENDOMETRIAL DISORDER ( 2 FDA reports)
ENDOTRACHEAL INTUBATION ( 2 FDA reports)
ENTHESOPATHY ( 2 FDA reports)
EXTRASYSTOLES ( 2 FDA reports)
EYE MOVEMENT DISORDER ( 2 FDA reports)
FEAR OF DISEASE ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
FIBRIN D DIMER INCREASED ( 2 FDA reports)
FLAT AFFECT ( 2 FDA reports)
FRUSTRATION ( 2 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 2 FDA reports)
GASTROINTESTINAL FUNGAL INFECTION ( 2 FDA reports)
GASTROINTESTINAL INFECTION ( 2 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 2 FDA reports)
GENITAL DISORDER FEMALE ( 2 FDA reports)
GLOMUS TUMOUR ( 2 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 2 FDA reports)
HAEMOLYSIS ( 2 FDA reports)
HALO VISION ( 2 FDA reports)
HEPATITIS C RNA POSITIVE ( 2 FDA reports)
HOARSENESS ( 2 FDA reports)
HUNGRY BONE SYNDROME ( 2 FDA reports)
HYPERCALCAEMIA ( 2 FDA reports)
HYPERCAPNIA ( 2 FDA reports)
HYPERPARATHYROIDISM ( 2 FDA reports)
HYPERSEXUALITY ( 2 FDA reports)
HYPERTONIC BLADDER ( 2 FDA reports)
HYPOSMIA ( 2 FDA reports)
HYPOTHALAMO-PITUITARY DISORDER ( 2 FDA reports)
HYSTERECTOMY ( 2 FDA reports)
ILEUS PARALYTIC ( 2 FDA reports)
IMPAIRED WORK ABILITY ( 2 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 2 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 2 FDA reports)
INCREASED TENDENCY TO BRUISE ( 2 FDA reports)
INFARCTION ( 2 FDA reports)
INFUSION SITE ERYTHEMA ( 2 FDA reports)
INJECTION SITE BRUISING ( 2 FDA reports)
INJECTION SITE BURNING ( 2 FDA reports)
INJECTION SITE EXTRAVASATION ( 2 FDA reports)
INJECTION SITE IRRITATION ( 2 FDA reports)
INJECTION SITE PRURITUS ( 2 FDA reports)
INJECTION SITE STINGING ( 2 FDA reports)
INJECTION SITE WARMTH ( 2 FDA reports)
INTESTINAL RESECTION ( 2 FDA reports)
INTRAOCULAR LENS IMPLANT ( 2 FDA reports)
ISCHAEMIA ( 2 FDA reports)
ISCHAEMIC HEPATITIS ( 2 FDA reports)
JAW DISORDER ( 2 FDA reports)
JOINT LOCK ( 2 FDA reports)
KIDNEY FIBROSIS ( 2 FDA reports)
KIDNEY SMALL ( 2 FDA reports)
LABYRINTHITIS ( 2 FDA reports)
LAPAROTOMY ( 2 FDA reports)
LERICHE SYNDROME ( 2 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 2 FDA reports)
LEUKOPLAKIA ORAL ( 2 FDA reports)
LIMB DEFORMITY ( 2 FDA reports)
LISTERIOSIS ( 2 FDA reports)
LIVER INJURY ( 2 FDA reports)
LIVER TENDERNESS ( 2 FDA reports)
LOBAR PNEUMONIA ( 2 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
LOWER LIMB FRACTURE ( 2 FDA reports)
LUNG HYPERINFLATION ( 2 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 2 FDA reports)
LYMPHADENITIS ( 2 FDA reports)
LYMPHOMA ( 2 FDA reports)
MACULAR CYST ( 2 FDA reports)
MALIGNANT HYPERTENSION ( 2 FDA reports)
MALIGNANT MELANOMA ( 2 FDA reports)
MATERNAL EXPOSURE BEFORE PREGNANCY ( 2 FDA reports)
MEDICAL DEVICE COMPLICATION ( 2 FDA reports)
MEDICATION TAMPERING ( 2 FDA reports)
MEGAKARYOCYTES INCREASED ( 2 FDA reports)
MENINGIOMA ( 2 FDA reports)
MESENTERIC LYMPHADENOPATHY ( 2 FDA reports)
METAPLASIA ( 2 FDA reports)
METATARSALGIA ( 2 FDA reports)
MILIA ( 2 FDA reports)
MIOSIS ( 2 FDA reports)
MITRAL VALVE DISEASE ( 2 FDA reports)
MIXED INCONTINENCE ( 2 FDA reports)
MOTOR DYSFUNCTION ( 2 FDA reports)
MUELLER'S MIXED TUMOUR ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ( 2 FDA reports)
MUSCLE DISORDER ( 2 FDA reports)
MUSCULOSKELETAL DEFORMITY ( 2 FDA reports)
MYDRIASIS ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME ( 2 FDA reports)
MYOSITIS ( 2 FDA reports)
MYRINGOTOMY ( 2 FDA reports)
NASAL CYST ( 2 FDA reports)
NASAL DISORDER ( 2 FDA reports)
NASAL DRYNESS ( 2 FDA reports)
NASAL SEPTUM PERFORATION ( 2 FDA reports)
NECROTISING FASCIITIS ( 2 FDA reports)
NEOPLASM PROGRESSION ( 2 FDA reports)
NERVE INJURY ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
NO ADVERSE EVENT ( 2 FDA reports)
NODAL RHYTHM ( 2 FDA reports)
NON-CARDIAC CHEST PAIN ( 2 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 2 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 2 FDA reports)
OESOPHAGEAL HYPOMOTILITY ( 2 FDA reports)
OESOPHAGEAL STENOSIS ( 2 FDA reports)
OPIATES POSITIVE ( 2 FDA reports)
