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

DYSPNOEA ( 1810 FDA reports)
DIZZINESS ( 1487 FDA reports)
NAUSEA ( 1355 FDA reports)
ANAPHYLACTIC REACTION ( 1311 FDA reports)
RASH ( 1208 FDA reports)
HYPERSENSITIVITY ( 1109 FDA reports)
ANXIETY ( 1085 FDA reports)
PAIN ( 1068 FDA reports)
DIARRHOEA ( 1018 FDA reports)
PRURITUS ( 959 FDA reports)
VOMITING ( 938 FDA reports)
ARTHRALGIA ( 881 FDA reports)
URTICARIA ( 880 FDA reports)
PAIN IN EXTREMITY ( 791 FDA reports)
ASTHENIA ( 785 FDA reports)
HEADACHE ( 757 FDA reports)
HYPOAESTHESIA ( 750 FDA reports)
OEDEMA PERIPHERAL ( 748 FDA reports)
PARAESTHESIA ( 696 FDA reports)
PYREXIA ( 669 FDA reports)
ERYTHEMA ( 666 FDA reports)
FATIGUE ( 661 FDA reports)
PNEUMONIA ( 647 FDA reports)
BACK PAIN ( 584 FDA reports)
HYPOTENSION ( 580 FDA reports)
CHEST PAIN ( 568 FDA reports)
PALPITATIONS ( 534 FDA reports)
ANAEMIA ( 522 FDA reports)
ABDOMINAL PAIN ( 519 FDA reports)
INSOMNIA ( 509 FDA reports)
LOSS OF CONSCIOUSNESS ( 502 FDA reports)
TREMOR ( 499 FDA reports)
SWELLING FACE ( 469 FDA reports)
FALL ( 444 FDA reports)
INJURY ( 442 FDA reports)
MUSCULAR WEAKNESS ( 439 FDA reports)
ANAPHYLACTIC SHOCK ( 435 FDA reports)
OSTEONECROSIS OF JAW ( 432 FDA reports)
DEPRESSION ( 420 FDA reports)
TENDONITIS ( 420 FDA reports)
COUGH ( 418 FDA reports)
RENAL FAILURE ( 405 FDA reports)
CONFUSIONAL STATE ( 403 FDA reports)
MALAISE ( 400 FDA reports)
BONE DISORDER ( 394 FDA reports)
FEELING ABNORMAL ( 377 FDA reports)
SYNCOPE ( 373 FDA reports)
MYALGIA ( 363 FDA reports)
SINUSITIS ( 361 FDA reports)
WEIGHT DECREASED ( 360 FDA reports)
GAIT DISTURBANCE ( 358 FDA reports)
SWELLING ( 358 FDA reports)
HYPERHIDROSIS ( 357 FDA reports)
OSTEOARTHRITIS ( 355 FDA reports)
TENDON RUPTURE ( 355 FDA reports)
TACHYCARDIA ( 347 FDA reports)
HEART RATE INCREASED ( 346 FDA reports)
PAIN IN JAW ( 345 FDA reports)
HYPERTENSION ( 328 FDA reports)
DEHYDRATION ( 324 FDA reports)
BRONCHITIS ( 314 FDA reports)
NEUROPATHY PERIPHERAL ( 314 FDA reports)
CONVULSION ( 311 FDA reports)
RENAL FAILURE ACUTE ( 307 FDA reports)
DYSPHAGIA ( 305 FDA reports)
PLEURAL EFFUSION ( 304 FDA reports)
MUSCLE SPASMS ( 299 FDA reports)
ABDOMINAL PAIN UPPER ( 297 FDA reports)
OSTEOMYELITIS ( 297 FDA reports)
CHEST DISCOMFORT ( 291 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 288 FDA reports)
EMOTIONAL DISTRESS ( 288 FDA reports)
DEATH ( 285 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 283 FDA reports)
ATRIAL FIBRILLATION ( 277 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 277 FDA reports)
BLOOD PRESSURE DECREASED ( 274 FDA reports)
LIP SWELLING ( 274 FDA reports)
PULMONARY EMBOLISM ( 260 FDA reports)
HALLUCINATION ( 255 FDA reports)
MUSCULOSKELETAL PAIN ( 250 FDA reports)
SPINAL OSTEOARTHRITIS ( 250 FDA reports)
INFECTION ( 249 FDA reports)
SEPSIS ( 247 FDA reports)
JOINT SWELLING ( 246 FDA reports)
SWOLLEN TONGUE ( 245 FDA reports)
CONSTIPATION ( 242 FDA reports)
CARDIAC ARREST ( 241 FDA reports)
CHILLS ( 240 FDA reports)
VISION BLURRED ( 240 FDA reports)
ATELECTASIS ( 237 FDA reports)
DRY MOUTH ( 234 FDA reports)
BURNING SENSATION ( 227 FDA reports)
URINARY TRACT INFECTION ( 227 FDA reports)
THROAT TIGHTNESS ( 226 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 223 FDA reports)
MYOCARDIAL INFARCTION ( 223 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 222 FDA reports)
RASH GENERALISED ( 222 FDA reports)
DEEP VEIN THROMBOSIS ( 219 FDA reports)
THROMBOCYTOPENIA ( 219 FDA reports)
ANHEDONIA ( 217 FDA reports)
LYMPHADENOPATHY ( 217 FDA reports)
TENDON PAIN ( 213 FDA reports)
NERVOUSNESS ( 211 FDA reports)
TOOTH EXTRACTION ( 211 FDA reports)
FLUSHING ( 209 FDA reports)
CEREBROVASCULAR ACCIDENT ( 208 FDA reports)
BLOOD PRESSURE INCREASED ( 206 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 204 FDA reports)
CELLULITIS ( 202 FDA reports)
NECK PAIN ( 200 FDA reports)
PHARYNGEAL OEDEMA ( 199 FDA reports)
RESPIRATORY FAILURE ( 198 FDA reports)
IMPAIRED HEALING ( 196 FDA reports)
OSTEOPOROSIS ( 195 FDA reports)
PRURITUS GENERALISED ( 195 FDA reports)
ASTHMA ( 191 FDA reports)
DYSPEPSIA ( 191 FDA reports)
ABDOMINAL DISCOMFORT ( 190 FDA reports)
CONTUSION ( 190 FDA reports)
DECREASED APPETITE ( 190 FDA reports)
ROTATOR CUFF SYNDROME ( 190 FDA reports)
DRUG HYPERSENSITIVITY ( 189 FDA reports)
DYSGEUSIA ( 184 FDA reports)
TOOTH DISORDER ( 182 FDA reports)
DENTAL CARIES ( 181 FDA reports)
HYPOGLYCAEMIA ( 180 FDA reports)
UNEVALUABLE EVENT ( 180 FDA reports)
SOMNOLENCE ( 179 FDA reports)
HAEMORRHOIDS ( 178 FDA reports)
ARRHYTHMIA ( 176 FDA reports)
EXOSTOSIS ( 176 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 172 FDA reports)
ABASIA ( 169 FDA reports)
PANCYTOPENIA ( 168 FDA reports)
DEFORMITY ( 167 FDA reports)
OSTEOPENIA ( 166 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 163 FDA reports)
RIB FRACTURE ( 163 FDA reports)
BLOOD GLUCOSE INCREASED ( 160 FDA reports)
HEPATIC ENZYME INCREASED ( 159 FDA reports)
DRUG INTERACTION ( 158 FDA reports)
BLOOD CREATININE INCREASED ( 157 FDA reports)
METASTASES TO BONE ( 157 FDA reports)
VISUAL IMPAIRMENT ( 157 FDA reports)
BONE PAIN ( 156 FDA reports)
SPEECH DISORDER ( 156 FDA reports)
OSTEONECROSIS ( 155 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 154 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 152 FDA reports)
WHEEZING ( 152 FDA reports)
HEPATIC FAILURE ( 151 FDA reports)
MITRAL VALVE INCOMPETENCE ( 151 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 150 FDA reports)
EYE PAIN ( 149 FDA reports)
NEURALGIA ( 149 FDA reports)
DISORIENTATION ( 148 FDA reports)
JAUNDICE ( 148 FDA reports)
NERVOUS SYSTEM DISORDER ( 147 FDA reports)
RESPIRATORY DISTRESS ( 147 FDA reports)
CLOSTRIDIAL INFECTION ( 146 FDA reports)
HYPOKALAEMIA ( 146 FDA reports)
CONDITION AGGRAVATED ( 144 FDA reports)
ABDOMINAL DISTENSION ( 142 FDA reports)
HYPOXIA ( 142 FDA reports)
EYE SWELLING ( 141 FDA reports)
NEUTROPENIA ( 141 FDA reports)
EAR PAIN ( 140 FDA reports)
TENDON DISORDER ( 140 FDA reports)
ECONOMIC PROBLEM ( 139 FDA reports)
FEELING HOT ( 139 FDA reports)
RASH MACULAR ( 139 FDA reports)
GASTRITIS ( 138 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 137 FDA reports)
VERTIGO ( 136 FDA reports)
TINNITUS ( 135 FDA reports)
CORONARY ARTERY DISEASE ( 134 FDA reports)
INFLAMMATION ( 134 FDA reports)
RASH ERYTHEMATOUS ( 133 FDA reports)
AMNESIA ( 130 FDA reports)
BURSITIS ( 130 FDA reports)
MULTI-ORGAN FAILURE ( 130 FDA reports)
PULMONARY OEDEMA ( 130 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 129 FDA reports)
DRUG INEFFECTIVE ( 129 FDA reports)
STEVENS-JOHNSON SYNDROME ( 129 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 128 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 128 FDA reports)
DIVERTICULUM ( 127 FDA reports)
HEPATIC STEATOSIS ( 127 FDA reports)
GENERALISED ERYTHEMA ( 125 FDA reports)
SUICIDAL IDEATION ( 125 FDA reports)
OROPHARYNGEAL PAIN ( 124 FDA reports)
TOOTH ABSCESS ( 123 FDA reports)
BRADYCARDIA ( 122 FDA reports)
HYPERLIPIDAEMIA ( 122 FDA reports)
MOBILITY DECREASED ( 122 FDA reports)
ANGIOEDEMA ( 121 FDA reports)
BALANCE DISORDER ( 121 FDA reports)
SLEEP APNOEA SYNDROME ( 121 FDA reports)
PURULENT DISCHARGE ( 120 FDA reports)
TOOTH LOSS ( 120 FDA reports)
ARTHRITIS ( 119 FDA reports)
MOUTH ULCERATION ( 119 FDA reports)
RECTAL HAEMORRHAGE ( 119 FDA reports)
PANIC ATTACK ( 118 FDA reports)
AGITATION ( 117 FDA reports)
CHOLELITHIASIS ( 117 FDA reports)
DEBRIDEMENT ( 117 FDA reports)
GINGIVITIS ( 116 FDA reports)
HIATUS HERNIA ( 116 FDA reports)
HYPOAESTHESIA ORAL ( 116 FDA reports)
HYPONATRAEMIA ( 115 FDA reports)
STOMATITIS ( 115 FDA reports)
ADVERSE EVENT ( 114 FDA reports)
CARDIOMEGALY ( 114 FDA reports)
STAPHYLOCOCCAL INFECTION ( 114 FDA reports)
SCOLIOSIS ( 113 FDA reports)
INTERSTITIAL LUNG DISEASE ( 111 FDA reports)
LETHARGY ( 111 FDA reports)
OSTEOLYSIS ( 111 FDA reports)
TOOTHACHE ( 110 FDA reports)
CATARACT ( 109 FDA reports)
DIABETES MELLITUS ( 109 FDA reports)
PRIMARY SEQUESTRUM ( 109 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 109 FDA reports)
APHASIA ( 108 FDA reports)
CARDIAC FAILURE ( 108 FDA reports)
MUSCLE TWITCHING ( 108 FDA reports)
DYSURIA ( 107 FDA reports)
HYPERGLYCAEMIA ( 107 FDA reports)
OEDEMA ( 107 FDA reports)
RASH PRURITIC ( 107 FDA reports)
DEAFNESS ( 106 FDA reports)
ENDODONTIC PROCEDURE ( 106 FDA reports)
MEMORY IMPAIRMENT ( 106 FDA reports)
NASAL CONGESTION ( 106 FDA reports)
TENDERNESS ( 106 FDA reports)
CANDIDIASIS ( 104 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 104 FDA reports)
HEPATITIS ( 104 FDA reports)
DISTURBANCE IN ATTENTION ( 103 FDA reports)
EPISTAXIS ( 103 FDA reports)
FEAR ( 102 FDA reports)
GINGIVAL PAIN ( 102 FDA reports)
PERIODONTITIS ( 102 FDA reports)
RESTLESSNESS ( 102 FDA reports)
LUNG INFILTRATION ( 101 FDA reports)
MIGRAINE ( 101 FDA reports)
VISUAL ACUITY REDUCED ( 101 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 100 FDA reports)
HAEMATOCHEZIA ( 100 FDA reports)
HEART RATE IRREGULAR ( 100 FDA reports)
METASTASES TO LIVER ( 100 FDA reports)
SHOCK ( 100 FDA reports)
ORAL PAIN ( 99 FDA reports)
PANCREATITIS ( 99 FDA reports)
TORSADE DE POINTES ( 99 FDA reports)
CYANOSIS ( 98 FDA reports)
BLOOD BILIRUBIN INCREASED ( 97 FDA reports)
CHRONIC SINUSITIS ( 97 FDA reports)
RENAL FAILURE CHRONIC ( 97 FDA reports)
ADVERSE DRUG REACTION ( 96 FDA reports)
DYSSTASIA ( 96 FDA reports)
HAEMOPTYSIS ( 96 FDA reports)
FISTULA ( 95 FDA reports)
HYPERKALAEMIA ( 95 FDA reports)
LUMBAR SPINAL STENOSIS ( 95 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 95 FDA reports)
PARAESTHESIA ORAL ( 95 FDA reports)
PLATELET COUNT DECREASED ( 95 FDA reports)
ARTHROPATHY ( 94 FDA reports)
CARDIO-RESPIRATORY ARREST ( 94 FDA reports)
FEBRILE NEUTROPENIA ( 94 FDA reports)
WEIGHT INCREASED ( 94 FDA reports)
GINGIVAL BLEEDING ( 93 FDA reports)
MENTAL STATUS CHANGES ( 93 FDA reports)
HAEMATURIA ( 92 FDA reports)
RENAL CYST ( 92 FDA reports)
DIPLOPIA ( 91 FDA reports)
HAEMOGLOBIN DECREASED ( 91 FDA reports)
NIGHT SWEATS ( 91 FDA reports)
URINARY RETENTION ( 91 FDA reports)
BLINDNESS ( 90 FDA reports)
DISABILITY ( 90 FDA reports)
PHOTOPHOBIA ( 90 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 89 FDA reports)
BLISTER ( 88 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 88 FDA reports)
CARDIAC DISORDER ( 88 FDA reports)
HYPOPHAGIA ( 88 FDA reports)
PERIODONTAL DISEASE ( 88 FDA reports)
MULTIPLE INJURIES ( 87 FDA reports)
CIRCULATORY COLLAPSE ( 86 FDA reports)
COMA ( 86 FDA reports)
LIVER DISORDER ( 86 FDA reports)
MULTIPLE MYELOMA ( 86 FDA reports)
NEOPLASM MALIGNANT ( 86 FDA reports)
SLEEP DISORDER ( 86 FDA reports)
SOFT TISSUE DISORDER ( 85 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 84 FDA reports)
AGEUSIA ( 84 FDA reports)
DELIRIUM ( 84 FDA reports)
LOOSE TOOTH ( 84 FDA reports)
RESPIRATORY ARREST ( 84 FDA reports)
RHABDOMYOLYSIS ( 84 FDA reports)
CHROMATURIA ( 83 FDA reports)
LEUKOCYTOSIS ( 83 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 83 FDA reports)
ANOREXIA ( 82 FDA reports)
BODY TEMPERATURE INCREASED ( 82 FDA reports)
BONE DEBRIDEMENT ( 82 FDA reports)
LEUKOPENIA ( 82 FDA reports)
ORAL DISORDER ( 82 FDA reports)
URINARY INCONTINENCE ( 82 FDA reports)
DYSPNOEA EXERTIONAL ( 81 FDA reports)
EMPHYSEMA ( 81 FDA reports)
FACE OEDEMA ( 81 FDA reports)
MENTAL DISORDER ( 81 FDA reports)
OCULAR HYPERAEMIA ( 81 FDA reports)
OXYGEN SATURATION DECREASED ( 81 FDA reports)
PULMONARY HYPERTENSION ( 81 FDA reports)
SKIN LESION ( 81 FDA reports)
STRESS ( 80 FDA reports)
CRYING ( 79 FDA reports)
FEMUR FRACTURE ( 79 FDA reports)
HERPES ZOSTER ( 79 FDA reports)
SPINAL COLUMN STENOSIS ( 79 FDA reports)
DISEASE PROGRESSION ( 78 FDA reports)
FUNGAL INFECTION ( 78 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 77 FDA reports)
SCAR ( 77 FDA reports)
VASCULITIS ( 77 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 77 FDA reports)
COMPRESSION FRACTURE ( 76 FDA reports)
GENERALISED OEDEMA ( 76 FDA reports)
SYNOVIAL CYST ( 76 FDA reports)
LUNG DISORDER ( 75 FDA reports)
NO ADVERSE EVENT ( 75 FDA reports)
PARANOIA ( 75 FDA reports)
BONE LESION ( 74 FDA reports)
COLITIS ( 74 FDA reports)
SKIN DISCOLOURATION ( 74 FDA reports)
HEPATIC CYST ( 73 FDA reports)
PHYSICAL DISABILITY ( 73 FDA reports)
SKIN EXFOLIATION ( 73 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 73 FDA reports)
CARPAL TUNNEL SYNDROME ( 72 FDA reports)
DISCOMFORT ( 72 FDA reports)
DRUG TOXICITY ( 72 FDA reports)
EATING DISORDER ( 72 FDA reports)
GINGIVAL SWELLING ( 72 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 72 FDA reports)
METASTASES TO LUNG ( 72 FDA reports)
OSTEITIS ( 72 FDA reports)
HAEMANGIOMA ( 71 FDA reports)
HYPERKERATOSIS ( 71 FDA reports)
MASTICATION DISORDER ( 71 FDA reports)
ORAL CAVITY FISTULA ( 71 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 71 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 70 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 70 FDA reports)
DECREASED INTEREST ( 70 FDA reports)
DYSPHONIA ( 70 FDA reports)
RASH MACULO-PAPULAR ( 70 FDA reports)
RHINORRHOEA ( 70 FDA reports)
RENAL IMPAIRMENT ( 69 FDA reports)
EXPOSED BONE IN JAW ( 68 FDA reports)
VENTRICULAR TACHYCARDIA ( 68 FDA reports)
ALOPECIA ( 67 FDA reports)
BACTERIAL INFECTION ( 67 FDA reports)
FACIAL PAIN ( 67 FDA reports)
IMPAIRED WORK ABILITY ( 67 FDA reports)
ORAL CANDIDIASIS ( 67 FDA reports)
SINUS TACHYCARDIA ( 67 FDA reports)
ABNORMAL BEHAVIOUR ( 66 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 66 FDA reports)
COORDINATION ABNORMAL ( 66 FDA reports)
HOT FLUSH ( 66 FDA reports)
JOINT DISLOCATION ( 66 FDA reports)
PSYCHOTIC DISORDER ( 66 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 66 FDA reports)
CARDIOMYOPATHY ( 65 FDA reports)
ROAD TRAFFIC ACCIDENT ( 65 FDA reports)
INFLUENZA ( 64 FDA reports)
NIGHTMARE ( 64 FDA reports)
OBESITY ( 64 FDA reports)
PRESYNCOPE ( 64 FDA reports)
RESPIRATORY DISORDER ( 64 FDA reports)
RHINITIS ALLERGIC ( 64 FDA reports)
ANGINA PECTORIS ( 63 FDA reports)
ANOSMIA ( 63 FDA reports)
AORTIC ANEURYSM ( 63 FDA reports)
GASTROINTESTINAL DISORDER ( 63 FDA reports)
MENISCUS LESION ( 63 FDA reports)
SURGERY ( 63 FDA reports)
TOOTH INFECTION ( 63 FDA reports)
VENTRICULAR FIBRILLATION ( 63 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 62 FDA reports)
COAGULOPATHY ( 62 FDA reports)
DYSARTHRIA ( 62 FDA reports)
FLATULENCE ( 62 FDA reports)
FOOT FRACTURE ( 62 FDA reports)
HAND FRACTURE ( 62 FDA reports)
HEPATOTOXICITY ( 62 FDA reports)
HIP FRACTURE ( 62 FDA reports)
MUCOSAL INFLAMMATION ( 62 FDA reports)
RHINITIS ( 62 FDA reports)
SEPTIC SHOCK ( 62 FDA reports)
ACTINOMYCOSIS ( 61 FDA reports)
DYSKINESIA ( 61 FDA reports)
NASOPHARYNGITIS ( 61 FDA reports)
PETECHIAE ( 61 FDA reports)
ASCITES ( 60 FDA reports)
BRONCHOPNEUMONIA ( 60 FDA reports)
DRY EYE ( 60 FDA reports)
GLOSSITIS ( 60 FDA reports)
OEDEMA MOUTH ( 60 FDA reports)
PULSE ABSENT ( 60 FDA reports)
SINUS HEADACHE ( 60 FDA reports)
SKIN DISORDER ( 60 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 60 FDA reports)
ASPIRATION ( 59 FDA reports)
ECZEMA ( 59 FDA reports)
FEELING JITTERY ( 59 FDA reports)
PALLOR ( 59 FDA reports)
SKIN ULCER ( 59 FDA reports)
FAECAL INCONTINENCE ( 58 FDA reports)
IRRITABLE BOWEL SYNDROME ( 58 FDA reports)
KYPHOSIS ( 58 FDA reports)
SPINAL COMPRESSION FRACTURE ( 58 FDA reports)
BLOOD CALCIUM DECREASED ( 57 FDA reports)
BLOOD UREA INCREASED ( 57 FDA reports)
BONE LOSS ( 57 FDA reports)
DENTURE WEARER ( 57 FDA reports)
HEART RATE DECREASED ( 57 FDA reports)
HUMERUS FRACTURE ( 57 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 57 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 57 FDA reports)
OSTEOSCLEROSIS ( 57 FDA reports)
PROTHROMBIN TIME PROLONGED ( 57 FDA reports)
UVEITIS ( 57 FDA reports)
COLONIC POLYP ( 56 FDA reports)
EMOTIONAL DISORDER ( 56 FDA reports)
HAEMATOCRIT DECREASED ( 56 FDA reports)
METABOLIC ACIDOSIS ( 56 FDA reports)
PLANTAR FASCIITIS ( 56 FDA reports)
BLOOD POTASSIUM DECREASED ( 55 FDA reports)
BONE OPERATION ( 55 FDA reports)
HYPERCHOLESTEROLAEMIA ( 55 FDA reports)
JOINT EFFUSION ( 55 FDA reports)
MOVEMENT DISORDER ( 55 FDA reports)
PARALYSIS ( 55 FDA reports)
COLITIS ULCERATIVE ( 54 FDA reports)
DERMATITIS ( 54 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 54 FDA reports)
DYSLIPIDAEMIA ( 54 FDA reports)
LACERATION ( 54 FDA reports)
POLLAKIURIA ( 54 FDA reports)
PRODUCTIVE COUGH ( 54 FDA reports)
SENSITIVITY OF TEETH ( 54 FDA reports)
UNRESPONSIVE TO STIMULI ( 54 FDA reports)
CARDIOVASCULAR DISORDER ( 53 FDA reports)
COLD SWEAT ( 53 FDA reports)
ENCEPHALOPATHY ( 53 FDA reports)
HAEMORRHAGE ( 53 FDA reports)
JOINT INJURY ( 53 FDA reports)
MYDRIASIS ( 53 FDA reports)
POLYNEUROPATHY ( 53 FDA reports)
SKIN BURNING SENSATION ( 53 FDA reports)
TOOTH FRACTURE ( 53 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 52 FDA reports)
CARDIAC MURMUR ( 52 FDA reports)
CYSTITIS ( 52 FDA reports)
FEELING COLD ( 52 FDA reports)
GROIN PAIN ( 52 FDA reports)
PHOTOSENSITIVITY REACTION ( 52 FDA reports)
TONGUE DISCOLOURATION ( 52 FDA reports)
BLOOD GLUCOSE DECREASED ( 51 FDA reports)
DENTAL OPERATION ( 51 FDA reports)
DIVERTICULITIS ( 51 FDA reports)
FOOT DEFORMITY ( 51 FDA reports)
INFLUENZA LIKE ILLNESS ( 51 FDA reports)
JOINT CREPITATION ( 51 FDA reports)
LUNG NEOPLASM ( 51 FDA reports)
SINUS CONGESTION ( 51 FDA reports)
THROMBOSIS ( 51 FDA reports)
ACUTE RESPIRATORY FAILURE ( 50 FDA reports)
AGRANULOCYTOSIS ( 50 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 50 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 50 FDA reports)
HYPERCALCAEMIA ( 50 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 50 FDA reports)
LOCAL SWELLING ( 50 FDA reports)
TYPE 2 DIABETES MELLITUS ( 50 FDA reports)
VISUAL DISTURBANCE ( 50 FDA reports)
BLOOD URINE PRESENT ( 49 FDA reports)
BONE DENSITY DECREASED ( 49 FDA reports)
BREATH ODOUR ( 49 FDA reports)
DEMENTIA ( 49 FDA reports)
EAR DISCOMFORT ( 49 FDA reports)
ENTERITIS ( 49 FDA reports)
FACIAL BONES FRACTURE ( 49 FDA reports)
HAEMATOMA ( 49 FDA reports)
HYPERTONIC BLADDER ( 49 FDA reports)
ILL-DEFINED DISORDER ( 49 FDA reports)
JAW OPERATION ( 49 FDA reports)
MELAENA ( 49 FDA reports)
SPONDYLOLISTHESIS ( 49 FDA reports)
DERMATITIS ALLERGIC ( 48 FDA reports)
ERECTILE DYSFUNCTION ( 48 FDA reports)
FAECES DISCOLOURED ( 48 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 48 FDA reports)
ORTHOSTATIC HYPOTENSION ( 48 FDA reports)
DIVERTICULUM INTESTINAL ( 47 FDA reports)
EAR DISORDER ( 47 FDA reports)
