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

PAIN ( 1140 FDA reports)
ANXIETY ( 1048 FDA reports)
DEPRESSION ( 989 FDA reports)
NAUSEA ( 850 FDA reports)
FATIGUE ( 730 FDA reports)
HEADACHE ( 719 FDA reports)
FALL ( 713 FDA reports)
DYSPNOEA ( 675 FDA reports)
ASTHENIA ( 649 FDA reports)
BACK PAIN ( 649 FDA reports)
INSOMNIA ( 640 FDA reports)
DIZZINESS ( 638 FDA reports)
ARTHRALGIA ( 632 FDA reports)
PAIN IN EXTREMITY ( 602 FDA reports)
CHEST PAIN ( 597 FDA reports)
OEDEMA PERIPHERAL ( 541 FDA reports)
VOMITING ( 539 FDA reports)
ANAEMIA ( 536 FDA reports)
DIARRHOEA ( 528 FDA reports)
HYPERTENSION ( 508 FDA reports)
PYREXIA ( 499 FDA reports)
HYPOAESTHESIA ( 481 FDA reports)
DRUG INEFFECTIVE ( 448 FDA reports)
INJURY ( 441 FDA reports)
WEIGHT DECREASED ( 439 FDA reports)
CONSTIPATION ( 435 FDA reports)
PAIN IN JAW ( 435 FDA reports)
OSTEOARTHRITIS ( 428 FDA reports)
OSTEONECROSIS OF JAW ( 421 FDA reports)
PNEUMONIA ( 408 FDA reports)
URINARY TRACT INFECTION ( 390 FDA reports)
BONE DISORDER ( 378 FDA reports)
ABDOMINAL PAIN ( 373 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 369 FDA reports)
CEREBROVASCULAR ACCIDENT ( 366 FDA reports)
DYSPHAGIA ( 353 FDA reports)
MYOCARDIAL INFARCTION ( 346 FDA reports)
NEUROPATHY PERIPHERAL ( 345 FDA reports)
OSTEOMYELITIS ( 339 FDA reports)
MYALGIA ( 336 FDA reports)
MUSCLE SPASMS ( 335 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 334 FDA reports)
WEIGHT INCREASED ( 332 FDA reports)
RASH ( 322 FDA reports)
CONFUSIONAL STATE ( 320 FDA reports)
PARAESTHESIA ( 314 FDA reports)
NECK PAIN ( 303 FDA reports)
IMPAIRED HEALING ( 301 FDA reports)
ANHEDONIA ( 297 FDA reports)
COUGH ( 297 FDA reports)
DIABETES MELLITUS ( 290 FDA reports)
MUSCULAR WEAKNESS ( 278 FDA reports)
SYNCOPE ( 277 FDA reports)
MUSCULOSKELETAL PAIN ( 272 FDA reports)
CORONARY ARTERY DISEASE ( 270 FDA reports)
EMOTIONAL DISTRESS ( 270 FDA reports)
TREMOR ( 268 FDA reports)
SINUSITIS ( 266 FDA reports)
SPINAL OSTEOARTHRITIS ( 263 FDA reports)
BRONCHITIS ( 262 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 260 FDA reports)
CONVULSION ( 258 FDA reports)
DEHYDRATION ( 250 FDA reports)
MALAISE ( 250 FDA reports)
ATRIAL FIBRILLATION ( 246 FDA reports)
RENAL FAILURE ( 245 FDA reports)
VISION BLURRED ( 245 FDA reports)
OSTEONECROSIS ( 239 FDA reports)
CONDITION AGGRAVATED ( 233 FDA reports)
HYPERLIPIDAEMIA ( 233 FDA reports)
CELLULITIS ( 230 FDA reports)
TOOTH EXTRACTION ( 229 FDA reports)
GAIT DISTURBANCE ( 226 FDA reports)
HYPERHIDROSIS ( 226 FDA reports)
LOSS OF CONSCIOUSNESS ( 226 FDA reports)
FIBROMYALGIA ( 224 FDA reports)
ABDOMINAL PAIN UPPER ( 218 FDA reports)
DENTAL CARIES ( 216 FDA reports)
DECREASED APPETITE ( 215 FDA reports)
SWELLING ( 215 FDA reports)
ARTHRITIS ( 212 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 211 FDA reports)
MIGRAINE ( 211 FDA reports)
SUICIDAL IDEATION ( 206 FDA reports)
BONE PAIN ( 204 FDA reports)
FEELING ABNORMAL ( 204 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 204 FDA reports)
HERPES ZOSTER ( 204 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 203 FDA reports)
SOMNOLENCE ( 203 FDA reports)
PRURITUS ( 202 FDA reports)
TYPE 2 DIABETES MELLITUS ( 202 FDA reports)
MITRAL VALVE INCOMPETENCE ( 197 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 196 FDA reports)
HAEMORRHOIDS ( 196 FDA reports)
BLOOD PRESSURE INCREASED ( 195 FDA reports)
DRY MOUTH ( 195 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 186 FDA reports)
BALANCE DISORDER ( 183 FDA reports)
DRUG DEPENDENCE ( 183 FDA reports)
CATARACT ( 182 FDA reports)
PALPITATIONS ( 181 FDA reports)
DYSPEPSIA ( 180 FDA reports)
INFECTION ( 179 FDA reports)
DEEP VEIN THROMBOSIS ( 177 FDA reports)
TOOTH LOSS ( 175 FDA reports)
ASTHMA ( 174 FDA reports)
MEMORY IMPAIRMENT ( 174 FDA reports)
ATELECTASIS ( 173 FDA reports)
OVERDOSE ( 172 FDA reports)
DEFORMITY ( 169 FDA reports)
HIATUS HERNIA ( 169 FDA reports)
PULMONARY EMBOLISM ( 168 FDA reports)
BLOOD GLUCOSE INCREASED ( 166 FDA reports)
RENAL FAILURE ACUTE ( 165 FDA reports)
GASTRITIS ( 164 FDA reports)
STOMATITIS ( 161 FDA reports)
AMNESIA ( 160 FDA reports)
BURSITIS ( 159 FDA reports)
CHOLELITHIASIS ( 157 FDA reports)
ERYTHEMA ( 157 FDA reports)
MOUTH ULCERATION ( 157 FDA reports)
PLEURAL EFFUSION ( 157 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 155 FDA reports)
TACHYCARDIA ( 153 FDA reports)
PANCYTOPENIA ( 152 FDA reports)
CARDIAC DISORDER ( 151 FDA reports)
HYPOTENSION ( 151 FDA reports)
NERVOUSNESS ( 151 FDA reports)
HAEMATOCHEZIA ( 150 FDA reports)
MENTAL DISORDER ( 150 FDA reports)
OSTEOPOROSIS ( 150 FDA reports)
CHILLS ( 149 FDA reports)
DEATH ( 149 FDA reports)
METASTASES TO BONE ( 149 FDA reports)
CARDIOMEGALY ( 147 FDA reports)
CONTUSION ( 146 FDA reports)
HAEMOGLOBIN DECREASED ( 144 FDA reports)
HYPOKALAEMIA ( 143 FDA reports)
AGITATION ( 142 FDA reports)
TOOTH DISORDER ( 141 FDA reports)
HYPERGLYCAEMIA ( 140 FDA reports)
SPINAL COLUMN STENOSIS ( 138 FDA reports)
SLEEP APNOEA SYNDROME ( 137 FDA reports)
MENTAL STATUS CHANGES ( 136 FDA reports)
RESPIRATORY FAILURE ( 136 FDA reports)
ANGINA PECTORIS ( 135 FDA reports)
JOINT SWELLING ( 135 FDA reports)
DECREASED INTEREST ( 134 FDA reports)
NEURALGIA ( 134 FDA reports)
RIB FRACTURE ( 134 FDA reports)
EAR PAIN ( 131 FDA reports)
OSTEOPENIA ( 130 FDA reports)
ROAD TRAFFIC ACCIDENT ( 129 FDA reports)
SEPSIS ( 126 FDA reports)
DISTURBANCE IN ATTENTION ( 125 FDA reports)
BONE LESION ( 124 FDA reports)
COLONIC POLYP ( 124 FDA reports)
DYSURIA ( 124 FDA reports)
LYMPHADENOPATHY ( 124 FDA reports)
TOOTH FRACTURE ( 124 FDA reports)
FISTULA ( 123 FDA reports)
RECTAL HAEMORRHAGE ( 123 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 122 FDA reports)
THROMBOCYTOPENIA ( 121 FDA reports)
PRIMARY SEQUESTRUM ( 120 FDA reports)
ROTATOR CUFF SYNDROME ( 119 FDA reports)
NEPHROLITHIASIS ( 117 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 117 FDA reports)
ARTHROPATHY ( 115 FDA reports)
MULTIPLE MYELOMA ( 115 FDA reports)
URINARY INCONTINENCE ( 115 FDA reports)
CHEST DISCOMFORT ( 114 FDA reports)
HAEMATURIA ( 114 FDA reports)
VERTIGO ( 111 FDA reports)
RENAL CYST ( 110 FDA reports)
RENAL DISORDER ( 110 FDA reports)
STAPHYLOCOCCAL INFECTION ( 110 FDA reports)
STRESS ( 110 FDA reports)
URINARY RETENTION ( 110 FDA reports)
URTICARIA ( 110 FDA reports)
CHRONIC SINUSITIS ( 109 FDA reports)
RHEUMATOID ARTHRITIS ( 109 FDA reports)
HEPATIC STEATOSIS ( 108 FDA reports)
CARPAL TUNNEL SYNDROME ( 107 FDA reports)
IRRITABLE BOWEL SYNDROME ( 107 FDA reports)
LETHARGY ( 107 FDA reports)
DIABETIC NEUROPATHY ( 106 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 106 FDA reports)
SLEEP DISORDER ( 106 FDA reports)
DYSPNOEA EXERTIONAL ( 105 FDA reports)
FOOT FRACTURE ( 105 FDA reports)
INFLUENZA LIKE ILLNESS ( 105 FDA reports)
EXOSTOSIS ( 103 FDA reports)
ARTERIOSCLEROSIS ( 102 FDA reports)
ORTHOSTATIC HYPOTENSION ( 102 FDA reports)
DIPLOPIA ( 101 FDA reports)
IRRITABILITY ( 101 FDA reports)
TINNITUS ( 101 FDA reports)
BASAL CELL CARCINOMA ( 100 FDA reports)
HYPERSENSITIVITY ( 100 FDA reports)
MASTICATION DISORDER ( 99 FDA reports)
TENDERNESS ( 99 FDA reports)
HYPOXIA ( 98 FDA reports)
CARDIAC MURMUR ( 97 FDA reports)
DIVERTICULUM ( 97 FDA reports)
SINUS TACHYCARDIA ( 97 FDA reports)
COMPLETED SUICIDE ( 96 FDA reports)
FEMUR FRACTURE ( 96 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 95 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 95 FDA reports)
EPISTAXIS ( 95 FDA reports)
LUNG INFILTRATION ( 95 FDA reports)
RENAL FAILURE CHRONIC ( 95 FDA reports)
ABDOMINAL DISTENSION ( 94 FDA reports)
DIVERTICULUM INTESTINAL ( 94 FDA reports)
OEDEMA ( 94 FDA reports)
ORAL PAIN ( 94 FDA reports)
OROPHARYNGEAL PAIN ( 94 FDA reports)
HALLUCINATION ( 93 FDA reports)
RADICULOPATHY ( 93 FDA reports)
PANCREATITIS ( 92 FDA reports)
ANOREXIA ( 91 FDA reports)
DISCOMFORT ( 91 FDA reports)
MENISCUS LESION ( 91 FDA reports)
NEOPLASM MALIGNANT ( 91 FDA reports)
SUICIDE ATTEMPT ( 91 FDA reports)
ADVERSE EVENT ( 90 FDA reports)
JOINT EFFUSION ( 89 FDA reports)
JOINT SPRAIN ( 89 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 89 FDA reports)
PURULENT DISCHARGE ( 89 FDA reports)
SWELLING FACE ( 89 FDA reports)
COMPRESSION FRACTURE ( 88 FDA reports)
DRUG INTERACTION ( 88 FDA reports)
NIGHT SWEATS ( 88 FDA reports)
PRODUCTIVE COUGH ( 88 FDA reports)
BLOOD CREATININE INCREASED ( 87 FDA reports)
DYSGEUSIA ( 87 FDA reports)
HAEMORRHAGE ( 87 FDA reports)
HEART RATE INCREASED ( 87 FDA reports)
CEREBRAL ATROPHY ( 86 FDA reports)
DISABILITY ( 86 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 85 FDA reports)
INFLAMMATION ( 85 FDA reports)
POLLAKIURIA ( 85 FDA reports)
DYSARTHRIA ( 84 FDA reports)
HYPERKERATOSIS ( 84 FDA reports)
HYPOPHAGIA ( 84 FDA reports)
JAW DISORDER ( 84 FDA reports)
CARDIAC ARREST ( 83 FDA reports)
DRUG HYPERSENSITIVITY ( 83 FDA reports)
HYPONATRAEMIA ( 83 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 83 FDA reports)
PULMONARY HYPERTENSION ( 83 FDA reports)
RESPIRATORY DISTRESS ( 83 FDA reports)
RHINITIS ALLERGIC ( 83 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 83 FDA reports)
HYPERCHOLESTEROLAEMIA ( 82 FDA reports)
IRON DEFICIENCY ANAEMIA ( 82 FDA reports)
PULMONARY OEDEMA ( 82 FDA reports)
AGGRESSION ( 81 FDA reports)
SKIN ULCER ( 81 FDA reports)
ECCHYMOSIS ( 80 FDA reports)
DRUG ABUSER ( 79 FDA reports)
FLUID RETENTION ( 79 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 79 FDA reports)
ORAL INFECTION ( 79 FDA reports)
SPEECH DISORDER ( 79 FDA reports)
ACCIDENTAL OVERDOSE ( 78 FDA reports)
COLITIS ( 78 FDA reports)
ENDODONTIC PROCEDURE ( 78 FDA reports)
EATING DISORDER ( 77 FDA reports)
GASTROENTERITIS ( 77 FDA reports)
MENTAL IMPAIRMENT ( 77 FDA reports)
PANIC ATTACK ( 77 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 77 FDA reports)
ABASIA ( 76 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 76 FDA reports)
DYSKINESIA ( 76 FDA reports)
HYPOGLYCAEMIA ( 76 FDA reports)
OSTEITIS ( 76 FDA reports)
PERIODONTAL DISEASE ( 76 FDA reports)
SKIN LESION ( 76 FDA reports)
TENDONITIS ( 76 FDA reports)
TOOTHACHE ( 76 FDA reports)
BONE DENSITY DECREASED ( 75 FDA reports)
BURNING SENSATION ( 75 FDA reports)
CYST ( 75 FDA reports)
HEPATIC CYST ( 75 FDA reports)
MULTIPLE SCLEROSIS ( 75 FDA reports)
TONGUE ULCERATION ( 75 FDA reports)
TOOTH ABSCESS ( 75 FDA reports)
WHEEZING ( 75 FDA reports)
ABNORMAL BEHAVIOUR ( 74 FDA reports)
ACTINOMYCOSIS ( 74 FDA reports)
GINGIVITIS ( 74 FDA reports)
HEPATIC ENZYME INCREASED ( 74 FDA reports)
KYPHOSIS ( 74 FDA reports)
MASS ( 74 FDA reports)
ALOPECIA ( 73 FDA reports)
ARRHYTHMIA ( 73 FDA reports)
DYSPHONIA ( 73 FDA reports)
HYPERTONIC BLADDER ( 73 FDA reports)
SCOLIOSIS ( 73 FDA reports)
ERECTILE DYSFUNCTION ( 72 FDA reports)
HYPOTHYROIDISM ( 72 FDA reports)
LEUKOPENIA ( 72 FDA reports)
ACUTE SINUSITIS ( 71 FDA reports)
CANDIDIASIS ( 71 FDA reports)
HAEMATOMA ( 71 FDA reports)
OSTEOSCLEROSIS ( 71 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 70 FDA reports)
DISORIENTATION ( 70 FDA reports)
MAJOR DEPRESSION ( 70 FDA reports)
BACK INJURY ( 69 FDA reports)
GINGIVAL DISORDER ( 69 FDA reports)
LUNG NEOPLASM ( 69 FDA reports)
OESOPHAGITIS ( 69 FDA reports)
RESTLESS LEGS SYNDROME ( 69 FDA reports)
VENTRICULAR TACHYCARDIA ( 69 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 68 FDA reports)
TOOTH INFECTION ( 68 FDA reports)
ANGER ( 67 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 67 FDA reports)
CHONDROMALACIA ( 67 FDA reports)
HYPOCALCAEMIA ( 67 FDA reports)
INCORRECT DOSE ADMINISTERED ( 67 FDA reports)
MEDICATION ERROR ( 67 FDA reports)
NEUTROPENIA ( 67 FDA reports)
PARANOIA ( 67 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 67 FDA reports)
RESTLESSNESS ( 67 FDA reports)
CARDIOMYOPATHY ( 66 FDA reports)
FOOT DEFORMITY ( 66 FDA reports)
GALLBLADDER DISORDER ( 66 FDA reports)
HERPES SIMPLEX ( 66 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 66 FDA reports)
HAEMATEMESIS ( 65 FDA reports)
JAW OPERATION ( 65 FDA reports)
SINUS DISORDER ( 65 FDA reports)
DEAFNESS ( 64 FDA reports)
GASTRIC ULCER ( 64 FDA reports)
LUMBAR SPINAL STENOSIS ( 64 FDA reports)
OBESITY ( 64 FDA reports)
ABSCESS ( 63 FDA reports)
CARDIAC FAILURE ( 63 FDA reports)
DERMATITIS ( 63 FDA reports)
FLUSHING ( 63 FDA reports)
LUNG DISORDER ( 63 FDA reports)
METASTASES TO LUNG ( 63 FDA reports)
SCIATICA ( 63 FDA reports)
SPINAL COMPRESSION FRACTURE ( 63 FDA reports)
THROMBOSIS ( 63 FDA reports)
MALNUTRITION ( 62 FDA reports)
ABDOMINAL DISCOMFORT ( 61 FDA reports)
FUNGAL INFECTION ( 61 FDA reports)
GINGIVAL RECESSION ( 61 FDA reports)
HIP FRACTURE ( 61 FDA reports)
ORAL CANDIDIASIS ( 61 FDA reports)
PERIODONTITIS ( 61 FDA reports)
PSORIASIS ( 61 FDA reports)
TREATMENT NONCOMPLIANCE ( 61 FDA reports)
UNRESPONSIVE TO STIMULI ( 61 FDA reports)
VIRAL INFECTION ( 61 FDA reports)
DELIRIUM ( 60 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 60 FDA reports)
DRUG TOXICITY ( 60 FDA reports)
HOT FLUSH ( 60 FDA reports)
INCONTINENCE ( 60 FDA reports)
METASTASES TO SPINE ( 60 FDA reports)
SKIN DISCOLOURATION ( 60 FDA reports)
COGNITIVE DISORDER ( 59 FDA reports)
EYE PAIN ( 59 FDA reports)
ORAL DISORDER ( 59 FDA reports)
PERICARDIAL EFFUSION ( 59 FDA reports)
VISUAL IMPAIRMENT ( 59 FDA reports)
DECUBITUS ULCER ( 58 FDA reports)
EJECTION FRACTION DECREASED ( 58 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 58 FDA reports)
LOOSE TOOTH ( 58 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 58 FDA reports)
PHARYNGITIS ( 58 FDA reports)
BLOOD GLUCOSE DECREASED ( 57 FDA reports)
DIVERTICULITIS ( 57 FDA reports)
FLANK PAIN ( 57 FDA reports)
GINGIVAL BLEEDING ( 57 FDA reports)
GLOSSODYNIA ( 57 FDA reports)
GOITRE ( 57 FDA reports)
HAND FRACTURE ( 57 FDA reports)
HEART RATE IRREGULAR ( 57 FDA reports)
NOCTURIA ( 57 FDA reports)
SCAR ( 57 FDA reports)
VAGINAL HAEMORRHAGE ( 57 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 56 FDA reports)
AZOTAEMIA ( 55 FDA reports)
CYSTITIS ( 55 FDA reports)
DRUG ABUSE ( 55 FDA reports)
ECONOMIC PROBLEM ( 55 FDA reports)
FEAR ( 55 FDA reports)
NASOPHARYNGITIS ( 55 FDA reports)
PNEUMONIA ASPIRATION ( 55 FDA reports)
ADVERSE DRUG REACTION ( 54 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 54 FDA reports)
INADEQUATE ANALGESIA ( 54 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 54 FDA reports)
AORTIC VALVE INCOMPETENCE ( 53 FDA reports)
BLOOD POTASSIUM DECREASED ( 53 FDA reports)
CARDIO-RESPIRATORY ARREST ( 53 FDA reports)
CHOLECYSTITIS CHRONIC ( 53 FDA reports)
HEPATITIS ( 53 FDA reports)
ABNORMAL DREAMS ( 52 FDA reports)
ASPIRATION ( 52 FDA reports)
DEBRIDEMENT ( 52 FDA reports)
FLATULENCE ( 52 FDA reports)
INTENTIONAL OVERDOSE ( 52 FDA reports)
MOBILITY DECREASED ( 52 FDA reports)
PATHOLOGICAL FRACTURE ( 52 FDA reports)
BONE DEBRIDEMENT ( 51 FDA reports)
HAEMATOCRIT DECREASED ( 51 FDA reports)