ORAL FUNGAL INFECTION ( 2 FDA reports)
OROPHARYNGEAL PLAQUE ( 2 FDA reports)
ORTHOPNOEA ( 2 FDA reports)
PACEMAKER COMPLICATION ( 2 FDA reports)
PAINFUL DEFAECATION ( 2 FDA reports)
PAINFUL RESPIRATION ( 2 FDA reports)
PANCREATITIS RELAPSING ( 2 FDA reports)
PAPILLARY THYROID CANCER ( 2 FDA reports)
PARALYSIS ( 2 FDA reports)
PARALYSIS FLACCID ( 2 FDA reports)
PARANOIA ( 2 FDA reports)
PARTIAL SEIZURES ( 2 FDA reports)
PERINEAL OPERATION ( 2 FDA reports)
PERIPHERAL COLDNESS ( 2 FDA reports)
PERIPHERAL ISCHAEMIA ( 2 FDA reports)
PERSONALITY DISORDER ( 2 FDA reports)
PETIT MAL EPILEPSY ( 2 FDA reports)
PHOTOPHOBIA ( 2 FDA reports)
PHYSICAL ASSAULT ( 2 FDA reports)
PLEURISY ( 2 FDA reports)
PNEUMONITIS ( 2 FDA reports)
POLYARTHRITIS ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 2 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 2 FDA reports)
POSTURE ABNORMAL ( 2 FDA reports)
PROCEDURAL PAIN ( 2 FDA reports)
PRODUCT ADHESION ISSUE ( 2 FDA reports)
PRODUCT ODOUR ABNORMAL ( 2 FDA reports)
PROTEIN C INCREASED ( 2 FDA reports)
PROTEIN TOTAL DECREASED ( 2 FDA reports)
PSEUDOMONAS INFECTION ( 2 FDA reports)
PULMONARY ARTERIAL WEDGE PRESSURE INCREASED ( 2 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 2 FDA reports)
PULMONARY VASCULAR DISORDER ( 2 FDA reports)
QUADRIPARESIS ( 2 FDA reports)
RADIOTHERAPY ( 2 FDA reports)
RASH PRURITIC ( 2 FDA reports)
RAYNAUD'S PHENOMENON ( 2 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 2 FDA reports)
RECTAL DISCHARGE ( 2 FDA reports)
RECTAL PROLAPSE REPAIR ( 2 FDA reports)
REFLUX GASTRITIS ( 2 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 2 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 2 FDA reports)
RENAL TUBULAR NECROSIS ( 2 FDA reports)
RESPIRATORY RATE DECREASED ( 2 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 2 FDA reports)
RETINOPEXY ( 2 FDA reports)
RIGHT ATRIAL DILATATION ( 2 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 2 FDA reports)
SENSATION OF HEAVINESS ( 2 FDA reports)
SENSORY DISTURBANCE ( 2 FDA reports)
SEROMA ( 2 FDA reports)
SIGMOIDECTOMY ( 2 FDA reports)
SINUSITIS FUNGAL ( 2 FDA reports)
SKIN ATROPHY ( 2 FDA reports)
SKIN CANCER ( 2 FDA reports)
SKIN HYPERTROPHY ( 2 FDA reports)
SKIN MASS ( 2 FDA reports)
SMEAR CERVIX ABNORMAL ( 2 FDA reports)
SPINAL COLUMN INJURY ( 2 FDA reports)
SPINAL CORD DISORDER ( 2 FDA reports)
SPINAL DEFORMITY ( 2 FDA reports)
SPIROMETRY ABNORMAL ( 2 FDA reports)
SPONDYLITIS ( 2 FDA reports)
SQUAMOUS CELL CARCINOMA ( 2 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 2 FDA reports)
STRESS URINARY INCONTINENCE ( 2 FDA reports)
SUBCUTANEOUS ABSCESS ( 2 FDA reports)
SYRINGOMYELIA ( 2 FDA reports)
TEARFULNESS ( 2 FDA reports)
TEMPORAL ARTERITIS ( 2 FDA reports)
TENDON DISORDER ( 2 FDA reports)
TENOSYNOVITIS STENOSANS ( 2 FDA reports)
THERAPEUTIC REACTION TIME DECREASED ( 2 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 2 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 2 FDA reports)
THINKING ABNORMAL ( 2 FDA reports)
THIRST ( 2 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 2 FDA reports)
THYMUS ENLARGEMENT ( 2 FDA reports)
TINEA PEDIS ( 2 FDA reports)
TOE DEFORMITY ( 2 FDA reports)
TONGUE BITING ( 2 FDA reports)
TONSILLECTOMY ( 2 FDA reports)
TRIGGER FINGER ( 2 FDA reports)
UMBILICAL HERNIA REPAIR ( 2 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
UPPER LIMB FRACTURE ( 2 FDA reports)
URINE LEUKOCYTE ESTERASE ( 2 FDA reports)
URINE OUTPUT DECREASED ( 2 FDA reports)
UTERINE CERVIX ATROPHY ( 2 FDA reports)
UTERINE DILATION AND CURETTAGE ( 2 FDA reports)
VAGINAL HAEMORRHAGE ( 2 FDA reports)
VASOGENIC CEREBRAL OEDEMA ( 2 FDA reports)
VASOMOTOR RHINITIS ( 2 FDA reports)
VERTEBROPLASTY ( 2 FDA reports)
VERTIGO POSITIONAL ( 2 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
VISUAL DISTURBANCE ( 2 FDA reports)
VITAMIN B COMPLEX DEFICIENCY ( 2 FDA reports)
VITAMIN D DECREASED ( 2 FDA reports)
VITREOUS HAEMORRHAGE ( 2 FDA reports)
VOMITING PROJECTILE ( 2 FDA reports)