HEAD INJURY ( 47 FDA reports)
LIGAMENT RUPTURE ( 47 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 47 FDA reports)
TONGUE ULCERATION ( 47 FDA reports)
UTERINE LEIOMYOMA ( 47 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 46 FDA reports)
EYE IRRITATION ( 46 FDA reports)
LIMB DISCOMFORT ( 46 FDA reports)
MITRAL VALVE PROLAPSE ( 46 FDA reports)
OESOPHAGITIS ( 46 FDA reports)
OLIGURIA ( 46 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 46 FDA reports)
TREATMENT NONCOMPLIANCE ( 46 FDA reports)
ARTERIOSCLEROSIS ( 45 FDA reports)
BACK DISORDER ( 45 FDA reports)
DEPRESSED MOOD ( 45 FDA reports)
EYE DISORDER ( 45 FDA reports)
FIBROSIS ( 45 FDA reports)
GINGIVAL INFECTION ( 45 FDA reports)
MENTAL IMPAIRMENT ( 45 FDA reports)
PERIPHERAL COLDNESS ( 45 FDA reports)
SPINAL DISORDER ( 45 FDA reports)
STRESS FRACTURE ( 45 FDA reports)
THINKING ABNORMAL ( 45 FDA reports)
THROAT IRRITATION ( 45 FDA reports)
ULCER ( 45 FDA reports)
ABSCESS ( 44 FDA reports)
BLOOD SODIUM DECREASED ( 44 FDA reports)
BRONCHOSPASM ( 44 FDA reports)
CHOLECYSTITIS ( 44 FDA reports)
HAEMOLYTIC ANAEMIA ( 44 FDA reports)
LUMBAR RADICULOPATHY ( 44 FDA reports)
MALNUTRITION ( 44 FDA reports)
METASTASES TO SPINE ( 44 FDA reports)
PNEUMONITIS ( 44 FDA reports)
PROTEINURIA ( 44 FDA reports)
TENDON INJURY ( 44 FDA reports)
DIALYSIS ( 43 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 43 FDA reports)
GYNAECOMASTIA ( 43 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 43 FDA reports)
NEURITIS ( 43 FDA reports)
ORAL DISCOMFORT ( 43 FDA reports)
RESTLESS LEGS SYNDROME ( 43 FDA reports)
TRANSAMINASES INCREASED ( 43 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 42 FDA reports)
ESCHERICHIA INFECTION ( 42 FDA reports)
EXTRASYSTOLES ( 42 FDA reports)
GASTROINTESTINAL PAIN ( 42 FDA reports)
GENITAL HERPES ( 42 FDA reports)
IRIDOCYCLITIS ( 42 FDA reports)
METASTATIC NEOPLASM ( 42 FDA reports)
PROCTALGIA ( 42 FDA reports)
PSEUDOMONAS INFECTION ( 42 FDA reports)
SEQUESTRECTOMY ( 42 FDA reports)
ABNORMAL DREAMS ( 41 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 41 FDA reports)
FLANK PAIN ( 41 FDA reports)
GOUT ( 41 FDA reports)
HALLUCINATION, VISUAL ( 41 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 41 FDA reports)
NEOPLASM ( 41 FDA reports)
ORAL INFECTION ( 41 FDA reports)
SPINAL LAMINECTOMY ( 41 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 40 FDA reports)
JOINT STIFFNESS ( 40 FDA reports)
LOBAR PNEUMONIA ( 40 FDA reports)
ONYCHOMYCOSIS ( 40 FDA reports)
SCIATICA ( 40 FDA reports)
SINUS BRADYCARDIA ( 40 FDA reports)
ENTEROCOCCAL INFECTION ( 39 FDA reports)
EYE INFECTION ( 39 FDA reports)
INCOHERENT ( 39 FDA reports)
INFUSION SITE ERYTHEMA ( 39 FDA reports)
LARYNGITIS ( 39 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 39 FDA reports)
MUSCLE RUPTURE ( 39 FDA reports)
NASAL SEPTUM DEVIATION ( 39 FDA reports)
PANCREATITIS ACUTE ( 39 FDA reports)
VIRAL INFECTION ( 39 FDA reports)
ATROPHY ( 38 FDA reports)
CHOLESTASIS ( 38 FDA reports)
COGNITIVE DISORDER ( 38 FDA reports)
GASTROENTERITIS ( 38 FDA reports)
GLOSSODYNIA ( 38 FDA reports)
HYPOTHYROIDISM ( 38 FDA reports)
PLASMACYTOSIS ( 38 FDA reports)
SENSATION OF HEAVINESS ( 38 FDA reports)
SENSORY LOSS ( 38 FDA reports)
SINUS DISORDER ( 38 FDA reports)
SYNOVITIS ( 38 FDA reports)
VITREOUS FLOATERS ( 38 FDA reports)
APNOEA ( 37 FDA reports)
APPENDICITIS ( 37 FDA reports)
DYSPLASTIC NAEVUS ( 37 FDA reports)
EJECTION FRACTION DECREASED ( 37 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 37 FDA reports)
GRAND MAL CONVULSION ( 37 FDA reports)
HAEMODIALYSIS ( 37 FDA reports)
LUNG NEOPLASM MALIGNANT ( 37 FDA reports)
PLATELET COUNT INCREASED ( 37 FDA reports)
PNEUMOTHORAX ( 37 FDA reports)
PULMONARY FIBROSIS ( 37 FDA reports)
RADICULAR PAIN ( 37 FDA reports)
RHEUMATOID ARTHRITIS ( 37 FDA reports)
SENSORY DISTURBANCE ( 37 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 37 FDA reports)
ACCIDENTAL OVERDOSE ( 36 FDA reports)
APTYALISM ( 36 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 36 FDA reports)
BEDRIDDEN ( 36 FDA reports)
BREAST CANCER ( 36 FDA reports)
EYE PRURITUS ( 36 FDA reports)
FURUNCLE ( 36 FDA reports)
ILEUS ( 36 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 36 FDA reports)
IRRITABILITY ( 36 FDA reports)
OVERDOSE ( 36 FDA reports)
PHOTOPSIA ( 36 FDA reports)
PURULENCE ( 36 FDA reports)
RESPIRATORY RATE INCREASED ( 36 FDA reports)
RHONCHI ( 36 FDA reports)
SCAB ( 36 FDA reports)
AREFLEXIA ( 35 FDA reports)
BONE FRAGMENTATION ( 35 FDA reports)
DELUSION ( 35 FDA reports)
DUODENITIS ( 35 FDA reports)
EAR PRURITUS ( 35 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 35 FDA reports)
HEPATITIS ACUTE ( 35 FDA reports)
HEPATOMEGALY ( 35 FDA reports)
JAW DISORDER ( 35 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 35 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 35 FDA reports)
MOTOR DYSFUNCTION ( 35 FDA reports)
NOCTURIA ( 35 FDA reports)
OSTEITIS DEFORMANS ( 35 FDA reports)
OTITIS MEDIA ( 35 FDA reports)
PANIC REACTION ( 35 FDA reports)
PERONEAL NERVE PALSY ( 35 FDA reports)
PLEURITIC PAIN ( 35 FDA reports)
SEROMA ( 35 FDA reports)
SPINAL CORD COMPRESSION ( 35 FDA reports)
WOUND DEHISCENCE ( 35 FDA reports)
ANAPHYLACTOID REACTION ( 34 FDA reports)
BREAST MASS ( 34 FDA reports)
CERVICAL SPINAL STENOSIS ( 34 FDA reports)
CHOLECYSTITIS CHRONIC ( 34 FDA reports)
DRUG DEPENDENCE ( 34 FDA reports)
ECCHYMOSIS ( 34 FDA reports)
GALLBLADDER DISORDER ( 34 FDA reports)
GANGRENE ( 34 FDA reports)
GASTRIC DISORDER ( 34 FDA reports)
GLAUCOMA ( 34 FDA reports)
HEMIPARESIS ( 34 FDA reports)
ISCHAEMIA ( 34 FDA reports)
MASS ( 34 FDA reports)
MUSCLE TIGHTNESS ( 34 FDA reports)
ODYNOPHAGIA ( 34 FDA reports)
OPEN WOUND ( 34 FDA reports)
SERUM SICKNESS ( 34 FDA reports)
ACUTE HEPATIC FAILURE ( 33 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 33 FDA reports)
BRAIN OEDEMA ( 33 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 33 FDA reports)
DEVICE FAILURE ( 33 FDA reports)
GASTRIC ULCER ( 33 FDA reports)
JAW FRACTURE ( 33 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 33 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 33 FDA reports)
MAJOR DEPRESSION ( 33 FDA reports)
PROCEDURAL PAIN ( 33 FDA reports)
PULMONARY MASS ( 33 FDA reports)
THYROID NEOPLASM ( 33 FDA reports)
AORTIC DISORDER ( 32 FDA reports)
DEVICE RELATED INFECTION ( 32 FDA reports)
DIASTOLIC DYSFUNCTION ( 32 FDA reports)
DRUG ERUPTION ( 32 FDA reports)
EPICONDYLITIS ( 32 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 32 FDA reports)
FACE INJURY ( 32 FDA reports)
GINGIVAL DISORDER ( 32 FDA reports)
HEARING IMPAIRED ( 32 FDA reports)
LACRIMATION INCREASED ( 32 FDA reports)
LIFE EXPECTANCY SHORTENED ( 32 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 32 FDA reports)
NEPHROLITHIASIS ( 32 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 32 FDA reports)
RENAL DISORDER ( 32 FDA reports)
SEBORRHOEIC KERATOSIS ( 32 FDA reports)
TOOTH DEPOSIT ( 32 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 32 FDA reports)
VENTRICULAR HYPERTROPHY ( 32 FDA reports)
VESSEL PUNCTURE SITE REACTION ( 32 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 31 FDA reports)
CEREBRAL HAEMORRHAGE ( 31 FDA reports)
CYST ( 31 FDA reports)
DIFFICULTY IN WALKING ( 31 FDA reports)
DYSPHEMIA ( 31 FDA reports)
ELECTROLYTE IMBALANCE ( 31 FDA reports)
HEPATIC NECROSIS ( 31 FDA reports)
HYPOPHOSPHATAEMIA ( 31 FDA reports)
LEFT ATRIAL DILATATION ( 31 FDA reports)
MUSCLE STRAIN ( 31 FDA reports)
MYOCARDIAL ISCHAEMIA ( 31 FDA reports)
MYOPATHY ( 31 FDA reports)
ORAL SURGERY ( 31 FDA reports)
PIGMENTATION DISORDER ( 31 FDA reports)
PURPURA ( 31 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 31 FDA reports)
THROMBOCYTOSIS ( 31 FDA reports)
TROPONIN INCREASED ( 31 FDA reports)
VAGINAL INFECTION ( 31 FDA reports)
BONE EROSION ( 30 FDA reports)
CERVICAL DYSPLASIA ( 30 FDA reports)
DRY SKIN ( 30 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 30 FDA reports)
EXCORIATION ( 30 FDA reports)
HAEMANGIOMA OF LIVER ( 30 FDA reports)
HYPERVENTILATION ( 30 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 30 FDA reports)
IMPAIRED DRIVING ABILITY ( 30 FDA reports)
METASTASES TO LYMPH NODES ( 30 FDA reports)
NEOPLASM PROGRESSION ( 30 FDA reports)
NEPHRITIS INTERSTITIAL ( 30 FDA reports)
PAROSMIA ( 30 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 30 FDA reports)
RETCHING ( 30 FDA reports)
SKIN REACTION ( 30 FDA reports)
TONGUE DISORDER ( 30 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 30 FDA reports)
BLINDNESS UNILATERAL ( 29 FDA reports)
CEREBRAL INFARCTION ( 29 FDA reports)
CERUMEN IMPACTION ( 29 FDA reports)
CHONDROMALACIA ( 29 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 29 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 29 FDA reports)
HOSPITALISATION ( 29 FDA reports)
HYPERPLASIA ( 29 FDA reports)
INFUSION SITE REACTION ( 29 FDA reports)
INTESTINAL OBSTRUCTION ( 29 FDA reports)
MALOCCLUSION ( 29 FDA reports)
POOR DENTAL CONDITION ( 29 FDA reports)
PULMONARY CONGESTION ( 29 FDA reports)
PULPITIS DENTAL ( 29 FDA reports)
RADIOTHERAPY ( 29 FDA reports)
RALES ( 29 FDA reports)
RESPIRATORY TRACT INFECTION ( 29 FDA reports)
SPLENOMEGALY ( 29 FDA reports)
STOMACH DISCOMFORT ( 29 FDA reports)
SUDDEN DEATH ( 29 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 29 FDA reports)
TOOTH INJURY ( 29 FDA reports)
DECUBITUS ULCER ( 28 FDA reports)
EARLY SATIETY ( 28 FDA reports)
FACIAL NEURALGIA ( 28 FDA reports)
FORMICATION ( 28 FDA reports)
GASTRITIS EROSIVE ( 28 FDA reports)
HEPATITIS FULMINANT ( 28 FDA reports)
HYPOKINESIA ( 28 FDA reports)
INCONTINENCE ( 28 FDA reports)
LABORATORY TEST ABNORMAL ( 28 FDA reports)
LIPASE INCREASED ( 28 FDA reports)
MICTURITION URGENCY ( 28 FDA reports)
NEURODERMATITIS ( 28 FDA reports)
OSTEORADIONECROSIS ( 28 FDA reports)
PELVIC FRACTURE ( 28 FDA reports)
POLYURIA ( 28 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 28 FDA reports)
SCLERODERMA ( 28 FDA reports)
SECONDARY SEQUESTRUM ( 28 FDA reports)
WEGENER'S GRANULOMATOSIS ( 28 FDA reports)
AFFECT LABILITY ( 27 FDA reports)
CAROTID ARTERY DISEASE ( 27 FDA reports)
CEREBRAL DISORDER ( 27 FDA reports)
CEREBRAL ISCHAEMIA ( 27 FDA reports)
CROHN'S DISEASE ( 27 FDA reports)
HAEMATEMESIS ( 27 FDA reports)
HYPOACUSIS ( 27 FDA reports)
HYPOMAGNESAEMIA ( 27 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 27 FDA reports)
MYOCLONUS ( 27 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 27 FDA reports)
PAIN OF SKIN ( 27 FDA reports)
PALMAR ERYTHEMA ( 27 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 27 FDA reports)
STEM CELL TRANSPLANT ( 27 FDA reports)
VARICOSE VEIN ( 27 FDA reports)
ABSCESS JAW ( 26 FDA reports)
AORTIC VALVE INCOMPETENCE ( 26 FDA reports)
BLOOD POTASSIUM INCREASED ( 26 FDA reports)
BREATH SOUNDS ABNORMAL ( 26 FDA reports)
HYPERAESTHESIA ( 26 FDA reports)
LIMB INJURY ( 26 FDA reports)
NEUROPATHY ( 26 FDA reports)
OCULAR ICTERUS ( 26 FDA reports)
PUPIL FIXED ( 26 FDA reports)
STREPTOCOCCAL INFECTION ( 26 FDA reports)
SUBCUTANEOUS ABSCESS ( 26 FDA reports)
TARDIVE DYSKINESIA ( 26 FDA reports)
VITREOUS DETACHMENT ( 26 FDA reports)
ABSCESS LIMB ( 25 FDA reports)
ABSCESS ORAL ( 25 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 25 FDA reports)
ACUTE SINUSITIS ( 25 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 25 FDA reports)
BACTERAEMIA ( 25 FDA reports)
BLADDER OPERATION ( 25 FDA reports)
BONE MARROW FAILURE ( 25 FDA reports)
CONJUNCTIVITIS ( 25 FDA reports)
FLUID OVERLOAD ( 25 FDA reports)
HEPATITIS TOXIC ( 25 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 25 FDA reports)
LUNG INFECTION ( 25 FDA reports)
NERVE INJURY ( 25 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 25 FDA reports)
PERICARDIAL EFFUSION ( 25 FDA reports)
POSTURE ABNORMAL ( 25 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 25 FDA reports)
SKIN PAPILLOMA ( 25 FDA reports)
WALKING AID USER ( 25 FDA reports)
WALKING DISABILITY ( 25 FDA reports)
WOUND ( 25 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 24 FDA reports)
BLOOD ALBUMIN DECREASED ( 24 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 24 FDA reports)
BREAST CANCER RECURRENT ( 24 FDA reports)
DEAFNESS NEUROSENSORY ( 24 FDA reports)
DISSOCIATION ( 24 FDA reports)
HEPATOCELLULAR DAMAGE ( 24 FDA reports)
INJECTION SITE IRRITATION ( 24 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 24 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 24 FDA reports)
METAPLASIA ( 24 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 24 FDA reports)
RENAL PAIN ( 24 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 24 FDA reports)
TENOSYNOVITIS ( 24 FDA reports)
ACNE ( 23 FDA reports)
ANURIA ( 23 FDA reports)
BLOOD PRESSURE ABNORMAL ( 23 FDA reports)
BRUXISM ( 23 FDA reports)
CHEST WALL MASS ( 23 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 23 FDA reports)
EAR INFECTION ( 23 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 23 FDA reports)
EOSINOPHILIA ( 23 FDA reports)
ERYTHEMA MULTIFORME ( 23 FDA reports)
FORAMEN MAGNUM STENOSIS ( 23 FDA reports)
HALLUCINATION, AUDITORY ( 23 FDA reports)
INTERMITTENT CLAUDICATION ( 23 FDA reports)
MOOD ALTERED ( 23 FDA reports)
MOUTH HAEMORRHAGE ( 23 FDA reports)
MULTIPLE SCLEROSIS ( 23 FDA reports)
MYELOPATHY ( 23 FDA reports)
MYOSITIS ( 23 FDA reports)
NASAL MUCOSAL DISORDER ( 23 FDA reports)
NECROSIS ( 23 FDA reports)
ORTHOPNOEA ( 23 FDA reports)
OTITIS EXTERNA ( 23 FDA reports)
PNEUMONIA ASPIRATION ( 23 FDA reports)
SKIN TIGHTNESS ( 23 FDA reports)
THIRST ( 23 FDA reports)
VASCULAR CALCIFICATION ( 23 FDA reports)
YELLOW SKIN ( 23 FDA reports)
ABDOMINAL HAEMATOMA ( 22 FDA reports)
AGGRESSION ( 22 FDA reports)
ANGIOPATHY ( 22 FDA reports)
APPENDICECTOMY ( 22 FDA reports)
ATRIAL FLUTTER ( 22 FDA reports)
CARDIOGENIC SHOCK ( 22 FDA reports)
CERVICOBRACHIAL SYNDROME ( 22 FDA reports)
DENTAL PROSTHESIS USER ( 22 FDA reports)
DERMAL CYST ( 22 FDA reports)
EMPYEMA ( 22 FDA reports)
FLUID RETENTION ( 22 FDA reports)
HYPOCALCAEMIA ( 22 FDA reports)
INGROWING NAIL ( 22 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 22 FDA reports)
LYMPHOEDEMA ( 22 FDA reports)
MALIGNANT MELANOMA ( 22 FDA reports)
MUSCLE DISORDER ( 22 FDA reports)
MUSCLE INJURY ( 22 FDA reports)
MYASTHENIA GRAVIS ( 22 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 22 FDA reports)
OVARIAN CANCER ( 22 FDA reports)
PATHOLOGICAL FRACTURE ( 22 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 22 FDA reports)
RADICULOPATHY ( 22 FDA reports)
SKIN HYPERTROPHY ( 22 FDA reports)
SKIN LACERATION ( 22 FDA reports)
SNEEZING ( 22 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 22 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 22 FDA reports)
URTICARIA GENERALISED ( 22 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 21 FDA reports)
ACUTE PULMONARY OEDEMA ( 21 FDA reports)
AORTIC STENOSIS ( 21 FDA reports)
AZOTAEMIA ( 21 FDA reports)
BLINDNESS TRANSIENT ( 21 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 21 FDA reports)
BRONCHIECTASIS ( 21 FDA reports)
CHOKING SENSATION ( 21 FDA reports)
CLAUSTROPHOBIA ( 21 FDA reports)
CYSTOCELE ( 21 FDA reports)
DERMATITIS BULLOUS ( 21 FDA reports)
DERMATITIS CONTACT ( 21 FDA reports)
DRUG INTOLERANCE ( 21 FDA reports)
EAR CONGESTION ( 21 FDA reports)
EYELID OEDEMA ( 21 FDA reports)
GALLBLADDER POLYP ( 21 FDA reports)
HEPATIC ENCEPHALOPATHY ( 21 FDA reports)
HYPOVOLAEMIA ( 21 FDA reports)
INJECTION SITE ERYTHEMA ( 21 FDA reports)
INJECTION SITE REACTION ( 21 FDA reports)
JOINT SPRAIN ( 21 FDA reports)
LIVER INJURY ( 21 FDA reports)
MASS EXCISION ( 21 FDA reports)
NASAL DISCOMFORT ( 21 FDA reports)
POOR QUALITY SLEEP ( 21 FDA reports)
RECTOCELE ( 21 FDA reports)
SERRATIA INFECTION ( 21 FDA reports)
SPINAL DECOMPRESSION ( 21 FDA reports)
TACHYPNOEA ( 21 FDA reports)
URINE OUTPUT DECREASED ( 21 FDA reports)
ABDOMINAL TENDERNESS ( 20 FDA reports)
ANGER ( 20 FDA reports)
ANGIONEUROTIC OEDEMA ( 20 FDA reports)
AORTIC CALCIFICATION ( 20 FDA reports)
CLOSTRIDIUM COLITIS ( 20 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 20 FDA reports)
EOSINOPHIL COUNT INCREASED ( 20 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 20 FDA reports)
HYPOAESTHESIA FACIAL ( 20 FDA reports)
LACTIC ACIDOSIS ( 20 FDA reports)
LUMBAR SPINE FLATTENING ( 20 FDA reports)
MAMMOGRAM ABNORMAL ( 20 FDA reports)
MANIA ( 20 FDA reports)
MIDDLE INSOMNIA ( 20 FDA reports)
MYCOSIS FUNGOIDES ( 20 FDA reports)
NEOPLASM RECURRENCE ( 20 FDA reports)
NO THERAPEUTIC RESPONSE ( 20 FDA reports)
OEDEMA MUCOSAL ( 20 FDA reports)
ORTHOSIS USER ( 20 FDA reports)
PERIARTHRITIS ( 20 FDA reports)
RECTAL FISSURE ( 20 FDA reports)
RENAL TUBULAR NECROSIS ( 20 FDA reports)
SCAN BONE MARROW ABNORMAL ( 20 FDA reports)
SKIN INDURATION ( 20 FDA reports)
SKIN WARM ( 20 FDA reports)
SOCIAL PROBLEM ( 20 FDA reports)
TELANGIECTASIA ( 20 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 20 FDA reports)
TENSION ( 20 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 20 FDA reports)
VITAMIN B12 DEFICIENCY ( 20 FDA reports)
WOUND DRAINAGE ( 20 FDA reports)
ABDOMINAL PAIN LOWER ( 19 FDA reports)
ANEURYSM ( 19 FDA reports)
APHAGIA ( 19 FDA reports)
ATAXIA ( 19 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 19 FDA reports)
BONE MARROW TRANSPLANT ( 19 FDA reports)
CACHEXIA ( 19 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 19 FDA reports)
CAROTID ARTERY STENOSIS ( 19 FDA reports)
CEREBRAL ATROPHY ( 19 FDA reports)
CHOLECYSTITIS ACUTE ( 19 FDA reports)
CORONARY ARTERY OCCLUSION ( 19 FDA reports)
DEAFNESS UNILATERAL ( 19 FDA reports)
DENTAL FISTULA ( 19 FDA reports)
DIABETIC KETOACIDOSIS ( 19 FDA reports)
DIZZINESS POSTURAL ( 19 FDA reports)
EDENTULOUS ( 19 FDA reports)
EXOPHTHALMOS ( 19 FDA reports)
EYE LASER SURGERY ( 19 FDA reports)
FACET JOINT SYNDROME ( 19 FDA reports)
FOREIGN BODY ( 19 FDA reports)
HEART VALVE INCOMPETENCE ( 19 FDA reports)
INFUSION RELATED REACTION ( 19 FDA reports)
KNEE ARTHROPLASTY ( 19 FDA reports)
MYOPIA ( 19 FDA reports)
NASAL POLYPS ( 19 FDA reports)
NASAL TURBINATE HYPERTROPHY ( 19 FDA reports)
NODULE ( 19 FDA reports)
OESOPHAGEAL DISORDER ( 19 FDA reports)
PELVIC PAIN ( 19 FDA reports)
PLEURISY ( 19 FDA reports)
RECTAL ABSCESS ( 19 FDA reports)
RENAL MASS ( 19 FDA reports)
STOMATOCYTES PRESENT ( 19 FDA reports)
SUICIDE ATTEMPT ( 19 FDA reports)
VASODILATATION ( 19 FDA reports)
ACCIDENT AT WORK ( 18 FDA reports)
ANGINA UNSTABLE ( 18 FDA reports)
BONE GRAFT ( 18 FDA reports)