HAEMOPTYSIS ( 51 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 51 FDA reports)
SKIN EXFOLIATION ( 51 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 51 FDA reports)
UTERINE LEIOMYOMA ( 51 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 51 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 50 FDA reports)
GASTROINTESTINAL DISORDER ( 50 FDA reports)
GINGIVAL ULCERATION ( 50 FDA reports)
HEAD INJURY ( 50 FDA reports)
JOINT INJURY ( 50 FDA reports)
MELAENA ( 50 FDA reports)
PROSTATITIS ( 50 FDA reports)
RENAL IMPAIRMENT ( 50 FDA reports)
RHABDOMYOLYSIS ( 50 FDA reports)
UNEVALUABLE EVENT ( 50 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 50 FDA reports)
COMA ( 49 FDA reports)
CRYING ( 49 FDA reports)
ENCEPHALOPATHY ( 49 FDA reports)
FACIAL BONES FRACTURE ( 49 FDA reports)
HYPOVOLAEMIA ( 49 FDA reports)
ATRIAL FLUTTER ( 48 FDA reports)
CAROTID ARTERY STENOSIS ( 48 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 48 FDA reports)
JAW FRACTURE ( 48 FDA reports)
ORAL CAVITY FISTULA ( 48 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 47 FDA reports)
ANGINA UNSTABLE ( 47 FDA reports)
BLISTER ( 47 FDA reports)
BONE NEOPLASM MALIGNANT ( 47 FDA reports)
DENTAL FISTULA ( 47 FDA reports)
LACERATION ( 47 FDA reports)
MYOPATHY ( 47 FDA reports)
NASAL CONGESTION ( 47 FDA reports)
NERVOUS SYSTEM DISORDER ( 47 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 47 FDA reports)
BLADDER DISORDER ( 46 FDA reports)
DEPRESSED MOOD ( 46 FDA reports)
INCREASED TENDENCY TO BRUISE ( 46 FDA reports)
LIMB INJURY ( 46 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 46 FDA reports)
SPONDYLOLISTHESIS ( 46 FDA reports)
THYROID DISORDER ( 46 FDA reports)
VISUAL ACUITY REDUCED ( 46 FDA reports)
BIPOLAR DISORDER ( 45 FDA reports)
CERVICAL SPINAL STENOSIS ( 45 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 45 FDA reports)
EYE DISORDER ( 45 FDA reports)
GASTRIC DISORDER ( 45 FDA reports)
METASTASES TO LIVER ( 45 FDA reports)
MYOCARDIAL ISCHAEMIA ( 45 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 45 FDA reports)
PLATELET COUNT DECREASED ( 45 FDA reports)
SKIN DISORDER ( 45 FDA reports)
VENTRICULAR HYPERTROPHY ( 45 FDA reports)
BLOOD UREA INCREASED ( 44 FDA reports)
BONE OPERATION ( 44 FDA reports)
DRY EYE ( 44 FDA reports)
EXCORIATION ( 44 FDA reports)
HALLUCINATION, AUDITORY ( 44 FDA reports)
INTRAOCULAR LENS IMPLANT ( 44 FDA reports)
LACUNAR INFARCTION ( 44 FDA reports)
PULMONARY CONGESTION ( 44 FDA reports)
PULMONARY FIBROSIS ( 44 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 44 FDA reports)
AORTIC ANEURYSM ( 43 FDA reports)
APHASIA ( 43 FDA reports)
BLOOD PRESSURE DECREASED ( 43 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 43 FDA reports)
DRUG DOSE OMISSION ( 43 FDA reports)
EMPHYSEMA ( 43 FDA reports)
FEBRILE NEUTROPENIA ( 43 FDA reports)
ILEUS ( 43 FDA reports)
JOINT DISLOCATION ( 43 FDA reports)
NIGHTMARE ( 43 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 43 FDA reports)
ANKLE FRACTURE ( 42 FDA reports)
ECZEMA ( 42 FDA reports)
GINGIVAL PAIN ( 42 FDA reports)
GLAUCOMA ( 42 FDA reports)
GROIN PAIN ( 42 FDA reports)
LEFT ATRIAL DILATATION ( 42 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 42 FDA reports)
OSTEOLYSIS ( 42 FDA reports)
PEPTIC ULCER ( 42 FDA reports)
RESPIRATORY ARREST ( 42 FDA reports)
SYNOVIAL CYST ( 42 FDA reports)
TENDON RUPTURE ( 42 FDA reports)
DEPENDENCE ( 41 FDA reports)
DRUG EFFECT DECREASED ( 41 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 41 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 41 FDA reports)
MUCOSAL INFLAMMATION ( 41 FDA reports)
MYOPIA ( 41 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 41 FDA reports)
PROTEINURIA ( 41 FDA reports)
PSYCHOTIC DISORDER ( 41 FDA reports)
SKIN LACERATION ( 41 FDA reports)
TYPE 1 DIABETES MELLITUS ( 41 FDA reports)
WOUND ( 41 FDA reports)
BREAST CANCER ( 40 FDA reports)
BRUXISM ( 40 FDA reports)
CARDIOVASCULAR DISORDER ( 40 FDA reports)
DRUG SCREEN POSITIVE ( 40 FDA reports)
EXPOSED BONE IN JAW ( 40 FDA reports)
INJECTION SITE PAIN ( 40 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 40 FDA reports)
SEQUESTRECTOMY ( 40 FDA reports)
STEM CELL TRANSPLANT ( 40 FDA reports)
ULCER ( 40 FDA reports)
DEVICE MALFUNCTION ( 39 FDA reports)
DYSSTASIA ( 39 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 39 FDA reports)
INTERMITTENT CLAUDICATION ( 39 FDA reports)
KNEE ARTHROPLASTY ( 39 FDA reports)
MANIA ( 39 FDA reports)
MULTI-ORGAN FAILURE ( 39 FDA reports)
MUSCLE STRAIN ( 39 FDA reports)
MUSCLE TWITCHING ( 39 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 39 FDA reports)
OFF LABEL USE ( 39 FDA reports)
PROSTATE CANCER ( 39 FDA reports)
SEDATION ( 39 FDA reports)
SENSITIVITY OF TEETH ( 39 FDA reports)
SEPTIC SHOCK ( 39 FDA reports)
ALVEOLOPLASTY ( 38 FDA reports)
APNOEA ( 38 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 38 FDA reports)
CROHN'S DISEASE ( 38 FDA reports)
DENTURE WEARER ( 38 FDA reports)
FAECAL INCONTINENCE ( 38 FDA reports)
HAEMOLYTIC ANAEMIA ( 38 FDA reports)
HOMICIDAL IDEATION ( 38 FDA reports)
INJECTION SITE REACTION ( 38 FDA reports)
LEUKOCYTOSIS ( 38 FDA reports)
POST PROCEDURAL COMPLICATION ( 38 FDA reports)
PRURITUS GENERALISED ( 38 FDA reports)
SINUS HEADACHE ( 38 FDA reports)
TARDIVE DYSKINESIA ( 38 FDA reports)
VITAMIN B12 DEFICIENCY ( 38 FDA reports)
ABSCESS ORAL ( 37 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 37 FDA reports)
BACTERAEMIA ( 37 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 37 FDA reports)
BUNION ( 37 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 37 FDA reports)
CORONARY ARTERY STENOSIS ( 37 FDA reports)
EYE INFECTION ( 37 FDA reports)
GINGIVAL SWELLING ( 37 FDA reports)
HEMIPARESIS ( 37 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 37 FDA reports)
JAUNDICE ( 37 FDA reports)
LIBIDO DECREASED ( 37 FDA reports)
METABOLIC ACIDOSIS ( 37 FDA reports)
NECK MASS ( 37 FDA reports)
NEURITIS ( 37 FDA reports)
PERONEAL NERVE PALSY ( 37 FDA reports)
PLANTAR FASCIITIS ( 37 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 37 FDA reports)
SPUTUM DISCOLOURED ( 37 FDA reports)
CERUMEN IMPACTION ( 36 FDA reports)
CHOLECYSTECTOMY ( 36 FDA reports)
DEMENTIA ( 36 FDA reports)
DIABETIC KETOACIDOSIS ( 36 FDA reports)
MOOD SWINGS ( 36 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 36 FDA reports)
OTITIS MEDIA ( 36 FDA reports)
PYELONEPHRITIS ( 36 FDA reports)
SPINAL FRACTURE ( 36 FDA reports)
ABSCESS JAW ( 35 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 35 FDA reports)
CERVICOBRACHIAL SYNDROME ( 35 FDA reports)
COORDINATION ABNORMAL ( 35 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 35 FDA reports)
EMOTIONAL DISORDER ( 35 FDA reports)
FEELING HOT ( 35 FDA reports)
PALLOR ( 35 FDA reports)
SQUAMOUS CELL CARCINOMA ( 35 FDA reports)
THYROID CANCER ( 35 FDA reports)
TONGUE DISCOLOURATION ( 35 FDA reports)
ABSCESS DRAINAGE ( 34 FDA reports)
CHEST WALL MASS ( 34 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 34 FDA reports)
DIFFICULTY IN WALKING ( 34 FDA reports)
FEELING JITTERY ( 34 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 34 FDA reports)
GRAND MAL CONVULSION ( 34 FDA reports)
INTENTIONAL DRUG MISUSE ( 34 FDA reports)
LIMB DISCOMFORT ( 34 FDA reports)
LUMBAR RADICULOPATHY ( 34 FDA reports)
PROTHROMBIN TIME PROLONGED ( 34 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 34 FDA reports)
SEXUAL DYSFUNCTION ( 34 FDA reports)
SINUS POLYP ( 34 FDA reports)
THINKING ABNORMAL ( 34 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 34 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 33 FDA reports)
BRADYCARDIA ( 33 FDA reports)
CEREBRAL INFARCTION ( 33 FDA reports)
CORONARY ARTERY OCCLUSION ( 33 FDA reports)
CYANOSIS ( 33 FDA reports)
DISEASE PROGRESSION ( 33 FDA reports)
EYE IRRITATION ( 33 FDA reports)
FRACTURE NONUNION ( 33 FDA reports)
GLOSSITIS ( 33 FDA reports)
HALLUCINATION, VISUAL ( 33 FDA reports)
ILL-DEFINED DISORDER ( 33 FDA reports)
INFLUENZA ( 33 FDA reports)
ORAL HERPES ( 33 FDA reports)
PRODUCT QUALITY ISSUE ( 33 FDA reports)
SNORING ( 33 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 33 FDA reports)
TRIGGER FINGER ( 33 FDA reports)
ANGIOPATHY ( 32 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 32 FDA reports)
BLOOD CALCIUM INCREASED ( 32 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 32 FDA reports)
DRY SKIN ( 32 FDA reports)
FRACTURE ( 32 FDA reports)
GASTRITIS EROSIVE ( 32 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 32 FDA reports)
LACRIMATION INCREASED ( 32 FDA reports)
LOBAR PNEUMONIA ( 32 FDA reports)
MOVEMENT DISORDER ( 32 FDA reports)
MULTIPLE DRUG OVERDOSE ( 32 FDA reports)
PELVIC PAIN ( 32 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 32 FDA reports)
POST HERPETIC NEURALGIA ( 32 FDA reports)
RHINITIS ( 32 FDA reports)
SURGERY ( 32 FDA reports)
VENOUS INSUFFICIENCY ( 32 FDA reports)
CATARACT OPERATION ( 31 FDA reports)
CERVICAL CORD COMPRESSION ( 31 FDA reports)
COAGULOPATHY ( 31 FDA reports)
DYSLIPIDAEMIA ( 31 FDA reports)
ELECTROLYTE IMBALANCE ( 31 FDA reports)
FAILURE TO THRIVE ( 31 FDA reports)
HEPATOTOXICITY ( 31 FDA reports)
IMPAIRED DRIVING ABILITY ( 31 FDA reports)
INJECTION SITE ERYTHEMA ( 31 FDA reports)
INTESTINAL OBSTRUCTION ( 31 FDA reports)
MOUTH HAEMORRHAGE ( 31 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 31 FDA reports)
RESPIRATORY DISORDER ( 31 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 31 FDA reports)
TOOTH REPAIR ( 31 FDA reports)
VISUAL DISTURBANCE ( 31 FDA reports)
HYPERSOMNIA ( 30 FDA reports)
LACTOSE INTOLERANCE ( 30 FDA reports)
NEUROPATHY ( 30 FDA reports)
OCULAR HYPERAEMIA ( 30 FDA reports)
PARAESTHESIA ORAL ( 30 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 30 FDA reports)
POLYURIA ( 30 FDA reports)
SINUS BRADYCARDIA ( 30 FDA reports)
SWOLLEN TONGUE ( 30 FDA reports)
TRISMUS ( 30 FDA reports)
WOUND DEHISCENCE ( 30 FDA reports)
ANIMAL BITE ( 29 FDA reports)
BLOOD ALBUMIN DECREASED ( 29 FDA reports)
BLOOD BILIRUBIN INCREASED ( 29 FDA reports)
BLOOD SODIUM DECREASED ( 29 FDA reports)
BONE GRAFT ( 29 FDA reports)
DELUSION ( 29 FDA reports)
FLUID OVERLOAD ( 29 FDA reports)
GINGIVAL INFECTION ( 29 FDA reports)
HERNIA ( 29 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 29 FDA reports)
LIVER DISORDER ( 29 FDA reports)
MENIERE'S DISEASE ( 29 FDA reports)
NEOPLASM PROGRESSION ( 29 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 29 FDA reports)
ODYNOPHAGIA ( 29 FDA reports)
OPEN WOUND ( 29 FDA reports)
PYURIA ( 29 FDA reports)
REFLUX OESOPHAGITIS ( 29 FDA reports)
RENAL PAIN ( 29 FDA reports)
SHOULDER ARTHROPLASTY ( 29 FDA reports)
STOMACH DISCOMFORT ( 29 FDA reports)
TEMPERATURE INTOLERANCE ( 29 FDA reports)
THROAT TIGHTNESS ( 29 FDA reports)
VITREOUS FLOATERS ( 29 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 28 FDA reports)
ASTIGMATISM ( 28 FDA reports)
BREAST CANCER RECURRENT ( 28 FDA reports)
CIRCULATORY COLLAPSE ( 28 FDA reports)
CUTIS LAXA ( 28 FDA reports)
DEVICE FAILURE ( 28 FDA reports)
DIABETIC RETINOPATHY ( 28 FDA reports)
GASTRIC POLYPS ( 28 FDA reports)
HEARING IMPAIRED ( 28 FDA reports)
INJECTION SITE HAEMORRHAGE ( 28 FDA reports)
MYELOMA RECURRENCE ( 28 FDA reports)
PHOTOPHOBIA ( 28 FDA reports)
PRESYNCOPE ( 28 FDA reports)
RENAL INJURY ( 28 FDA reports)
SPINAL DISORDER ( 28 FDA reports)
VAGINAL INFECTION ( 28 FDA reports)
ACCIDENT ( 27 FDA reports)
ATAXIA ( 27 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 27 FDA reports)
DERMAL CYST ( 27 FDA reports)
DRY THROAT ( 27 FDA reports)
FACIAL PALSY ( 27 FDA reports)
FAECES DISCOLOURED ( 27 FDA reports)
GENERALISED OEDEMA ( 27 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 27 FDA reports)
HYPOMAGNESAEMIA ( 27 FDA reports)
MELANOCYTIC NAEVUS ( 27 FDA reports)
NEPHROSCLEROSIS ( 27 FDA reports)
NODULE ( 27 FDA reports)
NON-CARDIAC CHEST PAIN ( 27 FDA reports)
OXYGEN SATURATION DECREASED ( 27 FDA reports)
PARALYSIS ( 27 FDA reports)
PERIPHERAL COLDNESS ( 27 FDA reports)
PNEUMOTHORAX ( 27 FDA reports)
PROSTATE CANCER METASTATIC ( 27 FDA reports)
RADIUS FRACTURE ( 27 FDA reports)
RASH PRURITIC ( 27 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 27 FDA reports)
TENSION ( 27 FDA reports)
AGEUSIA ( 26 FDA reports)
BONE EROSION ( 26 FDA reports)
BONE FRAGMENTATION ( 26 FDA reports)
BONE LOSS ( 26 FDA reports)
BONE SWELLING ( 26 FDA reports)
BRAIN INJURY ( 26 FDA reports)
BRAIN NEOPLASM ( 26 FDA reports)
BRONCHITIS ACUTE ( 26 FDA reports)
CACHEXIA ( 26 FDA reports)
CHOLECYSTITIS ( 26 FDA reports)
DRUG TOLERANCE ( 26 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 26 FDA reports)
FACIAL PAIN ( 26 FDA reports)
HYPERKALAEMIA ( 26 FDA reports)
HYPOGONADISM ( 26 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 26 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 26 FDA reports)
LUNG HYPERINFLATION ( 26 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 26 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 26 FDA reports)
PAROTITIS ( 26 FDA reports)
ACTINIC KERATOSIS ( 25 FDA reports)
ADRENAL INSUFFICIENCY ( 25 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 25 FDA reports)
BACK DISORDER ( 25 FDA reports)
BILE DUCT STENOSIS ( 25 FDA reports)
BLADDER OPERATION ( 25 FDA reports)
BODY HEIGHT DECREASED ( 25 FDA reports)
CONJUNCTIVITIS ( 25 FDA reports)
ESSENTIAL HYPERTENSION ( 25 FDA reports)
HYPOACUSIS ( 25 FDA reports)
INJECTION SITE SWELLING ( 25 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 25 FDA reports)
KIDNEY INFECTION ( 25 FDA reports)
LARYNGITIS ( 25 FDA reports)
MULTIPLE INJURIES ( 25 FDA reports)
ONYCHOMYCOSIS ( 25 FDA reports)
OSTEITIS DEFORMANS ( 25 FDA reports)
OTORRHOEA ( 25 FDA reports)
PANCREATITIS ACUTE ( 25 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 25 FDA reports)
RHINORRHOEA ( 25 FDA reports)
SELF-INJURIOUS IDEATION ( 25 FDA reports)
SKIN TIGHTNESS ( 25 FDA reports)
THROAT IRRITATION ( 25 FDA reports)
WITHDRAWAL SYNDROME ( 25 FDA reports)
ACROCHORDON ( 24 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 24 FDA reports)
BONE MARROW FAILURE ( 24 FDA reports)
BREAST CYST ( 24 FDA reports)
BREAST MASS ( 24 FDA reports)
CAROTID BRUIT ( 24 FDA reports)
CLOSTRIDIAL INFECTION ( 24 FDA reports)
DISEASE RECURRENCE ( 24 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 24 FDA reports)
GENERALISED ANXIETY DISORDER ( 24 FDA reports)
IMPAIRED WORK ABILITY ( 24 FDA reports)
INFUSION RELATED REACTION ( 24 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 24 FDA reports)
MENORRHAGIA ( 24 FDA reports)
MITRAL VALVE PROLAPSE ( 24 FDA reports)
NASAL SEPTUM DEVIATION ( 24 FDA reports)
OPEN REDUCTION OF FRACTURE ( 24 FDA reports)
PELVIC FRACTURE ( 24 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 24 FDA reports)
PHYSICAL DISABILITY ( 24 FDA reports)
PLASMACYTOSIS ( 24 FDA reports)
PNEUMONITIS ( 24 FDA reports)
RESORPTION BONE INCREASED ( 24 FDA reports)