ABORTION INDUCED ( 1 FDA reports)
ABSCESS ORAL ( 1 FDA reports)
ACANTHOSIS ( 1 FDA reports)
ACCIDENT AT WORK ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACCIDENTAL POISONING ( 1 FDA reports)
ACETABULUM FRACTURE ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACQUIRED CARDIAC SEPTAL DEFECT ( 1 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 1 FDA reports)
ACUTE HEPATIC FAILURE ( 1 FDA reports)
ADHESIOLYSIS ( 1 FDA reports)
ADRENAL ADENOMA ( 1 FDA reports)
ADRENAL DISORDER ( 1 FDA reports)
ADRENAL HAEMORRHAGE ( 1 FDA reports)
ADRENAL MASS ( 1 FDA reports)
AFFECT LABILITY ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
ALCOHOL POISONING ( 1 FDA reports)
ALLERGIC COLITIS ( 1 FDA reports)
ALOPECIA AREATA ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 1 FDA reports)
AMYLASE INCREASED ( 1 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 1 FDA reports)
ANAEMIA MACROCYTIC ( 1 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 1 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 1 FDA reports)
ANAL DISCOMFORT ( 1 FDA reports)
ANAL HAEMORRHAGE ( 1 FDA reports)
ANALGESIC DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANASTOMOTIC ULCER ( 1 FDA reports)
ANGIOGRAM ABNORMAL ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANGIOPLASTY ( 1 FDA reports)
ANHIDROSIS ( 1 FDA reports)
ANORECTAL DISCOMFORT ( 1 FDA reports)
ANORGASMIA ( 1 FDA reports)
ANTI-HBC IGM ANTIBODY POSITIVE ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 1 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 1 FDA reports)
ANTISOCIAL BEHAVIOUR ( 1 FDA reports)
AORTIC BYPASS ( 1 FDA reports)
AORTIC CALCIFICATION ( 1 FDA reports)
AORTIC DILATATION ( 1 FDA reports)
AORTIC DISORDER ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
AORTIC VALVE DISEASE ( 1 FDA reports)
AORTIC VALVE REPLACEMENT ( 1 FDA reports)
APHTHOUS STOMATITIS ( 1 FDA reports)
APLASTIC ANAEMIA ( 1 FDA reports)
APPARENT DEATH ( 1 FDA reports)
APPENDICECTOMY ( 1 FDA reports)
APPENDICITIS PERFORATED ( 1 FDA reports)
APPLICATION SITE DERMATITIS ( 1 FDA reports)
APPLICATION SITE IRRITATION ( 1 FDA reports)
APPLICATION SITE RASH ( 1 FDA reports)
APTYALISM ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ARTERIAL DISORDER ( 1 FDA reports)
ARTERIAL THROMBOSIS ( 1 FDA reports)
ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
ARTHROPOD BITE ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ATRIAL TACHYCARDIA ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 1 FDA reports)
AXILLARY VEIN THROMBOSIS ( 1 FDA reports)
BACTERIAL CULTURE POSITIVE ( 1 FDA reports)
BACTERIAL SEPSIS ( 1 FDA reports)
BACTERIURIA ( 1 FDA reports)
BALANITIS ( 1 FDA reports)
BAND SENSATION ( 1 FDA reports)
BENIGN GASTRIC NEOPLASM ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BILIARY DRAINAGE ( 1 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 1 FDA reports)
BIOPSY LIVER ABNORMAL ( 1 FDA reports)
BLADDER PROLAPSE ( 1 FDA reports)
BLEPHARITIS ( 1 FDA reports)
BLEPHAROSPASM ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLOOD CHLORIDE ABNORMAL ( 1 FDA reports)
BLOOD CHLORIDE INCREASED ( 1 FDA reports)
BLOOD FIBRINOGEN ABNORMAL ( 1 FDA reports)
BLOOD GASES ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 1 FDA reports)
BLOOD OESTROGEN DECREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD PROLACTIN INCREASED ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 1 FDA reports)
BLOOD UREA DECREASED ( 1 FDA reports)
BODY HEIGHT BELOW NORMAL ( 1 FDA reports)
BRACHYTHERAPY ( 1 FDA reports)
BRADYKINESIA ( 1 FDA reports)
BRAIN CONTUSION ( 1 FDA reports)
BRAIN INJURY ( 1 FDA reports)
BRAIN MIDLINE SHIFT ( 1 FDA reports)
BRAIN STEM STROKE ( 1 FDA reports)
BREAKTHROUGH PAIN ( 1 FDA reports)
BREAST CANCER STAGE I ( 1 FDA reports)
BREAST CANCER STAGE II ( 1 FDA reports)
BREAST CANCER STAGE III ( 1 FDA reports)
BREAST DISCHARGE ( 1 FDA reports)
BREAST DISORDER FEMALE ( 1 FDA reports)
BREAST HYPERPLASIA ( 1 FDA reports)
BREAST TENDERNESS ( 1 FDA reports)