CHEILITIS ( 18 FDA reports)
COLON ADENOMA ( 18 FDA reports)
COMMUNICATION DISORDER ( 18 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 18 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 18 FDA reports)
FAMILY STRESS ( 18 FDA reports)
FEELING DRUNK ( 18 FDA reports)
FISTULA REPAIR ( 18 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 18 FDA reports)
HYPERSOMNIA ( 18 FDA reports)
IMMUNODEFICIENCY ( 18 FDA reports)
IRIS TRANSILLUMINATION DEFECT ( 18 FDA reports)
MEDICAL DEVICE COMPLICATION ( 18 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 18 FDA reports)
MYELODYSPLASTIC SYNDROME ( 18 FDA reports)
ONYCHOMADESIS ( 18 FDA reports)
PHOTOPHERESIS ( 18 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 18 FDA reports)
RADIAL NERVE PALSY ( 18 FDA reports)
RASH PAPULAR ( 18 FDA reports)
SPINAL FRACTURE ( 18 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 18 FDA reports)
TACHYARRHYTHMIA ( 18 FDA reports)
URETHRAL STENOSIS ( 18 FDA reports)
ADENOCARCINOMA ( 17 FDA reports)
AMMONIA INCREASED ( 17 FDA reports)
ANORECTAL DISCOMFORT ( 17 FDA reports)
ANOXIC ENCEPHALOPATHY ( 17 FDA reports)
BASAL CELL CARCINOMA ( 17 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 17 FDA reports)
BONE SCAN ABNORMAL ( 17 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 17 FDA reports)
DENTAL CARE ( 17 FDA reports)
DRUG EFFECT DECREASED ( 17 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 17 FDA reports)
DYSTONIA ( 17 FDA reports)
FIBULA FRACTURE ( 17 FDA reports)
INFUSION SITE RASH ( 17 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 17 FDA reports)
IRIS HYPOPIGMENTATION ( 17 FDA reports)
IRON DEFICIENCY ( 17 FDA reports)
JOINT ARTHROPLASTY ( 17 FDA reports)
JOINT CONTRACTURE ( 17 FDA reports)
JOINT INSTABILITY ( 17 FDA reports)
LEUKAEMIA ( 17 FDA reports)
LIVER TRANSPLANT ( 17 FDA reports)
ONYCHALGIA ( 17 FDA reports)
PAPILLOEDEMA ( 17 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 17 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 17 FDA reports)
PRESBYOPIA ( 17 FDA reports)
PULMONARY INFARCTION ( 17 FDA reports)
QUALITY OF LIFE DECREASED ( 17 FDA reports)
RADIATION SKIN INJURY ( 17 FDA reports)
SUDDEN CARDIAC DEATH ( 17 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 17 FDA reports)
VOCAL CORD PARALYSIS ( 17 FDA reports)
WEIGHT BEARING DIFFICULTY ( 17 FDA reports)
ADRENAL DISORDER ( 16 FDA reports)
ANGIOFIBROMA ( 16 FDA reports)
ANOGENITAL WARTS ( 16 FDA reports)
AORTIC VALVE SCLEROSIS ( 16 FDA reports)
ATRIOVENTRICULAR BLOCK ( 16 FDA reports)
BREAST CANCER METASTATIC ( 16 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 16 FDA reports)
CARBUNCLE ( 16 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 16 FDA reports)
CHOLECYSTECTOMY ( 16 FDA reports)
CYSTITIS INTERSTITIAL ( 16 FDA reports)
DILATATION VENTRICULAR ( 16 FDA reports)
DRUG ABUSE ( 16 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 16 FDA reports)
FRACTURE ( 16 FDA reports)
GINGIVAL ULCERATION ( 16 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 16 FDA reports)
HYDROCEPHALUS ( 16 FDA reports)
HYPERPARATHYROIDISM ( 16 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 16 FDA reports)
INFUSION SITE PHLEBITIS ( 16 FDA reports)
INFUSION SITE PRURITUS ( 16 FDA reports)
LICHENOID KERATOSIS ( 16 FDA reports)
LIP BLISTER ( 16 FDA reports)
LOCALISED INFECTION ( 16 FDA reports)
LOCALISED OEDEMA ( 16 FDA reports)
MEDICATION ERROR ( 16 FDA reports)
MENORRHAGIA ( 16 FDA reports)
MULTIPLE ALLERGIES ( 16 FDA reports)
OESOPHAGEAL ULCER ( 16 FDA reports)
PAPILLOMA ( 16 FDA reports)
PERIODONTAL OPERATION ( 16 FDA reports)
PULMONARY CALCIFICATION ( 16 FDA reports)
RENAL ATROPHY ( 16 FDA reports)
THORACOTOMY ( 16 FDA reports)
TONGUE OEDEMA ( 16 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 16 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 15 FDA reports)
ADRENAL INSUFFICIENCY ( 15 FDA reports)
ARTHROPOD BITE ( 15 FDA reports)
AURICULAR SWELLING ( 15 FDA reports)
BIOPSY BONE MARROW ( 15 FDA reports)
BONE CYST ( 15 FDA reports)
CALCULUS URETERIC ( 15 FDA reports)
CATARACT OPERATION ( 15 FDA reports)
CHEST WALL OPERATION ( 15 FDA reports)
CHEST X-RAY ABNORMAL ( 15 FDA reports)
COMPLETED SUICIDE ( 15 FDA reports)
COR PULMONALE CHRONIC ( 15 FDA reports)
CORONARY ARTERY STENOSIS ( 15 FDA reports)
DECREASED ACTIVITY ( 15 FDA reports)
DERMATITIS EXFOLIATIVE ( 15 FDA reports)
DRUG LEVEL INCREASED ( 15 FDA reports)
EPIGASTRIC DISCOMFORT ( 15 FDA reports)
EYELID PTOSIS ( 15 FDA reports)
FAILURE TO THRIVE ( 15 FDA reports)
GASTRODUODENITIS ( 15 FDA reports)
GINGIVAL RECESSION ( 15 FDA reports)
HAEMOLYSIS ( 15 FDA reports)
HEPATIC LESION ( 15 FDA reports)
HYPOMANIA ( 15 FDA reports)
LIGAMENT SPRAIN ( 15 FDA reports)
LOSS OF EMPLOYMENT ( 15 FDA reports)
LUNG HYPERINFLATION ( 15 FDA reports)
MYELOMA RECURRENCE ( 15 FDA reports)
NEUROLOGICAL SYMPTOM ( 15 FDA reports)
OROPHARYNGEAL BLISTERING ( 15 FDA reports)
PHARYNGOESOPHAGEAL DIVERTICULUM ( 15 FDA reports)
POISONING ( 15 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 15 FDA reports)
PROCEDURAL HYPERTENSION ( 15 FDA reports)
PROSTATOMEGALY ( 15 FDA reports)
PULMONARY GRANULOMA ( 15 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 15 FDA reports)
RECTAL POLYP ( 15 FDA reports)
RENAL INJURY ( 15 FDA reports)
RETINAL DEPIGMENTATION ( 15 FDA reports)
RETINOPATHY ( 15 FDA reports)
SINUS POLYP ( 15 FDA reports)
SKIN HYPERPIGMENTATION ( 15 FDA reports)
STUPOR ( 15 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 15 FDA reports)
UTERINE ENLARGEMENT ( 15 FDA reports)
UTERINE POLYP ( 15 FDA reports)
ABSCESS DRAINAGE ( 14 FDA reports)
ACUTE CORONARY SYNDROME ( 14 FDA reports)
ACUTE PRERENAL FAILURE ( 14 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 14 FDA reports)
APALLIC SYNDROME ( 14 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 14 FDA reports)
ARTHROSCOPY ( 14 FDA reports)
ATROPHIC VULVOVAGINITIS ( 14 FDA reports)
BREAST PAIN ( 14 FDA reports)
CARDIAC VALVE DISEASE ( 14 FDA reports)
CARDIAC VALVE SCLEROSIS ( 14 FDA reports)
CATHETER PLACEMENT ( 14 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 14 FDA reports)
COSTOCHONDRITIS ( 14 FDA reports)
DIABETIC NEUROPATHY ( 14 FDA reports)
DROP ATTACKS ( 14 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 14 FDA reports)
EROSIVE OESOPHAGITIS ( 14 FDA reports)
FACIAL OPERATION ( 14 FDA reports)
FOAMING AT MOUTH ( 14 FDA reports)
HEAD DISCOMFORT ( 14 FDA reports)
HEARING AID USER ( 14 FDA reports)
HERPES SIMPLEX ( 14 FDA reports)
INTESTINAL PERFORATION ( 14 FDA reports)
KYPHOSCOLIOSIS ( 14 FDA reports)
LIBIDO DECREASED ( 14 FDA reports)
LUNG CONSOLIDATION ( 14 FDA reports)
MAXILLOFACIAL OPERATION ( 14 FDA reports)
MENISCUS REMOVAL ( 14 FDA reports)
OCCULT BLOOD POSITIVE ( 14 FDA reports)
ORAL HERPES ( 14 FDA reports)
PANCREATIC DISORDER ( 14 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 14 FDA reports)
PULMONARY RADIATION INJURY ( 14 FDA reports)
PYURIA ( 14 FDA reports)
RIGHT VENTRICULAR FAILURE ( 14 FDA reports)
SALPINGO-OOPHORECTOMY ( 14 FDA reports)
SENSATION OF FOREIGN BODY ( 14 FDA reports)
SPINAL FUSION SURGERY ( 14 FDA reports)
THERAPY NON-RESPONDER ( 14 FDA reports)
ASTIGMATISM ( 13 FDA reports)
ATRIAL SEPTAL DEFECT ( 13 FDA reports)
AUTOIMMUNE DISORDER ( 13 FDA reports)
BIPOLAR DISORDER ( 13 FDA reports)
CALCIFIC DEPOSITS REMOVAL ( 13 FDA reports)
COLITIS ISCHAEMIC ( 13 FDA reports)
CONGENITAL KNEE DEFORMITY ( 13 FDA reports)
CONTRAST MEDIA REACTION ( 13 FDA reports)
DEVICE OCCLUSION ( 13 FDA reports)
DILATATION ATRIAL ( 13 FDA reports)
DRUG SCREEN POSITIVE ( 13 FDA reports)
DYSAESTHESIA ( 13 FDA reports)
FEELING OF DESPAIR ( 13 FDA reports)
GASTRIC HAEMORRHAGE ( 13 FDA reports)
HAEMORRHAGIC DIATHESIS ( 13 FDA reports)
HAIR FOLLICLE TUMOUR BENIGN ( 13 FDA reports)
HEPATIC CIRRHOSIS ( 13 FDA reports)
HEPATORENAL SYNDROME ( 13 FDA reports)
HYPERNATRAEMIA ( 13 FDA reports)
HYPERTHYROIDISM ( 13 FDA reports)
ILIUM FRACTURE ( 13 FDA reports)
INTESTINAL MUCOSAL HYPERTROPHY ( 13 FDA reports)
ISCHAEMIC HEPATITIS ( 13 FDA reports)
LIGAMENT LAXITY ( 13 FDA reports)
MENINGITIS ( 13 FDA reports)
MOOD SWINGS ( 13 FDA reports)
NECK MASS ( 13 FDA reports)
NEPHROPATHY ( 13 FDA reports)
NEPHROSCLEROSIS ( 13 FDA reports)
OFF LABEL USE ( 13 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 13 FDA reports)
OROPHARYNGEAL SWELLING ( 13 FDA reports)
OSTEOCHONDROSIS ( 13 FDA reports)
PERIPHERAL ISCHAEMIA ( 13 FDA reports)
PERSONALITY DISORDER ( 13 FDA reports)
PHARYNGITIS ( 13 FDA reports)
POST PROCEDURAL COMPLICATION ( 13 FDA reports)
PROSTATITIS ( 13 FDA reports)
RADICULITIS ( 13 FDA reports)
RADICULITIS CERVICAL ( 13 FDA reports)
RADIOTHERAPY TO BRAIN ( 13 FDA reports)
RENAL TUBULAR ACIDOSIS ( 13 FDA reports)
RIGHT ATRIAL DILATATION ( 13 FDA reports)
SALPINGO-OOPHORECTOMY UNILATERAL ( 13 FDA reports)
SKIN CANCER ( 13 FDA reports)
SPUTUM DISCOLOURED ( 13 FDA reports)
SQUAMOUS CELL CARCINOMA ( 13 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 13 FDA reports)
THROMBOPHLEBITIS ( 13 FDA reports)
TOOTH EROSION ( 13 FDA reports)
TRIGEMINAL NEURALGIA ( 13 FDA reports)
VENOUS OCCLUSION ( 13 FDA reports)
VITAMIN D DEFICIENCY ( 13 FDA reports)
WOUND TREATMENT ( 13 FDA reports)
ACIDOSIS ( 12 FDA reports)
AFFECTIVE DISORDER ( 12 FDA reports)
ALCOHOL USE ( 12 FDA reports)
ANISOCYTOSIS ( 12 FDA reports)
APHTHOUS STOMATITIS ( 12 FDA reports)
APLASTIC ANAEMIA ( 12 FDA reports)
APPARENT DEATH ( 12 FDA reports)
ATRIAL TACHYCARDIA ( 12 FDA reports)
BENCE JONES PROTEINURIA ( 12 FDA reports)
BENIGN BREAST NEOPLASM ( 12 FDA reports)
BLEPHAROSPASM ( 12 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 12 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 12 FDA reports)
BREAST RECONSTRUCTION ( 12 FDA reports)
CARDIAC FLUTTER ( 12 FDA reports)
CHANGE OF BOWEL HABIT ( 12 FDA reports)
CONCUSSION ( 12 FDA reports)
DEAFNESS BILATERAL ( 12 FDA reports)
DIPLEGIA ( 12 FDA reports)
DUODENAL ULCER ( 12 FDA reports)
EPILEPSY ( 12 FDA reports)
EXERCISE TOLERANCE DECREASED ( 12 FDA reports)
FACIAL PALSY ( 12 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 12 FDA reports)
GOITRE ( 12 FDA reports)
GRIP STRENGTH DECREASED ( 12 FDA reports)
GUILLAIN-BARRE SYNDROME ( 12 FDA reports)
HAEMODYNAMIC INSTABILITY ( 12 FDA reports)
HEPATOSPLENOMEGALY ( 12 FDA reports)
HIP SURGERY ( 12 FDA reports)
HYPERPATHIA ( 12 FDA reports)
HYPERTHERMIA ( 12 FDA reports)
HYPERTROPHY ( 12 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 12 FDA reports)
KERATOMILEUSIS ( 12 FDA reports)
LONG QT SYNDROME ( 12 FDA reports)
MALIGNANT TUMOUR EXCISION ( 12 FDA reports)
METASTASES TO ADRENALS ( 12 FDA reports)
NAIL DISCOLOURATION ( 12 FDA reports)
NECK INJURY ( 12 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 12 FDA reports)
OPEN REDUCTION OF FRACTURE ( 12 FDA reports)
PANCREATIC CARCINOMA ( 12 FDA reports)
PERSONALITY CHANGE ( 12 FDA reports)
PHARYNGEAL ERYTHEMA ( 12 FDA reports)
PLASTIC SURGERY ( 12 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 12 FDA reports)
POOR PERSONAL HYGIENE ( 12 FDA reports)
PUPILS UNEQUAL ( 12 FDA reports)
RECTAL ULCER ( 12 FDA reports)
REFLUX OESOPHAGITIS ( 12 FDA reports)
RHINOPLASTY ( 12 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 12 FDA reports)
SKIN NECROSIS ( 12 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 12 FDA reports)
SUBDURAL HAEMATOMA ( 12 FDA reports)
TOBACCO ABUSE ( 12 FDA reports)
TOOTH IMPACTED ( 12 FDA reports)
TOOTH REPAIR ( 12 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 12 FDA reports)
VENOUS INSUFFICIENCY ( 12 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 12 FDA reports)
WOUND INFECTION ( 12 FDA reports)
ADVERSE REACTION ( 11 FDA reports)
ALVEOLOPLASTY ( 11 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 11 FDA reports)
APHONIA ( 11 FDA reports)
ASPIRATION PLEURAL CAVITY ( 11 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 11 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 11 FDA reports)
BILE DUCT STONE ( 11 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 11 FDA reports)
BONE SWELLING ( 11 FDA reports)
BORDERLINE PERSONALITY DISORDER ( 11 FDA reports)
BREAST ABSCESS ( 11 FDA reports)
CERVICITIS HUMAN PAPILLOMA VIRUS ( 11 FDA reports)
DENTAL NECROSIS ( 11 FDA reports)
DRUG DOSE OMISSION ( 11 FDA reports)
DRY THROAT ( 11 FDA reports)
DYSGRAPHIA ( 11 FDA reports)
DYSPHORIA ( 11 FDA reports)
ECZEMA INFECTED ( 11 FDA reports)
ENCEPHALITIS ( 11 FDA reports)
ENDOCARDITIS ( 11 FDA reports)
ENTEROVESICAL FISTULA ( 11 FDA reports)
ERYTHEMA NODOSUM ( 11 FDA reports)
EXTRASKELETAL OSSIFICATION ( 11 FDA reports)
EYE MOVEMENT DISORDER ( 11 FDA reports)
FAT NECROSIS ( 11 FDA reports)
FIBROMYALGIA ( 11 FDA reports)
GIANT CELL TUMOUR OF TENDON SHEATH ( 11 FDA reports)
HAEMOPHILUS INFECTION ( 11 FDA reports)
HEART RATE ABNORMAL ( 11 FDA reports)
HERNIA ( 11 FDA reports)
HYDRONEPHROSIS ( 11 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 11 FDA reports)
HYPERTENSIVE CRISIS ( 11 FDA reports)
HYPOTONIA ( 11 FDA reports)
INFLAMMATION OF WOUND ( 11 FDA reports)
INFUSION SITE EXTRAVASATION ( 11 FDA reports)
INITIAL INSOMNIA ( 11 FDA reports)
INJECTION SITE PAIN ( 11 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 11 FDA reports)
INTRAOSSEOUS ANGIOMA ( 11 FDA reports)
LIGHT CHAIN ANALYSIS ( 11 FDA reports)
LIP PAIN ( 11 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 11 FDA reports)
MENOPAUSE ( 11 FDA reports)
MONOCLONAL GAMMOPATHY ( 11 FDA reports)
MUSCLE RIGIDITY ( 11 FDA reports)
NAIL DISORDER ( 11 FDA reports)
NASAL OEDEMA ( 11 FDA reports)
NERVE BLOCK ( 11 FDA reports)
NIKOLSKY'S SIGN ( 11 FDA reports)
ORAL INTAKE REDUCED ( 11 FDA reports)
ORAL MUCOSAL BLISTERING ( 11 FDA reports)
PARATHYROID TUMOUR BENIGN ( 11 FDA reports)
PHLEBITIS ( 11 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 11 FDA reports)
PROTEIN URINE ABSENT ( 11 FDA reports)
PUBIS FRACTURE ( 11 FDA reports)
PULMONARY VALVE STENOSIS ( 11 FDA reports)
QRS AXIS ABNORMAL ( 11 FDA reports)
RENAL ARTERY STENOSIS ( 11 FDA reports)
RENAL STONE REMOVAL ( 11 FDA reports)
SUNBURN ( 11 FDA reports)
TEETH BRITTLE ( 11 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 11 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 11 FDA reports)
TONGUE BLISTERING ( 11 FDA reports)
TORTICOLLIS ( 11 FDA reports)
TOXIC SKIN ERUPTION ( 11 FDA reports)
TUMOUR INVASION ( 11 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 11 FDA reports)
VISUAL FIELD DEFECT ( 11 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 10 FDA reports)
ACUTE ABDOMEN ( 10 FDA reports)
AMYLOIDOSIS ( 10 FDA reports)
ASBESTOSIS ( 10 FDA reports)
ASPHYXIA ( 10 FDA reports)
BODY TEMPERATURE DECREASED ( 10 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 10 FDA reports)
CATHETER SEPSIS ( 10 FDA reports)
CHOKING ( 10 FDA reports)
COLON CANCER ( 10 FDA reports)
CONNECTIVE TISSUE DISORDER ( 10 FDA reports)
CREPITATIONS ( 10 FDA reports)
DEPRESSION SUICIDAL ( 10 FDA reports)
DYSTHYMIC DISORDER ( 10 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 10 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 10 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 10 FDA reports)
EOSINOPHILIC PNEUMONIA ( 10 FDA reports)
ERUCTATION ( 10 FDA reports)
ESCHERICHIA SEPSIS ( 10 FDA reports)
EXTREMITY CONTRACTURE ( 10 FDA reports)
EYELID DISORDER ( 10 FDA reports)
HAEMANGIOMA OF SPLEEN ( 10 FDA reports)
HAND DEFORMITY ( 10 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 10 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 10 FDA reports)
HERPES VIRUS INFECTION ( 10 FDA reports)
HICCUPS ( 10 FDA reports)
HODGKIN'S DISEASE ( 10 FDA reports)
HYPOGEUSIA ( 10 FDA reports)
HYSTERECTOMY ( 10 FDA reports)
IMMUNE SYSTEM DISORDER ( 10 FDA reports)
INGUINAL HERNIA ( 10 FDA reports)
IRON DEFICIENCY ANAEMIA ( 10 FDA reports)
KERATITIS ( 10 FDA reports)
LACUNAR INFARCTION ( 10 FDA reports)
LARYNGEAL OEDEMA ( 10 FDA reports)
LUNG CANCER METASTATIC ( 10 FDA reports)
LYMPHOCYTIC INFILTRATION ( 10 FDA reports)
METABOLIC DISORDER ( 10 FDA reports)
MITRAL VALVE STENOSIS ( 10 FDA reports)
MORTON'S NEUROMA ( 10 FDA reports)
MUSCLE ATROPHY ( 10 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 10 FDA reports)
NEUTROPHIL COUNT DECREASED ( 10 FDA reports)
NEUTROPHIL COUNT INCREASED ( 10 FDA reports)
NON-CARDIAC CHEST PAIN ( 10 FDA reports)
PANCREATIC CYST ( 10 FDA reports)
PAPILLOMA VIRAL INFECTION ( 10 FDA reports)
PLASMACYTOMA ( 10 FDA reports)
PNEUMONIA HAEMOPHILUS ( 10 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 10 FDA reports)
PRODUCT QUALITY ISSUE ( 10 FDA reports)
PROLAPSE REPAIR ( 10 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 10 FDA reports)
PYELONEPHRITIS ACUTE ( 10 FDA reports)
QUADRIPARESIS ( 10 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 10 FDA reports)
SICK SINUS SYNDROME ( 10 FDA reports)
SINUS ARRHYTHMIA ( 10 FDA reports)
SPONDYLOARTHROPATHY ( 10 FDA reports)
SYNCOPE VASOVAGAL ( 10 FDA reports)
TRANSFUSION ( 10 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 10 FDA reports)
UTERINE PROLAPSE REPAIR ( 10 FDA reports)
VENOUS STENOSIS ( 10 FDA reports)
VENTRICULAR ARRHYTHMIA ( 10 FDA reports)
VERTIGO POSITIONAL ( 10 FDA reports)
VESSEL PUNCTURE SITE PRURITUS ( 10 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 10 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 9 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 9 FDA reports)
ALVEOLAR OSTEITIS ( 9 FDA reports)
ANAL FISSURE EXCISION ( 9 FDA reports)
ANOPLASTY ( 9 FDA reports)
ANXIETY DISORDER ( 9 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 9 FDA reports)
AUTOIMMUNE HEPATITIS ( 9 FDA reports)
BACK INJURY ( 9 FDA reports)
BIOPSY BREAST ABNORMAL ( 9 FDA reports)
BLOOD MAGNESIUM DECREASED ( 9 FDA reports)
BODY HEIGHT DECREASED ( 9 FDA reports)
BONE MARROW DISORDER ( 9 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 9 FDA reports)
BRAIN INJURY ( 9 FDA reports)
BRAIN MASS ( 9 FDA reports)
BUNDLE BRANCH BLOCK ( 9 FDA reports)
CATARACT NUCLEAR ( 9 FDA reports)
CATHETER REMOVAL ( 9 FDA reports)
COLLAPSE OF LUNG ( 9 FDA reports)
COLONIC OBSTRUCTION ( 9 FDA reports)
CONDUCTION DISORDER ( 9 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 9 FDA reports)
DIABETIC RETINOPATHY ( 9 FDA reports)
DIAPHRAGMATIC HERNIA ( 9 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 9 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 9 FDA reports)
ENTHESOPATHY ( 9 FDA reports)
EUPHORIC MOOD ( 9 FDA reports)
EXTRAVASATION ( 9 FDA reports)