SPINAL CORD COMPRESSION ( 24 FDA reports)
STOMATITIS NECROTISING ( 24 FDA reports)
TENSION HEADACHE ( 24 FDA reports)
WHEELCHAIR USER ( 24 FDA reports)
ACUTE RESPIRATORY FAILURE ( 23 FDA reports)
ANOGENITAL WARTS ( 23 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 23 FDA reports)
CEREBRAL ARTERY STENOSIS ( 23 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 23 FDA reports)
EAR HAEMORRHAGE ( 23 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 23 FDA reports)
FEELING COLD ( 23 FDA reports)
GENITAL HERPES ( 23 FDA reports)
HEPATOMEGALY ( 23 FDA reports)
HYPOMANIA ( 23 FDA reports)
LARYNGEAL OEDEMA ( 23 FDA reports)
PATHOLOGICAL GAMBLING ( 23 FDA reports)
PHLEBITIS ( 23 FDA reports)
RAYNAUD'S PHENOMENON ( 23 FDA reports)
SKIN PAPILLOMA ( 23 FDA reports)
WEIGHT FLUCTUATION ( 23 FDA reports)
ABDOMINAL PAIN LOWER ( 22 FDA reports)
AGRANULOCYTOSIS ( 22 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 22 FDA reports)
BREAST CANCER FEMALE ( 22 FDA reports)
CAROTID ARTERY DISEASE ( 22 FDA reports)
CHROMATURIA ( 22 FDA reports)
CONNECTIVE TISSUE DISORDER ( 22 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 22 FDA reports)
INTERSTITIAL LUNG DISEASE ( 22 FDA reports)
LICHEN PLANUS ( 22 FDA reports)
LIFE EXPECTANCY SHORTENED ( 22 FDA reports)
LUNG INFECTION ( 22 FDA reports)
MENINGIOMA ( 22 FDA reports)
NECK INJURY ( 22 FDA reports)
OEDEMA MUCOSAL ( 22 FDA reports)
PLEURISY ( 22 FDA reports)
RETCHING ( 22 FDA reports)
RETINAL DETACHMENT ( 22 FDA reports)
ROSACEA ( 22 FDA reports)
SHOULDER PAIN ( 22 FDA reports)
VENTRICULAR DYSFUNCTION ( 22 FDA reports)
VIITH NERVE PARALYSIS ( 22 FDA reports)
BONE MARROW OEDEMA ( 21 FDA reports)
BONE SCAN ABNORMAL ( 21 FDA reports)
CEREBRAL ISCHAEMIA ( 21 FDA reports)
DYSTHYMIC DISORDER ( 21 FDA reports)
EARLY SATIETY ( 21 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 21 FDA reports)
EPICONDYLITIS ( 21 FDA reports)
EPILEPSY ( 21 FDA reports)
EXERCISE TOLERANCE DECREASED ( 21 FDA reports)
EYE INJURY ( 21 FDA reports)
FIBROSIS ( 21 FDA reports)
HAEMANGIOMA ( 21 FDA reports)
HEPATITIS C ( 21 FDA reports)
HYPERCALCAEMIA ( 21 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 21 FDA reports)
ISCHAEMIA ( 21 FDA reports)
LOCALISED INFECTION ( 21 FDA reports)
LOW TURNOVER OSTEOPATHY ( 21 FDA reports)
MYASTHENIA GRAVIS ( 21 FDA reports)
NEUTROPENIC SEPSIS ( 21 FDA reports)
ORAL DISCOMFORT ( 21 FDA reports)
ORAL SURGERY ( 21 FDA reports)
PANIC DISORDER ( 21 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 21 FDA reports)
SKIN BURNING SENSATION ( 21 FDA reports)
SKIN HYPERTROPHY ( 21 FDA reports)
STRESS SYMPTOMS ( 21 FDA reports)
TENDON INJURY ( 21 FDA reports)
THYROIDECTOMY ( 21 FDA reports)
VASCULITIS ( 21 FDA reports)
AFFECTIVE DISORDER ( 20 FDA reports)
BLINDNESS ( 20 FDA reports)
BLINDNESS UNILATERAL ( 20 FDA reports)
BLOOD CALCIUM DECREASED ( 20 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 20 FDA reports)
CYSTITIS INTERSTITIAL ( 20 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 20 FDA reports)
DRUG INTOLERANCE ( 20 FDA reports)
FELTY'S SYNDROME ( 20 FDA reports)
GRANULOMA ( 20 FDA reports)
GRAVITATIONAL OEDEMA ( 20 FDA reports)
HYPOALBUMINAEMIA ( 20 FDA reports)
INJECTION SITE DISCOLOURATION ( 20 FDA reports)
LUNG NEOPLASM MALIGNANT ( 20 FDA reports)
LYMPHOMA ( 20 FDA reports)
MALIGNANT MELANOMA ( 20 FDA reports)
MENSTRUATION IRREGULAR ( 20 FDA reports)
MICROGRAPHIC SKIN SURGERY ( 20 FDA reports)
MOUTH INJURY ( 20 FDA reports)
MUSCLE DISORDER ( 20 FDA reports)
NERVE INJURY ( 20 FDA reports)
RASH PAPULAR ( 20 FDA reports)
RECTAL POLYP ( 20 FDA reports)
SUBCUTANEOUS ABSCESS ( 20 FDA reports)
THYROID NEOPLASM ( 20 FDA reports)
TRIGEMINAL NEURALGIA ( 20 FDA reports)
ACUTE CORONARY SYNDROME ( 19 FDA reports)
BLADDER PROLAPSE ( 19 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 19 FDA reports)
CATHETERISATION CARDIAC ( 19 FDA reports)
COLD SWEAT ( 19 FDA reports)
COLITIS ISCHAEMIC ( 19 FDA reports)
CRANIAL NERVE DISORDER ( 19 FDA reports)
CYSTOCELE ( 19 FDA reports)
DENTAL DISCOMFORT ( 19 FDA reports)
DENTAL OPERATION ( 19 FDA reports)
FAT TISSUE INCREASED ( 19 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 19 FDA reports)
HEART RATE DECREASED ( 19 FDA reports)
HIP ARTHROPLASTY ( 19 FDA reports)
ILIOTIBIAL BAND SYNDROME ( 19 FDA reports)
JOINT STIFFNESS ( 19 FDA reports)
KERATITIS HERPETIC ( 19 FDA reports)
LEUKOPLAKIA ORAL ( 19 FDA reports)
LIGAMENT SPRAIN ( 19 FDA reports)
MICTURITION URGENCY ( 19 FDA reports)
MYELODYSPLASTIC SYNDROME ( 19 FDA reports)
NEUROMA ( 19 FDA reports)
ORAL PUSTULE ( 19 FDA reports)
OVARIAN CYST ( 19 FDA reports)
PAIN EXACERBATED ( 19 FDA reports)
PERICARDITIS ( 19 FDA reports)
PETECHIAE ( 19 FDA reports)
PLATELET DISORDER ( 19 FDA reports)
PROCTALGIA ( 19 FDA reports)
PULPITIS DENTAL ( 19 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 19 FDA reports)
SEROTONIN SYNDROME ( 19 FDA reports)
SHOCK ( 19 FDA reports)
SKIN CANCER ( 19 FDA reports)
SPINAL CORD OEDEMA ( 19 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 19 FDA reports)
TONGUE INJURY ( 19 FDA reports)
TOOTH INJURY ( 19 FDA reports)
URETHRAL STENOSIS ( 19 FDA reports)
VENOUS THROMBOSIS ( 19 FDA reports)
WALKING AID USER ( 19 FDA reports)
WOUND INFECTION ( 19 FDA reports)
ABORTION SPONTANEOUS ( 18 FDA reports)
ASCITES ( 18 FDA reports)
BARRETT'S OESOPHAGUS ( 18 FDA reports)
BRONCHITIS CHRONIC ( 18 FDA reports)
BURNING MOUTH SYNDROME ( 18 FDA reports)
CARDIAC VALVE DISEASE ( 18 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 18 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 18 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 18 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 18 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 18 FDA reports)
DEVICE RELATED INFECTION ( 18 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 18 FDA reports)
DIASTOLIC DYSFUNCTION ( 18 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 18 FDA reports)
EAR DISCOMFORT ( 18 FDA reports)
EUPHORIC MOOD ( 18 FDA reports)
FRACTURED SACRUM ( 18 FDA reports)
GASTROENTERITIS VIRAL ( 18 FDA reports)
HAEMANGIOMA OF LIVER ( 18 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 18 FDA reports)
INJECTION SITE HAEMATOMA ( 18 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 18 FDA reports)
KERATITIS ( 18 FDA reports)
LOCALISED OEDEMA ( 18 FDA reports)
LUNG CONSOLIDATION ( 18 FDA reports)
METASTATIC NEOPLASM ( 18 FDA reports)
MIDDLE INSOMNIA ( 18 FDA reports)
MOOD ALTERED ( 18 FDA reports)
MOTOR DYSFUNCTION ( 18 FDA reports)
MUSCLE TIGHTNESS ( 18 FDA reports)
PROCEDURAL PAIN ( 18 FDA reports)
RASH ERYTHEMATOUS ( 18 FDA reports)
RESPIRATORY TRACT INFECTION ( 18 FDA reports)
SPINAL FUSION SURGERY ( 18 FDA reports)
SUBCLAVIAN STEAL SYNDROME ( 18 FDA reports)
TENDON DISORDER ( 18 FDA reports)
TENOSYNOVITIS ( 18 FDA reports)
TIC ( 18 FDA reports)
TRANSAMINASES INCREASED ( 18 FDA reports)
TROPONIN INCREASED ( 18 FDA reports)
URINE ODOUR ABNORMAL ( 18 FDA reports)
VENTRICULAR FIBRILLATION ( 18 FDA reports)
VERTEBROPLASTY ( 18 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 18 FDA reports)
WOUND DRAINAGE ( 18 FDA reports)
ACNE ( 17 FDA reports)
ALCOHOLISM ( 17 FDA reports)
ANAPHYLACTIC REACTION ( 17 FDA reports)
ANOSMIA ( 17 FDA reports)
APPENDIX DISORDER ( 17 FDA reports)
ATROPHY ( 17 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 17 FDA reports)
BLADDER PAIN ( 17 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 17 FDA reports)
BONE CALLUS EXCESSIVE ( 17 FDA reports)
BONE CYST ( 17 FDA reports)
BONE GIANT CELL TUMOUR ( 17 FDA reports)
BREAST CANCER METASTATIC ( 17 FDA reports)
BREATH ODOUR ( 17 FDA reports)
BRONCHIAL SECRETION RETENTION ( 17 FDA reports)
CHOKING ( 17 FDA reports)
COLITIS ULCERATIVE ( 17 FDA reports)
CONCUSSION ( 17 FDA reports)
CORNEAL DYSTROPHY ( 17 FDA reports)
EAR INFECTION ( 17 FDA reports)
ENDOCARDITIS ( 17 FDA reports)
EPISCLERITIS ( 17 FDA reports)
FACIAL PARESIS ( 17 FDA reports)
HEPATIC FAILURE ( 17 FDA reports)
IMMUNOGLOBULINS DECREASED ( 17 FDA reports)
IMPRISONMENT ( 17 FDA reports)
INTENTIONAL SELF-INJURY ( 17 FDA reports)
LARYNGITIS VIRAL ( 17 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 17 FDA reports)
MUSCLE ATROPHY ( 17 FDA reports)
MUSCLE CRAMP ( 17 FDA reports)
MYOCLONUS ( 17 FDA reports)
OESOPHAGEAL ULCER ( 17 FDA reports)
POST PROCEDURAL FISTULA ( 17 FDA reports)
PROCEDURAL COMPLICATION ( 17 FDA reports)
PSEUDOMONAS INFECTION ( 17 FDA reports)
QUADRIPLEGIA ( 17 FDA reports)
RECTOCELE ( 17 FDA reports)
SKIN NEOPLASM EXCISION ( 17 FDA reports)
SOMNAMBULISM ( 17 FDA reports)
SPINAL FUSION ACQUIRED ( 17 FDA reports)
SUBCUTANEOUS NODULE ( 17 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 17 FDA reports)
VIRAL PHARYNGITIS ( 17 FDA reports)
APHAGIA ( 16 FDA reports)
AUTOIMMUNE THYROIDITIS ( 16 FDA reports)
BILE DUCT STONE ( 16 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 16 FDA reports)
BRONCHOSPASM ( 16 FDA reports)
CEREBRAL HAEMORRHAGE ( 16 FDA reports)
CHOLECYSTITIS INFECTIVE ( 16 FDA reports)
CRANIOTOMY ( 16 FDA reports)
DENTAL PULP DISORDER ( 16 FDA reports)
DUODENAL ULCER ( 16 FDA reports)
DYSTONIA ( 16 FDA reports)
EMBOLISM ( 16 FDA reports)
EXTREMITY CONTRACTURE ( 16 FDA reports)
FEELING DRUNK ( 16 FDA reports)
FRACTURE DELAYED UNION ( 16 FDA reports)
HEPATIC LESION ( 16 FDA reports)
HETEROTAXIA ( 16 FDA reports)
INCREASED APPETITE ( 16 FDA reports)
INJECTION SITE PRURITUS ( 16 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 16 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 16 FDA reports)
LIP DISORDER ( 16 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 16 FDA reports)
LUDWIG ANGINA ( 16 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 16 FDA reports)
NEUROGENIC BLADDER ( 16 FDA reports)
OESOPHAGEAL DISORDER ( 16 FDA reports)
ORTHOPNOEA ( 16 FDA reports)
OTITIS MEDIA ACUTE ( 16 FDA reports)
PARATHYROIDECTOMY ( 16 FDA reports)
PHYSICAL ABUSE ( 16 FDA reports)
PRESBYOPIA ( 16 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 16 FDA reports)
RASH MACULAR ( 16 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 16 FDA reports)
SELF-MEDICATION ( 16 FDA reports)
SNAKE BITE ( 16 FDA reports)
SOFT TISSUE DISORDER ( 16 FDA reports)
SPONDYLITIS ( 16 FDA reports)
SPONDYLOSIS ( 16 FDA reports)
STREPTOCOCCAL INFECTION ( 16 FDA reports)
TONGUE COATED ( 16 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 16 FDA reports)
VENTRICULAR SEPTAL DEFECT REPAIR ( 16 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 16 FDA reports)
VERTEBRAL WEDGING ( 16 FDA reports)
VOMITING PROJECTILE ( 16 FDA reports)
ABDOMINAL HERNIA ( 15 FDA reports)
ALCOHOL ABUSE ( 15 FDA reports)
ALCOHOL USE ( 15 FDA reports)
AORTIC VALVE SCLEROSIS ( 15 FDA reports)
APHTHOUS STOMATITIS ( 15 FDA reports)
ATRIAL TACHYCARDIA ( 15 FDA reports)
BENIGN COLONIC NEOPLASM ( 15 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 15 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 15 FDA reports)
CHRONIC FATIGUE SYNDROME ( 15 FDA reports)
CLOSTRIDIUM COLITIS ( 15 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 15 FDA reports)
DERMATITIS CONTACT ( 15 FDA reports)
DIALYSIS ( 15 FDA reports)
DILATATION ATRIAL ( 15 FDA reports)
DYSPHEMIA ( 15 FDA reports)
ESSENTIAL TREMOR ( 15 FDA reports)
GOUT ( 15 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 15 FDA reports)
HOSPITALISATION ( 15 FDA reports)
HYPERPLASIA ( 15 FDA reports)
HYPERREFLEXIA ( 15 FDA reports)
HYPERTENSIVE HEART DISEASE ( 15 FDA reports)
HYPOAESTHESIA ORAL ( 15 FDA reports)
HYPOPHOSPHATAEMIA ( 15 FDA reports)
HYSTERECTOMY ( 15 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 15 FDA reports)
LOWER EXTREMITY MASS ( 15 FDA reports)
MARROW HYPERPLASIA ( 15 FDA reports)
MASTOIDITIS ( 15 FDA reports)
METABOLIC DISORDER ( 15 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 15 FDA reports)
NARCOTIC INTOXICATION ( 15 FDA reports)
ORTHOSIS USER ( 15 FDA reports)
OVARIAN CANCER ( 15 FDA reports)
PELVIC ABSCESS ( 15 FDA reports)
PULSE ABSENT ( 15 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 15 FDA reports)
SENSORY LOSS ( 15 FDA reports)
SPINAL LAMINECTOMY ( 15 FDA reports)
SPLENOMEGALY ( 15 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 15 FDA reports)
TOBACCO USER ( 15 FDA reports)
VAGINAL DISCHARGE ( 15 FDA reports)
ANTI-THYROID ANTIBODY POSITIVE ( 14 FDA reports)
AORTIC CALCIFICATION ( 14 FDA reports)
APPENDICECTOMY ( 14 FDA reports)
BENIGN NEOPLASM ( 14 FDA reports)
BIPOLAR II DISORDER ( 14 FDA reports)
BLOOD URINE ( 14 FDA reports)
BODY TEMPERATURE INCREASED ( 14 FDA reports)
BUNION OPERATION ( 14 FDA reports)
CAROTID ARTERY OCCLUSION ( 14 FDA reports)
CHANGE OF BOWEL HABIT ( 14 FDA reports)
DIABETIC COMA ( 14 FDA reports)
DIABETIC GASTROPARESIS ( 14 FDA reports)
DIABETIC NEPHROPATHY ( 14 FDA reports)
DILATATION VENTRICULAR ( 14 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 14 FDA reports)
ECZEMA ASTEATOTIC ( 14 FDA reports)
EMPYEMA ( 14 FDA reports)
ENCEPHALOMALACIA ( 14 FDA reports)
ESCHERICHIA BACTERAEMIA ( 14 FDA reports)
FACE OEDEMA ( 14 FDA reports)
FIBROUS HISTIOCYTOMA ( 14 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 14 FDA reports)
GINGIVAL OEDEMA ( 14 FDA reports)
HAEMORRHOID OPERATION ( 14 FDA reports)
HAND DEFORMITY ( 14 FDA reports)
HYDROCELE ( 14 FDA reports)
ICHTHYOSIS ( 14 FDA reports)
INCISIONAL DRAINAGE ( 14 FDA reports)
LIPOMA ( 14 FDA reports)
LYMPHOEDEMA ( 14 FDA reports)
MEDICAL DEVICE REMOVAL ( 14 FDA reports)
NERVE ROOT INJURY ( 14 FDA reports)
NEURECTOMY ( 14 FDA reports)
OESOPHAGEAL MUCOSAL HYPERPLASIA ( 14 FDA reports)
ORAL FIBROMA ( 14 FDA reports)
ORAL MUCOSA ATROPHY ( 14 FDA reports)
ORTHODONTIC APPLIANCE USER ( 14 FDA reports)
PAPILLOMA ( 14 FDA reports)
PARAPLEGIA ( 14 FDA reports)
PARKINSON'S DISEASE ( 14 FDA reports)
PARKINSONISM ( 14 FDA reports)
PERSONALITY CHANGE ( 14 FDA reports)
PHARYNGEAL ERYTHEMA ( 14 FDA reports)
PRESCRIBED OVERDOSE ( 14 FDA reports)
RASH GENERALISED ( 14 FDA reports)
RECTAL PROLAPSE ( 14 FDA reports)
SECONDARY IMMUNODEFICIENCY ( 14 FDA reports)
SKELETAL SURVEY ABNORMAL ( 14 FDA reports)
SKIN INDURATION ( 14 FDA reports)
SPINAL MYELOGRAM ( 14 FDA reports)
SUBSTANCE ABUSE ( 14 FDA reports)
TUMOUR EXCISION ( 14 FDA reports)
VITAMIN D DEFICIENCY ( 14 FDA reports)
ABSCESS LIMB ( 13 FDA reports)
AFFECT LABILITY ( 13 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 13 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 13 FDA reports)
ANGIOPLASTY ( 13 FDA reports)
ASPIRATION JOINT ( 13 FDA reports)
BASOSQUAMOUS CARCINOMA ( 13 FDA reports)
BLEPHARITIS ( 13 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 13 FDA reports)
BLOODY DISCHARGE ( 13 FDA reports)
BUTTOCK PAIN ( 13 FDA reports)
CHEST WALL PAIN ( 13 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 13 FDA reports)
COSTOCHONDRITIS ( 13 FDA reports)
DEMYELINATION ( 13 FDA reports)