BRONCHIAL DISORDER ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
BURSA CALCIFICATION ( 1 FDA reports)
BURSAL OPERATION ( 1 FDA reports)
BUTTOCK PAIN ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
CARDIAC FIBRILLATION ( 1 FDA reports)
CARDIAC INFECTION ( 1 FDA reports)
CARDIAC PACEMAKER INSERTION ( 1 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
CARDIOVERSION ( 1 FDA reports)
CARDITIS ( 1 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 1 FDA reports)
CAROTID ARTERY ATHEROMA ( 1 FDA reports)
CAROTID ARTERY DISEASE ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CATHETER SEPSIS ( 1 FDA reports)
CATHETERISATION CARDIAC ( 1 FDA reports)
CAUSTIC INJURY ( 1 FDA reports)
CELLULITIS STREPTOCOCCAL ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 1 FDA reports)
CEREBRAL CALCIFICATION ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 1 FDA reports)
CERVICOBRACHIAL SYNDROME ( 1 FDA reports)
CHANGE OF BOWEL HABIT ( 1 FDA reports)
CHAPPED LIPS ( 1 FDA reports)
CHEMOTHERAPY ( 1 FDA reports)
CHEST WALL PAIN ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHOLECYSTITIS INFECTIVE ( 1 FDA reports)
CHORIORETINOPATHY ( 1 FDA reports)
CHOROIDAL NEOVASCULARISATION ( 1 FDA reports)
CHROMATOPSIA ( 1 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 1 FDA reports)
CLEFT PALATE ( 1 FDA reports)
CLUMSINESS ( 1 FDA reports)
COCCYDYNIA ( 1 FDA reports)
COELIAC DISEASE ( 1 FDA reports)
COLECTOMY ( 1 FDA reports)
COLON CANCER METASTATIC ( 1 FDA reports)
COLON NEOPLASM ( 1 FDA reports)
COMA SCALE ABNORMAL ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
COMPLEMENT FACTOR ABNORMAL ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED LUNG ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CONGENITAL ANOMALY ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
CONVERSION DISORDER ( 1 FDA reports)
CORNEAL TRANSPLANT ( 1 FDA reports)
CORONARY ARTERY ANEURYSM ( 1 FDA reports)
CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
CUSHING'S SYNDROME ( 1 FDA reports)
CUTIS LAXA ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
DELIRIUM TREMENS ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 1 FDA reports)
DEMYELINATION ( 1 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 1 FDA reports)
DERMATITIS ATOPIC ( 1 FDA reports)
DERMATITIS HERPETIFORMIS ( 1 FDA reports)
DEVICE DISLOCATION ( 1 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 1 FDA reports)
DIABETIC COMPLICATION ( 1 FDA reports)
DIABETIC GASTROPARESIS ( 1 FDA reports)
DIALYSIS DEVICE INSERTION ( 1 FDA reports)
DIAPHRAGMATIC DISORDER ( 1 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DISSOCIATION ( 1 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 1 FDA reports)
DRUG EFFECT INCREASED ( 1 FDA reports)
DRUG INTERACTION POTENTIATION ( 1 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 1 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 1 FDA reports)
EAR HAEMORRHAGE ( 1 FDA reports)
EAR INFECTION VIRAL ( 1 FDA reports)
EARLY SATIETY ( 1 FDA reports)
ECTOPIC PREGNANCY ( 1 FDA reports)
EJACULATION FAILURE ( 1 FDA reports)
ELECTROCARDIOGRAM ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM QT SHORTENED ( 1 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 1 FDA reports)
ELECTRON RADIATION THERAPY TO PROSTATE ( 1 FDA reports)
ENCEPHALITIS ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
ENDOMETRIAL ATROPHY ( 1 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 1 FDA reports)
ENERGY INCREASED ( 1 FDA reports)
ENLARGED UVULA ( 1 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
EPICONDYLITIS ( 1 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 1 FDA reports)
ERYTHEMA OF EYELID ( 1 FDA reports)
EXERCISE ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
EXOPHTHALMOS ( 1 FDA reports)
EXTRASKELETAL OSSIFICATION ( 1 FDA reports)
EXTRAVASATION BLOOD ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
EYE MUSCLE OPERATION ( 1 FDA reports)
EYE ROLLING ( 1 FDA reports)
EYELID CYST ( 1 FDA reports)
EYELID DISORDER ( 1 FDA reports)
FACIAL WASTING ( 1 FDA reports)