FEMORAL NECK FRACTURE ( 9 FDA reports)
GASTRIC POLYPS ( 9 FDA reports)
GRAFT VERSUS HOST DISEASE ( 9 FDA reports)
HAEMORRHAGE URINARY TRACT ( 9 FDA reports)
HAEMORRHOID OPERATION ( 9 FDA reports)
HEART INJURY ( 9 FDA reports)
HEPATIC CONGESTION ( 9 FDA reports)
HEPATITIS CHOLESTATIC ( 9 FDA reports)
HYPERMETROPIA ( 9 FDA reports)
HYPOVENTILATION ( 9 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 9 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 9 FDA reports)
INCREASED TENDENCY TO BRUISE ( 9 FDA reports)
INJECTION SITE HAEMORRHAGE ( 9 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 9 FDA reports)
INTESTINAL ISCHAEMIA ( 9 FDA reports)
INTRAOCULAR LENS IMPLANT ( 9 FDA reports)
LARGE INTESTINE PERFORATION ( 9 FDA reports)
LYMPHOMA ( 9 FDA reports)
MASTECTOMY ( 9 FDA reports)
METASTASES TO EYE ( 9 FDA reports)
METASTASES TO SKIN ( 9 FDA reports)
METASTASES TO STOMACH ( 9 FDA reports)
METATARSALGIA ( 9 FDA reports)
METATARSUS PRIMUS VARUS ( 9 FDA reports)
MUSCLE SWELLING ( 9 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 9 FDA reports)
ORAL PRURITUS ( 9 FDA reports)
PALATAL DISORDER ( 9 FDA reports)
PANCREATIC ENZYMES INCREASED ( 9 FDA reports)
PANIC DISORDER ( 9 FDA reports)
PEPTIC ULCER ( 9 FDA reports)
PERIPHERAL NERVE INJURY ( 9 FDA reports)
PHLEBITIS SUPERFICIAL ( 9 FDA reports)
PLASTIC SURGERY TO THE FACE ( 9 FDA reports)
POLYCYTHAEMIA ( 9 FDA reports)
POLYDIPSIA ( 9 FDA reports)
POLYP ( 9 FDA reports)
POLYP COLORECTAL ( 9 FDA reports)
POLYPECTOMY ( 9 FDA reports)
PULMONARY THROMBOSIS ( 9 FDA reports)
REHABILITATION THERAPY ( 9 FDA reports)
RENAL TUBULAR DISORDER ( 9 FDA reports)
RESPIRATORY TRACT CONGESTION ( 9 FDA reports)
SARCOIDOSIS ( 9 FDA reports)
SHOULDER PAIN ( 9 FDA reports)
SKIN EROSION ( 9 FDA reports)
SKIN INFECTION ( 9 FDA reports)
THROMBOCYTHAEMIA ( 9 FDA reports)
TOE OPERATION ( 9 FDA reports)
VENA CAVA INJURY ( 9 FDA reports)
VENOUS THROMBOSIS ( 9 FDA reports)
VENTRICULAR HYPOKINESIA ( 9 FDA reports)
VULVOVAGINAL PRURITUS ( 9 FDA reports)
ABSCESS INTESTINAL ( 8 FDA reports)
ACIDOSIS HYPERCHLORAEMIC ( 8 FDA reports)
ACTINOMYCES TEST POSITIVE ( 8 FDA reports)
APICECTOMY ( 8 FDA reports)
ASTHENOPIA ( 8 FDA reports)
AURA ( 8 FDA reports)
BLINDNESS CORTICAL ( 8 FDA reports)
BLOOD AMYLASE INCREASED ( 8 FDA reports)
BLOOD CHLORIDE DECREASED ( 8 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 8 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 8 FDA reports)
BLOOD TEST ABNORMAL ( 8 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 8 FDA reports)
BODY TINEA ( 8 FDA reports)
BONE FISTULA ( 8 FDA reports)
BRAIN DAMAGE ( 8 FDA reports)
BREAST SWELLING ( 8 FDA reports)
CATHETERISATION CARDIAC ( 8 FDA reports)
CEREBROVASCULAR DISORDER ( 8 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 8 FDA reports)
DENTAL IMPLANTATION ( 8 FDA reports)
DEPERSONALISATION ( 8 FDA reports)
DEVICE MALFUNCTION ( 8 FDA reports)
DYSPLASIA ( 8 FDA reports)
EFFUSION ( 8 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 8 FDA reports)
EXANTHEM ( 8 FDA reports)
FACET JOINT BLOCK ( 8 FDA reports)
FALLOT'S TETRALOGY ( 8 FDA reports)
FEAR OF DEATH ( 8 FDA reports)
FINGER AMPUTATION ( 8 FDA reports)
GAMMOPATHY ( 8 FDA reports)
HAEMATOCRIT INCREASED ( 8 FDA reports)
HAEMOGLOBIN INCREASED ( 8 FDA reports)
HYPERBILIRUBINAEMIA ( 8 FDA reports)
HYPERPROLACTINAEMIA ( 8 FDA reports)
HYPERTENSIVE HEART DISEASE ( 8 FDA reports)
HYPOTHERMIA ( 8 FDA reports)
IMMOBILE ( 8 FDA reports)
IMMUNOGLOBULINS DECREASED ( 8 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 8 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 8 FDA reports)
INJECTION SITE EXTRAVASATION ( 8 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 8 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 8 FDA reports)
INTRA-UTERINE DEATH ( 8 FDA reports)
IRIS ATROPHY ( 8 FDA reports)
IRITIS ( 8 FDA reports)
JAUNDICE CHOLESTATIC ( 8 FDA reports)
JUGULAR VEIN THROMBOSIS ( 8 FDA reports)
LEG AMPUTATION ( 8 FDA reports)
LIMB OPERATION ( 8 FDA reports)
LIVEDO RETICULARIS ( 8 FDA reports)
MEDICAL DEVICE REMOVAL ( 8 FDA reports)
MENSTRUATION IRREGULAR ( 8 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 8 FDA reports)
METASTATIC PAIN ( 8 FDA reports)
MICROVASCULAR ANGINA ( 8 FDA reports)
MITRAL VALVE CALCIFICATION ( 8 FDA reports)
MIXED CONNECTIVE TISSUE DISEASE ( 8 FDA reports)
MUSCULOSKELETAL DISORDER ( 8 FDA reports)
NAIL OPERATION ( 8 FDA reports)
NASOPHARYNGEAL DISORDER ( 8 FDA reports)
NEPHROTIC SYNDROME ( 8 FDA reports)
ODONTOGENIC CYST ( 8 FDA reports)
OESOPHAGEAL STENOSIS ( 8 FDA reports)
PAINFUL RESPIRATION ( 8 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 8 FDA reports)
PARTNER STRESS ( 8 FDA reports)
PERICARDITIS ( 8 FDA reports)
PERITONITIS ( 8 FDA reports)
PLEURAL FIBROSIS ( 8 FDA reports)
PLEURODESIS ( 8 FDA reports)
PNEUMONIA KLEBSIELLA ( 8 FDA reports)
PO2 DECREASED ( 8 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 8 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 8 FDA reports)
PSYCHOSOMATIC DISEASE ( 8 FDA reports)
PULMONARY HAEMORRHAGE ( 8 FDA reports)
PULMONARY HILUM MASS ( 8 FDA reports)
RASH PUSTULAR ( 8 FDA reports)
RETINAL DETACHMENT ( 8 FDA reports)
SEDATION ( 8 FDA reports)
SINUS OPERATION ( 8 FDA reports)
SJOGREN'S SYNDROME ( 8 FDA reports)
SKIN HAEMORRHAGE ( 8 FDA reports)
SKIN IRRITATION ( 8 FDA reports)
SKIN PLAQUE ( 8 FDA reports)
SOFT TISSUE INFLAMMATION ( 8 FDA reports)
SPINAL CORD DISORDER ( 8 FDA reports)
SPLENIC INFARCTION ( 8 FDA reports)
SPONDYLITIC MYELOPATHY ( 8 FDA reports)
SPONDYLOLYSIS ( 8 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 8 FDA reports)
STRIDOR ( 8 FDA reports)
THORACOSTOMY ( 8 FDA reports)
THYROID DISORDER ( 8 FDA reports)
TINEA PEDIS ( 8 FDA reports)
UPPER AIRWAY RESISTANCE SYNDROME ( 8 FDA reports)
UPPER LIMB FRACTURE ( 8 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 8 FDA reports)
UROSEPSIS ( 8 FDA reports)
VASCULAR PSEUDOANEURYSM ( 8 FDA reports)
ABDOMINAL ABSCESS ( 7 FDA reports)
ABDOMINAL HERNIA ( 7 FDA reports)
ABDOMINAL RIGIDITY ( 7 FDA reports)
ACUTE PSYCHOSIS ( 7 FDA reports)
AMENORRHOEA ( 7 FDA reports)
ANKLE FRACTURE ( 7 FDA reports)
ARTERIAL THROMBOSIS ( 7 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 7 FDA reports)
BACTERIAL SEPSIS ( 7 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 7 FDA reports)
BLOOD BLISTER ( 7 FDA reports)
BLOOD CULTURE POSITIVE ( 7 FDA reports)
BREAST CYST ( 7 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 7 FDA reports)
BRONCHITIS CHRONIC ( 7 FDA reports)
CARDIAC FAILURE ACUTE ( 7 FDA reports)
CORNEAL OEDEMA ( 7 FDA reports)
CORONARY ARTERY BYPASS ( 7 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 7 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 7 FDA reports)
DIABETIC NEPHROPATHY ( 7 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 7 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 7 FDA reports)
EMBOLISM ( 7 FDA reports)
EXCESSIVE EYE BLINKING ( 7 FDA reports)
EYE ALLERGY ( 7 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 7 FDA reports)
GAIT DEVIATION ( 7 FDA reports)
GENITAL BURNING SENSATION ( 7 FDA reports)
GLOMERULONEPHRITIS ( 7 FDA reports)
GRANULOMA ( 7 FDA reports)
HALLUCINATIONS, MIXED ( 7 FDA reports)
HEPATORENAL FAILURE ( 7 FDA reports)
INCISION SITE ABSCESS ( 7 FDA reports)
INCISIONAL DRAINAGE ( 7 FDA reports)
INCORRECT DOSE ADMINISTERED ( 7 FDA reports)
INFARCTION ( 7 FDA reports)
IRIS ADHESIONS ( 7 FDA reports)
IRIS DISORDER ( 7 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 7 FDA reports)
LYMPHADENECTOMY ( 7 FDA reports)
LYMPHANGITIS ( 7 FDA reports)
LYMPHOPENIA ( 7 FDA reports)
MACULAR OEDEMA ( 7 FDA reports)
MACULOPATHY ( 7 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 7 FDA reports)
METASTASIS ( 7 FDA reports)
METRORRHAGIA ( 7 FDA reports)
MIGRAINE WITH AURA ( 7 FDA reports)
MONOPLEGIA ( 7 FDA reports)
MORBID THOUGHTS ( 7 FDA reports)
MUSCLE FATIGUE ( 7 FDA reports)
OPTIC NEUROPATHY ( 7 FDA reports)
ORAL MUCOSA EROSION ( 7 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 7 FDA reports)
OS TRIGONUM SYNDROME ( 7 FDA reports)
OSTEOTOMY ( 7 FDA reports)
OVERWEIGHT ( 7 FDA reports)
PARAPARESIS ( 7 FDA reports)
PARKINSON'S DISEASE ( 7 FDA reports)
PNEUMONIA BACTERIAL ( 7 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 7 FDA reports)
POLYARTHRITIS ( 7 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 7 FDA reports)
PROTEIN URINE PRESENT ( 7 FDA reports)
PRURITUS GENITAL ( 7 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 7 FDA reports)
PSORIASIS ( 7 FDA reports)
PTERYGIUM ( 7 FDA reports)
PULMONARY AIR LEAKAGE ( 7 FDA reports)
PYELOCALIECTASIS ( 7 FDA reports)
RASH MORBILLIFORM ( 7 FDA reports)
RECTAL PROLAPSE ( 7 FDA reports)
REGURGITATION ( 7 FDA reports)
RESIDUAL URINE ( 7 FDA reports)
RESPIRATORY DEPRESSION ( 7 FDA reports)
RESPIRATORY RATE DECREASED ( 7 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 7 FDA reports)
RETROPERITONEAL HAEMATOMA ( 7 FDA reports)
REVERSIBLE AIRWAYS OBSTRUCTION ( 7 FDA reports)
SELF-INJURIOUS IDEATION ( 7 FDA reports)
SEPSIS SYNDROME ( 7 FDA reports)
SEROSITIS ( 7 FDA reports)
SERUM FERRITIN INCREASED ( 7 FDA reports)
SKELETAL INJURY ( 7 FDA reports)
SKIN OEDEMA ( 7 FDA reports)
SKIN ULCER HAEMORRHAGE ( 7 FDA reports)
SKIN WRINKLING ( 7 FDA reports)
SLEEP TERROR ( 7 FDA reports)
SPUTUM CULTURE POSITIVE ( 7 FDA reports)
STATUS ASTHMATICUS ( 7 FDA reports)
SUFFOCATION FEELING ( 7 FDA reports)
SUPERINFECTION ( 7 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 7 FDA reports)
TEMPERATURE INTOLERANCE ( 7 FDA reports)
TENDON SHEATH INCISION ( 7 FDA reports)
TENSION HEADACHE ( 7 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 7 FDA reports)
THERMAL BURN ( 7 FDA reports)
TIBIA FRACTURE ( 7 FDA reports)
TIC ( 7 FDA reports)
TRACHEAL STENOSIS ( 7 FDA reports)
TUBERCULOSIS ( 7 FDA reports)
TYPE III IMMUNE COMPLEX MEDIATED REACTION ( 7 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 7 FDA reports)
VAGINAL HAEMORRHAGE ( 7 FDA reports)
VENTRICULAR DYSFUNCTION ( 7 FDA reports)
ABNORMAL SENSATION IN EYE ( 6 FDA reports)
ACCOMMODATION DISORDER ( 6 FDA reports)
ACTINIC KERATOSIS ( 6 FDA reports)
ALCOHOL ABUSE ( 6 FDA reports)
ALLODYNIA ( 6 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 6 FDA reports)
ALVEOLITIS ( 6 FDA reports)
AMAUROSIS FUGAX ( 6 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 6 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 6 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 6 FDA reports)
B-CELL LYMPHOMA ( 6 FDA reports)
BACTERIA URINE ( 6 FDA reports)
BLADDER CATHETERISATION ( 6 FDA reports)
BLOOD IRON DECREASED ( 6 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 6 FDA reports)
BONE MARROW OEDEMA ( 6 FDA reports)
BRADYPHRENIA ( 6 FDA reports)
BREAST CANCER IN SITU ( 6 FDA reports)
CARDIAC OUTPUT DECREASED ( 6 FDA reports)
CARDIAC TAMPONADE ( 6 FDA reports)
CAROTID ARTERY OCCLUSION ( 6 FDA reports)
CAROTID BRUIT ( 6 FDA reports)
CHEST WALL PAIN ( 6 FDA reports)
CHOLANGITIS ( 6 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 6 FDA reports)
COLONOSCOPY ( 6 FDA reports)
COR PULMONALE ( 6 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 6 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 6 FDA reports)
DRUG-INDUCED LIVER INJURY ( 6 FDA reports)
DYSPLASTIC NAEVUS SYNDROME ( 6 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 6 FDA reports)
EXFOLIATIVE RASH ( 6 FDA reports)
EXTRAOCULAR MUSCLE PARESIS ( 6 FDA reports)
FAECALURIA ( 6 FDA reports)
FAECES PALE ( 6 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 6 FDA reports)
FIBRIN D DIMER INCREASED ( 6 FDA reports)
FRACTURE DISPLACEMENT ( 6 FDA reports)
FRACTURE NONUNION ( 6 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 6 FDA reports)
GENITAL LESION ( 6 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 6 FDA reports)
GRANULOCYTE COUNT DECREASED ( 6 FDA reports)
HEMIPLEGIA ( 6 FDA reports)
HEPATIC PAIN ( 6 FDA reports)
HILAR LYMPHADENOPATHY ( 6 FDA reports)
HYPOPROTEINAEMIA ( 6 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 6 FDA reports)
IMPETIGO ( 6 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 6 FDA reports)
INCREASED BRONCHIAL SECRETION ( 6 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 6 FDA reports)
INFUSION SITE SWELLING ( 6 FDA reports)
INJECTION SITE PRURITUS ( 6 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 6 FDA reports)
LARGE INTESTINAL ULCER ( 6 FDA reports)
LIGAMENT DISORDER ( 6 FDA reports)
LIGAMENT INJURY ( 6 FDA reports)
LOW TURNOVER OSTEOPATHY ( 6 FDA reports)
LUNG ADENOCARCINOMA ( 6 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 6 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 6 FDA reports)
MASTOIDITIS ( 6 FDA reports)
MECHANICAL VENTILATION ( 6 FDA reports)
MEGACOLON ( 6 FDA reports)
METASTASES TO MENINGES ( 6 FDA reports)
MIDDLE EAR EFFUSION ( 6 FDA reports)
MIOSIS ( 6 FDA reports)
MITRAL VALVE SCLEROSIS ( 6 FDA reports)
MULTIPLE FRACTURES ( 6 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 6 FDA reports)
NIGHT BLINDNESS ( 6 FDA reports)
NODAL RHYTHM ( 6 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 6 FDA reports)
OCCULT BLOOD ( 6 FDA reports)
OCULOMUCOCUTANEOUS SYNDROME ( 6 FDA reports)
ONYCHOCLASIS ( 6 FDA reports)
OPTIC NERVE DISORDER ( 6 FDA reports)
OXYGEN SUPPLEMENTATION ( 6 FDA reports)
PANCREATITIS CHRONIC ( 6 FDA reports)
PERIORBITAL OEDEMA ( 6 FDA reports)
PHARYNGOLARYNGEAL DISCOMFORT ( 6 FDA reports)
PLANTAR ERYTHEMA ( 6 FDA reports)
PNEUMONIA FUNGAL ( 6 FDA reports)
PNEUMONITIS CHEMICAL ( 6 FDA reports)
PO2 INCREASED ( 6 FDA reports)
PROCTOCOLITIS ( 6 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 6 FDA reports)
PSYCHIATRIC SYMPTOM ( 6 FDA reports)
PULSE ABNORMAL ( 6 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 6 FDA reports)
PYOGENIC GRANULOMA ( 6 FDA reports)
RADIUS FRACTURE ( 6 FDA reports)
RECTAL DISCHARGE ( 6 FDA reports)
RESUSCITATION ( 6 FDA reports)
ROSACEA ( 6 FDA reports)
SALIVARY HYPERSECRETION ( 6 FDA reports)
SEBORRHOEIC DERMATITIS ( 6 FDA reports)
SINUS ARREST ( 6 FDA reports)
SKIN FISSURES ( 6 FDA reports)
SOMNAMBULISM ( 6 FDA reports)
STENT PLACEMENT ( 6 FDA reports)
TENDON GRAFT ( 6 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 6 FDA reports)
TOE AMPUTATION ( 6 FDA reports)
TOOTH DISCOLOURATION ( 6 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 6 FDA reports)
TRAUMATIC RENAL INJURY ( 6 FDA reports)
TRIGGER FINGER ( 6 FDA reports)
TRISMUS ( 6 FDA reports)
TUMOUR LYSIS SYNDROME ( 6 FDA reports)
TYPE 1 DIABETES MELLITUS ( 6 FDA reports)
URINE ANALYSIS ABNORMAL ( 6 FDA reports)
VASCULAR ENCEPHALOPATHY ( 6 FDA reports)
VASCULAR GRAFT OCCLUSION ( 6 FDA reports)
VASCULAR RUPTURE ( 6 FDA reports)
VEIN DISORDER ( 6 FDA reports)
VESTIBULAR DISORDER ( 6 FDA reports)
VOCAL CORD DISORDER ( 6 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 6 FDA reports)
WHEELCHAIR USER ( 6 FDA reports)
X-RAY ( 6 FDA reports)
ABNORMAL FAECES ( 5 FDA reports)
ACUTE LUNG INJURY ( 5 FDA reports)
ADNEXA UTERI MASS ( 5 FDA reports)
AKATHISIA ( 5 FDA reports)
ALBUMIN URINE PRESENT ( 5 FDA reports)
ANKYLOSING SPONDYLITIS ( 5 FDA reports)
ANORECTAL DISORDER ( 5 FDA reports)
ARTERITIS ( 5 FDA reports)
ASPERGILLOSIS ( 5 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 5 FDA reports)
BACTERIA URINE IDENTIFIED ( 5 FDA reports)
BILIARY TRACT DISORDER ( 5 FDA reports)
BIPOLAR I DISORDER ( 5 FDA reports)
BLEPHARITIS ( 5 FDA reports)
BLOOD COUNT ABNORMAL ( 5 FDA reports)
BLOOD DISORDER ( 5 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 5 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 5 FDA reports)
BLOOD MAGNESIUM INCREASED ( 5 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 5 FDA reports)
BONE NEOPLASM ( 5 FDA reports)
BRAIN ABSCESS ( 5 FDA reports)
BRONCHIAL DISORDER ( 5 FDA reports)
BRONCHIAL OBSTRUCTION ( 5 FDA reports)
BRONCHITIS ACUTE ( 5 FDA reports)
BRONCHITIS VIRAL ( 5 FDA reports)
CARDIAC PACEMAKER INSERTION ( 5 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 5 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 5 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 5 FDA reports)
CARTILAGE INJURY ( 5 FDA reports)
CATATONIA ( 5 FDA reports)
CEREBROSPINAL FLUID RESERVOIR PLACEMENT ( 5 FDA reports)
CHONDROPLASTY ( 5 FDA reports)
CHROMATOPSIA ( 5 FDA reports)
COLECTOMY ( 5 FDA reports)
COMPULSIONS ( 5 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 5 FDA reports)
CULTURE URINE POSITIVE ( 5 FDA reports)
CUSHINGOID ( 5 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 5 FDA reports)
DIABETIC FOOT ( 5 FDA reports)
DROOLING ( 5 FDA reports)
DRUG ADMINISTRATION ERROR ( 5 FDA reports)
EMERGENCY CARE ( 5 FDA reports)
ESSENTIAL HYPERTENSION ( 5 FDA reports)
EYE OEDEMA ( 5 FDA reports)
EYE ROLLING ( 5 FDA reports)
FAECALOMA ( 5 FDA reports)
FEMALE STERILISATION ( 5 FDA reports)
FLATBACK SYNDROME ( 5 FDA reports)
FLUID INTAKE REDUCED ( 5 FDA reports)
FOOD ALLERGY ( 5 FDA reports)
FOREIGN BODY TRAUMA ( 5 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 5 FDA reports)
GENITAL INFECTION FUNGAL ( 5 FDA reports)
GENITAL ULCERATION ( 5 FDA reports)
GINGIVAL CYST ( 5 FDA reports)
HAEMOCHROMATOSIS ( 5 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 5 FDA reports)
HEART SOUNDS ABNORMAL ( 5 FDA reports)
HELICOBACTER GASTRITIS ( 5 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 5 FDA reports)
HOMICIDAL IDEATION ( 5 FDA reports)
HYDROURETER ( 5 FDA reports)
HYPERACUSIS ( 5 FDA reports)
HYPERAMYLASAEMIA ( 5 FDA reports)
HYPOCHONDRIASIS ( 5 FDA reports)
HYPOSMIA ( 5 FDA reports)
INCISIONAL HERNIA ( 5 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 5 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 5 FDA reports)
INFUSION SITE IRRITATION ( 5 FDA reports)
INJECTION SITE SWELLING ( 5 FDA reports)
INTESTINAL HAEMORRHAGE ( 5 FDA reports)
KIDNEY INFECTION ( 5 FDA reports)
LABYRINTHITIS ( 5 FDA reports)
LICHEN PLANUS ( 5 FDA reports)
LIVER TRANSPLANT REJECTION ( 5 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 5 FDA reports)
LUNG INJURY ( 5 FDA reports)
LYMPH NODE PAIN ( 5 FDA reports)
MACULAR DEGENERATION ( 5 FDA reports)
MALIGNANT HYPERTENSION ( 5 FDA reports)
MEDIASTINAL MASS ( 5 FDA reports)
METABOLIC ENCEPHALOPATHY ( 5 FDA reports)
MICTURITION FREQUENCY DECREASED ( 5 FDA reports)
MILLER FISHER SYNDROME ( 5 FDA reports)
MUCOUS STOOLS ( 5 FDA reports)
MUSCLE SPASTICITY ( 5 FDA reports)
NASAL OBSTRUCTION ( 5 FDA reports)
NEPHRITIS ALLERGIC ( 5 FDA reports)