DERMATITIS EXFOLIATIVE ( 13 FDA reports)
EDENTULOUS ( 13 FDA reports)
EMBOLISM ARTERIAL ( 13 FDA reports)
EMBOLISM VENOUS ( 13 FDA reports)
EROSIVE OESOPHAGITIS ( 13 FDA reports)
EYE SWELLING ( 13 FDA reports)
FACET JOINT SYNDROME ( 13 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 13 FDA reports)
HAEMORRHAGIC ANAEMIA ( 13 FDA reports)
HORMONE LEVEL ABNORMAL ( 13 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 13 FDA reports)
HYPERVENTILATION ( 13 FDA reports)
KLEBSIELLA TEST POSITIVE ( 13 FDA reports)
KNEE OPERATION ( 13 FDA reports)
MALLORY-WEISS SYNDROME ( 13 FDA reports)
MUSCLE SPASTICITY ( 13 FDA reports)
ORAL NEOPLASM ( 13 FDA reports)
PERIPHERAL ISCHAEMIA ( 13 FDA reports)
PNEUMONIA VIRAL ( 13 FDA reports)
POLYTRAUMATISM ( 13 FDA reports)
PREMATURE MENOPAUSE ( 13 FDA reports)
PSYCHIATRIC SYMPTOM ( 13 FDA reports)
PURULENCE ( 13 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 13 FDA reports)
SENSATION OF HEAVINESS ( 13 FDA reports)
SENSORY DISTURBANCE ( 13 FDA reports)
SERUM FERRITIN INCREASED ( 13 FDA reports)
SJOGREN'S SYNDROME ( 13 FDA reports)
STRABISMUS ( 13 FDA reports)
SUBDURAL HAEMATOMA ( 13 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 13 FDA reports)
THERAPY NON-RESPONDER ( 13 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 13 FDA reports)
ABDOMINAL SEPSIS ( 12 FDA reports)
ANXIETY DISORDER ( 12 FDA reports)
AORTIC BRUIT ( 12 FDA reports)
APPLICATION SITE ERYTHEMA ( 12 FDA reports)
AUTOIMMUNE HEPATITIS ( 12 FDA reports)
B-CELL LYMPHOMA ( 12 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 12 FDA reports)
BREAST ENLARGEMENT ( 12 FDA reports)
BREAST TENDERNESS ( 12 FDA reports)
BREATH SOUNDS ABNORMAL ( 12 FDA reports)
CARDIAC ASTHMA ( 12 FDA reports)
CARDIAC FLUTTER ( 12 FDA reports)
CATARACT NUCLEAR ( 12 FDA reports)
CEREBROVASCULAR DISORDER ( 12 FDA reports)
CHEST X-RAY ABNORMAL ( 12 FDA reports)
CHOLESTASIS ( 12 FDA reports)
CHRONIC INFLAMMATORY DEMYELINATING POLYRADICULONEUROPATHY ( 12 FDA reports)
COMPLEX PARTIAL SEIZURES ( 12 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 12 FDA reports)
CONGO-CRIMEAN HAEMORRHAGIC FEVER ( 12 FDA reports)
DRUG DISPENSING ERROR ( 12 FDA reports)
ERUCTATION ( 12 FDA reports)
EYELID OEDEMA ( 12 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 12 FDA reports)
FIBROMA ( 12 FDA reports)
FINGER AMPUTATION ( 12 FDA reports)
GINGIVAL GRAFT ( 12 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 12 FDA reports)
HAEMODIALYSIS ( 12 FDA reports)
HALLUCINATIONS, MIXED ( 12 FDA reports)
HEPATIC NEOPLASM ( 12 FDA reports)
ILIUM FRACTURE ( 12 FDA reports)
IMMUNOSUPPRESSION ( 12 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 12 FDA reports)
LHERMITTE'S SIGN ( 12 FDA reports)
LOWER LIMB FRACTURE ( 12 FDA reports)
MEAN CELL VOLUME INCREASED ( 12 FDA reports)
METASTASES TO BONE MARROW ( 12 FDA reports)
METASTASES TO LYMPH NODES ( 12 FDA reports)
MONARTHRITIS ( 12 FDA reports)
MUNCHAUSEN'S SYNDROME ( 12 FDA reports)
MUSCLE RIGIDITY ( 12 FDA reports)
MYDRIASIS ( 12 FDA reports)
MYOSITIS ( 12 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 12 FDA reports)
PANCREATITIS RELAPSING ( 12 FDA reports)
PAPULE ( 12 FDA reports)
PARAPROTEINAEMIA ( 12 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 12 FDA reports)
PIRIFORMIS SYNDROME ( 12 FDA reports)
POLYSUBSTANCE ABUSE ( 12 FDA reports)
PULMONARY MASS ( 12 FDA reports)
QUALITY OF LIFE DECREASED ( 12 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 12 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 12 FDA reports)
SKIN INFECTION ( 12 FDA reports)
SPINAL X-RAY ABNORMAL ( 12 FDA reports)
TANDEM GAIT TEST ABNORMAL ( 12 FDA reports)
THERMAL BURN ( 12 FDA reports)
THIRST ( 12 FDA reports)
TOOTH DEPOSIT ( 12 FDA reports)
TOOTH DISCOLOURATION ( 12 FDA reports)
TRACHEITIS ( 12 FDA reports)
UPPER LIMB FRACTURE ( 12 FDA reports)
UTERINE DISORDER ( 12 FDA reports)
VAGINITIS BACTERIAL ( 12 FDA reports)
VENOUS THROMBOSIS LIMB ( 12 FDA reports)
VULVAL DISORDER ( 12 FDA reports)
WRIST FRACTURE ( 12 FDA reports)
ABSCESS INTESTINAL ( 11 FDA reports)
ACIDOSIS ( 11 FDA reports)
ANGIOEDEMA ( 11 FDA reports)
APPETITE DISORDER ( 11 FDA reports)
APPLICATION SITE VESICLES ( 11 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 11 FDA reports)
BACTERIAL INFECTION ( 11 FDA reports)
BEDRIDDEN ( 11 FDA reports)
BIOPSY ( 11 FDA reports)
BLADDER DYSFUNCTION ( 11 FDA reports)
BLOOD CHLORIDE DECREASED ( 11 FDA reports)
BREAST CANCER IN SITU ( 11 FDA reports)
BRONCHIECTASIS ( 11 FDA reports)
CARDIAC VALVE SCLEROSIS ( 11 FDA reports)
CORONARY ARTERY BYPASS ( 11 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 11 FDA reports)
DIABETIC EYE DISEASE ( 11 FDA reports)
DIURETIC THERAPY ( 11 FDA reports)
EROSIVE DUODENITIS ( 11 FDA reports)
EXPLORATORY OPERATION ( 11 FDA reports)
FIBULA FRACTURE ( 11 FDA reports)
FOOT OPERATION ( 11 FDA reports)
GANGRENE ( 11 FDA reports)
GASTRIC HAEMORRHAGE ( 11 FDA reports)
GASTROENTERITIS RADIATION ( 11 FDA reports)
HEART INJURY ( 11 FDA reports)
HEMIPLEGIA ( 11 FDA reports)
HEPATIC CIRRHOSIS ( 11 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 11 FDA reports)
HYPERTHYROIDISM ( 11 FDA reports)
IMMUNE SYSTEM DISORDER ( 11 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 11 FDA reports)
INTRACRANIAL ANEURYSM ( 11 FDA reports)
KETOACIDOSIS ( 11 FDA reports)
KLEBSIELLA INFECTION ( 11 FDA reports)
LAGOPHTHALMOS ( 11 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE 0 ( 11 FDA reports)
LUPUS-LIKE SYNDROME ( 11 FDA reports)
MACULAR DEGENERATION ( 11 FDA reports)
MENSTRUAL DISORDER ( 11 FDA reports)
METABOLIC ENCEPHALOPATHY ( 11 FDA reports)
METAPLASIA ( 11 FDA reports)
MULTIPLE FRACTURES ( 11 FDA reports)
MYOFASCITIS ( 11 FDA reports)
NERVE COMPRESSION ( 11 FDA reports)
OCULAR HYPERTENSION ( 11 FDA reports)
OEDEMA MOUTH ( 11 FDA reports)
OPEN FRACTURE ( 11 FDA reports)
PANCREATIC DISORDER ( 11 FDA reports)
PERITONITIS ( 11 FDA reports)
PHARYNGEAL OEDEMA ( 11 FDA reports)
PLATELET COUNT INCREASED ( 11 FDA reports)
PLEURITIC PAIN ( 11 FDA reports)
POLYNEUROPATHY ( 11 FDA reports)
POLYPECTOMY ( 11 FDA reports)
POOR QUALITY SLEEP ( 11 FDA reports)
PROCTITIS ( 11 FDA reports)
RENAL ANEURYSM ( 11 FDA reports)
RETINOPATHY ( 11 FDA reports)
ROTATOR CUFF REPAIR ( 11 FDA reports)
SEBORRHOEIC KERATOSIS ( 11 FDA reports)
SERUM SICKNESS ( 11 FDA reports)
SKIN FIBROSIS ( 11 FDA reports)
SOFT TISSUE INFECTION ( 11 FDA reports)
SPINAL CORPECTOMY ( 11 FDA reports)
STRESS FRACTURE ( 11 FDA reports)
SUDDEN DEATH ( 11 FDA reports)
SYNOVITIS ( 11 FDA reports)
TEMPORAL ARTERITIS ( 11 FDA reports)
TESTICULAR PAIN ( 11 FDA reports)
TINEA PEDIS ( 11 FDA reports)
TINEL'S SIGN ( 11 FDA reports)
WOUND SECRETION ( 11 FDA reports)
ABDOMINAL ADHESIONS ( 10 FDA reports)
ADENOCARCINOMA ( 10 FDA reports)
ADJUSTMENT DISORDER ( 10 FDA reports)
AKATHISIA ( 10 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 10 FDA reports)
ANEURYSM ( 10 FDA reports)
ANORECTAL DISORDER ( 10 FDA reports)
AORTIC ATHEROSCLEROSIS ( 10 FDA reports)
ARTHRODESIS ( 10 FDA reports)
AUTONOMIC NEUROPATHY ( 10 FDA reports)
BILIARY COLIC ( 10 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 10 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 10 FDA reports)
BREAST HYPERPLASIA ( 10 FDA reports)
CARTILAGE INJURY ( 10 FDA reports)
CATHETER PLACEMENT ( 10 FDA reports)
CEREBROSCLEROSIS ( 10 FDA reports)
CLOSED HEAD INJURY ( 10 FDA reports)
COLON NEOPLASM ( 10 FDA reports)
COLON POLYPECTOMY ( 10 FDA reports)
COLONOSCOPY ABNORMAL ( 10 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 10 FDA reports)
CORONARY ANGIOPLASTY ( 10 FDA reports)
DIAPHRAGMATIC DISORDER ( 10 FDA reports)
DRUG ADMINISTRATION ERROR ( 10 FDA reports)
DRUG ERUPTION ( 10 FDA reports)
DRUG PRESCRIBING ERROR ( 10 FDA reports)
DUODENITIS ( 10 FDA reports)
DYSAESTHESIA ( 10 FDA reports)
EYE OPERATION ( 10 FDA reports)
FAECALOMA ( 10 FDA reports)
FOOD CRAVING ( 10 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 10 FDA reports)
GINGIVAL ATROPHY ( 10 FDA reports)
GRANULAR CELL TUMOUR ( 10 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 10 FDA reports)
HEART DISEASE CONGENITAL ( 10 FDA reports)
HOSTILITY ( 10 FDA reports)
HYDRONEPHROSIS ( 10 FDA reports)
HYPERBILIRUBINAEMIA ( 10 FDA reports)
HYPERPHAGIA ( 10 FDA reports)
INFUSION SITE HAEMORRHAGE ( 10 FDA reports)
INTRADUCTAL PAPILLOMA OF BREAST ( 10 FDA reports)
LABORATORY TEST ABNORMAL ( 10 FDA reports)
LIPOMATOSIS ( 10 FDA reports)
MACROPHAGES INCREASED ( 10 FDA reports)
MENINGITIS ( 10 FDA reports)
METASTASES TO SKIN ( 10 FDA reports)
METASTATIC SQUAMOUS CELL CARCINOMA ( 10 FDA reports)
METRORRHAGIA ( 10 FDA reports)
MITRAL VALVE CALCIFICATION ( 10 FDA reports)
NASAL DISCOMFORT ( 10 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 10 FDA reports)
NO THERAPEUTIC RESPONSE ( 10 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 10 FDA reports)
OESOPHAGEAL STENOSIS ( 10 FDA reports)
OPEN ANGLE GLAUCOMA ( 10 FDA reports)
OPTIC NEURITIS ( 10 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 10 FDA reports)
PARTIAL SEIZURES ( 10 FDA reports)
PROTEIN TOTAL INCREASED ( 10 FDA reports)
RADIOTHERAPY ( 10 FDA reports)
RALES ( 10 FDA reports)
RENAL CANCER METASTATIC ( 10 FDA reports)
RENAL TUBULAR NECROSIS ( 10 FDA reports)
RESPIRATORY DEPRESSION ( 10 FDA reports)
SCAB ( 10 FDA reports)
SCLERODERMA ( 10 FDA reports)
SHOULDER OPERATION ( 10 FDA reports)
SKIN FRAGILITY ( 10 FDA reports)
SLEEP TERROR ( 10 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 10 FDA reports)
STERNOTOMY ( 10 FDA reports)
TONGUE DISORDER ( 10 FDA reports)
ULNA FRACTURE ( 10 FDA reports)
URINARY TRACT DISORDER ( 10 FDA reports)
VARICOCELE ( 10 FDA reports)
VASCULAR INSUFFICIENCY ( 10 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 9 FDA reports)
ADRENAL MASS ( 9 FDA reports)
AORTIC STENOSIS ( 9 FDA reports)
APPLICATION SITE RASH ( 9 FDA reports)
ARACHNOID CYST ( 9 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 9 FDA reports)
BIPOLAR I DISORDER ( 9 FDA reports)
BLOOD CULTURE POSITIVE ( 9 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 9 FDA reports)
BLOOD OESTROGEN DECREASED ( 9 FDA reports)
BLOOD PRESSURE ABNORMAL ( 9 FDA reports)
BREAST FIBROSIS ( 9 FDA reports)
BREAST NECROSIS ( 9 FDA reports)
CARDIAC ENZYMES INCREASED ( 9 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 9 FDA reports)
COMMUNICATION DISORDER ( 9 FDA reports)
DEAFNESS UNILATERAL ( 9 FDA reports)
DENTAL ALVEOLAR ANOMALY ( 9 FDA reports)
DIZZINESS POSTURAL ( 9 FDA reports)
ENTERITIS ( 9 FDA reports)
EPIDERMAL NECROSIS ( 9 FDA reports)
EPIDIDYMAL CYST ( 9 FDA reports)
EXCESSIVE EYE BLINKING ( 9 FDA reports)
EYE HAEMORRHAGE ( 9 FDA reports)
FACIAL NERVE DISORDER ( 9 FDA reports)
FORMICATION ( 9 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 9 FDA reports)
GRIMACING ( 9 FDA reports)
GUN SHOT WOUND ( 9 FDA reports)
HAEMORRHAGIC DIATHESIS ( 9 FDA reports)
HEPATITIS CHOLESTATIC ( 9 FDA reports)
HIP DEFORMITY ( 9 FDA reports)
HORNER'S SYNDROME ( 9 FDA reports)
HYPERAESTHESIA ( 9 FDA reports)
HYPERCAPNIA ( 9 FDA reports)
HYPERPARATHYROIDISM ( 9 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 9 FDA reports)
INCISION SITE COMPLICATION ( 9 FDA reports)
INCOHERENT ( 9 FDA reports)
INCREASED BRONCHIAL SECRETION ( 9 FDA reports)
INITIAL INSOMNIA ( 9 FDA reports)
INTENTIONAL MISUSE ( 9 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 9 FDA reports)
ISCHAEMIC STROKE ( 9 FDA reports)
JOINT CONTRACTURE ( 9 FDA reports)
JOINT LOCK ( 9 FDA reports)
LIGAMENT INJURY ( 9 FDA reports)
LIPASE INCREASED ( 9 FDA reports)
LOCALISED OSTEOARTHRITIS ( 9 FDA reports)
MALOCCLUSION ( 9 FDA reports)
MENOPAUSE ( 9 FDA reports)
MYOMECTOMY ( 9 FDA reports)
NASAL CYST ( 9 FDA reports)
NEPHRITIS ( 9 FDA reports)
NEPHROPATHY ( 9 FDA reports)
NEURODERMATITIS ( 9 FDA reports)
OBSTRUCTION ( 9 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 9 FDA reports)
OOPHORECTOMY ( 9 FDA reports)
ORAL INTAKE REDUCED ( 9 FDA reports)
OSTEORADIONECROSIS ( 9 FDA reports)
PAIN OF SKIN ( 9 FDA reports)
PERIARTHRITIS ( 9 FDA reports)
POLYDIPSIA ( 9 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 9 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 9 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 9 FDA reports)
PROSTATE CANCER RECURRENT ( 9 FDA reports)
PROSTATOMEGALY ( 9 FDA reports)
RASH MACULO-PAPULAR ( 9 FDA reports)
RETINAL HAEMORRHAGE ( 9 FDA reports)
RETINAL TEAR ( 9 FDA reports)
RETINAL VEIN OCCLUSION ( 9 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 9 FDA reports)
SACROILIITIS ( 9 FDA reports)
SARCOIDOSIS ( 9 FDA reports)
SCAPULA FRACTURE ( 9 FDA reports)
SCRATCH ( 9 FDA reports)
SICK SINUS SYNDROME ( 9 FDA reports)
SIGMOIDITIS ( 9 FDA reports)
SINUS CONGESTION ( 9 FDA reports)
SINUS OPERATION ( 9 FDA reports)
SKIN HYPERPIGMENTATION ( 9 FDA reports)
SKIN WARM ( 9 FDA reports)
SLEEP WALKING ( 9 FDA reports)
SNEEZING ( 9 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 9 FDA reports)
THYROID CYST ( 9 FDA reports)
TIBIA FRACTURE ( 9 FDA reports)
URINE OUTPUT DECREASED ( 9 FDA reports)
UROSEPSIS ( 9 FDA reports)
VASCULAR CALCIFICATION ( 9 FDA reports)
VIRAL MYOCARDITIS ( 9 FDA reports)
WHIPLASH INJURY ( 9 FDA reports)
ACCIDENT AT WORK ( 8 FDA reports)
ACCIDENTAL DEATH ( 8 FDA reports)
AMENORRHOEA ( 8 FDA reports)
ANAL FISSURE ( 8 FDA reports)
AORTIC VALVE REPLACEMENT ( 8 FDA reports)
AREFLEXIA ( 8 FDA reports)
ARNOLD-CHIARI MALFORMATION ( 8 FDA reports)
ARTERIAL DISORDER ( 8 FDA reports)
ATRIAL SEPTAL DEFECT ( 8 FDA reports)
BENIGN NEOPLASM OF SPINAL CORD ( 8 FDA reports)
BLOOD POTASSIUM INCREASED ( 8 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 8 FDA reports)
BODY TEMPERATURE DECREASED ( 8 FDA reports)
BODY TINEA ( 8 FDA reports)
CALCULUS URINARY ( 8 FDA reports)
CERVICAL DYSPLASIA ( 8 FDA reports)
CHEST TUBE INSERTION ( 8 FDA reports)
CHONDROPLASTY ( 8 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 8 FDA reports)
COLON ADENOMA ( 8 FDA reports)
COLON CANCER ( 8 FDA reports)
COLOSTOMY ( 8 FDA reports)
COMPRESSION STOCKINGS APPLICATION ( 8 FDA reports)
CORONARY ARTERY EMBOLISM ( 8 FDA reports)
DIABETIC COMPLICATION ( 8 FDA reports)
DRUG TOLERANCE INCREASED ( 8 FDA reports)
ESCHERICHIA INFECTION ( 8 FDA reports)
FEELING OF DESPAIR ( 8 FDA reports)
GASTROINTESTINAL PAIN ( 8 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 8 FDA reports)
GINGIVAL EROSION ( 8 FDA reports)
GINGIVAL ERYTHEMA ( 8 FDA reports)
GLIOSIS ( 8 FDA reports)
HAEMARTHROSIS ( 8 FDA reports)
HIDRADENITIS ( 8 FDA reports)
HYPERTONIA ( 8 FDA reports)
HYPOKINESIA ( 8 FDA reports)
HYPOTHERMIA ( 8 FDA reports)
ILEUS PARALYTIC ( 8 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 8 FDA reports)
INJECTION SITE EXTRAVASATION ( 8 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 8 FDA reports)
KELOID SCAR ( 8 FDA reports)
LABYRINTHITIS ( 8 FDA reports)
LENTIGO ( 8 FDA reports)