FACTITIOUS DISORDER ( 1 FDA reports)
FACTOR V LEIDEN MUTATION ( 1 FDA reports)
FAECALOMA ( 1 FDA reports)
FAMILIAL TREMOR ( 1 FDA reports)
FASCIITIS ( 1 FDA reports)
FAT NECROSIS ( 1 FDA reports)
FAT TISSUE INCREASED ( 1 FDA reports)
FEAR OF DEATH ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
FEELING GUILTY ( 1 FDA reports)
FEELING HOT AND COLD ( 1 FDA reports)
FEELINGS OF WORTHLESSNESS ( 1 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 1 FDA reports)
FLASHBACK ( 1 FDA reports)
FOLLICULITIS ( 1 FDA reports)
FOOD ALLERGY ( 1 FDA reports)
FOOD CRAVING ( 1 FDA reports)
FOOT OPERATION ( 1 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 1 FDA reports)
FRACTURE MALUNION ( 1 FDA reports)
FUNGAL TEST POSITIVE ( 1 FDA reports)
GALLBLADDER PERFORATION ( 1 FDA reports)
GALLBLADDER POLYP ( 1 FDA reports)
GASTRIC DILATATION ( 1 FDA reports)
GASTRIC MUCOSA ERYTHEMA ( 1 FDA reports)
GASTRIC PH DECREASED ( 1 FDA reports)
GASTRIC STENOSIS ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTROENTERITIS VIRAL ( 1 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
GASTROINTESTINAL DISORDER POSTOPERATIVE ( 1 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 1 FDA reports)
GASTROINTESTINAL STENOSIS ( 1 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 1 FDA reports)
GASTROINTESTINAL ULCER ( 1 FDA reports)
GENITAL PRURITUS FEMALE ( 1 FDA reports)
GLIOSIS ( 1 FDA reports)
GLOBAL AMNESIA ( 1 FDA reports)
GOUTY ARTHRITIS ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
GRANULOMA ( 1 FDA reports)
GRANULOMA SKIN ( 1 FDA reports)
GRIEF REACTION ( 1 FDA reports)
GROWING PAINS ( 1 FDA reports)
HAEMANGIOMA OF LIVER ( 1 FDA reports)
HAEMANGIOMA OF SKIN ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMOCHROMATOSIS ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 1 FDA reports)
HAEMORRHAGIC DIATHESIS ( 1 FDA reports)
HAEMORRHAGIC DISORDER ( 1 FDA reports)
HAEMORRHAGIC INFARCTION ( 1 FDA reports)
HALITOSIS ( 1 FDA reports)
HAND FRACTURE ( 1 FDA reports)
HEART RATE ABNORMAL ( 1 FDA reports)
HEART TRANSPLANT ( 1 FDA reports)
HEART TRANSPLANT REJECTION ( 1 FDA reports)
HELICOBACTER TEST POSITIVE ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC ENZYME ABNORMAL ( 1 FDA reports)
HEPATIC FIBROSIS ( 1 FDA reports)
HEPATIC ISCHAEMIA ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 1 FDA reports)
HEPATITIS C VIRUS ( 1 FDA reports)
HEPATITIS FULMINANT ( 1 FDA reports)
HEPATITIS VIRAL ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HERPES DERMATITIS ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
HILAR LYMPHADENOPATHY ( 1 FDA reports)
HISTOPLASMOSIS DISSEMINATED ( 1 FDA reports)
HORNER'S SYNDROME ( 1 FDA reports)
HUNGER ( 1 FDA reports)
HUNTINGTON'S CHOREA ( 1 FDA reports)
HUNTINGTON'S DISEASE ( 1 FDA reports)
HYPERKINESIA ( 1 FDA reports)
HYPERMOBILITY SYNDROME ( 1 FDA reports)
HYPERREFLEXIA ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPERTENSIVE EMERGENCY ( 1 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPERTONIA ( 1 FDA reports)
HYPERTRICHOSIS ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOGEUSIA ( 1 FDA reports)
HYPOGLYCAEMIC COMA ( 1 FDA reports)
HYPOMENORRHOEA ( 1 FDA reports)
HYPOPROTEINAEMIA ( 1 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
ILEUS ( 1 FDA reports)
ILIAC ARTERY STENOSIS ( 1 FDA reports)
IMMUNODEFICIENCY ( 1 FDA reports)
IMMUNOGLOBULINS DECREASED ( 1 FDA reports)
IMPATIENCE ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR MALFUNCTION ( 1 FDA reports)
IMPULSIVE BEHAVIOUR ( 1 FDA reports)
INAPPROPRIATE AFFECT ( 1 FDA reports)
INCISION SITE ERYTHEMA ( 1 FDA reports)
INCISION SITE HAEMORRHAGE ( 1 FDA reports)
INCISION SITE PAIN ( 1 FDA reports)
INCISIONAL HERNIA REPAIR ( 1 FDA reports)
INCREASED BRONCHIAL SECRETION ( 1 FDA reports)
INDURATION ( 1 FDA reports)
INFECTION TRANSMISSION VIA PERSONAL CONTACT ( 1 FDA reports)
INGROWING NAIL ( 1 FDA reports)
INJECTION SITE INDURATION ( 1 FDA reports)
INJECTION SITE INFECTION ( 1 FDA reports)