NEPHROPATHY TOXIC ( 5 FDA reports)
NERVE ROOT COMPRESSION ( 5 FDA reports)
NERVE ROOT INJURY LUMBAR ( 5 FDA reports)
NEUTROPHILIA ( 5 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 5 FDA reports)
OESOPHAGEAL DILATATION ( 5 FDA reports)
ORAL TORUS ( 5 FDA reports)
ORBITAL OEDEMA ( 5 FDA reports)
OSTEOMYELITIS CHRONIC ( 5 FDA reports)
OTITIS MEDIA CHRONIC ( 5 FDA reports)
OTOTOXICITY ( 5 FDA reports)
PANCREATIC MASS ( 5 FDA reports)
PARESIS ( 5 FDA reports)
PEMPHIGOID ( 5 FDA reports)
PERIRECTAL ABSCESS ( 5 FDA reports)
PHARYNGEAL DISORDER ( 5 FDA reports)
PHARYNGEAL ULCERATION ( 5 FDA reports)
PLATELET DISORDER ( 5 FDA reports)
PORTAL VEIN THROMBOSIS ( 5 FDA reports)
POSTNASAL DRIP ( 5 FDA reports)
POSTURING ( 5 FDA reports)
PRESCRIBED OVERDOSE ( 5 FDA reports)
PROSTHESIS USER ( 5 FDA reports)
PROTEIN TOTAL DECREASED ( 5 FDA reports)
PROTHROMBIN TIME SHORTENED ( 5 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 5 FDA reports)
PYLORIC STENOSIS ( 5 FDA reports)
ROTATOR CUFF REPAIR ( 5 FDA reports)
SELF-MEDICATION ( 5 FDA reports)
SLEEP WALKING ( 5 FDA reports)
STATUS EPILEPTICUS ( 5 FDA reports)
SUBCUTANEOUS NODULE ( 5 FDA reports)
TARSAL TUNNEL SYNDROME ( 5 FDA reports)
TEMPERATURE REGULATION DISORDER ( 5 FDA reports)
TEMPORAL ARTERITIS ( 5 FDA reports)
TRANSPLANT ( 5 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 5 FDA reports)
UPPER EXTREMITY MASS ( 5 FDA reports)
URETERIC DILATATION ( 5 FDA reports)
URETHRAL PAIN ( 5 FDA reports)
VEIN DISCOLOURATION ( 5 FDA reports)
VESSEL PUNCTURE SITE SWELLING ( 5 FDA reports)
VIRAL RASH ( 5 FDA reports)
VITAMIN D DECREASED ( 5 FDA reports)
VITH NERVE PARALYSIS ( 5 FDA reports)
VULVOVAGINAL DRYNESS ( 5 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 5 FDA reports)
ABDOMINAL MASS ( 4 FDA reports)
ABDOMINAL WALL ABSCESS ( 4 FDA reports)
ABORTION INDUCED ( 4 FDA reports)
ABORTION SPONTANEOUS ( 4 FDA reports)
ABSCESS BACTERIAL ( 4 FDA reports)
ACQUIRED EPIDERMOLYSIS BULLOSA ( 4 FDA reports)
ADNEXA UTERI CYST ( 4 FDA reports)
ADRENAL NEOPLASM ( 4 FDA reports)
ALBINISM ( 4 FDA reports)
ANAL DISCOMFORT ( 4 FDA reports)
ANORECTAL OPERATION ( 4 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 4 FDA reports)
APHAKIA ( 4 FDA reports)
APPLICATION SITE RASH ( 4 FDA reports)
APRAXIA ( 4 FDA reports)
AZOOSPERMIA ( 4 FDA reports)
BARRETT'S OESOPHAGUS ( 4 FDA reports)
BENIGN NEOPLASM OF ADRENAL GLAND ( 4 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 4 FDA reports)
BILIARY DYSKINESIA ( 4 FDA reports)
BLADDER SPASM ( 4 FDA reports)
BLOOD CALCIUM INCREASED ( 4 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 4 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 4 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ABNORMAL ( 4 FDA reports)
BONE DENSITY INCREASED ( 4 FDA reports)
BONE MARROW DEPRESSION ( 4 FDA reports)
BONE NEOPLASM MALIGNANT ( 4 FDA reports)
BREAST CALCIFICATIONS ( 4 FDA reports)
BREAST DISCHARGE ( 4 FDA reports)
BRONCHIAL SECRETION RETENTION ( 4 FDA reports)
CARDIAC DISCOMFORT ( 4 FDA reports)
CARDIAC ENZYMES INCREASED ( 4 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 4 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 4 FDA reports)
CEREBRAL HAEMORRHAGE TRAUMATIC ( 4 FDA reports)
CHRONIC HEPATITIS ( 4 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 4 FDA reports)
COLONIC STENOSIS ( 4 FDA reports)
COMMINUTED FRACTURE ( 4 FDA reports)
CONJUNCTIVAL PRIMARY ACQUIRED MELANOSIS ( 4 FDA reports)
CONNECTIVE TISSUE INFLAMMATION ( 4 FDA reports)
CONVERSION DISORDER ( 4 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 4 FDA reports)
CRYSTAL URINE ( 4 FDA reports)
CYTOLYTIC HEPATITIS ( 4 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 4 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 4 FDA reports)
DECEREBRATION ( 4 FDA reports)
DELUSIONAL PERCEPTION ( 4 FDA reports)
DEVICE BREAKAGE ( 4 FDA reports)
DIABETIC KETOACIDOTIC HYPERGLYCAEMIC COMA ( 4 FDA reports)
DIVERTICULAR PERFORATION ( 4 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 4 FDA reports)
DRUG DISPENSING ERROR ( 4 FDA reports)
DRUG RESISTANCE ( 4 FDA reports)
DRUG USE FOR UNKNOWN INDICATION ( 4 FDA reports)
DUPUYTREN'S CONTRACTURE ( 4 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 4 FDA reports)
EAR CANAL STENOSIS ( 4 FDA reports)
ELECTROCARDIOGRAM QT INTERVAL ABNORMAL ( 4 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 4 FDA reports)
ENDOTRACHEAL INTUBATION ( 4 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 4 FDA reports)
ERYTHEMA INFECTIOSUM ( 4 FDA reports)
ESCHERICHIA TEST POSITIVE ( 4 FDA reports)
EYE HAEMORRHAGE ( 4 FDA reports)
EYE INFLAMMATION ( 4 FDA reports)
FACE LIFT ( 4 FDA reports)
FEELING HOT AND COLD ( 4 FDA reports)
FEMORAL ARTERY OCCLUSION ( 4 FDA reports)
FISTULA DISCHARGE ( 4 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 4 FDA reports)
FOOD AVERSION ( 4 FDA reports)
FOOD CRAVING ( 4 FDA reports)
FULL BLOOD COUNT DECREASED ( 4 FDA reports)
FUNGAL SKIN INFECTION ( 4 FDA reports)
GALLBLADDER OPERATION ( 4 FDA reports)
GASTRIC BYPASS ( 4 FDA reports)
GASTRIC INFECTION ( 4 FDA reports)
GASTRIC MUCOSAL HYPERTROPHY ( 4 FDA reports)
GASTROINTESTINAL SURGERY ( 4 FDA reports)
GAZE PALSY ( 4 FDA reports)
GLUCOSE URINE PRESENT ( 4 FDA reports)
GUN SHOT WOUND ( 4 FDA reports)
HAEMORRHAGIC ANAEMIA ( 4 FDA reports)
HAEMOTHORAX ( 4 FDA reports)
HAIR DISORDER ( 4 FDA reports)
HEAD TITUBATION ( 4 FDA reports)
HEAT RASH ( 4 FDA reports)
HEPATIC ENZYME ABNORMAL ( 4 FDA reports)
HEPATIC MASS ( 4 FDA reports)
HEPATITIS VIRAL ( 4 FDA reports)
HIV INFECTION ( 4 FDA reports)
HOSTILITY ( 4 FDA reports)
HUNGER ( 4 FDA reports)
HYPERCOAGULATION ( 4 FDA reports)
HYPOALBUMINAEMIA ( 4 FDA reports)
HYPOGLYCAEMIC COMA ( 4 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 4 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 4 FDA reports)
IGA NEPHROPATHY ( 4 FDA reports)
INADEQUATE ANALGESIA ( 4 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 4 FDA reports)
INJECTION SITE THROMBOSIS ( 4 FDA reports)
INJURY CORNEAL ( 4 FDA reports)
INTESTINAL PROLAPSE ( 4 FDA reports)
ISCHAEMIC STROKE ( 4 FDA reports)
KLEBSIELLA INFECTION ( 4 FDA reports)
LACTOSE INTOLERANCE ( 4 FDA reports)
LARYNGOSPASM ( 4 FDA reports)
LIGAMENT PAIN ( 4 FDA reports)
LIMB DEFORMITY ( 4 FDA reports)
LIP EROSION ( 4 FDA reports)
LIP OEDEMA ( 4 FDA reports)
LISTLESS ( 4 FDA reports)
LOWER LIMB FRACTURE ( 4 FDA reports)
LUNG ABSCESS ( 4 FDA reports)
MALLORY-WEISS SYNDROME ( 4 FDA reports)
MARROW HYPERPLASIA ( 4 FDA reports)
MASTITIS ( 4 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 4 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 4 FDA reports)
MELANOSIS COLI ( 4 FDA reports)
MENINGITIS ASEPTIC ( 4 FDA reports)
MENINGITIS TUBERCULOUS ( 4 FDA reports)
MENINGOCOCCAL SEPSIS ( 4 FDA reports)
METASTASES TO PELVIS ( 4 FDA reports)
MICROANGIOPATHY ( 4 FDA reports)
MITRAL VALVE DISEASE ( 4 FDA reports)
MOUTH BREATHING ( 4 FDA reports)
MUCOSAL EROSION ( 4 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 4 FDA reports)
MUSCLE CONTRACTURE ( 4 FDA reports)
MYOCARDITIS ( 4 FDA reports)
NEOPLASM SKIN ( 4 FDA reports)
NERVE COMPRESSION ( 4 FDA reports)
NO ADVERSE DRUG EFFECT ( 4 FDA reports)
NONSPECIFIC REACTION ( 4 FDA reports)
OBSESSIVE THOUGHTS ( 4 FDA reports)
OESOPHAGEAL SPASM ( 4 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 4 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 4 FDA reports)
ORTHOSTATIC INTOLERANCE ( 4 FDA reports)
OVARIAN CYST ( 4 FDA reports)
PAROTID GLAND ENLARGEMENT ( 4 FDA reports)
PATHOGEN RESISTANCE ( 4 FDA reports)
PATHOLOGICAL GAMBLING ( 4 FDA reports)
PERFORMANCE STATUS DECREASED ( 4 FDA reports)
PERIPHERAL NERVE DECOMPRESSION ( 4 FDA reports)
PERITONEAL HAEMATOMA ( 4 FDA reports)
PERSECUTORY DELUSION ( 4 FDA reports)
PERTUSSIS ( 4 FDA reports)
PETIT MAL EPILEPSY ( 4 FDA reports)
PHARYNGEAL INFLAMMATION ( 4 FDA reports)
PLATELET COUNT ABNORMAL ( 4 FDA reports)
POLYMYALGIA RHEUMATICA ( 4 FDA reports)
POLYNEUROPATHY IDIOPATHIC PROGRESSIVE ( 4 FDA reports)
PORTAL HYPERTENSION ( 4 FDA reports)
PRE-EXISTING CONDITION IMPROVED ( 4 FDA reports)
PREGNANCY ( 4 FDA reports)
PROSTATIC PAIN ( 4 FDA reports)
PULMONARY TUBERCULOSIS ( 4 FDA reports)
PURPURA SENILE ( 4 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 4 FDA reports)
RESORPTION BONE INCREASED ( 4 FDA reports)
RESPIRATORY RATE ( 4 FDA reports)
SCREAMING ( 4 FDA reports)
SENSORY NEUROPATHY HEREDITARY ( 4 FDA reports)
SKIN LESION EXCISION ( 4 FDA reports)
SLUGGISHNESS ( 4 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 4 FDA reports)
SMALL INTESTINE CARCINOMA ( 4 FDA reports)
STREPTOCOCCAL SEPSIS ( 4 FDA reports)
STRESS INCONTINENCE ( 4 FDA reports)
SUDDEN HEARING LOSS ( 4 FDA reports)
TACHYPHRENIA ( 4 FDA reports)
TERMINAL STATE ( 4 FDA reports)
TESTICULAR SWELLING ( 4 FDA reports)
THROMBOCYTOPENIC PURPURA ( 4 FDA reports)
TOBACCO USER ( 4 FDA reports)
TONGUE BITING ( 4 FDA reports)
TOXIC ENCEPHALOPATHY ( 4 FDA reports)
TRANSPLANT FAILURE ( 4 FDA reports)
TREATMENT FAILURE ( 4 FDA reports)
TUNNEL VISION ( 4 FDA reports)
ULCER HAEMORRHAGE ( 4 FDA reports)
URGE INCONTINENCE ( 4 FDA reports)
URINARY HESITATION ( 4 FDA reports)
URINE BILIRUBIN INCREASED ( 4 FDA reports)
URINE KETONE BODY PRESENT ( 4 FDA reports)
UTERINE MASS ( 4 FDA reports)
VAGINAL DISCHARGE ( 4 FDA reports)
VARICES OESOPHAGEAL ( 4 FDA reports)
VASCULAR GRAFT COMPLICATION ( 4 FDA reports)
VENA CAVA THROMBOSIS ( 4 FDA reports)
VIITH NERVE PARALYSIS ( 4 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 4 FDA reports)
VITILIGO ( 4 FDA reports)
VOMITING PROJECTILE ( 4 FDA reports)
WITHDRAWAL SYNDROME ( 4 FDA reports)
ABDOMINAL INFECTION ( 3 FDA reports)
ABDOMINAL SEPSIS ( 3 FDA reports)
ABSCESS OF EYELID ( 3 FDA reports)
ACTINIC ELASTOSIS ( 3 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 3 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 3 FDA reports)
ACUTE LEUKAEMIA ( 3 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 3 FDA reports)
ALCOHOLISM ( 3 FDA reports)
ALKALOSIS ( 3 FDA reports)
ANAL FISSURE ( 3 FDA reports)
ANTITHROMBIN III DECREASED ( 3 FDA reports)
APATHY ( 3 FDA reports)
APLASIA ( 3 FDA reports)
APNOEIC ATTACK ( 3 FDA reports)
APPETITE DISORDER ( 3 FDA reports)
ARTERIAL DISORDER ( 3 FDA reports)
ARTERIOSPASM CORONARY ( 3 FDA reports)
ARTHRITIS INFECTIVE ( 3 FDA reports)
ARTHRITIS REACTIVE ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK THIRD DEGREE ( 3 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 3 FDA reports)
AVULSION FRACTURE ( 3 FDA reports)
BACTERIA STOOL IDENTIFIED ( 3 FDA reports)
BALANITIS CANDIDA ( 3 FDA reports)
BASEDOW'S DISEASE ( 3 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 3 FDA reports)
BIOPSY ( 3 FDA reports)
BLOOD ALBUMIN INCREASED ( 3 FDA reports)
BLOOD BICARBONATE DECREASED ( 3 FDA reports)
BLOOD CHLORIDE INCREASED ( 3 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 3 FDA reports)
BLOOD CREATINE ABNORMAL ( 3 FDA reports)
BLOOD GASES ABNORMAL ( 3 FDA reports)
BLOOD PH DECREASED ( 3 FDA reports)
BLOODY DISCHARGE ( 3 FDA reports)
BONE CALLUS EXCESSIVE ( 3 FDA reports)
BONE MARROW TOXICITY ( 3 FDA reports)
BRAIN CONTUSION ( 3 FDA reports)
BRAIN DEATH ( 3 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 3 FDA reports)
BRAIN SCAN ABNORMAL ( 3 FDA reports)
BREAST CANCER FEMALE ( 3 FDA reports)
BREAST DISORDER ( 3 FDA reports)
BREAST MILK DISCOLOURATION ( 3 FDA reports)
BREAST NECROSIS ( 3 FDA reports)
BREATH HOLDING ( 3 FDA reports)
BRONCHITIS BACTERIAL ( 3 FDA reports)
BUDD-CHIARI SYNDROME ( 3 FDA reports)
BULIMIA NERVOSA ( 3 FDA reports)
BURSA DISORDER ( 3 FDA reports)
CALCINOSIS ( 3 FDA reports)
CANDIDA SEPSIS ( 3 FDA reports)
CARDIOPULMONARY FAILURE ( 3 FDA reports)
CARDIOVERSION ( 3 FDA reports)
CAROTID ARTERY ANEURYSM ( 3 FDA reports)
CATHETER RELATED INFECTION ( 3 FDA reports)
CD4 LYMPHOCYTES INCREASED ( 3 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 3 FDA reports)
CHAPPED LIPS ( 3 FDA reports)
CHLAMYDIAL INFECTION ( 3 FDA reports)
CHOLECYSTITIS INFECTIVE ( 3 FDA reports)
CHONDROPATHY ( 3 FDA reports)
CHOREA ( 3 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 3 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 3 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 3 FDA reports)
CLAVICLE FRACTURE ( 3 FDA reports)
CLOSTRIDIUM DIFFICILE SEPSIS ( 3 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 3 FDA reports)
COAGULATION TIME PROLONGED ( 3 FDA reports)
COMA HEPATIC ( 3 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 3 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 3 FDA reports)
CONGENITAL ANOMALY ( 3 FDA reports)
CONJUNCTIVITIS VIRAL ( 3 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 3 FDA reports)
CONVULSIVE THRESHOLD LOWERED ( 3 FDA reports)
CORNEAL DEPOSITS ( 3 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 3 FDA reports)
CORONARY ARTERY RESTENOSIS ( 3 FDA reports)
CULTURE WOUND POSITIVE ( 3 FDA reports)
CYTOMEGALOVIRUS HEPATITIS ( 3 FDA reports)
DEPENDENCE ( 3 FDA reports)
DERMATITIS ATOPIC ( 3 FDA reports)
DIABETIC COMPLICATION ( 3 FDA reports)
DIABETIC GASTROPARESIS ( 3 FDA reports)
DIAPHRAGMALGIA ( 3 FDA reports)
DIAPHRAGMATIC DISORDER ( 3 FDA reports)
DISEASE RECURRENCE ( 3 FDA reports)
DISSEMINATED TUBERCULOSIS ( 3 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 3 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 3 FDA reports)
DYSPHASIA ( 3 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 3 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 3 FDA reports)
ELECTROCARDIOGRAM QT SHORTENED ( 3 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 3 FDA reports)
EMBOLIC STROKE ( 3 FDA reports)
ENANTHEMA ( 3 FDA reports)
ENCEPHALOMALACIA ( 3 FDA reports)
ENDOCRINE DISORDER ( 3 FDA reports)
ENTEROCOCCAL SEPSIS ( 3 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 3 FDA reports)
EOSINOPHIL COUNT DECREASED ( 3 FDA reports)
EOSINOPHILIC PNEUMONIA ACUTE ( 3 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 3 FDA reports)
EXTRAVASATION BLOOD ( 3 FDA reports)
FANCONI SYNDROME ( 3 FDA reports)
FINGER DEFORMITY ( 3 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 3 FDA reports)
FUNGAEMIA ( 3 FDA reports)
GALLBLADDER ENLARGEMENT ( 3 FDA reports)
GASTRIC DILATATION ( 3 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 3 FDA reports)
GASTRIC ULCER PERFORATION ( 3 FDA reports)
GASTROENTERITIS EOSINOPHILIC ( 3 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 3 FDA reports)
GENERALISED ANXIETY DISORDER ( 3 FDA reports)
GINGIVAL DISCOLOURATION ( 3 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 3 FDA reports)
HALO VISION ( 3 FDA reports)
HELICOBACTER INFECTION ( 3 FDA reports)
HEPATIC FIBROSIS ( 3 FDA reports)
HEPATIC ISCHAEMIA ( 3 FDA reports)
HEPATIC NEOPLASM ( 3 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 3 FDA reports)
HEPATIC VEIN OCCLUSION ( 3 FDA reports)
HEPATITIS A ( 3 FDA reports)
HIP ARTHROPLASTY ( 3 FDA reports)
HIP DEFORMITY ( 3 FDA reports)
HISTOPLASMOSIS ( 3 FDA reports)
HOARSENESS ( 3 FDA reports)
HODGKIN'S DISEASE STAGE IV ( 3 FDA reports)
HYPERALBUMINAEMIA ( 3 FDA reports)
HYPERCAPNIA ( 3 FDA reports)
HYPERLACTACIDAEMIA ( 3 FDA reports)
HYPOGONADISM ( 3 FDA reports)
IMPINGEMENT SYNDROME ( 3 FDA reports)
INCISION SITE COMPLICATION ( 3 FDA reports)
INFUSION SITE PAIN ( 3 FDA reports)
INJECTION SITE HAEMATOMA ( 3 FDA reports)
INJECTION SITE INDURATION ( 3 FDA reports)
INJECTION SITE RASH ( 3 FDA reports)
INJECTION SITE URTICARIA ( 3 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 3 FDA reports)
ISCHAEMIC ULCER ( 3 FDA reports)
JUGULAR VEIN DISTENSION ( 3 FDA reports)
KNEE DEFORMITY ( 3 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 3 FDA reports)
LID LAG ( 3 FDA reports)
LIP ULCERATION ( 3 FDA reports)
LOCKED-IN SYNDROME ( 3 FDA reports)
LOGORRHOEA ( 3 FDA reports)
LYMPHATIC DISORDER ( 3 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 3 FDA reports)
MARITAL PROBLEM ( 3 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 3 FDA reports)
MEDIASTINAL DISORDER ( 3 FDA reports)
MEDIASTINOSCOPY ( 3 FDA reports)
MEDICATION RESIDUE ( 3 FDA reports)
MELANOCYTIC NAEVUS ( 3 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 3 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 3 FDA reports)
METASTASES TO SPLEEN ( 3 FDA reports)
MICROSPORIDIA INFECTION ( 3 FDA reports)
MONOCYTE COUNT DECREASED ( 3 FDA reports)
MONONEURITIS ( 3 FDA reports)
MOUNTAIN SICKNESS ACUTE ( 3 FDA reports)
MOUTH INJURY ( 3 FDA reports)
MUSCLE HAEMORRHAGE ( 3 FDA reports)
MYASTHENIC SYNDROME ( 3 FDA reports)
MYCOPLASMA INFECTION ( 3 FDA reports)
MYOSCLEROSIS ( 3 FDA reports)
NARCOLEPSY ( 3 FDA reports)
NASAL DISORDER ( 3 FDA reports)
NASAL DRYNESS ( 3 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 3 FDA reports)
NIPPLE EXUDATE BLOODY ( 3 FDA reports)
OESOPHAGEAL PAIN ( 3 FDA reports)
ORAL PAPILLOMA ( 3 FDA reports)
ORGANIC ERECTILE DYSFUNCTION ( 3 FDA reports)
OSTEOGENESIS IMPERFECTA ( 3 FDA reports)
OXYGEN SATURATION ABNORMAL ( 3 FDA reports)
PANCREATIC INSUFFICIENCY ( 3 FDA reports)
PANCREATITIS RELAPSING ( 3 FDA reports)
PARAPLEGIA ( 3 FDA reports)
PAROTITIS ( 3 FDA reports)
PERINEAL ABSCESS ( 3 FDA reports)
PERIPHERAL NERVE LESION ( 3 FDA reports)
PHLEBOLITH ( 3 FDA reports)
PHONOPHOBIA ( 3 FDA reports)
PHYSICAL ASSAULT ( 3 FDA reports)
PIGMENT DISPERSION SYNDROME ( 3 FDA reports)
PITUITARY TUMOUR ( 3 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 3 FDA reports)
PNEUMONIA VIRAL ( 3 FDA reports)
POLYCYSTIC LIVER DISEASE ( 3 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 3 FDA reports)
POST LAMINECTOMY SYNDROME ( 3 FDA reports)
POST PROCEDURAL HAEMATOMA ( 3 FDA reports)
POTENTIATING DRUG INTERACTION ( 3 FDA reports)
PRE-ECLAMPSIA ( 3 FDA reports)
PROCEDURAL HYPOTENSION ( 3 FDA reports)
PROSTATE CANCER ( 3 FDA reports)
PROSTATE CANCER METASTATIC ( 3 FDA reports)
PROTEIN TOTAL INCREASED ( 3 FDA reports)
PROTEUS INFECTION ( 3 FDA reports)
PSYCHOTIC DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 3 FDA reports)
PULMONARY ARTERY STENOSIS CONGENITAL ( 3 FDA reports)
PULMONARY EOSINOPHILIA ( 3 FDA reports)
PULMONARY MYCOSIS ( 3 FDA reports)
PULMONARY TOXICITY ( 3 FDA reports)
PULSE PRESSURE DECREASED ( 3 FDA reports)
PYELONEPHRITIS ( 3 FDA reports)
PYODERMA GANGRENOSUM ( 3 FDA reports)
PYOTHORAX ( 3 FDA reports)
QUADRIPLEGIA ( 3 FDA reports)
RADIATION FIBROSIS - LUNG ( 3 FDA reports)
RECTAL ADENOMA ( 3 FDA reports)
RECTAL TENESMUS ( 3 FDA reports)