LOCAL SWELLING ( 8 FDA reports)
LORDOSIS ( 8 FDA reports)
MASTECTOMY ( 8 FDA reports)
METABOLIC SYNDROME ( 8 FDA reports)
OCCULT BLOOD POSITIVE ( 8 FDA reports)
PANIC REACTION ( 8 FDA reports)
PAROTID GLAND ENLARGEMENT ( 8 FDA reports)
PHOTOSENSITIVITY REACTION ( 8 FDA reports)
POSTNASAL DRIP ( 8 FDA reports)
POSTURE ABNORMAL ( 8 FDA reports)
PREGNANCY ( 8 FDA reports)
PRESSURE OF SPEECH ( 8 FDA reports)
RECURRENT CANCER ( 8 FDA reports)
RESPIRATORY TRACT CONGESTION ( 8 FDA reports)
RIB DEFORMITY ( 8 FDA reports)
SALIVARY HYPERSECRETION ( 8 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 8 FDA reports)
SCHIZOPHRENIA ( 8 FDA reports)
SECRETION DISCHARGE ( 8 FDA reports)
SPINAL CORD NEOPLASM ( 8 FDA reports)
SUDDEN CARDIAC DEATH ( 8 FDA reports)
THORACOTOMY ( 8 FDA reports)
THROMBOCYTHAEMIA ( 8 FDA reports)
TOBACCO ABUSE ( 8 FDA reports)
TONGUE BITING ( 8 FDA reports)
TONSILLITIS ( 8 FDA reports)
TOOTH EROSION ( 8 FDA reports)
URINE ABNORMALITY ( 8 FDA reports)
UTERINE PAIN ( 8 FDA reports)
VERTEBRAL COLUMN MASS ( 8 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 8 FDA reports)
VOCAL CORD DISORDER ( 8 FDA reports)
ABDOMINAL MASS ( 7 FDA reports)
ACCIDENTAL EXPOSURE ( 7 FDA reports)
ANAEMIA POSTOPERATIVE ( 7 FDA reports)
ANAL SPHINCTER ATONY ( 7 FDA reports)
ANGIOMYOLIPOMA ( 7 FDA reports)
ANGIONEUROTIC OEDEMA ( 7 FDA reports)
ANOMALOUS PULMONARY VENOUS CONNECTION ( 7 FDA reports)
APPARENT DEATH ( 7 FDA reports)
APPLICATION SITE PRURITUS ( 7 FDA reports)
ASBESTOSIS ( 7 FDA reports)
ATRIOVENTRICULAR SEPTAL DEFECT ( 7 FDA reports)
BENIGN GASTRIC NEOPLASM ( 7 FDA reports)
BILIARY DYSKINESIA ( 7 FDA reports)
BLADDER DISCOMFORT ( 7 FDA reports)
BLADDER SPASM ( 7 FDA reports)
BLOOD PROLACTIN INCREASED ( 7 FDA reports)
BONE TRIMMING ( 7 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 7 FDA reports)
BREAKTHROUGH PAIN ( 7 FDA reports)
BULLOUS IMPETIGO ( 7 FDA reports)
BUNDLE BRANCH BLOCK ( 7 FDA reports)
CARDIAC FAILURE CHRONIC ( 7 FDA reports)
CARDIAC HYPERTROPHY ( 7 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 7 FDA reports)
CATHETER SITE HAEMORRHAGE ( 7 FDA reports)
CEREBELLAR INFARCTION ( 7 FDA reports)
CHOLECYSTITIS ACUTE ( 7 FDA reports)
CLAUSTROPHOBIA ( 7 FDA reports)
DECREASED ACTIVITY ( 7 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 7 FDA reports)
DROOLING ( 7 FDA reports)
DYSGRAPHIA ( 7 FDA reports)
DYSPHORIA ( 7 FDA reports)
EAR DISORDER ( 7 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 7 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 7 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 7 FDA reports)
EMBOLIC STROKE ( 7 FDA reports)
ESCHERICHIA SEPSIS ( 7 FDA reports)
EXTRASKELETAL OSSIFICATION ( 7 FDA reports)
FACE INJURY ( 7 FDA reports)
FAMILY STRESS ( 7 FDA reports)
FEAR OF DEATH ( 7 FDA reports)
FEELING GUILTY ( 7 FDA reports)
FEMORAL ARTERY OCCLUSION ( 7 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 7 FDA reports)
FRACTURED COCCYX ( 7 FDA reports)
GASTRODUODENITIS ( 7 FDA reports)
GASTROSTOMY TUBE INSERTION ( 7 FDA reports)
GENERALISED ERYTHEMA ( 7 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 7 FDA reports)
HAEMOTHORAX ( 7 FDA reports)
HEART VALVE INCOMPETENCE ( 7 FDA reports)
HEPATIC ENCEPHALOPATHY ( 7 FDA reports)
HICCUPS ( 7 FDA reports)
HOARSENESS ( 7 FDA reports)
HYPOPNOEA ( 7 FDA reports)
HYPOTONIA ( 7 FDA reports)
INJECTION SITE IRRITATION ( 7 FDA reports)
INJECTION SITE URTICARIA ( 7 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 7 FDA reports)
INTESTINAL ULCER ( 7 FDA reports)
LARGE INTESTINAL ULCER ( 7 FDA reports)
LICHENOID KERATOSIS ( 7 FDA reports)
LIP INJURY ( 7 FDA reports)
LIP ULCERATION ( 7 FDA reports)
LIPOATROPHY ( 7 FDA reports)
LOSS OF EMPLOYMENT ( 7 FDA reports)
LYMPHADENITIS ( 7 FDA reports)
MASTOCYTOSIS ( 7 FDA reports)
MEAN CELL HAEMOGLOBIN ( 7 FDA reports)
MICTURITION DISORDER ( 7 FDA reports)
MITRAL VALVE STENOSIS ( 7 FDA reports)
MUSCULOSKELETAL DISORDER ( 7 FDA reports)
NASAL SEPTUM DISORDER ( 7 FDA reports)
NASOPHARYNGEAL DISORDER ( 7 FDA reports)
OESOPHAGEAL DILATATION ( 7 FDA reports)
OESOPHAGEAL DILATION PROCEDURE ( 7 FDA reports)
OESOPHAGEAL RUPTURE ( 7 FDA reports)
ORAL TORUS ( 7 FDA reports)
OVERWEIGHT ( 7 FDA reports)
PAINFUL RESPIRATION ( 7 FDA reports)
PARONYCHIA ( 7 FDA reports)
PAROSMIA ( 7 FDA reports)
PERFORATED ULCER ( 7 FDA reports)
PERINEURIAL CYST ( 7 FDA reports)
PERIODONTAL INFECTION ( 7 FDA reports)
PHYSICAL ASSAULT ( 7 FDA reports)
PLEURAL DECORTICATION ( 7 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 7 FDA reports)
POOR DENTAL CONDITION ( 7 FDA reports)
PRODUCT ADHESION ISSUE ( 7 FDA reports)
PSORIATIC ARTHROPATHY ( 7 FDA reports)
PSYCHOLOGICAL TRAUMA ( 7 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 7 FDA reports)
PULMONARY ARTERY ATRESIA ( 7 FDA reports)
PULMONARY GRANULOMA ( 7 FDA reports)
PYODERMA GANGRENOSUM ( 7 FDA reports)
QUADRIPARESIS ( 7 FDA reports)
RAPID EYE MOVEMENTS SLEEP ABNORMAL ( 7 FDA reports)
READING DISORDER ( 7 FDA reports)
RENAL MASS ( 7 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 7 FDA reports)
SINUS ARRHYTHMIA ( 7 FDA reports)
SKIN INJURY ( 7 FDA reports)
SKIN PLAQUE ( 7 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 7 FDA reports)
SPLENIC RUPTURE ( 7 FDA reports)
STENT REMOVAL ( 7 FDA reports)
THROAT CANCER ( 7 FDA reports)
THROMBOPHLEBITIS ( 7 FDA reports)
TRANSFUSION ( 7 FDA reports)
TRANSPOSITION OF THE GREAT VESSELS ( 7 FDA reports)
TRAUMATIC LIVER INJURY ( 7 FDA reports)
ULCER HAEMORRHAGE ( 7 FDA reports)
ULCERATIVE KERATITIS ( 7 FDA reports)
VASOMOTOR RHINITIS ( 7 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 7 FDA reports)
VERTIGO POSITIONAL ( 7 FDA reports)
VESTIBULAR NEURONITIS ( 7 FDA reports)
VICTIM OF CRIME ( 7 FDA reports)
ABDOMINAL WALL ABSCESS ( 6 FDA reports)
ACUTE HEPATIC FAILURE ( 6 FDA reports)
ALCOHOL DETOXIFICATION ( 6 FDA reports)
ALLERGIC COUGH ( 6 FDA reports)
ANOXIC ENCEPHALOPATHY ( 6 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 6 FDA reports)
ANURIA ( 6 FDA reports)
APATHY ( 6 FDA reports)
APPENDICITIS ( 6 FDA reports)
APPLICATION SITE REACTION ( 6 FDA reports)
ARTERIAL BYPASS OPERATION ( 6 FDA reports)
ASEPTIC NECROSIS BONE ( 6 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 6 FDA reports)
ATROPHIC VULVOVAGINITIS ( 6 FDA reports)
BACTERIAL SEPSIS ( 6 FDA reports)
BLADDER CANCER ( 6 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 6 FDA reports)
BLOOD DISORDER ( 6 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 6 FDA reports)
BLOOD URIC ACID INCREASED ( 6 FDA reports)
BLOOD URINE PRESENT ( 6 FDA reports)
BONE FISTULA ( 6 FDA reports)
BONE MARROW TRANSPLANT ( 6 FDA reports)
BORDERLINE PERSONALITY DISORDER ( 6 FDA reports)
BRAIN DEATH ( 6 FDA reports)
BRAIN OEDEMA ( 6 FDA reports)
BREAST DISORDER ( 6 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 6 FDA reports)
CARDIOPULMONARY FAILURE ( 6 FDA reports)
CATHETERISATION VENOUS ( 6 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 6 FDA reports)
COLONIC STENOSIS ( 6 FDA reports)
CONVERSION DISORDER ( 6 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 6 FDA reports)
CYSTIC FIBROSIS PANCREATIC ( 6 FDA reports)
DENTAL IMPLANTATION ( 6 FDA reports)
DERMATITIS ACNEIFORM ( 6 FDA reports)
DIAPHRAGMATIC HERNIA ( 6 FDA reports)
DRUG EFFECT INCREASED ( 6 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 6 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 6 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 6 FDA reports)
ENERGY INCREASED ( 6 FDA reports)
ERECTION INCREASED ( 6 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 6 FDA reports)
ETHMOID SINUS SURGERY ( 6 FDA reports)
EXFOLIATIVE RASH ( 6 FDA reports)
EXPIRED DRUG ADMINISTERED ( 6 FDA reports)
EXTRASYSTOLES ( 6 FDA reports)
FASCIITIS ( 6 FDA reports)
FISTULA REPAIR ( 6 FDA reports)
FLUID INTAKE REDUCED ( 6 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 6 FDA reports)
FOLLICULITIS ( 6 FDA reports)
FUNGAL SKIN INFECTION ( 6 FDA reports)
FUNGUS CERVICAL SPECIMEN IDENTIFIED ( 6 FDA reports)
GUILLAIN-BARRE SYNDROME ( 6 FDA reports)
HAIR GROWTH ABNORMAL ( 6 FDA reports)
HEART RATE ABNORMAL ( 6 FDA reports)
HEPATOCELLULAR DAMAGE ( 6 FDA reports)
HIP SURGERY ( 6 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 6 FDA reports)
HYPERTHERMIA ( 6 FDA reports)
HYPOAESTHESIA FACIAL ( 6 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 6 FDA reports)
IMPAIRED REASONING ( 6 FDA reports)
IMPULSIVE BEHAVIOUR ( 6 FDA reports)
INCISIONAL HERNIA ( 6 FDA reports)
LACTIC ACIDOSIS ( 6 FDA reports)
LIP SWELLING ( 6 FDA reports)
LIPIDS INCREASED ( 6 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 6 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 6 FDA reports)
MAXILLOFACIAL OPERATION ( 6 FDA reports)
MELANOSIS COLI ( 6 FDA reports)
MERALGIA PARAESTHETICA ( 6 FDA reports)
MICTURITION FREQUENCY DECREASED ( 6 FDA reports)
MIGRAINE WITHOUT AURA ( 6 FDA reports)
MITRAL VALVE DISEASE ( 6 FDA reports)
MONOPLEGIA ( 6 FDA reports)
MULTI-ORGAN DISORDER ( 6 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 6 FDA reports)
NAIL DYSTROPHY ( 6 FDA reports)
NARCOLEPSY ( 6 FDA reports)
NASAL DISORDER ( 6 FDA reports)
NECROSIS ( 6 FDA reports)
NEGATIVE THOUGHTS ( 6 FDA reports)
NEOPLASM ( 6 FDA reports)
NEUTROPHIL COUNT INCREASED ( 6 FDA reports)
NICOTINE DEPENDENCE ( 6 FDA reports)
NIPPLE PAIN ( 6 FDA reports)
OSTECTOMY ( 6 FDA reports)
OSTEOMYELITIS CHRONIC ( 6 FDA reports)
OSTEOSARCOMA METASTATIC ( 6 FDA reports)
PANIC DISORDER WITH AGORAPHOBIA ( 6 FDA reports)
PAPILLARY THYROID CANCER ( 6 FDA reports)
PARANASAL SINUS MUCOSAL HYPERTROPHY ( 6 FDA reports)
PERSONALITY DISORDER ( 6 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 6 FDA reports)
PHLEBOSCLEROSIS ( 6 FDA reports)
PHYSIOTHERAPY ( 6 FDA reports)
PLASMAPHERESIS ( 6 FDA reports)
PLASTIC SURGERY TO THE FACE ( 6 FDA reports)
PNEUMONIA BACTERIAL ( 6 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 6 FDA reports)
POLYNEUROPATHY CHRONIC ( 6 FDA reports)
POST-TRAUMATIC PAIN ( 6 FDA reports)
PROLAPSE REPAIR ( 6 FDA reports)
PROSTATISM ( 6 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 6 FDA reports)
SEASONAL ALLERGY ( 6 FDA reports)
SENSORY LEVEL ABNORMAL ( 6 FDA reports)
SINUS ANTROSTOMY ( 6 FDA reports)
SOMATISATION DISORDER ( 6 FDA reports)
SPLEEN DISORDER ( 6 FDA reports)
SPLENIC CYST ( 6 FDA reports)
STAB WOUND ( 6 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 6 FDA reports)
STATUS EPILEPTICUS ( 6 FDA reports)
STENT OCCLUSION ( 6 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 6 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 6 FDA reports)
TONGUE OEDEMA ( 6 FDA reports)
TONSILLAR DISORDER ( 6 FDA reports)
TOOTH IMPACTED ( 6 FDA reports)
TRACHEAL OPERATION ( 6 FDA reports)
TREATMENT FAILURE ( 6 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 6 FDA reports)
URINE ANALYSIS ABNORMAL ( 6 FDA reports)
UTEROVAGINAL PROLAPSE ( 6 FDA reports)
VENTRICULAR HYPOKINESIA ( 6 FDA reports)
VITREOUS DETACHMENT ( 6 FDA reports)
WOUND DECOMPOSITION ( 6 FDA reports)
ABDOMINAL TENDERNESS ( 5 FDA reports)
ACANTHOMA ( 5 FDA reports)
ACCIDENT AT HOME ( 5 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 5 FDA reports)
ANAPHYLACTIC SHOCK ( 5 FDA reports)
ANASTOMOTIC STENOSIS ( 5 FDA reports)
ANASTOMOTIC ULCER ( 5 FDA reports)
ANTICHOLINERGIC SYNDROME ( 5 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 5 FDA reports)
AORTIC BYPASS ( 5 FDA reports)
APPLICATION SITE IRRITATION ( 5 FDA reports)
APPLICATION SITE SCAR ( 5 FDA reports)
ARTERIOSPASM CORONARY ( 5 FDA reports)
ARTHROPOD BITE ( 5 FDA reports)
AUTOIMMUNE DISORDER ( 5 FDA reports)
BILIARY SEPSIS ( 5 FDA reports)
BLOOD TEST ABNORMAL ( 5 FDA reports)
BLUE TOE SYNDROME ( 5 FDA reports)
BONE MARROW DEPRESSION ( 5 FDA reports)
BOWEL SOUNDS ABNORMAL ( 5 FDA reports)
BRADYPHRENIA ( 5 FDA reports)
BREAST NEOPLASM ( 5 FDA reports)
CARDIAC OUTPUT DECREASED ( 5 FDA reports)
CARDIAC PACEMAKER INSERTION ( 5 FDA reports)
CARDIOGENIC SHOCK ( 5 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 5 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 5 FDA reports)
CERVICITIS ( 5 FDA reports)
COAGULATION TIME PROLONGED ( 5 FDA reports)
COMPARTMENT SYNDROME ( 5 FDA reports)
COR PULMONALE ( 5 FDA reports)
CORONARY ARTERY THROMBOSIS ( 5 FDA reports)
CULTURE URINE POSITIVE ( 5 FDA reports)
DEAFNESS NEUROSENSORY ( 5 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 5 FDA reports)
DENTAL PROSTHESIS USER ( 5 FDA reports)
DIVERTICULUM DUODENAL ( 5 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 5 FDA reports)
DUANE'S SYNDROME ( 5 FDA reports)
DYSKINESIA OESOPHAGEAL ( 5 FDA reports)
DYSPAREUNIA ( 5 FDA reports)
EJACULATION DELAYED ( 5 FDA reports)
ELBOW OPERATION ( 5 FDA reports)
ELECTROCUTION ( 5 FDA reports)
ENCEPHALITIS ( 5 FDA reports)
ENDOMETRIOSIS ( 5 FDA reports)
EPIDIDYMITIS ( 5 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 5 FDA reports)
ERYTHEMA MULTIFORME ( 5 FDA reports)
EXOPHTHALMOS ( 5 FDA reports)
FACTOR VII DEFICIENCY ( 5 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 5 FDA reports)
GASTRIC CANCER ( 5 FDA reports)
GASTRITIS HAEMORRHAGIC ( 5 FDA reports)
GASTROINTESTINAL TRACT IRRITATION ( 5 FDA reports)
GINGIVAL ABSCESS ( 5 FDA reports)
HANGOVER ( 5 FDA reports)
HELICOBACTER INFECTION ( 5 FDA reports)
HEPATITIS ACUTE ( 5 FDA reports)
HERPES VIRUS INFECTION ( 5 FDA reports)
HYPOCHONDRIASIS ( 5 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 5 FDA reports)
ILEAL STENOSIS ( 5 FDA reports)
IMMUNODEFICIENCY ( 5 FDA reports)
INFARCTION ( 5 FDA reports)
INJECTION SITE CELLULITIS ( 5 FDA reports)
INJECTION SITE MASS ( 5 FDA reports)
INJECTION SITE SCAR ( 5 FDA reports)
INJECTION SITE WARMTH ( 5 FDA reports)
INNER EAR DISORDER ( 5 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 5 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 5 FDA reports)
JUDGEMENT IMPAIRED ( 5 FDA reports)
JUVENILE ARTHRITIS ( 5 FDA reports)
KYPHOSCOLIOSIS ( 5 FDA reports)
LARYNGOSPASM ( 5 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 5 FDA reports)
LIGAMENT RUPTURE ( 5 FDA reports)
LIP BLISTER ( 5 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 5 FDA reports)
MALIGNANT HYPERTENSION ( 5 FDA reports)
MANDIBULAR PROSTHESIS USER ( 5 FDA reports)
MANDIBULECTOMY ( 5 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 5 FDA reports)
MENISCUS REMOVAL ( 5 FDA reports)
METASTASES TO MOUTH ( 5 FDA reports)
METASTASIS ( 5 FDA reports)
MICROCYTIC ANAEMIA ( 5 FDA reports)
MIOSIS ( 5 FDA reports)
MONONEURITIS ( 5 FDA reports)
MOUTH CYST ( 5 FDA reports)
MULTIPLE ALLERGIES ( 5 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 5 FDA reports)
NAIL DISORDER ( 5 FDA reports)
NASAL POLYPS ( 5 FDA reports)
NEUROPATHIC PAIN ( 5 FDA reports)
NEUTROPHIL COUNT DECREASED ( 5 FDA reports)
NYSTAGMUS ( 5 FDA reports)
OESOPHAGOSCOPY ABNORMAL ( 5 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 5 FDA reports)