INJECTION SITE NODULE ( 1 FDA reports)
INJECTION SITE VESICLES ( 1 FDA reports)
INTENTIONAL MISUSE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 1 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 1 FDA reports)
INTESTINAL DILATATION ( 1 FDA reports)
INTESTINAL ULCER ( 1 FDA reports)
INTRA-UTERINE CONTRACEPTIVE DEVICE EXPELLED ( 1 FDA reports)
IRON DEFICIENCY ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 1 FDA reports)
IUCD COMPLICATION ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
JOINT ANKYLOSIS ( 1 FDA reports)
JOINT HYPEREXTENSION ( 1 FDA reports)
KERATOACANTHOMA ( 1 FDA reports)
KETOACIDOSIS ( 1 FDA reports)
LACTOSE INTOLERANCE ( 1 FDA reports)
LARGE INTESTINAL ULCER ( 1 FDA reports)
LEG AMPUTATION ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LICHENOID KERATOSIS ( 1 FDA reports)
LIGAMENT RUPTURE ( 1 FDA reports)
LIMB TRAUMATIC AMPUTATION ( 1 FDA reports)
LIP DISORDER ( 1 FDA reports)
LIP DRY ( 1 FDA reports)
LIP NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 1 FDA reports)
LIP OEDEMA ( 1 FDA reports)
LIPASE DECREASED ( 1 FDA reports)
LISTLESS ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
LOSS OF LIBIDO ( 1 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
LUNG ADENOCARCINOMA STAGE IV ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
LUNG TRANSPLANT REJECTION ( 1 FDA reports)
LUNG WEDGE RESECTION ( 1 FDA reports)
LYMPH NODE CALCIFICATION ( 1 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
MACULAR FIBROSIS ( 1 FDA reports)
MAJOR DEPRESSION ( 1 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 1 FDA reports)
MARITAL PROBLEM ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MASTECTOMY ( 1 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 1 FDA reports)
MECHANICAL VENTILATION ( 1 FDA reports)
MEDICAL DEVICE REMOVAL ( 1 FDA reports)
MEDICATION RESIDUE ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MENINGIOMA BENIGN ( 1 FDA reports)
MENINGITIS ( 1 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 1 FDA reports)
MENOPAUSAL SYMPTOMS ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
METABOLIC ALKALOSIS ( 1 FDA reports)
METANEPHRINE URINE INCREASED ( 1 FDA reports)
METASTASES TO ADRENALS ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
METASTASES TO OVARY ( 1 FDA reports)
METASTASIS ( 1 FDA reports)
MICROALBUMINURIA ( 1 FDA reports)
MICROANGIOPATHY ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
MIGRAINE WITH AURA ( 1 FDA reports)
MILK ALLERGY ( 1 FDA reports)
MITRAL VALVE CALCIFICATION ( 1 FDA reports)
MITRAL VALVE REPAIR ( 1 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
MOUTH PLAQUE ( 1 FDA reports)
MUCOSAL HAEMORRHAGE ( 1 FDA reports)
MULTI-ORGAN DISORDER ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
MUSCLE HAEMORRHAGE ( 1 FDA reports)
MUSCLE STRAIN ( 1 FDA reports)
MUSCULAR DYSTROPHY ( 1 FDA reports)
MYELITIS TRANSVERSE ( 1 FDA reports)
MYOCARDIAL REPERFUSION INJURY ( 1 FDA reports)
NAIL INFECTION ( 1 FDA reports)
NASAL MUCOSAL DISORDER ( 1 FDA reports)
NASAL OPERATION ( 1 FDA reports)
NASAL SEPTUM DEVIATION ( 1 FDA reports)
NASAL ULCER ( 1 FDA reports)
NECK MASS ( 1 FDA reports)
NECROSIS ISCHAEMIC ( 1 FDA reports)
NEEDLE ISSUE ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NEPHROCALCINOSIS ( 1 FDA reports)
NEURODEGENERATIVE DISORDER ( 1 FDA reports)
NEUROGENIC BLADDER ( 1 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 1 FDA reports)
NEUROMYOPATHY ( 1 FDA reports)
NEUROSIS ( 1 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
NYSTAGMUS ( 1 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 1 FDA reports)
OBSTRUCTION GASTRIC ( 1 FDA reports)
ODYNOPHAGIA ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
OESOPHAGEAL ADENOCARCINOMA ( 1 FDA reports)
OESOPHAGEAL CARCINOMA ( 1 FDA reports)
OESOPHAGEAL DILATATION ( 1 FDA reports)
OESOPHAGEAL ULCER ( 1 FDA reports)
OESOPHAGITIS ULCERATIVE ( 1 FDA reports)
ONYCHOMYCOSIS ( 1 FDA reports)
ORAL INFECTION ( 1 FDA reports)
ORAL MUCOSA EROSION ( 1 FDA reports)
ORAL MUCOSAL DISORDER ( 1 FDA reports)