RED MAN SYNDROME ( 3 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 3 FDA reports)
RENAL CELL CARCINOMA ( 3 FDA reports)
RESPIRATION ABNORMAL ( 3 FDA reports)
RHINALGIA ( 3 FDA reports)
SCROTAL ULCER ( 3 FDA reports)
SEROTONIN SYNDROME ( 3 FDA reports)
SHOCK HAEMORRHAGIC ( 3 FDA reports)
SKIN CANDIDA ( 3 FDA reports)
SKIN DISCOMFORT ( 3 FDA reports)
SKIN INFLAMMATION ( 3 FDA reports)
SKIN SWELLING ( 3 FDA reports)
SKULL FRACTURE ( 3 FDA reports)
SKULL FRACTURED BASE ( 3 FDA reports)
SKULL X-RAY ABNORMAL ( 3 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 3 FDA reports)
SMALL INTESTINE ULCER ( 3 FDA reports)
SPINAL PAIN ( 3 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 3 FDA reports)
STARING ( 3 FDA reports)
STRABISMUS ( 3 FDA reports)
STRESS URINARY INCONTINENCE ( 3 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 3 FDA reports)
SURGICAL FAILURE ( 3 FDA reports)
TENDINOUS CONTRACTURE ( 3 FDA reports)
TETANY ( 3 FDA reports)
TONIC CLONIC MOVEMENTS ( 3 FDA reports)
TONSILLITIS ( 3 FDA reports)
TRACHEAL HAEMORRHAGE ( 3 FDA reports)
TRANSFUSION REACTION ( 3 FDA reports)
TRANSIENT PSYCHOSIS ( 3 FDA reports)
TRAUMATIC LUNG INJURY ( 3 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 3 FDA reports)
ULNA FRACTURE ( 3 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 3 FDA reports)
UMBILICAL HERNIA ( 3 FDA reports)
URETERIC OBSTRUCTION ( 3 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 3 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 3 FDA reports)
URINARY TRACT OBSTRUCTION ( 3 FDA reports)
URINE ABNORMALITY ( 3 FDA reports)
VAGINAL CANDIDIASIS ( 3 FDA reports)
VAGINITIS BACTERIAL ( 3 FDA reports)
VASCULAR INJURY ( 3 FDA reports)
VASCULAR OCCLUSION ( 3 FDA reports)
VASCULAR PUNCTURE SITE SEALING ( 3 FDA reports)
VASCULAR RESISTANCE SYSTEMIC INCREASED ( 3 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 3 FDA reports)
VIRAEMIA ( 3 FDA reports)
VITAMIN B COMPLEX DEFICIENCY ( 3 FDA reports)
WOUND ABSCESS ( 3 FDA reports)
WOUND INFECTION BACTERIAL ( 3 FDA reports)
WRIST FRACTURE ( 3 FDA reports)
XEROPHTHALMIA ( 3 FDA reports)
ABDOMINAL ADHESIONS ( 2 FDA reports)
ABDOMINAL AORTIC BRUIT ( 2 FDA reports)
ABDOMINAL SYMPTOM ( 2 FDA reports)
ABDOMINAL WALL DISORDER ( 2 FDA reports)
ABORTION ( 2 FDA reports)
ABORTION MISSED ( 2 FDA reports)
ABSCESS NECK ( 2 FDA reports)
ABSCESS SOFT TISSUE ( 2 FDA reports)
ACANTHOSIS ( 2 FDA reports)
ACCIDENT ( 2 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 2 FDA reports)
ADAMS-STOKES SYNDROME ( 2 FDA reports)
ADDISON'S DISEASE ( 2 FDA reports)
ADENOMA BENIGN ( 2 FDA reports)
ADHESION ( 2 FDA reports)
ADRENAL ADENOMA ( 2 FDA reports)
ADRENAL HAEMORRHAGE ( 2 FDA reports)
AGORAPHOBIA ( 2 FDA reports)
AIDS ENCEPHALOPATHY ( 2 FDA reports)
ALBUMINURIA ( 2 FDA reports)
ALLERGIC OEDEMA ( 2 FDA reports)
ALPHA 1 MICROGLOBULIN URINE INCREASED ( 2 FDA reports)
ALVEOLITIS ALLERGIC ( 2 FDA reports)
AMBLYOPIA ( 2 FDA reports)
ANAEMIA MACROCYTIC ( 2 FDA reports)
ANAEMIA MEGALOBLASTIC ( 2 FDA reports)
ANAEMIA POSTOPERATIVE ( 2 FDA reports)
ANAL CANDIDIASIS ( 2 FDA reports)
ANAL ULCER ( 2 FDA reports)
ANGIOGRAM ABNORMAL ( 2 FDA reports)
ANGIOPLASTY ( 2 FDA reports)
ANTASTHMATIC DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST ( 2 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 2 FDA reports)
AORTIC VALVE DISEASE ( 2 FDA reports)
AORTIC VALVE PROLAPSE ( 2 FDA reports)
APPARENT LIFE THREATENING EVENT ( 2 FDA reports)
APPENDICEAL ABSCESS ( 2 FDA reports)
APPENDIX DISORDER ( 2 FDA reports)
ARRESTED LABOUR ( 2 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 2 FDA reports)
ASEPTIC NECROSIS BONE ( 2 FDA reports)
ASPIRATION BREAST ( 2 FDA reports)
ASTHMATIC CRISIS ( 2 FDA reports)
ATHEROSCLEROSIS ( 2 FDA reports)
ATRIOVENTRICULAR DISSOCIATION ( 2 FDA reports)
AV DISSOCIATION ( 2 FDA reports)
AXILLARY PAIN ( 2 FDA reports)
AZYGOS LOBE ( 2 FDA reports)
BACTERIA TISSUE SPECIMEN IDENTIFIED ( 2 FDA reports)
BILE DUCT STENOSIS ( 2 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 2 FDA reports)
BINOCULAR EYE MOVEMENT DISORDER ( 2 FDA reports)
BIOPSY SITE UNSPECIFIED ABNORMAL ( 2 FDA reports)
BIOPSY SKIN ( 2 FDA reports)
BIOPSY SMALL INTESTINE ABNORMAL ( 2 FDA reports)
BIOPSY STOMACH ( 2 FDA reports)
BITE ( 2 FDA reports)
BLADDER ADENOCARCINOMA STAGE UNSPECIFIED ( 2 FDA reports)
BLADDER CANCER ( 2 FDA reports)
BLADDER DISORDER ( 2 FDA reports)
BLADDER NEOPLASM ( 2 FDA reports)
BLADDER OBSTRUCTION ( 2 FDA reports)
BLADDER PAIN ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE ( 2 FDA reports)
BLOOD BICARBONATE INCREASED ( 2 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 2 FDA reports)
BLOOD CORTISOL DECREASED ( 2 FDA reports)
BLOOD CREATININE ABNORMAL ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 2 FDA reports)
BLOOD LACTIC ACID INCREASED ( 2 FDA reports)
BLOOD PRESSURE ( 2 FDA reports)
BLOOD SODIUM INCREASED ( 2 FDA reports)
BLOOD UREA DECREASED ( 2 FDA reports)
BLOOD URIC ACID INCREASED ( 2 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 2 FDA reports)
BRADYARRHYTHMIA ( 2 FDA reports)
BREAST FIBROSIS ( 2 FDA reports)
BREAST TENDERNESS ( 2 FDA reports)
BRONCHOALVEOLAR LAVAGE ( 2 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 2 FDA reports)
BRONCHOSCOPY NORMAL ( 2 FDA reports)
BUNION ( 2 FDA reports)
CAECITIS ( 2 FDA reports)
CAESAREAN SECTION ( 2 FDA reports)
CALCULUS URINARY ( 2 FDA reports)
CANDIDURIA ( 2 FDA reports)
CARBOHYDRATE INTOLERANCE ( 2 FDA reports)
CARBON DIOXIDE ABNORMAL ( 2 FDA reports)
CARBON DIOXIDE DECREASED ( 2 FDA reports)
CARCINOID TUMOUR ( 2 FDA reports)
CARDIAC FAILURE HIGH OUTPUT ( 2 FDA reports)
CARDIAC HYPERTROPHY ( 2 FDA reports)
CARDIAC INFECTION ( 2 FDA reports)
CARDIOTOXICITY ( 2 FDA reports)
CATHETER SITE HAEMORRHAGE ( 2 FDA reports)
CATHETER SITE PAIN ( 2 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 2 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 2 FDA reports)
CENTRAL LINE INFECTION ( 2 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 2 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 2 FDA reports)
CEREBRAL ARTERY STENOSIS ( 2 FDA reports)
CEREBRAL THROMBOSIS ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT PROPHYLAXIS ( 2 FDA reports)
CERVIX CARCINOMA RECURRENT ( 2 FDA reports)
CHLAMYDIA SEROLOGY POSITIVE ( 2 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 2 FDA reports)
CITROBACTER INFECTION ( 2 FDA reports)
CLONIC CONVULSION ( 2 FDA reports)
CLONUS ( 2 FDA reports)
CLUBBING ( 2 FDA reports)
CLUMSINESS ( 2 FDA reports)
COGWHEEL RIGIDITY ( 2 FDA reports)
COLLAGEN DISORDER ( 2 FDA reports)
COLONOSCOPY ABNORMAL ( 2 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 2 FDA reports)
COMPULSIVE SHOPPING ( 2 FDA reports)
CONGENITAL AORTIC VALVE STENOSIS ( 2 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 2 FDA reports)
CONJUNCTIVAL OEDEMA ( 2 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 2 FDA reports)
COOMBS TEST POSITIVE ( 2 FDA reports)
CORNEAL OPACITY ( 2 FDA reports)
CORONARY ARTERY THROMBOSIS ( 2 FDA reports)
CRANIOCEREBRAL INJURY ( 2 FDA reports)
CRANIOTOMY ( 2 FDA reports)
CREST SYNDROME ( 2 FDA reports)
CUBITAL TUNNEL SYNDROME ( 2 FDA reports)
CUTIS LAXA ( 2 FDA reports)
DEPENDENCE ON RESPIRATOR ( 2 FDA reports)
DERMATITIS INFECTED ( 2 FDA reports)
DEVICE RELATED SEPSIS ( 2 FDA reports)
DIABETES INSIPIDUS ( 2 FDA reports)
DIABETIC COMA ( 2 FDA reports)
DRUG EFFECT INCREASED ( 2 FDA reports)
DRUG TOLERANCE ( 2 FDA reports)
DYSACUSIS ( 2 FDA reports)
DYSPNOEA EXACERBATED ( 2 FDA reports)
EAR HAEMORRHAGE ( 2 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 2 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 2 FDA reports)
ELEVATED MOOD ( 2 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 2 FDA reports)
ENCEPHALITIS VIRAL ( 2 FDA reports)
ENERGY INCREASED ( 2 FDA reports)
ENLARGED UVULA ( 2 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 2 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 2 FDA reports)
EROSIVE DUODENITIS ( 2 FDA reports)
ESSENTIAL TREMOR ( 2 FDA reports)
EUSTACHIAN TUBE OBSTRUCTION ( 2 FDA reports)
EYE DISCHARGE ( 2 FDA reports)
EYE INJURY ( 2 FDA reports)
EYE PENETRATION ( 2 FDA reports)
EYELID FUNCTION DISORDER ( 2 FDA reports)
FACIAL LESION EXCISION ( 2 FDA reports)
FAILED INDUCTION OF LABOUR ( 2 FDA reports)
FEBRILE CONVULSION ( 2 FDA reports)
FEELING GUILTY ( 2 FDA reports)
FLAT AFFECT ( 2 FDA reports)
FLIGHT OF IDEAS ( 2 FDA reports)
FOETAL DISORDER ( 2 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 2 FDA reports)
FOOD INTOLERANCE ( 2 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 2 FDA reports)
FUNGUS URINE TEST POSITIVE ( 2 FDA reports)
GAIT SPASTIC ( 2 FDA reports)
GALLBLADDER FISTULA ( 2 FDA reports)
GALLBLADDER INJURY ( 2 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 2 FDA reports)
GALLOP RHYTHM PRESENT ( 2 FDA reports)
GASTRIC CANCER ( 2 FDA reports)
GASTROENTERITIS VIRAL ( 2 FDA reports)
GASTROINTESTINAL INFECTION ( 2 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 2 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 2 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 2 FDA reports)
GENITAL DISCOMFORT ( 2 FDA reports)
GENITAL PRURITUS FEMALE ( 2 FDA reports)
GENITAL SWELLING ( 2 FDA reports)
GOUTY ARTHRITIS ( 2 FDA reports)
GRANULOCYTOPENIA ( 2 FDA reports)
GRIMACING ( 2 FDA reports)
HAIR COLOUR CHANGES ( 2 FDA reports)
HAIR TEXTURE ABNORMAL ( 2 FDA reports)
HEARING DISABILITY ( 2 FDA reports)
HELICOBACTER TEST POSITIVE ( 2 FDA reports)
HEPATIC HAEMATOMA ( 2 FDA reports)
HEPATIC SIDEROSIS ( 2 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 2 FDA reports)
HEPATITIS B ( 2 FDA reports)
HEPATITIS C ( 2 FDA reports)
HERNIA REPAIR ( 2 FDA reports)
HUMAN EHRLICHIOSIS ( 2 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 2 FDA reports)
HYPERAMMONAEMIA ( 2 FDA reports)
HYPERPHOSPHATAEMIA ( 2 FDA reports)
HYPERPYREXIA ( 2 FDA reports)
HYPERTENSIVE EMERGENCY ( 2 FDA reports)
HYPERTROPHIC OBSTRUCTIVE CARDIOMYOPATHY ( 2 FDA reports)
HYPOREFLEXIA ( 2 FDA reports)
HYPOVOLAEMIC SHOCK ( 2 FDA reports)
IATROGENIC INJURY ( 2 FDA reports)
ILEOSTOMY ( 2 FDA reports)
ILEOSTOMY CLOSURE ( 2 FDA reports)
ILIAC ARTERY OCCLUSION ( 2 FDA reports)
ILIAC ARTERY STENOSIS ( 2 FDA reports)
ILLUSION ( 2 FDA reports)
IMPLANT SITE INFECTION ( 2 FDA reports)
INAPPROPRIATE AFFECT ( 2 FDA reports)
INCISION SITE INFECTION ( 2 FDA reports)
INCISION SITE PAIN ( 2 FDA reports)
INCREASED APPETITE ( 2 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 2 FDA reports)
INFUSION SITE INFLAMMATION ( 2 FDA reports)
INFUSION SITE URTICARIA ( 2 FDA reports)
INFUSION SITE VESICLES ( 2 FDA reports)
INGROWN HAIR ( 2 FDA reports)
INHIBITORY DRUG INTERACTION ( 2 FDA reports)
INJECTION RELATED REACTION ( 2 FDA reports)
INJECTION SITE OEDEMA ( 2 FDA reports)
INSPIRATORY CAPACITY DECREASED ( 2 FDA reports)
INTENTIONAL MISUSE ( 2 FDA reports)
INTENTIONAL OVERDOSE ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 2 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 2 FDA reports)
INTESTINAL STENOSIS ( 2 FDA reports)
INTRACARDIAC THROMBUS ( 2 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 2 FDA reports)
INTRAOCULAR PRESSURE TEST ABNORMAL ( 2 FDA reports)
INTUBATION COMPLICATION ( 2 FDA reports)
IUCD COMPLICATION ( 2 FDA reports)
JARISCH-HERXHEIMER REACTION ( 2 FDA reports)
JAUNDICE ACHOLURIC ( 2 FDA reports)
JC VIRUS INFECTION ( 2 FDA reports)
JC VIRUS TEST POSITIVE ( 2 FDA reports)
JOINT LOCK ( 2 FDA reports)
JUDGEMENT IMPAIRED ( 2 FDA reports)
KETONURIA ( 2 FDA reports)
KNEE OPERATION ( 2 FDA reports)
KOEBNER PHENOMENON ( 2 FDA reports)
LACRIMAL DISORDER ( 2 FDA reports)
LACRIMATION DECREASED ( 2 FDA reports)
LARYNGITIS BACTERIAL ( 2 FDA reports)
LARYNGITIS FUNGAL ( 2 FDA reports)
LEARNING DISORDER ( 2 FDA reports)
LEFT VENTRICULAR FAILURE ( 2 FDA reports)
LEGIONELLA INFECTION ( 2 FDA reports)
LEIOMYOMA ( 2 FDA reports)
LEUKOPLAKIA ORAL ( 2 FDA reports)
LIP INJURY ( 2 FDA reports)
LIPOMA ( 2 FDA reports)
LIVER TENDERNESS ( 2 FDA reports)
LIVIDITY ( 2 FDA reports)
LOCALISED EXFOLIATION ( 2 FDA reports)
LOOSE STOOLS ( 2 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 2 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 2 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 2 FDA reports)
LYMPHOCELE ( 2 FDA reports)
LYMPHOHISTIOCYTOSIS ( 2 FDA reports)
MACULAR CYST ( 2 FDA reports)
MACULAR HOLE ( 2 FDA reports)
MALABSORPTION ( 2 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 2 FDA reports)
MAMMOPLASTY ( 2 FDA reports)
MANDIBULECTOMY ( 2 FDA reports)
MENINGISM ( 2 FDA reports)
MENINGITIS BACTERIAL ( 2 FDA reports)
MENINGITIS VIRAL ( 2 FDA reports)
MENSTRUAL DISCOMFORT ( 2 FDA reports)
MENSTRUAL DISORDER ( 2 FDA reports)
METABOLIC ALKALOSIS ( 2 FDA reports)
METASTASES TO BREAST ( 2 FDA reports)
METASTASES TO CHEST WALL ( 2 FDA reports)
METASTASES TO RETROPERITONEUM ( 2 FDA reports)
METEOROPATHY ( 2 FDA reports)
MICROCYTIC ANAEMIA ( 2 FDA reports)
MILIA ( 2 FDA reports)
MONARTHRITIS ( 2 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 2 FDA reports)
MOUTH PLAQUE ( 2 FDA reports)
MUCOSAL DISCOLOURATION ( 2 FDA reports)
MUCOSAL DRYNESS ( 2 FDA reports)
MUCOUS MEMBRANE DISORDER ( 2 FDA reports)
MULTIMORBIDITY ( 2 FDA reports)
MUSCLE CRAMP ( 2 FDA reports)
MYCOBACTERIUM KANSASII INFECTION ( 2 FDA reports)
MYOCLONIC EPILEPSY ( 2 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 2 FDA reports)
MYRINGOTOMY ( 2 FDA reports)
NASAL SEPTAL OPERATION ( 2 FDA reports)
NEAR DROWNING ( 2 FDA reports)
NECROTISING COLITIS ( 2 FDA reports)
NEGATIVISM ( 2 FDA reports)
NEPHRITIS ( 2 FDA reports)
NEPHROCALCINOSIS ( 2 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 2 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 2 FDA reports)
NEUROTOXICITY ( 2 FDA reports)
NEUTROPENIC INFECTION ( 2 FDA reports)
NICOTINE DEPENDENCE ( 2 FDA reports)
NITRITE URINE PRESENT ( 2 FDA reports)
NOCARDIOSIS ( 2 FDA reports)
NYSTAGMUS ( 2 FDA reports)
OBSTRUCTION GASTRIC ( 2 FDA reports)
OCULAR DISCOMFORT ( 2 FDA reports)
OESOPHAGITIS ULCERATIVE ( 2 FDA reports)
OESTROGEN DEFICIENCY ( 2 FDA reports)
OLIGODENDROGLIOMA ( 2 FDA reports)
OPTIC ATROPHY ( 2 FDA reports)
ORAL FUNGAL INFECTION ( 2 FDA reports)
ORAL MUCOSAL ERUPTION ( 2 FDA reports)
ORGAN FAILURE ( 2 FDA reports)
ORTHOSTATIC HYPERTENSION ( 2 FDA reports)
OTORRHOEA ( 2 FDA reports)
OVERGROWTH BACTERIAL ( 2 FDA reports)
OVERLAP SYNDROME ( 2 FDA reports)
PANCREATIC ABSCESS ( 2 FDA reports)
PANCREATIC ENLARGEMENT ( 2 FDA reports)
PANCREATIC NECROSIS ( 2 FDA reports)
PANCREATIC NEOPLASM ( 2 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 2 FDA reports)
PARKINSONISM ( 2 FDA reports)
PEAK EXPIRATORY FLOW RATE DECREASED ( 2 FDA reports)
PELVIC FLUID COLLECTION ( 2 FDA reports)
PELVIC VENOUS THROMBOSIS ( 2 FDA reports)
PENILE OEDEMA ( 2 FDA reports)
PEPTIC ULCER REACTIVATED ( 2 FDA reports)
PERIDIVERTICULITIS ( 2 FDA reports)
PERINEAL PAIN ( 2 FDA reports)
PH BODY FLUID ABNORMAL ( 2 FDA reports)
PHAEOCHROMOCYTOMA ( 2 FDA reports)
PHIMOSIS ( 2 FDA reports)
PILOERECTION ( 2 FDA reports)
PNEUMOCOCCAL SEPSIS ( 2 FDA reports)
PNEUMOCYSTIS CARINII INFECTION ( 2 FDA reports)
PNEUMOMEDIASTINUM ( 2 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 2 FDA reports)
PNEUMONIA HERPES VIRAL ( 2 FDA reports)
PNEUMONIA MYCOPLASMAL ( 2 FDA reports)
POLYSEROSITIS ( 2 FDA reports)
POLYTRAUMATISM ( 2 FDA reports)
POOR PERIPHERAL CIRCULATION ( 2 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 2 FDA reports)
POST PROCEDURAL INFECTION ( 2 FDA reports)
PROCALCITONIN INCREASED ( 2 FDA reports)
PROCEDURAL COMPLICATION ( 2 FDA reports)
PROCTITIS ( 2 FDA reports)
PRODUCT TASTE ABNORMAL ( 2 FDA reports)
PROSTATISM ( 2 FDA reports)
PROTEIN-LOSING GASTROENTEROPATHY ( 2 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 2 FDA reports)
PROTRUSION TONGUE ( 2 FDA reports)
PSEUDARTHROSIS ( 2 FDA reports)
PSEUDOMONAL SEPSIS ( 2 FDA reports)
PSYCHOLOGICAL TRAUMA ( 2 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 2 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 2 FDA reports)
RADIATION OESOPHAGITIS ( 2 FDA reports)
RADICULITIS LUMBOSACRAL ( 2 FDA reports)
RASH VESICULAR ( 2 FDA reports)
RAYNAUD'S PHENOMENON ( 2 FDA reports)
REFLUX GASTRITIS ( 2 FDA reports)
REFRACTION DISORDER ( 2 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 2 FDA reports)
RENAL INFARCT ( 2 FDA reports)
RENAL TRANSPLANT ( 2 FDA reports)
REPETITIVE SPEECH ( 2 FDA reports)
RESPIRATORY TRACT INFLAMMATION ( 2 FDA reports)
RESPIRATORY TRACT OEDEMA ( 2 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 2 FDA reports)
RETINAL ARTERY OCCLUSION ( 2 FDA reports)
RETINAL ARTERY THROMBOSIS ( 2 FDA reports)
RETINAL HAEMORRHAGE ( 2 FDA reports)
RETINAL TEAR ( 2 FDA reports)
RETROPERITONEAL NEOPLASM ( 2 FDA reports)
RHEUMATIC FEVER ( 2 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 2 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 2 FDA reports)
SACROILIITIS ( 2 FDA reports)
SALIVARY GLAND CANCER ( 2 FDA reports)
SALIVARY GLAND DISORDER ( 2 FDA reports)
SCAN ABDOMEN ABNORMAL ( 2 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 2 FDA reports)
SCLERAL DISCOLOURATION ( 2 FDA reports)
SCLERITIS ( 2 FDA reports)
SCROTAL PAIN ( 2 FDA reports)
SCROTAL SWELLING ( 2 FDA reports)
SEASONAL ALLERGY ( 2 FDA reports)
SENSATION OF BLOOD FLOW ( 2 FDA reports)
SENSATION OF PRESSURE ( 2 FDA reports)
SERUM FERRITIN DECREASED ( 2 FDA reports)
SHOCK HYPOGLYCAEMIC ( 2 FDA reports)
SKIN BACTERIAL INFECTION ( 2 FDA reports)
SKIN DEPIGMENTATION ( 2 FDA reports)
SKIN INJURY ( 2 FDA reports)
SKIN NODULE ( 2 FDA reports)
SKIN TURGOR DECREASED ( 2 FDA reports)
SLEEP TALKING ( 2 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 2 FDA reports)
SNORING ( 2 FDA reports)
SPERM COUNT ZERO ( 2 FDA reports)
SPIDER NAEVUS ( 2 FDA reports)
SPINAL DEFORMITY ( 2 FDA reports)
SPIROMETRY ABNORMAL ( 2 FDA reports)
SPLENIC CYST ( 2 FDA reports)
SPLENIC HAEMORRHAGE ( 2 FDA reports)
SPONDYLOSIS ( 2 FDA reports)
SPUTUM PURULENT ( 2 FDA reports)
STASIS DERMATITIS ( 2 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 2 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 2 FDA reports)
SUBSTANCE ABUSE ( 2 FDA reports)
SUICIDAL BEHAVIOUR ( 2 FDA reports)
SUSPICIOUSNESS ( 2 FDA reports)
SWEAT DISCOLOURATION ( 2 FDA reports)
TENDON OPERATION ( 2 FDA reports)
TESTICULAR DISORDER ( 2 FDA reports)
THYROID MASS ( 2 FDA reports)
TINEA CRURIS ( 2 FDA reports)