OPTIC NEUROPATHY ( 5 FDA reports)
ORAL SOFT TISSUE DISORDER ( 5 FDA reports)
OROANTRAL FISTULA ( 5 FDA reports)
OROPHARYNGEAL SPASM ( 5 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 5 FDA reports)
PHARYNGOESOPHAGEAL DIVERTICULUM ( 5 FDA reports)
PLEURAL FIBROSIS ( 5 FDA reports)
PNEUMATOSIS CYSTOIDES INTESTINALIS ( 5 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 5 FDA reports)
POLYP ( 5 FDA reports)
POST PROCEDURAL INFECTION ( 5 FDA reports)
POST PROCEDURAL NAUSEA ( 5 FDA reports)
POST PROCEDURAL PAIN ( 5 FDA reports)
PROSTHESIS IMPLANTATION ( 5 FDA reports)
PROSTHESIS USER ( 5 FDA reports)
PULMONARY MYCOSIS ( 5 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 5 FDA reports)
PYOGENIC GRANULOMA ( 5 FDA reports)
RASH PUSTULAR ( 5 FDA reports)
RECTAL PERFORATION ( 5 FDA reports)
REFLEX SYMPATHETIC DYSTROPHY ( 5 FDA reports)
RENAL ATROPHY ( 5 FDA reports)
RHABDOMYOMA ( 5 FDA reports)
SCIATIC NERVE INJURY ( 5 FDA reports)
SCLERITIS ( 5 FDA reports)
SCOTOMA ( 5 FDA reports)
SEROMA ( 5 FDA reports)
SKELETAL INJURY ( 5 FDA reports)
SKIN HYPOPIGMENTATION ( 5 FDA reports)
SKIN WRINKLING ( 5 FDA reports)
SPINAL CORD DISORDER ( 5 FDA reports)
STASIS DERMATITIS ( 5 FDA reports)
STEVENS-JOHNSON SYNDROME ( 5 FDA reports)
STRESS INCONTINENCE ( 5 FDA reports)
TARSAL TUNNEL SYNDROME ( 5 FDA reports)
TEARFULNESS ( 5 FDA reports)
TEETH BRITTLE ( 5 FDA reports)
THORACOSTOMY ( 5 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 5 FDA reports)
TINEA CRURIS ( 5 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 5 FDA reports)
TORSADE DE POINTES ( 5 FDA reports)
TRICUSPID VALVE STENOSIS ( 5 FDA reports)
TUBEROUS SCLEROSIS ( 5 FDA reports)
UNDERDOSE ( 5 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 5 FDA reports)
URETHRAL CARUNCLE ( 5 FDA reports)
URGE INCONTINENCE ( 5 FDA reports)
URINARY HESITATION ( 5 FDA reports)
UTERINE POLYP ( 5 FDA reports)
VENOUS OCCLUSION ( 5 FDA reports)
VIRAL CARDIOMYOPATHY ( 5 FDA reports)
VISUAL FIELD DEFECT ( 5 FDA reports)
VITREOUS HAEMORRHAGE ( 5 FDA reports)
WOLFF-PARKINSON-WHITE SYNDROME ( 5 FDA reports)
WOUND COMPLICATION ( 5 FDA reports)
WRIST SURGERY ( 5 FDA reports)
ABDOMINAL INFECTION ( 4 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 4 FDA reports)
ABORTION COMPLETE ( 4 FDA reports)
ACCELERATED HYPERTENSION ( 4 FDA reports)
ALCOHOL POISONING ( 4 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 4 FDA reports)
ANAL ABSCESS ( 4 FDA reports)
ANAL SKIN TAGS ( 4 FDA reports)
ANKLE OPERATION ( 4 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 4 FDA reports)
ANTIDEPRESSANT DRUG LEVEL ABOVE THERAPEUTIC ( 4 FDA reports)
ANTISOCIAL BEHAVIOUR ( 4 FDA reports)
AORTIC ANEURYSM REPAIR ( 4 FDA reports)
AORTIC DILATATION ( 4 FDA reports)
ARACHNOPHOBIA ( 4 FDA reports)
ARTERIOGRAM CORONARY ( 4 FDA reports)
ASTHENOPIA ( 4 FDA reports)
ATHEROSCLEROSIS ( 4 FDA reports)
ATRIOVENTRICULAR BLOCK ( 4 FDA reports)
BILIARY DILATATION ( 4 FDA reports)
BLADDER CANCER RECURRENT ( 4 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 4 FDA reports)
BLOOD IRON INCREASED ( 4 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 4 FDA reports)
BRADYARRHYTHMIA ( 4 FDA reports)
BRAIN CANCER METASTATIC ( 4 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 4 FDA reports)
BREAST OPERATION ( 4 FDA reports)
BREAST PAIN ( 4 FDA reports)
BRONCHOPNEUMONIA ( 4 FDA reports)
BURKITT'S LYMPHOMA ( 4 FDA reports)
BURNS SECOND DEGREE ( 4 FDA reports)
CARBON MONOXIDE POISONING ( 4 FDA reports)
CARDIAC SEPTAL DEFECT ( 4 FDA reports)
CARDIAC STRESS TEST ( 4 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 4 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 4 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 4 FDA reports)
CERVICAL CYST ( 4 FDA reports)
CERVICAL MYELOPATHY ( 4 FDA reports)
CHOKING SENSATION ( 4 FDA reports)
CLUMSINESS ( 4 FDA reports)
CLUSTER HEADACHE ( 4 FDA reports)
COLECTOMY ( 4 FDA reports)
COLONOSCOPY ( 4 FDA reports)
CRYPTORCHISM ( 4 FDA reports)
CYTOLYTIC HEPATITIS ( 4 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 4 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 4 FDA reports)
DENERVATION ATROPHY ( 4 FDA reports)
DERMATILLOMANIA ( 4 FDA reports)
DEVICE DISLOCATION ( 4 FDA reports)
DIABETIC ULCER ( 4 FDA reports)
DISTURBANCE IN SEXUAL AROUSAL ( 4 FDA reports)
DRUG DELIVERY DEVICE IMPLANTATION ( 4 FDA reports)
DRUG LEVEL DECREASED ( 4 FDA reports)
EAR CONGESTION ( 4 FDA reports)
EJACULATION DISORDER ( 4 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 4 FDA reports)
EOSINOPHIL COUNT INCREASED ( 4 FDA reports)
EXTRADURAL ABSCESS ( 4 FDA reports)
EYE MOVEMENT DISORDER ( 4 FDA reports)
EYELID PTOSIS ( 4 FDA reports)
FACTOR II DEFICIENCY ( 4 FDA reports)
FACTOR V DEFICIENCY ( 4 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 4 FDA reports)
FEAR OF FALLING ( 4 FDA reports)
FLASHBACK ( 4 FDA reports)
FOAMING AT MOUTH ( 4 FDA reports)
FOCAL NODULAR HYPERPLASIA ( 4 FDA reports)
FRUSTRATION ( 4 FDA reports)
GALACTORRHOEA ( 4 FDA reports)
GASTRIC ULCER PERFORATION ( 4 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 4 FDA reports)
HAIR TEXTURE ABNORMAL ( 4 FDA reports)
HEAD DISCOMFORT ( 4 FDA reports)
HEPATIC MASS ( 4 FDA reports)
HERNIA OBSTRUCTIVE ( 4 FDA reports)
HERNIA REPAIR ( 4 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 4 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 4 FDA reports)
HYPERGAMMAGLOBULINAEMIA BENIGN MONOCLONAL ( 4 FDA reports)
HYPERPATHIA ( 4 FDA reports)
HYPERTENSIVE CRISIS ( 4 FDA reports)
HYPOVENTILATION ( 4 FDA reports)
IMMOBILE ( 4 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 4 FDA reports)
INFECTED SKIN ULCER ( 4 FDA reports)
INGUINAL HERNIA ( 4 FDA reports)
INGUINAL HERNIA REPAIR ( 4 FDA reports)
INJECTION SITE ULCER ( 4 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 4 FDA reports)
INTESTINAL RESECTION ( 4 FDA reports)
INTESTINAL STENOSIS ( 4 FDA reports)
INTRACRANIAL HAEMATOMA ( 4 FDA reports)
LEG AMPUTATION ( 4 FDA reports)
LICHENIFICATION ( 4 FDA reports)
LIMB MALFORMATION ( 4 FDA reports)
LIP DISCOLOURATION ( 4 FDA reports)
LIP DRY ( 4 FDA reports)
LIVER INJURY ( 4 FDA reports)
LOGORRHOEA ( 4 FDA reports)
LOOSE STOOLS ( 4 FDA reports)
LYMPHOCYTOSIS ( 4 FDA reports)
MALABSORPTION ( 4 FDA reports)
MAMMOGRAM ( 4 FDA reports)
MEGACOLON ( 4 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 4 FDA reports)
MITRAL VALVE REPLACEMENT ( 4 FDA reports)
MUSCLE FIBROSIS ( 4 FDA reports)
MUSCLE INJURY ( 4 FDA reports)
MUSCLE RELAXANT DRUG LEVEL ABOVE THERAPEUTIC ( 4 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 4 FDA reports)
NAIL HYPERTROPHY ( 4 FDA reports)
NASAL MUCOSAL DISORDER ( 4 FDA reports)
NASAL SINUS DRAINAGE ( 4 FDA reports)
NECROSIS ISCHAEMIC ( 4 FDA reports)
NEUROLOGICAL SYMPTOM ( 4 FDA reports)
NODULE ON EXTREMITY ( 4 FDA reports)
NON-SMALL CELL LUNG CANCER ( 4 FDA reports)
NOSOCOMIAL INFECTION ( 4 FDA reports)
NUCHAL RIGIDITY ( 4 FDA reports)
OESOPHAGEAL PAIN ( 4 FDA reports)
OLIGOMENORRHOEA ( 4 FDA reports)
OPTIC NERVE INJURY ( 4 FDA reports)
ORAL FUNGAL INFECTION ( 4 FDA reports)
PANCREATIC ENZYMES INCREASED ( 4 FDA reports)
PANCREATITIS CHRONIC ( 4 FDA reports)
PARATHYROID TUMOUR BENIGN ( 4 FDA reports)
PCO2 DECREASED ( 4 FDA reports)
PEAU D'ORANGE ( 4 FDA reports)
PHARYNGEAL LESION ( 4 FDA reports)
PLASMA PROTEIN METABOLISM DISORDER ( 4 FDA reports)
PNEUMATOSIS INTESTINALIS ( 4 FDA reports)
PNEUMONIA KLEBSIELLA ( 4 FDA reports)
POISONING ( 4 FDA reports)
POLYARTHRITIS ( 4 FDA reports)
POSTOPERATIVE RENAL FAILURE ( 4 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 4 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 4 FDA reports)
PULMONARY HAEMORRHAGE ( 4 FDA reports)
PULMONARY INFARCTION ( 4 FDA reports)
PULMONARY THROMBOSIS ( 4 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 4 FDA reports)
PUPIL FIXED ( 4 FDA reports)
RADICULITIS LUMBOSACRAL ( 4 FDA reports)
RASH VESICULAR ( 4 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 4 FDA reports)
RESPIRATORY RATE INCREASED ( 4 FDA reports)
RETROVIRAL INFECTION ( 4 FDA reports)
RHONCHI ( 4 FDA reports)
RIGHT ATRIAL HYPERTROPHY ( 4 FDA reports)
SCAN MYOCARDIAL PERFUSION ( 4 FDA reports)
SCLERAL DISORDER ( 4 FDA reports)
SEBORRHOEA ( 4 FDA reports)
SENSATION OF FOREIGN BODY ( 4 FDA reports)
SERRATIA INFECTION ( 4 FDA reports)
SHIFT TO THE LEFT ( 4 FDA reports)
SKIN ATROPHY ( 4 FDA reports)
SKIN GRAFT ( 4 FDA reports)
SKIN IRRITATION ( 4 FDA reports)
SKULL FRACTURE ( 4 FDA reports)
SMEAR CERVIX ABNORMAL ( 4 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 4 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 4 FDA reports)
SUPERINFECTION ( 4 FDA reports)
SYMBOLIC DYSFUNCTION ( 4 FDA reports)
SYNCOPE VASOVAGAL ( 4 FDA reports)
TACHYARRHYTHMIA ( 4 FDA reports)
TENOSYNOVITIS STENOSANS ( 4 FDA reports)
TESTICULAR SWELLING ( 4 FDA reports)
THROAT LESION ( 4 FDA reports)
THROMBOCYTOSIS ( 4 FDA reports)
TINEA CAPITIS ( 4 FDA reports)
TOE AMPUTATION ( 4 FDA reports)
TOE OPERATION ( 4 FDA reports)
TORTICOLLIS ( 4 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 4 FDA reports)
TUBERCULOSIS ( 4 FDA reports)
URINARY TRACT OBSTRUCTION ( 4 FDA reports)
VARICOSE VEIN ( 4 FDA reports)
VASOGENIC CEREBRAL OEDEMA ( 4 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 4 FDA reports)
WITHDRAWAL BLEEDING IRREGULAR ( 4 FDA reports)
ABDOMINAL RIGIDITY ( 3 FDA reports)
ABNORMAL SENSATION IN EYE ( 3 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 3 FDA reports)
ACINETOBACTER BACTERAEMIA ( 3 FDA reports)
ACINETOBACTER INFECTION ( 3 FDA reports)
ACUTE PRERENAL FAILURE ( 3 FDA reports)
ACUTE PULMONARY OEDEMA ( 3 FDA reports)
ADHESION ( 3 FDA reports)
ADNEXA UTERI MASS ( 3 FDA reports)
AKINESIA ( 3 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 3 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 3 FDA reports)
AMYLOIDOSIS ( 3 FDA reports)
ANAEMIA MACROCYTIC ( 3 FDA reports)
ANAESTHETIC COMPLICATION NEUROLOGICAL ( 3 FDA reports)
ANDROGEN DEFICIENCY ( 3 FDA reports)
ANDROGENS DECREASED ( 3 FDA reports)
ANTIANDROGEN THERAPY ( 3 FDA reports)
ANTICOAGULANT THERAPY ( 3 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 3 FDA reports)
ANTIMITOCHONDRIAL ANTIBODY POSITIVE ( 3 FDA reports)
AORTIC DISORDER ( 3 FDA reports)
AORTIC DISSECTION ( 3 FDA reports)
APHONIA ( 3 FDA reports)
APPLICATION SITE PAIN ( 3 FDA reports)
APPLICATION SITE URTICARIA ( 3 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 3 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 3 FDA reports)
ARTHRITIS INFECTIVE ( 3 FDA reports)
ARTHROSCOPY ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 3 FDA reports)
ATRIAL THROMBOSIS ( 3 FDA reports)
BACTERIA URINE IDENTIFIED ( 3 FDA reports)
BACTERIURIA ( 3 FDA reports)
BENIGN ANORECTAL NEOPLASM ( 3 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 3 FDA reports)
BLEPHAROSPASM ( 3 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 3 FDA reports)
BLOOD IRON DECREASED ( 3 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 3 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 3 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 3 FDA reports)
BLOOD UREA DECREASED ( 3 FDA reports)
BODY MASS INDEX INCREASED ( 3 FDA reports)
BRAIN DAMAGE ( 3 FDA reports)
BRAIN MASS ( 3 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 3 FDA reports)
BRAIN STEM INFARCTION ( 3 FDA reports)
BREAST CALCIFICATIONS ( 3 FDA reports)
BREAST CANCER STAGE I ( 3 FDA reports)
BREAST LUMP REMOVAL ( 3 FDA reports)
BRONCHIOLITIS ( 3 FDA reports)
CALCULUS URETHRAL ( 3 FDA reports)
CANDIDA SEPSIS ( 3 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 3 FDA reports)
CARCINOMA ( 3 FDA reports)
CARDIAC MYXOMA ( 3 FDA reports)
CARDIAC OPERATION ( 3 FDA reports)
CARDIAC PERFORATION ( 3 FDA reports)
CARDIORENAL SYNDROME ( 3 FDA reports)
CATHETER RELATED COMPLICATION ( 3 FDA reports)
CATHETER SITE INFECTION ( 3 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 3 FDA reports)
CEREBRAL CYST ( 3 FDA reports)
CERVIX DISORDER ( 3 FDA reports)
CHEST WALL OPERATION ( 3 FDA reports)
CHONDROPATHY ( 3 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 3 FDA reports)
COELIAC DISEASE ( 3 FDA reports)
COLLAPSE OF LUNG ( 3 FDA reports)
CORNEAL ABRASION ( 3 FDA reports)
CORNEAL OEDEMA ( 3 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 3 FDA reports)
CYCLIC VOMITING SYNDROME ( 3 FDA reports)
DARK CIRCLES UNDER EYES ( 3 FDA reports)
DEATH OF RELATIVE ( 3 FDA reports)
DELIRIUM FEBRILE ( 3 FDA reports)
DELIRIUM TREMENS ( 3 FDA reports)
DEPRESSION SUICIDAL ( 3 FDA reports)
DERMATOPHYTOSIS ( 3 FDA reports)
DERMATOSIS ( 3 FDA reports)
DEVICE BREAKAGE ( 3 FDA reports)
DISEASE COMPLICATION ( 3 FDA reports)
DISSOCIATIVE DISORDER ( 3 FDA reports)
DIVERTICULAR PERFORATION ( 3 FDA reports)
DRUG ADDICT ( 3 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 3 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 3 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 3 FDA reports)
DRUG SCREEN NEGATIVE ( 3 FDA reports)
DUODENAL PERFORATION ( 3 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 3 FDA reports)
DYSHIDROSIS ( 3 FDA reports)
DYSPHASIA ( 3 FDA reports)
EAR LOBE INFECTION ( 3 FDA reports)
EFFUSION ( 3 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 3 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 3 FDA reports)
ENCEPHALITIS HERPES ( 3 FDA reports)
ENTEROCUTANEOUS FISTULA ( 3 FDA reports)
ENURESIS ( 3 FDA reports)
EPSTEIN-BARR VIRAEMIA ( 3 FDA reports)
EXPOSURE TO TOXIC AGENT ( 3 FDA reports)
EYE INFLAMMATION ( 3 FDA reports)
EYE ROLLING ( 3 FDA reports)
FAECES HARD ( 3 FDA reports)
FALSE POSITIVE INVESTIGATION RESULT ( 3 FDA reports)
FEELINGS OF WORTHLESSNESS ( 3 FDA reports)
FINGER DEFORMITY ( 3 FDA reports)
GALLBLADDER ENLARGEMENT ( 3 FDA reports)
GAMBLING ( 3 FDA reports)
GAS POISONING ( 3 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 3 FDA reports)
GASTROENTERITIS NORWALK VIRUS ( 3 FDA reports)
GASTROINTESTINAL INFECTION ( 3 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 3 FDA reports)
GENERAL SYMPTOM ( 3 FDA reports)
GLOBULINS INCREASED ( 3 FDA reports)
GLYCOSURIA ( 3 FDA reports)
GRIP STRENGTH DECREASED ( 3 FDA reports)
HAEMATOCRIT INCREASED ( 3 FDA reports)
HAEMOLYSIS ( 3 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 3 FDA reports)
HEPATIC ENZYME ABNORMAL ( 3 FDA reports)
HEPATIC FIBROSIS ( 3 FDA reports)
HEPATIC NECROSIS ( 3 FDA reports)
HEPATITIS B ( 3 FDA reports)
HERNIA CONGENITAL ( 3 FDA reports)
HISTOPLASMOSIS ( 3 FDA reports)
HISTOPLASMOSIS DISSEMINATED ( 3 FDA reports)
HOSPICE CARE ( 3 FDA reports)
HUNGER ( 3 FDA reports)
HYPER IGE SYNDROME ( 3 FDA reports)
HYPERCOAGULATION ( 3 FDA reports)
HYPERGLOBULINAEMIA ( 3 FDA reports)
HYPERSEXUALITY ( 3 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 3 FDA reports)
HYPOCHLORAEMIA ( 3 FDA reports)