ORAL PRURITUS ( 1 FDA reports)
ORAL SOFT TISSUE DISORDER ( 1 FDA reports)
OROANTRAL FISTULA ( 1 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 1 FDA reports)
OTITIS EXTERNA ( 1 FDA reports)
OVARIAN CANCER ( 1 FDA reports)
OVARIAN CYST ( 1 FDA reports)
OXYGEN CONSUMPTION INCREASED ( 1 FDA reports)
OXYGEN SUPPLEMENTATION ( 1 FDA reports)
PALATAL DISORDER ( 1 FDA reports)
PANCREATIC CARCINOMA ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PANIC DISORDER WITH AGORAPHOBIA ( 1 FDA reports)
PANIC REACTION ( 1 FDA reports)
PANNICULITIS ( 1 FDA reports)
PAPILLOMA VIRAL INFECTION ( 1 FDA reports)
PARANOID PERSONALITY DISORDER ( 1 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PAROTID GLAND ENLARGEMENT ( 1 FDA reports)
PAROXYSMAL NOCTURNAL HAEMOGLOBINURIA ( 1 FDA reports)
PELVIC FLUID COLLECTION ( 1 FDA reports)
PELVIC VENOUS THROMBOSIS ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PERIORBITAL HAEMATOMA ( 1 FDA reports)
PERIORBITAL OEDEMA ( 1 FDA reports)
PERIPHERAL NERVE DECOMPRESSION ( 1 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 1 FDA reports)
PERITONEAL HAEMORRHAGE ( 1 FDA reports)
PERNICIOUS ANAEMIA ( 1 FDA reports)
PHAEOCHROMOCYTOMA ( 1 FDA reports)
PHANTOM PAIN ( 1 FDA reports)
PHARYNGEAL ERYTHEMA ( 1 FDA reports)
PHARYNGEAL NEOPLASM ( 1 FDA reports)
PHARYNGEAL ULCERATION ( 1 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 1 FDA reports)
PLASMACYTOMA ( 1 FDA reports)
PLEURAL CALCIFICATION ( 1 FDA reports)
PLEURAL DISORDER ( 1 FDA reports)
PNEUMOCONIOSIS ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
PNEUMONIA BACTERIAL ( 1 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 1 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 1 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 1 FDA reports)
POLYMYALGIA RHEUMATICA ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 1 FDA reports)
POLYTRAUMATISM ( 1 FDA reports)
POOR PERSONAL HYGIENE ( 1 FDA reports)
POOR QUALITY SLEEP ( 1 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 1 FDA reports)
POST HERPETIC NEURALGIA ( 1 FDA reports)
POST PROCEDURAL BILE LEAK ( 1 FDA reports)
POST PROCEDURAL CELLULITIS ( 1 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 1 FDA reports)
POSTICTAL STATE ( 1 FDA reports)
POSTOPERATIVE ADHESION ( 1 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 1 FDA reports)
PREMATURE MENOPAUSE ( 1 FDA reports)
PRESSURE OF SPEECH ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PRODUCT LABEL CONFUSION ( 1 FDA reports)
PRODUCT MEASURED POTENCY ISSUE ( 1 FDA reports)
PRODUCT PACKAGING ISSUE ( 1 FDA reports)
PROGESTERONE DECREASED ( 1 FDA reports)
PROSTATE CANCER METASTATIC ( 1 FDA reports)
PROSTATE CANCER STAGE II ( 1 FDA reports)
PROSTATIC INTRAEPITHELIAL NEOPLASIA ( 1 FDA reports)
PROTEIN S INCREASED ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PROTRUSION TONGUE ( 1 FDA reports)
PSEUDOCYST ( 1 FDA reports)
PSEUDOMONAS BRONCHITIS ( 1 FDA reports)
PSORIATIC ARTHROPATHY ( 1 FDA reports)
PSYCHOLOGICAL TRAUMA ( 1 FDA reports)
PSYCHOSOMATIC DISEASE ( 1 FDA reports)
PTOSIS REPAIR ( 1 FDA reports)
PUBIS FRACTURE ( 1 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 1 FDA reports)
PULMONARY BULLA ( 1 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
PULMONARY MASS ( 1 FDA reports)
PULSE ABNORMAL ( 1 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 1 FDA reports)
PUNCTATE KERATITIS ( 1 FDA reports)
PYLORIC STENOSIS ( 1 FDA reports)
RADIUS FRACTURE ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RASH VESICULAR ( 1 FDA reports)
REACTION TO COLOURING ( 1 FDA reports)
REFLUX OESOPHAGITIS ( 1 FDA reports)
REGURGITATION ( 1 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL ATROPHY ( 1 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 1 FDA reports)
RENAL MASS ( 1 FDA reports)
REOCCLUSION ( 1 FDA reports)
RESPIRATION ABNORMAL ( 1 FDA reports)
RESPIRATORY ACIDOSIS ( 1 FDA reports)
RETINAL ARTERY THROMBOSIS ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
RETINAL TEAR ( 1 FDA reports)