TONGUE COATED ( 2 FDA reports)
TONGUE PRURITUS ( 2 FDA reports)
TONGUE SPASM ( 2 FDA reports)
TONSILLAR DISORDER ( 2 FDA reports)
TONSILLAR HYPERTROPHY ( 2 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 2 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 2 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 2 FDA reports)
TYPHUS ( 2 FDA reports)
ULNAR NEURITIS ( 2 FDA reports)
UNEMPLOYMENT ( 2 FDA reports)
URETERIC STENOSIS ( 2 FDA reports)
URINARY TRACT DISORDER ( 2 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 2 FDA reports)
URINE KETONE BODY ( 2 FDA reports)
VASCULAR GRAFT ( 2 FDA reports)
VASCULAR SKIN DISORDER ( 2 FDA reports)
VASCULITIS NECROTISING ( 2 FDA reports)
VENIPUNCTURE SITE SWELLING ( 2 FDA reports)
VENOUS STASIS ( 2 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 2 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 2 FDA reports)
VIRAL MYOCARDITIS ( 2 FDA reports)
VITAL CAPACITY DECREASED ( 2 FDA reports)
VITAMIN B12 DECREASED ( 2 FDA reports)
VITREOUS HAEMORRHAGE ( 2 FDA reports)
VULVAR EROSION ( 2 FDA reports)
WINGED SCAPULA ( 2 FDA reports)
WOUND DEBRIDEMENT ( 2 FDA reports)
WOUND SECRETION ( 2 FDA reports)
X-RAY ABNORMAL ( 2 FDA reports)
ZYGOMYCOSIS ( 2 FDA reports)
ABDOMINAL PANNICULECTOMY ( 1 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 1 FDA reports)
ABNORMAL WEIGHT GAIN ( 1 FDA reports)
ACETONAEMIA ( 1 FDA reports)
ACOUSTIC NEUROMA ( 1 FDA reports)
ACROCHORDON ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 1 FDA reports)
ACUTE INTERSTITIAL PNEUMONITIS ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 1 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA ( 1 FDA reports)
ACUTE STRESS DISORDER ( 1 FDA reports)
ADJUSTMENT DISORDER ( 1 FDA reports)
ADJUSTMENT DISORDER WITH MIXED ANXIETY AND DEPRESSED MOOD ( 1 FDA reports)
ADNEXA UTERI PAIN ( 1 FDA reports)
ADRENAL MASS ( 1 FDA reports)
ADRENOMEGALY ( 1 FDA reports)
AGNOSIA ( 1 FDA reports)
AGRAPHIA ( 1 FDA reports)
AIR EMBOLISM ( 1 FDA reports)
AKINESIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ( 1 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 1 FDA reports)
ALLEN'S TEST ( 1 FDA reports)
ALLERGY TO ANIMAL ( 1 FDA reports)
ALLERGY TO ARTHROPOD STING ( 1 FDA reports)
ALLERGY TO CHEMICALS ( 1 FDA reports)
ALLERGY TO PLANTS ( 1 FDA reports)
ALPHA-1 ANTI-TRYPSIN DEFICIENCY ( 1 FDA reports)
AMAUROSIS ( 1 FDA reports)
AMNESTIC DISORDER ( 1 FDA reports)
AMNIOTIC FLUID VOLUME DECREASED ( 1 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 1 FDA reports)
ANAESTHETIC COMPLICATION CARDIAC ( 1 FDA reports)
ANAESTHETIC COMPLICATION PULMONARY ( 1 FDA reports)
ANAL FUNGAL INFECTION ( 1 FDA reports)
ANAL SKIN TAGS ( 1 FDA reports)
ANAL SPHINCTER ATONY ( 1 FDA reports)
ANALGESIC DRUG LEVEL INCREASED ( 1 FDA reports)
ANASTOMOTIC STENOSIS ( 1 FDA reports)
ANASTOMOTIC ULCER ( 1 FDA reports)
ANDROGEN DEFICIENCY ( 1 FDA reports)
ANGIOGRAM ( 1 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 1 FDA reports)
ANION GAP INCREASED ( 1 FDA reports)
ANKLE BRACHIAL INDEX DECREASED ( 1 FDA reports)
ANTEPARTUM HAEMORRHAGE ( 1 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 1 FDA reports)
ANTIBIOTIC LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTICHOLINERGIC SYNDROME ( 1 FDA reports)
ANTICOAGULANT THERAPY ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTIMICROBIAL SUSCEPTIBILITY TEST RESISTANT ( 1 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTISOCIAL BEHAVIOUR ( 1 FDA reports)
AORTIC ATHEROSCLEROSIS ( 1 FDA reports)
AORTIC EMBOLUS ( 1 FDA reports)
AORTIC VALVE CALCIFICATION ( 1 FDA reports)
AORTIC VALVE STENOSIS ( 1 FDA reports)
AORTOGRAM ABNORMAL ( 1 FDA reports)
APLASIA PURE RED CELL ( 1 FDA reports)
APPLICATION SITE ERYTHEMA ( 1 FDA reports)
APPLICATION SITE HYPERSENSITIVITY ( 1 FDA reports)
APPLICATION SITE IRRITATION ( 1 FDA reports)
APPLICATION SITE PAIN ( 1 FDA reports)
APPLICATION SITE PRURITUS ( 1 FDA reports)
ARACHNOIDITIS ( 1 FDA reports)
ARNOLD-CHIARI MALFORMATION ( 1 FDA reports)
ARTERIAL STENOSIS ( 1 FDA reports)
ARTERIOGRAM ABNORMAL ( 1 FDA reports)
ARTERIOGRAM CORONARY ( 1 FDA reports)
ARTERIOGRAM CORONARY ABNORMAL ( 1 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 1 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 1 FDA reports)
ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
ARTHRITIS BACTERIAL ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ASTERIXIS ( 1 FDA reports)
ATHETOSIS ( 1 FDA reports)
ATONIC URINARY BLADDER ( 1 FDA reports)
ATRIAL CONDUCTION TIME PROLONGATION ( 1 FDA reports)
ATRIAL PRESSURE INCREASED ( 1 FDA reports)
ATTENTION-SEEKING BEHAVIOUR ( 1 FDA reports)
AUTOANTIBODY POSITIVE ( 1 FDA reports)
AUTOIMMUNE THYROIDITIS ( 1 FDA reports)
AUTOLOGOUS BONE MARROW TRANSPLANTATION THERAPY ( 1 FDA reports)
AUTONOMIC NEUROPATHY ( 1 FDA reports)
AXILLARY MASS ( 1 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 1 FDA reports)
BACTERIA WOUND IDENTIFIED ( 1 FDA reports)
BAND NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
BARTTER'S SYNDROME ( 1 FDA reports)
BASE EXCESS POSITIVE ( 1 FDA reports)
BENIGN MESOTHELIOMA ( 1 FDA reports)
BENIGN SOFT TISSUE NEOPLASM ( 1 FDA reports)
BEREAVEMENT REACTION ( 1 FDA reports)
BILE DUCT OBSTRUCTION ( 1 FDA reports)
BILE DUCT PRESSURE INCREASED ( 1 FDA reports)
BILIARY CIRRHOSIS ( 1 FDA reports)
BILIARY COLIC ( 1 FDA reports)
BILIARY FISTULA ( 1 FDA reports)
BILIARY TRACT INFECTION ( 1 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 1 FDA reports)
BIOPSY CARTILAGE ABNORMAL ( 1 FDA reports)
BIOPSY LIVER ABNORMAL ( 1 FDA reports)
BLADDER DILATATION ( 1 FDA reports)
BLADDER DYSFUNCTION ( 1 FDA reports)
BLADDER INJURY ( 1 FDA reports)
BLADDER MASS ( 1 FDA reports)
BLADDER NEOPLASM SURGERY ( 1 FDA reports)
BLADDER OUTLET OBSTRUCTION ( 1 FDA reports)
BLEEDING TIME PROLONGED ( 1 FDA reports)
BLEEDING TIME SHORTENED ( 1 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 1 FDA reports)
BLOOD BILIRUBIN ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 1 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 1 FDA reports)
BLOOD ERYTHROPOIETIN INCREASED ( 1 FDA reports)
BLOOD FOLATE INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 1 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 1 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 1 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 1 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE ABNORMAL ( 1 FDA reports)
BLOOD URIC ACID DECREASED ( 1 FDA reports)
BODY TEMPERATURE ( 1 FDA reports)
BONE INFECTION ( 1 FDA reports)
BONE MARROW MYELOGRAM ABNORMAL ( 1 FDA reports)
BRADYPNOEA ( 1 FDA reports)
BRAIN COMPRESSION ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
BRAIN HYPOXIA ( 1 FDA reports)
BRAIN NEOPLASM BENIGN ( 1 FDA reports)
BREAST CELLULITIS ( 1 FDA reports)
BREAST CYST EXCISION ( 1 FDA reports)
BREAST HYPERPLASIA ( 1 FDA reports)
BREAST INFECTION ( 1 FDA reports)
BREAST LUMP REMOVAL ( 1 FDA reports)
BRONCHIAL CARCINOMA ( 1 FDA reports)
BRONCHIAL HYPERACTIVITY ( 1 FDA reports)
BUNION OPERATION ( 1 FDA reports)
BURSITIS INFECTIVE ( 1 FDA reports)
CALCIPHYLAXIS ( 1 FDA reports)
CALCIUM METABOLISM DISORDER ( 1 FDA reports)
CANDIDA PNEUMONIA ( 1 FDA reports)
CAPILLARY LEAK SYNDROME ( 1 FDA reports)
CARBON DIOXIDE INCREASED ( 1 FDA reports)
CARBON MONOXIDE POISONING ( 1 FDA reports)
CARDIAC ANEURYSM ( 1 FDA reports)
CARDIAC FAILURE CHRONIC ( 1 FDA reports)
CARDIAC FIBRILLATION ( 1 FDA reports)
CARDIAC IMAGING PROCEDURE ABNORMAL ( 1 FDA reports)
CARDIAC PACEMAKER MALFUNCTION ( 1 FDA reports)
CARDIAC PERFORATION ( 1 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 1 FDA reports)
CARDIAC VALVE VEGETATION ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 1 FDA reports)
CARDITIS ( 1 FDA reports)
CAROTID ARTERY ATHEROMA ( 1 FDA reports)
CAROTID ENDARTERECTOMY ( 1 FDA reports)
CASTLEMAN'S DISEASE ( 1 FDA reports)
CATABOLIC STATE ( 1 FDA reports)
CATARACT DIABETIC ( 1 FDA reports)
CATHETER SITE CELLULITIS ( 1 FDA reports)
CATHETER SITE HAEMATOMA ( 1 FDA reports)
CD4/CD8 RATIO INCREASED ( 1 FDA reports)
CD8 LYMPHOCYTES DECREASED ( 1 FDA reports)
CELLS IN URINE ( 1 FDA reports)
CELLULITIS ORBITAL ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM STIMULATION ( 1 FDA reports)
CEREBELLAR INFARCTION ( 1 FDA reports)
CEREBELLAR ISCHAEMIA ( 1 FDA reports)
CEREBELLAR SYNDROME ( 1 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 1 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 1 FDA reports)
CEREBRAL CALCIFICATION ( 1 FDA reports)
CEREBRAL CIRCULATORY FAILURE ( 1 FDA reports)
CEREBRAL CYST ( 1 FDA reports)
CEREBRAL FUNGAL INFECTION ( 1 FDA reports)
CEREBRAL HYPOPERFUSION ( 1 FDA reports)
CEREBRAL MICROANGIOPATHY ( 1 FDA reports)
CEREBRAL VASOCONSTRICTION ( 1 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 1 FDA reports)
CERVICAL CORD COMPRESSION ( 1 FDA reports)
CERVICAL CYST ( 1 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 1 FDA reports)
CERVIX CARCINOMA ( 1 FDA reports)
CHEMOTHERAPY ( 1 FDA reports)
CHEST TUBE INSERTION ( 1 FDA reports)
CHILD ABUSE ( 1 FDA reports)
CHOLANGITIS SCLEROSING ( 1 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 1 FDA reports)
CHORIOAMNIONITIS ( 1 FDA reports)
CHORIORETINOPATHY ( 1 FDA reports)
CHRONIC FATIGUE SYNDROME ( 1 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 1 FDA reports)
CITROBACTER SEPSIS ( 1 FDA reports)
CLOSED HEAD INJURY ( 1 FDA reports)
CLOSTRIDIUM BACTERAEMIA ( 1 FDA reports)
COAGULATION FACTOR VIII LEVEL INCREASED ( 1 FDA reports)
COAGULATION TEST ABNORMAL ( 1 FDA reports)
COCCYDYNIA ( 1 FDA reports)
COELIAC DISEASE ( 1 FDA reports)
COLLATERAL CIRCULATION ( 1 FDA reports)
COLON NEOPLASM ( 1 FDA reports)
COLONIC PSEUDO-OBSTRUCTION ( 1 FDA reports)
COLOSTOMY ( 1 FDA reports)
COLOUR BLINDNESS ( 1 FDA reports)
COMPARTMENT SYNDROME ( 1 FDA reports)
COMPLEMENT FACTOR C3 INCREASED ( 1 FDA reports)
COMPLICATED MIGRAINE ( 1 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 1 FDA reports)
CONDUCTIVE DEAFNESS ( 1 FDA reports)
CONJUNCTIVAL PALLOR ( 1 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 1 FDA reports)
CORNEAL EROSION ( 1 FDA reports)
CORNEAL PERFORATION ( 1 FDA reports)
CORNEAL SCAR ( 1 FDA reports)
CORNEAL ULCER ( 1 FDA reports)
CORONARY ANGIOPLASTY ( 1 FDA reports)
CORONARY ARTERY EMBOLISM ( 1 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 1 FDA reports)
CRACKLES LUNG ( 1 FDA reports)
CRANIAL NERVE DISORDER ( 1 FDA reports)
CRANIAL NERVE PARALYSIS ( 1 FDA reports)
CRANIOPHARYNGIOMA ( 1 FDA reports)
CSF GLUCOSE INCREASED ( 1 FDA reports)
CULTURE STOOL POSITIVE ( 1 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 1 FDA reports)
CUTANEOUS VASCULITIS ( 1 FDA reports)
CYANOPSIA ( 1 FDA reports)
CYST REMOVAL ( 1 FDA reports)
CYST RUPTURE ( 1 FDA reports)
CYSTITIS HAEMORRHAGIC ( 1 FDA reports)
CYSTITIS PSEUDOMONAL ( 1 FDA reports)
CYSTOID MACULAR OEDEMA ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS GASTROINTESTINAL INFECTION ( 1 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 1 FDA reports)
DAYDREAMING ( 1 FDA reports)
DEFAECATION URGENCY ( 1 FDA reports)
DEMYELINATION ( 1 FDA reports)
DERMATITIS ACNEIFORM ( 1 FDA reports)
DERMATITIS EXFOLIATIVE GENERALISED ( 1 FDA reports)
DESQUAMATION MOUTH ( 1 FDA reports)
DEVELOPMENTAL DELAY ( 1 FDA reports)
DEVICE COLOUR ISSUE ( 1 FDA reports)
DEVICE DISLOCATION ( 1 FDA reports)
DIABETES WITH HYPEROSMOLARITY ( 1 FDA reports)
DIABETIC BLINDNESS ( 1 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 1 FDA reports)
DIABETIC ULCER ( 1 FDA reports)
DIET REFUSAL ( 1 FDA reports)
DISEASE COMPLICATION ( 1 FDA reports)
DISSOCIATIVE DISORDER ( 1 FDA reports)
DISTRACTIBILITY ( 1 FDA reports)
DIVERTICULUM DUODENAL ( 1 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DIVORCED ( 1 FDA reports)
DOUBLE STRANDED DNA ANTIBODY POSITIVE ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG EFFECT DELAYED ( 1 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 1 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 1 FDA reports)
DRUG INTERACTION POTENTIATION ( 1 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 1 FDA reports)
DUODENAL NEOPLASM ( 1 FDA reports)
DUODENAL POLYP ( 1 FDA reports)
DYSAESTHESIA PHARYNX ( 1 FDA reports)
DYSMORPHISM ( 1 FDA reports)
DYSPNOEA AT REST ( 1 FDA reports)
EATING DISORDER SYMPTOM ( 1 FDA reports)
ECTOPIC ACTH SYNDROME ( 1 FDA reports)
EJACULATION DISORDER ( 1 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 1 FDA reports)
ELECTROLYTE DEPLETION ( 1 FDA reports)
EMBOLISM VENOUS ( 1 FDA reports)
EMERGENCY CARE EXAMINATION ( 1 FDA reports)
ENCEPHALITIC INFECTION ( 1 FDA reports)
ENCEPHALITIS TOXIC ( 1 FDA reports)
ENDOCARDIAL DISEASE ( 1 FDA reports)
ENDOCARDIAL FIBROSIS ( 1 FDA reports)
ENDOSCOPIC RETROGRADE CHOLANGIOPANCREATOGRAPHY ( 1 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ABNORMAL ( 1 FDA reports)
ENDOTOXIC SHOCK ( 1 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 1 FDA reports)
ENTERITIS INFECTIOUS ( 1 FDA reports)
ENTEROBACTER INFECTION ( 1 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 1 FDA reports)
ENTEROCUTANEOUS FISTULA ( 1 FDA reports)
ENZYME ABNORMALITY ( 1 FDA reports)
EOSINOPHIL PERCENTAGE DECREASED ( 1 FDA reports)
EOSINOPHILIC MYOCARDITIS ( 1 FDA reports)
EOSINOPHILS URINE PRESENT ( 1 FDA reports)
EPIDERMOLYSIS ( 1 FDA reports)
EPIDIDYMITIS ( 1 FDA reports)
EPIDURAL LIPOMATOSIS ( 1 FDA reports)
EPIGLOTTIC CYST ( 1 FDA reports)
EPIGLOTTITIS ( 1 FDA reports)
ERYSIPELAS ( 1 FDA reports)
ERYTHEMA OF EYELID ( 1 FDA reports)
EX-TOBACCO USER ( 1 FDA reports)
EXSANGUINATION ( 1 FDA reports)
EXTERNAL EAR DISORDER ( 1 FDA reports)
EXTRAOCULAR MUSCLE DISORDER ( 1 FDA reports)
EYE BURNS ( 1 FDA reports)
EYE DEGENERATIVE DISORDER ( 1 FDA reports)
EYE INFECTION VIRAL ( 1 FDA reports)
EYE OPERATION ( 1 FDA reports)
EYELID CYST ( 1 FDA reports)
EYELIDS PRURITUS ( 1 FDA reports)
FACIAL PARESIS ( 1 FDA reports)
FACIAL WASTING ( 1 FDA reports)
FAILURE TO ANASTOMOSE ( 1 FDA reports)
FALLOT'S PENTALOGY ( 1 FDA reports)
FAMILIAL TREMOR ( 1 FDA reports)
FEAR OF DISEASE ( 1 FDA reports)
FEMORAL ARTERY ANEURYSM ( 1 FDA reports)
FLUID IMBALANCE ( 1 FDA reports)
FLUOROSIS ( 1 FDA reports)
FOETAL DISTRESS SYNDROME ( 1 FDA reports)
FOETAL GROWTH RETARDATION ( 1 FDA reports)
FOLATE DEFICIENCY ( 1 FDA reports)
FOREARM FRACTURE ( 1 FDA reports)
FOREIGN BODY ASPIRATION ( 1 FDA reports)
FRACTION OF INSPIRED OXYGEN ( 1 FDA reports)
FRACTURED SACRUM ( 1 FDA reports)
FRONTOTEMPORAL DEMENTIA ( 1 FDA reports)
FRUSTRATION ( 1 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 1 FDA reports)
FUNGAL TEST POSITIVE ( 1 FDA reports)
FUNISITIS ( 1 FDA reports)
GALACTORRHOEA ( 1 FDA reports)
GALLBLADDER ABSCESS ( 1 FDA reports)
GALLBLADDER EMPYEMA ( 1 FDA reports)
GALLBLADDER OEDEMA ( 1 FDA reports)
GALLBLADDER PAIN ( 1 FDA reports)
GALLBLADDER PERFORATION ( 1 FDA reports)
GASTRIC PH INCREASED ( 1 FDA reports)
GASTRITIS HAEMORRHAGIC ( 1 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA HAEMORRHAGIC ( 1 FDA reports)
GASTROINTESTINAL EROSION ( 1 FDA reports)
GASTROINTESTINAL FUNGAL INFECTION ( 1 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 1 FDA reports)
GASTROINTESTINAL ISCHAEMIA ( 1 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 1 FDA reports)
GASTROINTESTINAL NECROSIS ( 1 FDA reports)
GASTROINTESTINAL ULCER ( 1 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
GASTROOESOPHAGEAL SPHINCTER INSUFFICIENCY ( 1 FDA reports)
GASTROSTOMY TUBE INSERTION ( 1 FDA reports)
GENITAL HAEMORRHAGE ( 1 FDA reports)
GENITAL PAIN FEMALE ( 1 FDA reports)
GENITAL RASH ( 1 FDA reports)
GESTATIONAL DIABETES ( 1 FDA reports)
GINGIVAL BLISTER ( 1 FDA reports)
GINGIVAL OEDEMA ( 1 FDA reports)
GLABELLAR REFLEX ABNORMAL ( 1 FDA reports)
GLARE ( 1 FDA reports)
GLIOSIS ( 1 FDA reports)
GLOMERULONEPHRITIS RAPIDLY PROGRESSIVE ( 1 FDA reports)
GLUCOSE URINE ( 1 FDA reports)
GOUTY TOPHUS ( 1 FDA reports)
GRAFT COMPLICATION ( 1 FDA reports)
GRANULOCYTES MATURATION ARREST ( 1 FDA reports)
GRANULOMA SKIN ( 1 FDA reports)
GRIEF REACTION ( 1 FDA reports)
GUM NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 1 FDA reports)
H1N1 INFLUENZA ( 1 FDA reports)
HAEMANGIOMA OF SKIN ( 1 FDA reports)
HAEMARTHROSIS ( 1 FDA reports)
HAEMATOCRIT ( 1 FDA reports)
HAEMATOLOGICAL MALIGNANCY ( 1 FDA reports)
HAEMATOTOXICITY ( 1 FDA reports)
HAEMOPERFUSION ( 1 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 1 FDA reports)
HAEMORRHAGIC DISORDER ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HALLUCINATION, TACTILE ( 1 FDA reports)
HEART VALVE OPERATION ( 1 FDA reports)
HEMIANOPIA ( 1 FDA reports)
HEPATIC CANCER METASTATIC ( 1 FDA reports)
HEPATIC INFECTION FUNGAL ( 1 FDA reports)
HEPATIC TRAUMA ( 1 FDA reports)
HEPATITIS ALCOHOLIC ( 1 FDA reports)
HEPATITIS E ( 1 FDA reports)
HEPATO-LENTICULAR DEGENERATION ( 1 FDA reports)
HEPATOBILIARY SCAN ABNORMAL ( 1 FDA reports)
HERNIA PAIN ( 1 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 1 FDA reports)
HERPES ZOSTER MULTI-DERMATOMAL ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN ( 1 FDA reports)
HIGH RISK PREGNANCY ( 1 FDA reports)
HIV WASTING SYNDROME ( 1 FDA reports)
HORMONE LEVEL ABNORMAL ( 1 FDA reports)
HOSPICE CARE ( 1 FDA reports)
HYALOSIS ASTEROID ( 1 FDA reports)
HYDROCHOLECYSTIS ( 1 FDA reports)
HYPERADRENALISM ( 1 FDA reports)
HYPERAEMIA ( 1 FDA reports)
HYPERCHLORAEMIA ( 1 FDA reports)
HYPEREOSINOPHILIC SYNDROME ( 1 FDA reports)
HYPERINSULINAEMIA ( 1 FDA reports)
HYPERMETABOLISM ( 1 FDA reports)
HYPEROSMOLAR STATE ( 1 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 1 FDA reports)
HYPERPHAGIA ( 1 FDA reports)
HYPERREFLEXIA ( 1 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 1 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 1 FDA reports)
HYPERTHERMIA MALIGNANT ( 1 FDA reports)
HYPERTONIA ( 1 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 1 FDA reports)
HYPERURICAEMIA ( 1 FDA reports)
HYPERVIGILANCE ( 1 FDA reports)
HYPHAEMA ( 1 FDA reports)
HYPOCHLORAEMIA ( 1 FDA reports)
HYPOCHROMIC ANAEMIA ( 1 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 1 FDA reports)
HYPOMENORRHOEA ( 1 FDA reports)
HYPOPERFUSION ( 1 FDA reports)
HYPORESPONSIVE TO STIMULI ( 1 FDA reports)
HYPOTHROMBINAEMIA ( 1 FDA reports)
HYPOVITAMINOSIS ( 1 FDA reports)
IDIOPATHIC URTICARIA ( 1 FDA reports)
IIIRD NERVE PARALYSIS ( 1 FDA reports)
ILEAL PERFORATION ( 1 FDA reports)
ILIAC ARTERY THROMBOSIS ( 1 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