HYPOTRICHOSIS ( 3 FDA reports)
HYPOVOLAEMIC SHOCK ( 3 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 3 FDA reports)
IMPATIENCE ( 3 FDA reports)
INCISION SITE INFECTION ( 3 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 3 FDA reports)
INDURATION ( 3 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 3 FDA reports)
INJECTION SITE ATROPHY ( 3 FDA reports)
INJECTION SITE INDURATION ( 3 FDA reports)
INJECTION SITE INFECTION ( 3 FDA reports)
INJECTION SITE NECROSIS ( 3 FDA reports)
INJECTION SITE NERVE DAMAGE ( 3 FDA reports)
INJECTION SITE NODULE ( 3 FDA reports)
INJECTION SITE RASH ( 3 FDA reports)
INJECTION SITE STREAKING ( 3 FDA reports)
INJURY ASPHYXIATION ( 3 FDA reports)
INTESTINAL ANASTOMOSIS COMPLICATION ( 3 FDA reports)
INTESTINAL DILATATION ( 3 FDA reports)
INTESTINAL PERFORATION ( 3 FDA reports)
INTRACARDIAC THROMBUS ( 3 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 3 FDA reports)
IRON DEFICIENCY ( 3 FDA reports)
KIDNEY FIBROSIS ( 3 FDA reports)
KNEE DEFORMITY ( 3 FDA reports)
LARGE INTESTINE PERFORATION ( 3 FDA reports)
LIGAMENT DISORDER ( 3 FDA reports)
LIMB OPERATION ( 3 FDA reports)
LIVER ABSCESS ( 3 FDA reports)
LUNG ABSCESS ( 3 FDA reports)
LYMPH NODE PALPABLE ( 3 FDA reports)
MACULAR OEDEMA ( 3 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 3 FDA reports)
MATERNAL EXPOSURE BEFORE PREGNANCY ( 3 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 3 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 3 FDA reports)
MECHANICAL VENTILATION ( 3 FDA reports)
MEDICAL DEVICE COMPLICATION ( 3 FDA reports)
MENINGITIS ASEPTIC ( 3 FDA reports)
METABOLIC ALKALOSIS ( 3 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 3 FDA reports)
MITRAL VALVE REPAIR ( 3 FDA reports)
MOANING ( 3 FDA reports)
MONOCYTE COUNT INCREASED ( 3 FDA reports)
MORPHOEA ( 3 FDA reports)
MOTION SICKNESS ( 3 FDA reports)
MUCOEPIDERMOID CARCINOMA ( 3 FDA reports)
MUCOSAL DISCOLOURATION ( 3 FDA reports)
MUSCLE CONTRACTURE ( 3 FDA reports)
MUSCULAR DYSTROPHY ( 3 FDA reports)
NASAL OEDEMA ( 3 FDA reports)
NEUROTOXICITY ( 3 FDA reports)
NO ADVERSE EVENT ( 3 FDA reports)
NODAL ARRHYTHMIA ( 3 FDA reports)
OBSESSIVE THOUGHTS ( 3 FDA reports)
OLIGURIA ( 3 FDA reports)
ORGAN FAILURE ( 3 FDA reports)
OSTEOCHONDROMA ( 3 FDA reports)
OTITIS EXTERNA ( 3 FDA reports)
PANCREATIC CARCINOMA ( 3 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 3 FDA reports)
PEDAL PULSE DECREASED ( 3 FDA reports)
PERICARDITIS CONSTRICTIVE ( 3 FDA reports)
PERITONEAL ADHESIONS ( 3 FDA reports)
PERNICIOUS ANAEMIA ( 3 FDA reports)
PETIT MAL EPILEPSY ( 3 FDA reports)
PHARYNGEAL DISORDER ( 3 FDA reports)
PHARYNGEAL MASS ( 3 FDA reports)
PHOTOPSIA ( 3 FDA reports)
PILOERECTION ( 3 FDA reports)
PITTING OEDEMA ( 3 FDA reports)
PITUITARY TUMOUR BENIGN ( 3 FDA reports)
POLYP COLORECTAL ( 3 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 3 FDA reports)
POOR PERIPHERAL CIRCULATION ( 3 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 3 FDA reports)
PROCEDURAL DIZZINESS ( 3 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 3 FDA reports)
PROTEIN C DEFICIENCY ( 3 FDA reports)
PROTEIN TOTAL DECREASED ( 3 FDA reports)
PROTEIN URINE PRESENT ( 3 FDA reports)
PULMONARY ARTERIAL WEDGE PRESSURE INCREASED ( 3 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 3 FDA reports)
RADIAL NERVE PALSY ( 3 FDA reports)
RADIATION OESOPHAGITIS ( 3 FDA reports)
REFLUX LARYNGITIS ( 3 FDA reports)
REFRACTORY ANAEMIA ( 3 FDA reports)
RENAL ARTERY STENOSIS ( 3 FDA reports)
RESPIRATION ABNORMAL ( 3 FDA reports)
RESUSCITATION ( 3 FDA reports)
RETINAL ISCHAEMIA ( 3 FDA reports)
RETROPERITONEAL HAEMATOMA ( 3 FDA reports)
RIGHT VENTRICULAR FAILURE ( 3 FDA reports)
ROSAI-DORFMAN SYNDROME ( 3 FDA reports)
SCHIZOID PERSONALITY DISORDER ( 3 FDA reports)
SEBORRHOEIC DERMATITIS ( 3 FDA reports)
SENSATION OF PRESSURE ( 3 FDA reports)
SINUS PAIN ( 3 FDA reports)
SINUSITIS BACTERIAL ( 3 FDA reports)
SKIN EROSION ( 3 FDA reports)
SKIN FISSURES ( 3 FDA reports)
SKIN NECROSIS ( 3 FDA reports)
SKIN ODOUR ABNORMAL ( 3 FDA reports)
SKIN OEDEMA ( 3 FDA reports)
SKIN REACTION ( 3 FDA reports)
SKIN SWELLING ( 3 FDA reports)
SKULL FRACTURED BASE ( 3 FDA reports)
SMALL INTESTINAL PERFORATION ( 3 FDA reports)
SOFT TISSUE MASS ( 3 FDA reports)
SOMATOFORM DISORDER ( 3 FDA reports)
SPEECH REHABILITATION ( 3 FDA reports)
SPINAL CORD INFECTION ( 3 FDA reports)
SPINAL PAIN ( 3 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 3 FDA reports)
STATUS ASTHMATICUS ( 3 FDA reports)
STENT PLACEMENT ( 3 FDA reports)
STEREOTYPY ( 3 FDA reports)
STOOL ANALYSIS ABNORMAL ( 3 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 3 FDA reports)
STRESS URINARY INCONTINENCE ( 3 FDA reports)
STUPOR ( 3 FDA reports)
SUPRAPUBIC PAIN ( 3 FDA reports)
TACHYPNOEA ( 3 FDA reports)
TENDON PAIN ( 3 FDA reports)
THALASSAEMIA ( 3 FDA reports)
THERAPEUTIC EMBOLISATION ( 3 FDA reports)
TONSILLAR CYST ( 3 FDA reports)
TONSILLITIS STREPTOCOCCAL ( 3 FDA reports)
TOXIC ENCEPHALOPATHY ( 3 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 3 FDA reports)
TRUNCUS ARTERIOSUS PERSISTENT ( 3 FDA reports)
TUMOUR MARKER INCREASED ( 3 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 3 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 3 FDA reports)
URINE KETONE BODY PRESENT ( 3 FDA reports)
URTICARIA GENERALISED ( 3 FDA reports)
UTERINE HAEMORRHAGE ( 3 FDA reports)
UVULECTOMY ( 3 FDA reports)
VAGINAL BURNING SENSATION ( 3 FDA reports)
VASCULAR DEMENTIA ( 3 FDA reports)
VEIN DISORDER ( 3 FDA reports)
VENTRICULAR ARRHYTHMIA ( 3 FDA reports)
VITAMIN D DECREASED ( 3 FDA reports)
VULVAL ABSCESS ( 3 FDA reports)
VULVOVAGINAL PRURITUS ( 3 FDA reports)
WEST NILE VIRAL INFECTION ( 3 FDA reports)
WOUND DEBRIDEMENT ( 3 FDA reports)
YELLOW SKIN ( 3 FDA reports)
ABDOMINAL PANNICULECTOMY ( 2 FDA reports)
ABNORMAL FAECES ( 2 FDA reports)
ACCIDENTAL NEEDLE STICK ( 2 FDA reports)
ACETABULUM FRACTURE ( 2 FDA reports)
ACQUIRED CARDIAC SEPTAL DEFECT ( 2 FDA reports)
ACUTE PULMONARY HISTOPLASMOSIS ( 2 FDA reports)
ADDISON'S DISEASE ( 2 FDA reports)
ADENOCARCINOMA PANCREAS ( 2 FDA reports)
ADENOMYOSIS ( 2 FDA reports)
ADRENAL DISORDER ( 2 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 2 FDA reports)
ALCOHOL PROBLEM ( 2 FDA reports)
ALCOHOLIC PANCREATITIS ( 2 FDA reports)
ANAESTHETIC COMPLICATION ( 2 FDA reports)
ANAL FISTULA ( 2 FDA reports)
ANAPHYLACTOID REACTION ( 2 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 2 FDA reports)
ANORGASMIA ( 2 FDA reports)
ANTICONVULSANT TOXICITY ( 2 FDA reports)
ANTIDEPRESSANT DRUG LEVEL DECREASED ( 2 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 2 FDA reports)
ANTISOCIAL PERSONALITY DISORDER ( 2 FDA reports)
AORTIC VALVE DISEASE ( 2 FDA reports)
APPLICATION SITE EROSION ( 2 FDA reports)
ARACHNOIDITIS ( 2 FDA reports)
ARTERIAL REPAIR ( 2 FDA reports)
ARTERIAL THROMBOSIS ( 2 FDA reports)
ARTHROFIBROSIS ( 2 FDA reports)
ASOCIAL BEHAVIOUR ( 2 FDA reports)
ASPIRATION BONE MARROW ABNORMAL ( 2 FDA reports)
ATRIAL NATRIURETIC PEPTIDE INCREASED ( 2 FDA reports)
AXILLARY PAIN ( 2 FDA reports)
AXONAL NEUROPATHY ( 2 FDA reports)
AZYGOS LOBE ( 2 FDA reports)
BAND SENSATION ( 2 FDA reports)
BENIGN BREAST NEOPLASM ( 2 FDA reports)
BENIGN CARDIAC NEOPLASM ( 2 FDA reports)
BENIGN LUNG NEOPLASM ( 2 FDA reports)
BILIARY TRACT DISORDER ( 2 FDA reports)
BINGE EATING ( 2 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 2 FDA reports)
BIOPSY LIVER ABNORMAL ( 2 FDA reports)
BLADDER DIVERTICULUM ( 2 FDA reports)
BLADDER HYPERTROPHY ( 2 FDA reports)
BLADDER OBSTRUCTION ( 2 FDA reports)
BLINDNESS TRANSIENT ( 2 FDA reports)
BLOOD ALCOHOL INCREASED ( 2 FDA reports)
BLOOD AMYLASE INCREASED ( 2 FDA reports)
BLOOD BICARBONATE DECREASED ( 2 FDA reports)
BLOOD CHLORIDE INCREASED ( 2 FDA reports)
BLOOD COUNT ABNORMAL ( 2 FDA reports)
BLOOD CREATINE INCREASED ( 2 FDA reports)
BLOOD CREATININE ABNORMAL ( 2 FDA reports)
BLOOD CREATININE DECREASED ( 2 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 2 FDA reports)
BLOOD MAGNESIUM INCREASED ( 2 FDA reports)
BLOOD PH INCREASED ( 2 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 2 FDA reports)
BLOOD PRESSURE ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 2 FDA reports)
BLOOD SODIUM INCREASED ( 2 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 2 FDA reports)
BONE FORMATION INCREASED ( 2 FDA reports)
BONE INFARCTION ( 2 FDA reports)
BONE MARROW DISORDER ( 2 FDA reports)
BONE MARROW TOXICITY ( 2 FDA reports)
BREAST ABSCESS ( 2 FDA reports)
BREAST DISCHARGE ( 2 FDA reports)
BREAST MICROCALCIFICATION ( 2 FDA reports)
BUCCAL MUCOSAL ROUGHENING ( 2 FDA reports)
BURSA DISORDER ( 2 FDA reports)
CARDIAC REHABILITATION THERAPY ( 2 FDA reports)
CARDIAC TAMPONADE ( 2 FDA reports)
CARDIAC VALVE ABSCESS ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 2 FDA reports)
CARDIOVERSION ( 2 FDA reports)
CAROTIDYNIA ( 2 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 2 FDA reports)
CATHETER RELATED INFECTION ( 2 FDA reports)
CELLULITIS PHARYNGEAL ( 2 FDA reports)
CEREBELLAR ATROPHY ( 2 FDA reports)
CEREBELLAR SYNDROME ( 2 FDA reports)
CEREBRAL CALCIFICATION ( 2 FDA reports)
CEREBRAL DISORDER ( 2 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 2 FDA reports)
CHEYNE-STOKES RESPIRATION ( 2 FDA reports)
CHOLANGITIS ( 2 FDA reports)
CHONDRITIS ( 2 FDA reports)
CHOREA ( 2 FDA reports)
CHOROIDAL NEOVASCULARISATION ( 2 FDA reports)
CHROMATOPSIA ( 2 FDA reports)
CHRONIC HEPATITIS ( 2 FDA reports)
CLAVICLE FRACTURE ( 2 FDA reports)
CLUBBING ( 2 FDA reports)
COLON OPERATION ( 2 FDA reports)
COLONIC PERFORATION POSTOPERATIVE ( 2 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 2 FDA reports)
COMPULSIVE SHOPPING ( 2 FDA reports)
CONDUCTION DISORDER ( 2 FDA reports)
CONGENITAL ANOMALY ( 2 FDA reports)
CONTRAST MEDIA ALLERGY ( 2 FDA reports)
CONTRAST MEDIA REACTION ( 2 FDA reports)
COR PULMONALE CHRONIC ( 2 FDA reports)
CORNEAL DEPOSITS ( 2 FDA reports)
CORNEAL EROSION ( 2 FDA reports)
CORONARY ARTERY RESTENOSIS ( 2 FDA reports)
CRUSH INJURY ( 2 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 2 FDA reports)
CSF TEST ABNORMAL ( 2 FDA reports)
CUSHING'S SYNDROME ( 2 FDA reports)
CUSHINGOID ( 2 FDA reports)
CYSTITIS RADIATION ( 2 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 2 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 2 FDA reports)
DENTAL CARE ( 2 FDA reports)
DENTAL PLAQUE ( 2 FDA reports)
DERMATITIS ALLERGIC ( 2 FDA reports)
DEVICE INEFFECTIVE ( 2 FDA reports)
DEVICE OCCLUSION ( 2 FDA reports)
DEVICE RELATED SEPSIS ( 2 FDA reports)
DIABETES INSIPIDUS ( 2 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 2 FDA reports)
DIABETIC VASCULAR DISORDER ( 2 FDA reports)
DIARRHOEA INFECTIOUS ( 2 FDA reports)
DIRECTIONAL DOPPLER FLOW TESTS ABNORMAL ( 2 FDA reports)
DISSEMINATED TUBERCULOSIS ( 2 FDA reports)
DOUBLE STRANDED DNA ANTIBODY ( 2 FDA reports)
DRESSLER'S SYNDROME ( 2 FDA reports)
DRUG DIVERSION ( 2 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
DRUG RESISTANCE ( 2 FDA reports)
DRUG WITHDRAWAL HEADACHE ( 2 FDA reports)
DRY GANGRENE ( 2 FDA reports)
DYSMORPHISM ( 2 FDA reports)
ECZEMA NUMMULAR ( 2 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 2 FDA reports)
EMPHYSEMATOUS CYSTITIS ( 2 FDA reports)
ENDOCARDITIS BACTERIAL ( 2 FDA reports)
ENDOMETRIAL ABLATION ( 2 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 2 FDA reports)
ENDOTRACHEAL INTUBATION ( 2 FDA reports)
ENTEROCOLITIS ( 2 FDA reports)
EPHELIDES ( 2 FDA reports)
EPIDERMAL NAEVUS ( 2 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 2 FDA reports)
ESCHAR ( 2 FDA reports)
EXCITABILITY ( 2 FDA reports)
EXTERNAL EAR PAIN ( 2 FDA reports)
EXTRAVASATION ( 2 FDA reports)
EYE PRURITUS ( 2 FDA reports)
FACTOR V LEIDEN MUTATION ( 2 FDA reports)
FAECES PALE ( 2 FDA reports)
FEBRILE INFECTION ( 2 FDA reports)
FEELING HOT AND COLD ( 2 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 2 FDA reports)
FIBRIN D DIMER INCREASED ( 2 FDA reports)
FINE MOTOR DELAY ( 2 FDA reports)
FLAIL CHEST ( 2 FDA reports)
FOETAL ALCOHOL SYNDROME ( 2 FDA reports)
FOOD ALLERGY ( 2 FDA reports)
FOOD INTOLERANCE ( 2 FDA reports)
FOREIGN BODY ( 2 FDA reports)
FOREIGN BODY ASPIRATION ( 2 FDA reports)
FOREIGN BODY TRAUMA ( 2 FDA reports)
FUNGAL OESOPHAGITIS ( 2 FDA reports)
FUNGAL TEST POSITIVE ( 2 FDA reports)
GALLBLADDER OPERATION ( 2 FDA reports)
GAMMOPATHY ( 2 FDA reports)
GASTROINTESTINAL ULCER ( 2 FDA reports)
GENITAL BURNING SENSATION ( 2 FDA reports)
GENITAL PRURITUS FEMALE ( 2 FDA reports)
GILBERT'S SYNDROME ( 2 FDA reports)
GLOBULINS DECREASED ( 2 FDA reports)
GLOMERULONEPHRITIS ACUTE ( 2 FDA reports)
GLOMERULOSCLEROSIS ( 2 FDA reports)
GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
GRANDIOSITY ( 2 FDA reports)
GRANULOMA ANNULARE ( 2 FDA reports)
HAEMOCONCENTRATION ( 2 FDA reports)
HAEMODYNAMIC INSTABILITY ( 2 FDA reports)
HAEMOGLOBIN INCREASED ( 2 FDA reports)
HALLUCINATION, OLFACTORY ( 2 FDA reports)
HALLUCINATION, TACTILE ( 2 FDA reports)
HAND-FOOT-AND-MOUTH DISEASE ( 2 FDA reports)
HEART TRANSPLANT REJECTION ( 2 FDA reports)
HEAT EXHAUSTION ( 2 FDA reports)
HEPATITIS ALCOHOLIC ( 2 FDA reports)
HERPES OPHTHALMIC ( 2 FDA reports)
HOMANS' SIGN ( 2 FDA reports)
HOMICIDE ( 2 FDA reports)
HYDROCEPHALUS ( 2 FDA reports)
HYPERACUSIS ( 2 FDA reports)
HYPERAEMIA ( 2 FDA reports)
HYPERKINETIC HEART SYNDROME ( 2 FDA reports)
HYPERNATRAEMIA ( 2 FDA reports)
HYPOGLYCAEMIA UNAWARENESS ( 2 FDA reports)
HYPOGLYCAEMIC COMA ( 2 FDA reports)
HYPOMENORRHOEA ( 2 FDA reports)
HYPOMETABOLISM ( 2 FDA reports)
HYPOPITUITARISM ( 2 FDA reports)
HYPOPROTEINAEMIA ( 2 FDA reports)
HYPOSMIA ( 2 FDA reports)
IATROGENIC INJURY ( 2 FDA reports)
ILIAC ARTERY STENOSIS ( 2 FDA reports)
IMPAIRED SELF-CARE ( 2 FDA reports)
IMPLANT SITE REACTION ( 2 FDA reports)
INFUSION SITE PAIN ( 2 FDA reports)
INFUSION SITE REACTION ( 2 FDA reports)
INJECTION SITE ABSCESS ( 2 FDA reports)
INJECTION SITE DISCOMFORT ( 2 FDA reports)
INJECTION SITE DRYNESS ( 2 FDA reports)
INJECTION SITE PAPULE ( 2 FDA reports)
INJECTION SITE VESICLES ( 2 FDA reports)
INSULIN RESISTANCE ( 2 FDA reports)
INTUBATION ( 2 FDA reports)
IODINE ALLERGY ( 2 FDA reports)
JOINT CREPITATION ( 2 FDA reports)
JUGULAR VEIN DISTENSION ( 2 FDA reports)
KIDNEY ENLARGEMENT ( 2 FDA reports)
KIDNEY SMALL ( 2 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 2 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 2 FDA reports)
LARYNGEAL PAIN ( 2 FDA reports)
LARYNGEAL POLYP ( 2 FDA reports)
LATERAL MEDULLARY SYNDROME ( 2 FDA reports)
LEFT VENTRICULAR FAILURE ( 2 FDA reports)
LEGAL PROBLEM ( 2 FDA reports)
LEUKAEMIA ( 2 FDA reports)
LIBIDO INCREASED ( 2 FDA reports)
LIMB CRUSHING INJURY ( 2 FDA reports)
LIP PAIN ( 2 FDA reports)
LIVEDO RETICULARIS ( 2 FDA reports)
LOSS OF LIBIDO ( 2 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 2 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