RETINAL VASCULAR THROMBOSIS ( 1 FDA reports)
RETINAL VEIN THROMBOSIS ( 1 FDA reports)
RHEUMATIC FEVER ( 1 FDA reports)
RHONCHI ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
ROSACEA ( 1 FDA reports)
SALIVARY GLAND CALCULUS ( 1 FDA reports)
SALIVARY GLAND PAIN ( 1 FDA reports)
SALPINGO-OOPHORECTOMY UNILATERAL ( 1 FDA reports)
SARCOMA ( 1 FDA reports)
SCLERODERMA ( 1 FDA reports)
SEASONAL ALLERGY ( 1 FDA reports)
SEBORRHOEIC DERMATITIS ( 1 FDA reports)
SENSATION OF PRESSURE ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SEPSIS SYNDROME ( 1 FDA reports)
SERUM FERRITIN DECREASED ( 1 FDA reports)
SEXUAL DYSFUNCTION ( 1 FDA reports)
SHOCK HYPOGLYCAEMIC ( 1 FDA reports)
SHOULDER PAIN ( 1 FDA reports)
SIMILAR REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
SIMPLE PARTIAL SEIZURES ( 1 FDA reports)
SINOBRONCHITIS ( 1 FDA reports)
SKIN HYPERPIGMENTATION ( 1 FDA reports)
SKIN INFECTION ( 1 FDA reports)
SKIN PAPILLOMA ( 1 FDA reports)
SKIN PLAQUE ( 1 FDA reports)
SKIN TEST POSITIVE ( 1 FDA reports)
SLEEP DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 1 FDA reports)
SMALL INTESTINAL STENOSIS ( 1 FDA reports)
SMALL INTESTINE ULCER ( 1 FDA reports)
SOCIAL PROBLEM ( 1 FDA reports)
SOFT TISSUE INFECTION ( 1 FDA reports)
SPINAL CORD DRAINAGE ( 1 FDA reports)
SPINAL DECOMPRESSION ( 1 FDA reports)
SPINAL PAIN ( 1 FDA reports)
SPLEEN DISORDER ( 1 FDA reports)
SPLENIC LESION ( 1 FDA reports)
SPUTUM ABNORMAL ( 1 FDA reports)
SPUTUM PURULENT ( 1 FDA reports)
STATUS ASTHMATICUS ( 1 FDA reports)
STENOTROPHOMONAS INFECTION ( 1 FDA reports)
STEREOTYPY ( 1 FDA reports)
STRABISMUS ( 1 FDA reports)
STRESS ULCER ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 1 FDA reports)
SUDDEN CARDIAC DEATH ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
TEMPERATURE INTOLERANCE ( 1 FDA reports)
TENDON CALCIFICATION ( 1 FDA reports)
TERMINAL INSOMNIA ( 1 FDA reports)
TESTICULAR MASS ( 1 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 1 FDA reports)
THERAPY CESSATION ( 1 FDA reports)
THROMBOCYTHAEMIA ( 1 FDA reports)
THROMBOPHLEBITIS ( 1 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 1 FDA reports)
TINEA VERSICOLOUR ( 1 FDA reports)
TONGUE BLISTERING ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TONGUE OEDEMA ( 1 FDA reports)
TONGUE SPASM ( 1 FDA reports)
TONSILLAR DISORDER ( 1 FDA reports)
TONSILLAR HYPERTROPHY ( 1 FDA reports)
TONSILLITIS ( 1 FDA reports)
TOOTH DISCOLOURATION ( 1 FDA reports)
TOOTH INJURY ( 1 FDA reports)
TRANSFUSION ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TRI-IODOTHYRONINE DECREASED ( 1 FDA reports)
TRIGEMINAL NEURALGIA ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
TUNNEL VISION ( 1 FDA reports)
TYPE III IMMUNE COMPLEX MEDIATED REACTION ( 1 FDA reports)
ULCER HAEMORRHAGE ( 1 FDA reports)
ULNA FRACTURE ( 1 FDA reports)
UNINTENDED PREGNANCY ( 1 FDA reports)
URAEMIC ENCEPHALOPATHY ( 1 FDA reports)
URETERIC OBSTRUCTION ( 1 FDA reports)
URINARY HESITATION ( 1 FDA reports)
URINARY SEDIMENT PRESENT ( 1 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 1 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 1 FDA reports)
UTERINE CANCER ( 1 FDA reports)
UTERINE POLYP ( 1 FDA reports)
UVULITIS ( 1 FDA reports)
VAGINAL DISORDER ( 1 FDA reports)
VAGINAL INFECTION ( 1 FDA reports)
VAGINITIS ( 1 FDA reports)
VARICELLA ( 1 FDA reports)
VASCULAR GRAFT OCCLUSION ( 1 FDA reports)
VASCULAR GRAFT THROMBOSIS ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VASOCONSTRICTION ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 1 FDA reports)
VERTEBRAL INJURY ( 1 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 1 FDA reports)
VISCERAL CONGESTION ( 1 FDA reports)
VOCAL CORD DISORDER ( 1 FDA reports)
VULVITIS ( 1 FDA reports)
WHITE BLOOD CELL DISORDER ( 1 FDA reports)
WOUND ABSCESS ( 1 FDA reports)
WOUND COMPLICATION ( 1 FDA reports)
WOUND NECROSIS ( 1 FDA reports)
WRIST DEFORMITY ( 1 FDA reports)
X-RAY ABNORMAL ( 1 FDA reports)
YAWNING ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use