IMPAIRED FASTING GLUCOSE ( 1 FDA reports)
IMPAIRED SELF-CARE ( 1 FDA reports)
IMPATIENCE ( 1 FDA reports)
IMPLANT SITE RASH ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR REPLACEMENT ( 1 FDA reports)
IMPULSIVE BEHAVIOUR ( 1 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
INCISION SITE ERYTHEMA ( 1 FDA reports)
INDIFFERENCE ( 1 FDA reports)
INDURATION ( 1 FDA reports)
INFECTIVE GLOSSITIS ( 1 FDA reports)
INFECTIVE MYOSITIS ( 1 FDA reports)
INFECTIVE TENOSYNOVITIS ( 1 FDA reports)
INFUSION SITE DISCOLOURATION ( 1 FDA reports)
INFUSION SITE DISCOMFORT ( 1 FDA reports)
INFUSION SITE HYPERSENSITIVITY ( 1 FDA reports)
INFUSION SITE MASS ( 1 FDA reports)
INJECTION SITE ABSCESS ( 1 FDA reports)
INJECTION SITE NODULE ( 1 FDA reports)
INJECTION SITE PAPULE ( 1 FDA reports)
INJECTION SITE PHLEBITIS ( 1 FDA reports)
INJECTION SITE VESICLES ( 1 FDA reports)
INSULIN RESISTANCE ( 1 FDA reports)
INSULIN-REQUIRING TYPE II DIABETES MELLITUS ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTERCAPILLARY GLOMERULOSCLEROSIS ( 1 FDA reports)
INTERCEPTED MEDICATION ERROR ( 1 FDA reports)
INTERNAL HERNIA ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 1 FDA reports)
INTERVENTRICULAR SEPTUM RUPTURE ( 1 FDA reports)
INTERVERTEBRAL DISCITIS ( 1 FDA reports)
INTESTINAL DILATATION ( 1 FDA reports)
INTESTINAL POLYP ( 1 FDA reports)
INTESTINAL SPASM ( 1 FDA reports)
INTRAMEDULLARY ROD INSERTION ( 1 FDA reports)
INTUBATION ( 1 FDA reports)
INTUSSUSCEPTION ( 1 FDA reports)
INVESTIGATION ABNORMAL ( 1 FDA reports)
IRIS HYPERPIGMENTATION ( 1 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 1 FDA reports)
IRON OVERLOAD ( 1 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 1 FDA reports)
IVTH NERVE PARALYSIS ( 1 FDA reports)
JOB DISSATISFACTION ( 1 FDA reports)
JOINT ABSCESS ( 1 FDA reports)
JOINT DESTRUCTION ( 1 FDA reports)
JOINT FLUID DRAINAGE ( 1 FDA reports)
JOINT SURGERY ( 1 FDA reports)
KERATITIS HERPETIC ( 1 FDA reports)
KERATOACANTHOMA ( 1 FDA reports)
KIDNEY SMALL ( 1 FDA reports)
KWASHIORKOR ( 1 FDA reports)
LARYNGEAL DISORDER ( 1 FDA reports)
LARYNGEAL REPAIR ( 1 FDA reports)
LATEX ALLERGY ( 1 FDA reports)
LAZINESS ( 1 FDA reports)
LEAD DISLODGEMENT ( 1 FDA reports)
LEISHMANIASIS ( 1 FDA reports)
LENS DISORDER ( 1 FDA reports)
LENTIGO ( 1 FDA reports)
LEUKOCYTURIA ( 1 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 1 FDA reports)
LIP DISCOLOURATION ( 1 FDA reports)
LIP DISORDER ( 1 FDA reports)
LIP EXFOLIATION ( 1 FDA reports)
LIP HAEMORRHAGE ( 1 FDA reports)
LIP INFECTION ( 1 FDA reports)
LIP NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 1 FDA reports)
LIP PRURITUS ( 1 FDA reports)
LIPID METABOLISM DISORDER ( 1 FDA reports)
LIPIDS ABNORMAL ( 1 FDA reports)
LIVER ABSCESS ( 1 FDA reports)
LOCAL REACTION ( 1 FDA reports)
LORDOSIS ( 1 FDA reports)
LOSS OF CONTROL OF LEGS ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION FUNGAL ( 1 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 1 FDA reports)
LUNG ADENOCARCINOMA STAGE III ( 1 FDA reports)
LUNG ADENOCARCINOMA STAGE IV ( 1 FDA reports)
LUNG HERNIA ( 1 FDA reports)
LUNG LOBECTOMY ( 1 FDA reports)
LYMPH GLAND INFECTION ( 1 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
LYMPHOCYTOSIS ( 1 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
MADAROSIS ( 1 FDA reports)
MALIGNANT NEOPLASM OF SPINAL CORD ( 1 FDA reports)
MALIGNANT PALATE NEOPLASM ( 1 FDA reports)
MANTLE CELL LYMPHOMA ( 1 FDA reports)
MEASLES ( 1 FDA reports)
MECONIUM ABNORMAL ( 1 FDA reports)
MEDICAL DIET ( 1 FDA reports)
MEIGE'S SYNDROME ( 1 FDA reports)
MENIERE'S DISEASE ( 1 FDA reports)
MENINGEAL DISORDER ( 1 FDA reports)
MENINGIOMA ( 1 FDA reports)
MENINGOMYELOCELE ( 1 FDA reports)
MENISCAL DEGENERATION ( 1 FDA reports)
MENOPAUSAL SYMPTOMS ( 1 FDA reports)
MENTAL RETARDATION SEVERITY UNSPECIFIED ( 1 FDA reports)
MESANGIOPROLIFERATIVE GLOMERULONEPHRITIS ( 1 FDA reports)
MESOTHELIOMA MALIGNANT ( 1 FDA reports)
METANEPHRINE URINE INCREASED ( 1 FDA reports)
METASTASES TO PLEURA ( 1 FDA reports)
METASTASES TO THE RESPIRATORY SYSTEM ( 1 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST POSITIVE ( 1 FDA reports)
MICTURITION DISORDER ( 1 FDA reports)
MILK ALLERGY ( 1 FDA reports)
MINERAL DEFICIENCY ( 1 FDA reports)
MITOCHONDRIAL DNA MUTATION ( 1 FDA reports)
MITRAL VALVE REPLACEMENT ( 1 FDA reports)
MIXED DEAFNESS ( 1 FDA reports)
MIXED LIVER INJURY ( 1 FDA reports)
MOANING ( 1 FDA reports)
MONOCYTE COUNT INCREASED ( 1 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MORAXELLA INFECTION ( 1 FDA reports)
MUCOSAL HAEMORRHAGE ( 1 FDA reports)
MULTI-ORGAN DISORDER ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 1 FDA reports)
MUMPS ( 1 FDA reports)
MUSCLE HYPERTROPHY ( 1 FDA reports)
MUSCULAR DYSTROPHY ( 1 FDA reports)
MYCOBACTERIAL INFECTION ( 1 FDA reports)
MYCOBACTERIUM TUBERCULOSIS COMPLEX TEST POSITIVE ( 1 FDA reports)
MYOCARDIAL RUPTURE ( 1 FDA reports)
MYODESOPSIA ( 1 FDA reports)
MYOGLOBINURIA ( 1 FDA reports)
NAIL AVULSION ( 1 FDA reports)
NAIL GROWTH ABNORMAL ( 1 FDA reports)
NAIL TINEA ( 1 FDA reports)
NASAL DISCHARGE DISCOLOURATION ( 1 FDA reports)
NASAL TURBINATE ABNORMALITY ( 1 FDA reports)
NECROTISING FASCIITIS ( 1 FDA reports)
NEEDLE TRACK MARKS ( 1 FDA reports)
NEGATIVE THOUGHTS ( 1 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 1 FDA reports)
NEONATAL ASPIRATION ( 1 FDA reports)
NERVE ROOT INJURY ( 1 FDA reports)
NEUROFIBROMA ( 1 FDA reports)
NEUROGENIC BLADDER ( 1 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 1 FDA reports)
NEUTROPHIL TOXIC GRANULATION PRESENT ( 1 FDA reports)
NIGHT CRAMPS ( 1 FDA reports)
NO ADVERSE EFFECT ( 1 FDA reports)
NOCTURNAL DYSPNOEA ( 1 FDA reports)
NODULAR VASCULITIS ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER RECURRENT ( 1 FDA reports)
NOSOCOMIAL INFECTION ( 1 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 1 FDA reports)
OCULOGYRATION ( 1 FDA reports)
OESOPHAGEAL HYPOMOTILITY ( 1 FDA reports)
OESOPHAGEAL INJURY ( 1 FDA reports)
OESOPHAGEAL MASS ( 1 FDA reports)
OESOPHAGEAL OEDEMA ( 1 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 1 FDA reports)
OESOPHAGOGASTRODUODENOSCOPY ( 1 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 1 FDA reports)
OLIGODIPSIA ( 1 FDA reports)
ONYCHOLYSIS ( 1 FDA reports)
OPHTHALMOPLEGIA ( 1 FDA reports)
OPPORTUNISTIC INFECTION ( 1 FDA reports)
OPTIC NEURITIS ( 1 FDA reports)
ORAL ALLERGY SYNDROME ( 1 FDA reports)
ORAL MUCOSAL DISORDER ( 1 FDA reports)
ORCHITIS NONINFECTIVE ( 1 FDA reports)
ORGANISING PNEUMONIA ( 1 FDA reports)
OSTEOMYELITIS ACUTE ( 1 FDA reports)
OVARIAN CYST RUPTURED ( 1 FDA reports)
OXYGEN CONSUMPTION ( 1 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 1 FDA reports)
PALATAL OEDEMA ( 1 FDA reports)
PANNICULITIS ( 1 FDA reports)
PARAESTHESIA EAR ( 1 FDA reports)
PARANEOPLASTIC SYNDROME ( 1 FDA reports)
PARANOID PERSONALITY DISORDER ( 1 FDA reports)
PARAPROTEINAEMIA ( 1 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 1 FDA reports)
PAROTID ABSCESS ( 1 FDA reports)
PARTIAL SEIZURES ( 1 FDA reports)
PARVOVIRUS B19 SEROLOGY POSITIVE ( 1 FDA reports)
PATELLA FRACTURE ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PCO2 INCREASED ( 1 FDA reports)
PEAK EXPIRATORY FLOW RATE ( 1 FDA reports)
PEDAL PULSE ABSENT ( 1 FDA reports)
PELVIC ABSCESS ( 1 FDA reports)
PELVIC INFECTION ( 1 FDA reports)
PEMPHIGUS ( 1 FDA reports)
PENILE SWELLING ( 1 FDA reports)
PENIS DISORDER ( 1 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 1 FDA reports)
PERFUME SENSITIVITY ( 1 FDA reports)
PERICARDITIS RHEUMATIC ( 1 FDA reports)
PERIODIC LIMB MOVEMENT DISORDER ( 1 FDA reports)
PERIODONTAL INFECTION ( 1 FDA reports)
PERIPHERAL ARTERY ANEURYSM ( 1 FDA reports)
PERIPHERAL EMBOLISM ( 1 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 1 FDA reports)
PERITONEAL EFFUSION ( 1 FDA reports)
PERITONEAL HAEMORRHAGE ( 1 FDA reports)
PERITONEAL TUBERCULOSIS ( 1 FDA reports)
PERIVASCULAR DERMATITIS ( 1 FDA reports)
PERNICIOUS ANAEMIA ( 1 FDA reports)
PERONEAL MUSCULAR ATROPHY ( 1 FDA reports)
PERSONALITY CHANGE DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
PHANTOM PAIN ( 1 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 1 FDA reports)
PHARYNGEAL HYPOAESTHESIA ( 1 FDA reports)
PHOBIA ( 1 FDA reports)
PICKWICKIAN SYNDROME ( 1 FDA reports)
PIGMENTARY GLAUCOMA ( 1 FDA reports)
PILONIDAL CYST ( 1 FDA reports)
PIRIFORMIS SYNDROME ( 1 FDA reports)
PITTING OEDEMA ( 1 FDA reports)
PITUITARY TUMOUR BENIGN ( 1 FDA reports)
PLACENTAL NECROSIS ( 1 FDA reports)
PLASMAPHERESIS ( 1 FDA reports)
PNEUMOCOCCAL BACTERAEMIA ( 1 FDA reports)
PNEUMOCOCCAL INFECTION ( 1 FDA reports)
PNEUMONIA LEGIONELLA ( 1 FDA reports)
PNEUMONIA RESPIRATORY SYNCYTIAL VIRAL ( 1 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 1 FDA reports)
PNEUMOTHORAX TRAUMATIC ( 1 FDA reports)
POLYCYTHAEMIA VERA ( 1 FDA reports)
POLYMENORRHOEA ( 1 FDA reports)
POPLITEAL PULSE DECREASED ( 1 FDA reports)
POST CONCUSSION SYNDROME ( 1 FDA reports)
POST PROCEDURAL BILE LEAK ( 1 FDA reports)
POST PROCEDURAL CELLULITIS ( 1 FDA reports)
POST PROCEDURAL DISCOMFORT ( 1 FDA reports)
POST PROCEDURAL OEDEMA ( 1 FDA reports)
POST PROCEDURAL PULMONARY EMBOLISM ( 1 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 1 FDA reports)
POSTICTAL STATE ( 1 FDA reports)
POSTMATURE BABY ( 1 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 1 FDA reports)
POSTOPERATIVE ILEUS ( 1 FDA reports)
POSTOPERATIVE INFECTION ( 1 FDA reports)
PREALBUMIN DECREASED ( 1 FDA reports)
PREGNANCY WITH CONTRACEPTIVE DEVICE ( 1 FDA reports)
PREMATURE LABOUR ( 1 FDA reports)
PRESBYACUSIS ( 1 FDA reports)
PRESSURE OF SPEECH ( 1 FDA reports)
PROCEDURAL SITE REACTION ( 1 FDA reports)
PROCEDURAL VOMITING ( 1 FDA reports)
PRODUCT ADHESION ISSUE ( 1 FDA reports)
PRODUCT COUNTERFEIT ( 1 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 1 FDA reports)
PROSTATIC DISORDER ( 1 FDA reports)
PROSTATIC OBSTRUCTION ( 1 FDA reports)
PROSTATIC OPERATION ( 1 FDA reports)
PROSTRATION ( 1 FDA reports)
PROTEIN C DECREASED ( 1 FDA reports)
PROTEIN INDUCED BY VITAMIN K ABSENCE OR ANTAGONIST II INCREASED ( 1 FDA reports)
PROTEIN S DECREASED ( 1 FDA reports)
PROTEIN URINE ( 1 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 1 FDA reports)
PRURITUS ALLERGIC ( 1 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 1 FDA reports)
PSITTACOSIS ( 1 FDA reports)
PSYCHIATRIC EVALUATION ABNORMAL ( 1 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 1 FDA reports)
PULMONARY NECROSIS ( 1 FDA reports)
PULMONARY SEPSIS ( 1 FDA reports)
PULMONARY VASCULAR DISORDER ( 1 FDA reports)
PUNCTATE KERATITIS ( 1 FDA reports)
PUPILLARY DEFORMITY ( 1 FDA reports)
PUPILLARY DISORDER ( 1 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 1 FDA reports)
RADIAL PULSE ABNORMAL ( 1 FDA reports)
RADIATION INJURY ( 1 FDA reports)
RASH FOLLICULAR ( 1 FDA reports)
RASH SCALY ( 1 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 1 FDA reports)
READING DISORDER ( 1 FDA reports)
RECTAL CANCER ( 1 FDA reports)
RECTAL ULCER HAEMORRHAGE ( 1 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE ABNORMAL ( 1 FDA reports)
REFRACTORY ANAEMIA WITH AN EXCESS OF BLASTS ( 1 FDA reports)
REFRACTORY ANAEMIA WITH RINGED SIDEROBLASTS ( 1 FDA reports)
RELAPSING FEVER ( 1 FDA reports)
RENAL ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL CANCER ( 1 FDA reports)
RENAL EMBOLISM ( 1 FDA reports)
RENAL VEIN OCCLUSION ( 1 FDA reports)
RENAL VESSEL DISORDER ( 1 FDA reports)
RESPIRATORY ACIDOSIS ( 1 FDA reports)
RESPIRATORY ALKALOSIS ( 1 FDA reports)
RESPIRATORY FUME INHALATION DISORDER ( 1 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 1 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS TEST POSITIVE ( 1 FDA reports)
RESTRICTIVE CARDIOMYOPATHY ( 1 FDA reports)
RETICULOCYTE COUNT INCREASED ( 1 FDA reports)
RETINAL VEIN OCCLUSION ( 1 FDA reports)
RETROGRADE AMNESIA ( 1 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 1 FDA reports)
RHEUMATOID FACTOR INCREASED ( 1 FDA reports)
RHINITIS SEASONAL ( 1 FDA reports)
RHYTHM IDIOVENTRICULAR ( 1 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
RUBELLA ANTIBODY POSITIVE ( 1 FDA reports)
SACCADIC EYE MOVEMENT ( 1 FDA reports)
SALIVA ALTERED ( 1 FDA reports)
SALIVARY GLAND MASS ( 1 FDA reports)
SALIVARY GLAND PAIN ( 1 FDA reports)
SALPINGITIS ( 1 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 1 FDA reports)
SCHIZOPHRENIA ( 1 FDA reports)
SCHIZOPHRENIFORM DISORDER ( 1 FDA reports)
SCIATIC NERVE NEUROPATHY ( 1 FDA reports)
SCLERODACTYLIA ( 1 FDA reports)
SCOTOMA ( 1 FDA reports)
SECRETION DISCHARGE ( 1 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 1 FDA reports)
SENILE DEMENTIA ( 1 FDA reports)
SENSATION OF PRESSURE IN EAR ( 1 FDA reports)
SERRATIA TEST POSITIVE ( 1 FDA reports)
SERUM FERRITIN ABNORMAL ( 1 FDA reports)
SEXUAL DYSFUNCTION ( 1 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 1 FDA reports)
SIGMOIDOSCOPY ( 1 FDA reports)
SIGMOIDOSCOPY ABNORMAL ( 1 FDA reports)
SIMILAR REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
SINOATRIAL BLOCK ( 1 FDA reports)
SKIN ATROPHY ( 1 FDA reports)
SKIN CHAPPED ( 1 FDA reports)
SKIN DESQUAMATION ( 1 FDA reports)
SKIN GRAFT ( 1 FDA reports)
SKIN HYPOPIGMENTATION ( 1 FDA reports)
SKIN MASS ( 1 FDA reports)
SKIN ODOUR ABNORMAL ( 1 FDA reports)
SKIN OPERATION ( 1 FDA reports)
SMALL INTESTINAL STENOSIS ( 1 FDA reports)
SMEAR CERVIX ABNORMAL ( 1 FDA reports)
SMOOTH MUSCLE ANTIBODY POSITIVE ( 1 FDA reports)
SOFT TISSUE NEOPLASM ( 1 FDA reports)
SOPOR ( 1 FDA reports)
SPINAL X-RAY ABNORMAL ( 1 FDA reports)
SPLENIC HAEMATOMA ( 1 FDA reports)
SPONDYLITIS ( 1 FDA reports)
SPUTUM TEST ( 1 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 1 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 1 FDA reports)
STENOTROPHOMONAS INFECTION ( 1 FDA reports)
STENOTROPHOMONAS TEST POSITIVE ( 1 FDA reports)
STILLBIRTH ( 1 FDA reports)
STOMATITIS HAEMORRHAGIC ( 1 FDA reports)
STRAWBERRY TONGUE ( 1 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 1 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 1 FDA reports)
SUBILEUS ( 1 FDA reports)
SUPERIOR VENA CAVAL STENOSIS ( 1 FDA reports)
SUTURE RELATED COMPLICATION ( 1 FDA reports)
SYMBLEPHARON ( 1 FDA reports)
SYMBOLIC DYSFUNCTION ( 1 FDA reports)
SYSTEMIC CANDIDA ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 1 FDA reports)
SYSTEMIC MYCOSIS ( 1 FDA reports)
SYSTEMIC SCLEROSIS ( 1 FDA reports)
SYSTOLIC HYPERTENSION ( 1 FDA reports)
T-CELL LYMPHOMA ( 1 FDA reports)
TACHYCARDIA PAROXYSMAL ( 1 FDA reports)
TEARFULNESS ( 1 FDA reports)
TEMPERATURE PERCEPTION TEST ABNORMAL ( 1 FDA reports)
TENDON NEOPLASM ( 1 FDA reports)
TENONECTOMY ( 1 FDA reports)
TERTIARY SYPHILIS ( 1 FDA reports)
TESTICULAR ABSCESS ( 1 FDA reports)
TESTICULAR PAIN ( 1 FDA reports)
THALAMIC INFARCTION ( 1 FDA reports)
THERAPEUTIC PRODUCT CONTAMINATION ( 1 FDA reports)
THERAPY CESSATION ( 1 FDA reports)
THERAPY REGIMEN CHANGED ( 1 FDA reports)
THORACIC OUTLET SYNDROME ( 1 FDA reports)
THROMBIN TIME PROLONGED ( 1 FDA reports)
THROMBOSIS IN DEVICE ( 1 FDA reports)
THYROIDITIS ( 1 FDA reports)
THYROTOXIC CRISIS ( 1 FDA reports)
TINEA VERSICOLOUR ( 1 FDA reports)
TOBACCO WITHDRAWAL SYMPTOMS ( 1 FDA reports)
TONGUE DRY ( 1 FDA reports)
TONGUE ERUPTION ( 1 FDA reports)
TONGUE INJURY ( 1 FDA reports)
TONIC CONVULSION ( 1 FDA reports)
TORULOPSIS INFECTION ( 1 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO ( 1 FDA reports)
TOXIC OPTIC NEUROPATHY ( 1 FDA reports)
TRACHEAL DILATATION ( 1 FDA reports)
TRACHEAL DISORDER ( 1 FDA reports)
TRACHEAL PAIN ( 1 FDA reports)
TRACHEITIS ( 1 FDA reports)
TRACHEOBRONCHITIS ( 1 FDA reports)
TRANCE ( 1 FDA reports)
TRAUMATIC BRAIN INJURY ( 1 FDA reports)
TRAUMATIC HAEMATOMA ( 1 FDA reports)
TRAUMATIC INTRACRANIAL HAEMORRHAGE ( 1 FDA reports)
TRAUMATIC LIVER INJURY ( 1 FDA reports)
TRICHOMONIASIS ( 1 FDA reports)
TRICUSPID VALVE DISEASE ( 1 FDA reports)
TRISOMY 21 ( 1 FDA reports)
TROPONIN I INCREASED ( 1 FDA reports)
TUBERCULIN TEST POSITIVE ( 1 FDA reports)
TUBERCULOSIS GASTROINTESTINAL ( 1 FDA reports)
TUMOUR MARKER INCREASED ( 1 FDA reports)
TUMOUR PAIN ( 1 FDA reports)
TYPE I HYPERSENSITIVITY ( 1 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 1 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 1 FDA reports)
ULTRASOUND SCAN VAGINA ABNORMAL ( 1 FDA reports)
UNDERDOSE ( 1 FDA reports)
URETERAL DISORDER ( 1 FDA reports)
URETHRAL OBSTRUCTION ( 1 FDA reports)
URETHRITIS ( 1 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
URINE FLOW DECREASED ( 1 FDA reports)
UROBILIN URINE PRESENT ( 1 FDA reports)
UROGRAM ABNORMAL ( 1 FDA reports)
URTICARIA LOCALISED ( 1 FDA reports)
URTICARIA PAPULAR ( 1 FDA reports)
UTERINE CANCER ( 1 FDA reports)
UTERINE CONTRACTIONS ABNORMAL ( 1 FDA reports)
UTERINE DISORDER ( 1 FDA reports)
UTERINE PAIN ( 1 FDA reports)
VAGINAL BURNING SENSATION ( 1 FDA reports)
VAGINAL MYCOSIS ( 1 FDA reports)
VAGINAL PAIN ( 1 FDA reports)
VAGUS NERVE DISORDER ( 1 FDA reports)
VANISHING BILE DUCT SYNDROME ( 1 FDA reports)
VARICELLA ZOSTER VIRUS SEROLOGY POSITIVE ( 1 FDA reports)
VASCULAR BYPASS DYSFUNCTION ( 1 FDA reports)
VASCULAR BYPASS GRAFT ( 1 FDA reports)
VASCULAR GRAFT THROMBOSIS ( 1 FDA reports)
VASCULAR INSUFFICIENCY ( 1 FDA reports)
VASCULITIC RASH ( 1 FDA reports)
VASECTOMY ( 1 FDA reports)
VASODILATION PROCEDURE ( 1 FDA reports)
VENOUS INJURY ( 1 FDA reports)
VENTILATION/PERFUSION SCAN ABNORMAL ( 1 FDA reports)
VENTRICULAR FLUTTER ( 1 FDA reports)
VERBIGERATION ( 1 FDA reports)
VESSEL PUNCTURE SITE PAIN ( 1 FDA reports)
VESTIBULAR NEURONITIS ( 1 FDA reports)
VICTIM OF ELDER ABUSE ( 1 FDA reports)
VIRAL MYOSITIS ( 1 FDA reports)
VISCERAL ARTERIAL ISCHAEMIA ( 1 FDA reports)
VISUAL ACUITY REDUCED TRANSIENTLY ( 1 FDA reports)
VITAL FUNCTIONS ABNORMAL ( 1 FDA reports)
VITAMIN B12 INCREASED ( 1 FDA reports)
VITAMIN K DECREASED ( 1 FDA reports)
VOCAL CORD PARESIS ( 1 FDA reports)
VOLVULUS ( 1 FDA reports)
VON WILLEBRAND'S FACTOR MULTIMERS ABNORMAL ( 1 FDA reports)
VULVAL ULCERATION ( 1 FDA reports)
WALDENSTROM'S MACROGLOBULINAEMIA ( 1 FDA reports)
WEIGHT FLUCTUATION ( 1 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
WHITE BLOOD CELL DISORDER ( 1 FDA reports)
WHITE BLOOD CELLS URINE ( 1 FDA reports)
WOUND CLOSURE ( 1 FDA reports)
WOUND HAEMATOMA ( 1 FDA reports)
WOUND HAEMORRHAGE ( 1 FDA reports)
X-RAY LIMB ABNORMAL ( 1 FDA reports)
XANTHOPSIA ( 1 FDA reports)

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