LUMBAR SPINE FLATTENING ( 2 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 2 FDA reports)
LUNG CREPITATION ( 2 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 2 FDA reports)
LYMPH NODES SCAN ABNORMAL ( 2 FDA reports)
LYMPHANGITIS ( 2 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 2 FDA reports)
MACROCYTOSIS ( 2 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 2 FDA reports)
MALIGNANT URINARY TRACT NEOPLASM ( 2 FDA reports)
MAMMOGRAM ABNORMAL ( 2 FDA reports)
MARFAN'S SYNDROME ( 2 FDA reports)
MARITAL PROBLEM ( 2 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 2 FDA reports)
MEDICAL DEVICE IMPLANTATION ( 2 FDA reports)
MEDICATION RESIDUE ( 2 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 2 FDA reports)
MILK ALLERGY ( 2 FDA reports)
MITRAL VALVE SCLEROSIS ( 2 FDA reports)
MORTON'S NEUROMA ( 2 FDA reports)
MUSCLE ABSCESS ( 2 FDA reports)
MUSCLE FATIGUE ( 2 FDA reports)
MYCOTIC ANEURYSM ( 2 FDA reports)
MYOGLOBIN URINE PRESENT ( 2 FDA reports)
NAIL INFECTION ( 2 FDA reports)
NEPHRITIC SYNDROME ( 2 FDA reports)
NEPHRITIS INTERSTITIAL ( 2 FDA reports)
NEPHROCALCINOSIS ( 2 FDA reports)
NEURILEMMOMA ( 2 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 2 FDA reports)
NEUTROPHIL TOXIC GRANULATION PRESENT ( 2 FDA reports)
NIGHT CRAMPS ( 2 FDA reports)
NO ADVERSE DRUG EFFECT ( 2 FDA reports)
NONSPECIFIC REACTION ( 2 FDA reports)
OBSTRUCTIVE UROPATHY ( 2 FDA reports)
OCULAR ICTERUS ( 2 FDA reports)
OPERATIVE HAEMORRHAGE ( 2 FDA reports)
OPHTHALMOPLEGIA ( 2 FDA reports)
ORCHITIS NONINFECTIVE ( 2 FDA reports)
OROPHARYNGEAL BLISTERING ( 2 FDA reports)
OTOTOXICITY ( 2 FDA reports)
OVARIAN CANCER METASTATIC ( 2 FDA reports)
OVARIAN CYST RUPTURED ( 2 FDA reports)
OXYGEN SUPPLEMENTATION ( 2 FDA reports)
PALMAR ERYTHEMA ( 2 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 2 FDA reports)
PANCREATIC INSUFFICIENCY ( 2 FDA reports)
PANCREATIC MASS ( 2 FDA reports)
PANCREATIC PSEUDOCYST ( 2 FDA reports)
PANCREATITIS NECROTISING ( 2 FDA reports)
PARANEOPLASTIC CEREBELLAR DEGENERATION ( 2 FDA reports)
PARESIS ( 2 FDA reports)
PARTNER STRESS ( 2 FDA reports)
PCO2 INCREASED ( 2 FDA reports)
PELVIC VENOUS THROMBOSIS ( 2 FDA reports)
PERIORBITAL HAEMATOMA ( 2 FDA reports)
PERIORBITAL OEDEMA ( 2 FDA reports)
PERIRENAL HAEMATOMA ( 2 FDA reports)
PHANTOM PAIN ( 2 FDA reports)
PHARMACOPHOBIA ( 2 FDA reports)
PHONOPHOBIA ( 2 FDA reports)
PIGMENTATION DISORDER ( 2 FDA reports)
PLATELET AGGREGATION INCREASED ( 2 FDA reports)
PNEUMOMEDIASTINUM ( 2 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 2 FDA reports)
PO2 DECREASED ( 2 FDA reports)
POLYMYALGIA RHEUMATICA ( 2 FDA reports)
POLYMYOSITIS ( 2 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 2 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 2 FDA reports)
POST LAMINECTOMY SYNDROME ( 2 FDA reports)
POST PROCEDURAL HAEMATOMA ( 2 FDA reports)
POSTICTAL STATE ( 2 FDA reports)
POSTMENOPAUSE ( 2 FDA reports)
POSTOPERATIVE ADHESION ( 2 FDA reports)
POSTOPERATIVE INFECTION ( 2 FDA reports)
PRESENILE DEMENTIA ( 2 FDA reports)
PRIAPISM ( 2 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 2 FDA reports)
PROTEIN S DEFICIENCY ( 2 FDA reports)
PROTRUSION TONGUE ( 2 FDA reports)
PSEUDARTHROSIS ( 2 FDA reports)
PSEUDOMENINGOCELE ( 2 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 2 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 2 FDA reports)
PULMONARY VASCULAR DISORDER ( 2 FDA reports)
PULSE ABNORMAL ( 2 FDA reports)
PULSE PRESSURE DECREASED ( 2 FDA reports)
PUNCTATE KERATITIS ( 2 FDA reports)
PUPILLARY DISORDER ( 2 FDA reports)
PYODERMA ( 2 FDA reports)
RADIAL PULSE INCREASED ( 2 FDA reports)
RADICULAR PAIN ( 2 FDA reports)
RADICULITIS ( 2 FDA reports)
RADICULOTOMY ( 2 FDA reports)
RASH MORBILLIFORM ( 2 FDA reports)
RASH SCARLATINIFORM ( 2 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 2 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 2 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 2 FDA reports)
REFLUX GASTRITIS ( 2 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 2 FDA reports)
RENAL INFARCT ( 2 FDA reports)
RENAL NEOPLASM ( 2 FDA reports)
RENAL SURGERY ( 2 FDA reports)
RESPIRATORY TRACT IRRITATION ( 2 FDA reports)
RETINAL EXUDATES ( 2 FDA reports)
RETROSTERNAL FLUID EVACUATION ( 2 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 2 FDA reports)
RHYTHM IDIOVENTRICULAR ( 2 FDA reports)
SCREAMING ( 2 FDA reports)
SECONDARY PROGRESSIVE MULTIPLE SCLEROSIS ( 2 FDA reports)
SELF ESTEEM DECREASED ( 2 FDA reports)
SELF MUTILATION ( 2 FDA reports)
SEPSIS SYNDROME ( 2 FDA reports)
SERUM SEROTONIN DECREASED ( 2 FDA reports)
SHOCK HAEMORRHAGIC ( 2 FDA reports)
SKIN LESION EXCISION ( 2 FDA reports)
SMOKER ( 2 FDA reports)
SOCIAL PROBLEM ( 2 FDA reports)
SPINAL DEFORMITY ( 2 FDA reports)
SPINAL OPERATION ( 2 FDA reports)
SPIROMETRY ABNORMAL ( 2 FDA reports)
SPLENIC INFARCTION ( 2 FDA reports)
SPONDYLOLYSIS ( 2 FDA reports)
SPUTUM PURULENT ( 2 FDA reports)
STARING ( 2 FDA reports)
STEATORRHOEA ( 2 FDA reports)
STIFF-MAN SYNDROME ( 2 FDA reports)
STOOLS WATERY ( 2 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 2 FDA reports)
SUICIDAL BEHAVIOUR ( 2 FDA reports)
SUNBURN ( 2 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 2 FDA reports)
SWEAT GLAND INFECTION ( 2 FDA reports)
SYRINGOMYELIA ( 2 FDA reports)
SYSTEMIC SCLEROSIS ( 2 FDA reports)
TACHYPHRENIA ( 2 FDA reports)
TAKAYASU'S ARTERITIS ( 2 FDA reports)
TEMPERATURE REGULATION DISORDER ( 2 FDA reports)
TENDON REPAIR ( 2 FDA reports)
TERMINAL INSOMNIA ( 2 FDA reports)
TESTICULAR DISORDER ( 2 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 2 FDA reports)
THERAPY CESSATION ( 2 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
THYROID CANCER METASTATIC ( 2 FDA reports)
TONGUE BLACK HAIRY ( 2 FDA reports)
TONGUE NEOPLASM ( 2 FDA reports)
TONSILLAR NEOPLASM ( 2 FDA reports)
TOOTH RESORPTION ( 2 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 2 FDA reports)
TRAUMATIC BRAIN INJURY ( 2 FDA reports)
TRAUMATIC FRACTURE ( 2 FDA reports)
TRAUMATIC LUNG INJURY ( 2 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 2 FDA reports)
TUNNEL VISION ( 2 FDA reports)
UMBILICAL HERNIA ( 2 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 2 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 2 FDA reports)
URETERAL NEOPLASM ( 2 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 2 FDA reports)
UVEITIS ( 2 FDA reports)
VAGINAL FISTULA ( 2 FDA reports)
VAGINAL MYCOSIS ( 2 FDA reports)
VAGINAL ULCERATION ( 2 FDA reports)
VASCULAR GRAFT ( 2 FDA reports)
VASCULAR GRAFT OCCLUSION ( 2 FDA reports)
VASCULAR OCCLUSION ( 2 FDA reports)
VENA CAVA THROMBOSIS ( 2 FDA reports)
VENOUS STASIS ( 2 FDA reports)
VENTRICULAR ASYSTOLE ( 2 FDA reports)
VENTRICULAR DYSKINESIA ( 2 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 2 FDA reports)
VIRAL LOAD INCREASED ( 2 FDA reports)
VOCAL CORD POLYP ( 2 FDA reports)
VOLVULUS ( 2 FDA reports)
VULVAL ULCERATION ( 2 FDA reports)
VULVITIS ( 2 FDA reports)
WHITE BLOOD CELL DISORDER ( 2 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 2 FDA reports)
WOUND ABSCESS ( 2 FDA reports)
WOUND HAEMORRHAGE ( 2 FDA reports)
XEROSIS ( 2 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 1 FDA reports)
ABDOMINAL SYMPTOM ( 1 FDA reports)
ABNORMAL CHEST SOUND ( 1 FDA reports)
ABNORMAL WEIGHT GAIN ( 1 FDA reports)
ABSCESS BACTERIAL ( 1 FDA reports)
ACCIDENTAL POISONING ( 1 FDA reports)
ACCOMMODATION DISORDER ( 1 FDA reports)
ACID-BASE BALANCE DISORDER MIXED ( 1 FDA reports)
ACNE CYSTIC ( 1 FDA reports)
ACNE PUSTULAR ( 1 FDA reports)
ACQUIRED CLAW TOE ( 1 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ABNORMAL ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 1 FDA reports)
ACUTE ENDOCARDITIS ( 1 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
ACUTE PSYCHOSIS ( 1 FDA reports)
ADENOIDECTOMY ( 1 FDA reports)
ADENOMATOUS POLYPOSIS COLI ( 1 FDA reports)
ADJUSTMENT DISORDER WITH MIXED ANXIETY AND DEPRESSED MOOD ( 1 FDA reports)
ADRENAL ADENOMA ( 1 FDA reports)
ADRENOMEGALY ( 1 FDA reports)
AEROPHAGIA ( 1 FDA reports)
AFFERENT LOOP SYNDROME ( 1 FDA reports)
AGE INDETERMINATE MYOCARDIAL INFARCTION ( 1 FDA reports)
AGNOSIA ( 1 FDA reports)
AGORAPHOBIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
ALBUMIN GLOBULIN RATIO INCREASED ( 1 FDA reports)
ALCOHOL INTOLERANCE ( 1 FDA reports)
ALLERGIC SINUSITIS ( 1 FDA reports)
ALLODYNIA ( 1 FDA reports)
ALVEOLITIS ALLERGIC ( 1 FDA reports)
AMAUROSIS FUGAX ( 1 FDA reports)
AMMONIA INCREASED ( 1 FDA reports)
AMPUTATION STUMP PAIN ( 1 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 1 FDA reports)
ANAL PRURITUS ( 1 FDA reports)
ANALGESIC THERAPY ( 1 FDA reports)
ANASTOMOTIC LEAK ( 1 FDA reports)
ANGIOTENSIN CONVERTING ENZYME INCREASED ( 1 FDA reports)
ANHIDROSIS ( 1 FDA reports)
ANION GAP ABNORMAL ( 1 FDA reports)
ANION GAP INCREASED ( 1 FDA reports)
ANISOCHROMIA ( 1 FDA reports)
ANISOCYTOSIS ( 1 FDA reports)
ANKYLOSING SPONDYLITIS ( 1 FDA reports)
ANOSOGNOSIA ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL ABNORMAL ( 1 FDA reports)
AORTIC OCCLUSION ( 1 FDA reports)
AORTIC VALVE CALCIFICATION ( 1 FDA reports)
APGAR SCORE LOW ( 1 FDA reports)
APICECTOMY ( 1 FDA reports)
APLASIA PURE RED CELL ( 1 FDA reports)
APPLICATION SITE BURNING ( 1 FDA reports)
APPLICATION SITE DISCOLOURATION ( 1 FDA reports)
APPLICATION SITE SWELLING ( 1 FDA reports)
APTYALISM ( 1 FDA reports)
ARM AMPUTATION ( 1 FDA reports)
ARRESTED LABOUR ( 1 FDA reports)
ARTERECTOMY ( 1 FDA reports)
ARTERIAL HAEMORRHAGE ( 1 FDA reports)
ARTERIAL RUPTURE ( 1 FDA reports)
ARTERIAL STENOSIS LIMB ( 1 FDA reports)
ARTERIAL STENT INSERTION ( 1 FDA reports)
ARTERIOVENOUS FISTULA OPERATION ( 1 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 1 FDA reports)
ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
ARTHRITIS BACTERIAL ( 1 FDA reports)
ARTHROSCOPIC SURGERY ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
ASPIRATION PLEURAL CAVITY ( 1 FDA reports)
ATHETOSIS ( 1 FDA reports)
ATONIC URINARY BLADDER ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 1 FDA reports)
ATTENTION-SEEKING BEHAVIOUR ( 1 FDA reports)
AURA ( 1 FDA reports)
AURICULAR PERICHONDRITIS ( 1 FDA reports)
AURICULAR SWELLING ( 1 FDA reports)
AUTONOMIC FAILURE SYNDROME ( 1 FDA reports)
AVULSION FRACTURE ( 1 FDA reports)
AXILLARY MASS ( 1 FDA reports)
B-CELL LYMPHOMA RECURRENT ( 1 FDA reports)
BACTERIA STOOL IDENTIFIED ( 1 FDA reports)
BACTERIAL CULTURE POSITIVE ( 1 FDA reports)
BASEDOW'S DISEASE ( 1 FDA reports)
BENIGN HEPATIC NEOPLASM ( 1 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 1 FDA reports)
BENIGN TUMOUR EXCISION ( 1 FDA reports)
BETA GLOBULIN INCREASED ( 1 FDA reports)
BILE DUCT OBSTRUCTION ( 1 FDA reports)
BILIARY CIRRHOSIS ( 1 FDA reports)
BILIARY NEOPLASM ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BILIRUBIN URINE ( 1 FDA reports)
BIOPSY ARTERY ( 1 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 1 FDA reports)
BIOPSY SKIN ABNORMAL ( 1 FDA reports)
BIOPSY STOMACH ( 1 FDA reports)
BLADDER CATHETERISATION ( 1 FDA reports)
BLADDER NEOPLASM ( 1 FDA reports)
BLADDER NEOPLASM SURGERY ( 1 FDA reports)
BLEEDING TIME PROLONGED ( 1 FDA reports)
BLOOD ACID PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE ( 1 FDA reports)
BLOOD ARSENIC INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 1 FDA reports)
BLOOD CHOLESTEROL ( 1 FDA reports)
BLOOD ETHANOL INCREASED ( 1 FDA reports)
BLOOD FOLLICLE STIMULATING HORMONE DECREASED ( 1 FDA reports)
BLOOD GLUCOSE ( 1 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 1 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN POSITIVE ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 1 FDA reports)
BLOOD KETONE BODY PRESENT ( 1 FDA reports)
BLOOD LUTEINISING HORMONE DECREASED ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD MERCURY ABNORMAL ( 1 FDA reports)
BLOOD OSMOLARITY DECREASED ( 1 FDA reports)
BLOOD PARATHYROID HORMONE DECREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 1 FDA reports)
BLOOD PROLACTIN ABNORMAL ( 1 FDA reports)
BLOOD PYRUVIC ACID DECREASED ( 1 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 1 FDA reports)
BLOOD URIC ACID DECREASED ( 1 FDA reports)
BLOOD VISCOSITY INCREASED ( 1 FDA reports)
BODY HEIGHT ABNORMAL ( 1 FDA reports)
BODY HEIGHT INCREASED ( 1 FDA reports)
BONE FORMATION DECREASED ( 1 FDA reports)
BORDERLINE LEPROSY ( 1 FDA reports)
BRADYKINESIA ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
BRAIN HYPOXIA ( 1 FDA reports)
BRAIN SCAN ABNORMAL ( 1 FDA reports)
BRAIN STEM HAEMORRHAGE ( 1 FDA reports)
BRAIN STEM ISCHAEMIA ( 1 FDA reports)
BREAST CELLULITIS ( 1 FDA reports)
BREAST COSMETIC SURGERY ( 1 FDA reports)
BREAST DISCOMFORT ( 1 FDA reports)
BREAST INDURATION ( 1 FDA reports)
BREATHING-RELATED SLEEP DISORDER ( 1 FDA reports)
BRONCHIAL CARCINOMA ( 1 FDA reports)
BRONCHIAL HYPERACTIVITY ( 1 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 1 FDA reports)
BRONCHIAL IRRITATION ( 1 FDA reports)
BRONCHIAL OEDEMA ( 1 FDA reports)
BRONCHITIS VIRAL ( 1 FDA reports)
BRONCHOPLEURAL FISTULA ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 1 FDA reports)
BURN OESOPHAGEAL ( 1 FDA reports)
BURN OPERATION ( 1 FDA reports)
BURSA REMOVAL ( 1 FDA reports)
BUTTERFLY RASH ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)
CALCIPHYLAXIS ( 1 FDA reports)
CALCIUM DEFICIENCY ( 1 FDA reports)
CALCIUM IONISED ABNORMAL ( 1 FDA reports)
CALCULUS URETERIC ( 1 FDA reports)
CANCER GENE CARRIER ( 1 FDA reports)
CAPILLARY DISORDER ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 27.29 INCREASED ( 1 FDA reports)
CARBOXYHAEMOGLOBIN INCREASED ( 1 FDA reports)
CARCINOID SYNDROME ( 1 FDA reports)
CARCINOID TUMOUR ( 1 FDA reports)
CARCINOID TUMOUR OF THE STOMACH ( 1 FDA reports)
CARDIAC ANEURYSM ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
CARDIAC MURMUR FUNCTIONAL ( 1 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 1 FDA reports)
CARDIAC PSEUDOANEURYSM ( 1 FDA reports)
CARDIAC VALVE REPLACEMENT COMPLICATION ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
CARDIOTOXICITY ( 1 FDA reports)
CARDIOVASCULAR DECONDITIONING ( 1 FDA reports)
CARDITIS ( 1 FDA reports)
CAROTID ARTERY ATHEROMA ( 1 FDA reports)
CAROTID ARTERY DISSECTION ( 1 FDA reports)
CATHETER REMOVAL ( 1 FDA reports)
CATHETER SEPSIS ( 1 FDA reports)
CATHETER SITE ERYTHEMA ( 1 FDA reports)
CATHETER SITE PAIN ( 1 FDA reports)
CATHETER SITE RELATED REACTION ( 1 FDA reports)
CELL DEATH ( 1 FDA reports)
CELLULITIS GANGRENOUS ( 1 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM MASS ( 1 FDA reports)
CENTRAL OBESITY ( 1 FDA reports)
CENTRAL PAIN SYNDROME ( 1 FDA reports)
CEREBELLAR ATAXIA ( 1 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 1 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 1 FDA reports)
CEREBRAL ATHEROSCLEROSIS ( 1 FDA reports)
CERVIX CARCINOMA ( 1 FDA reports)
CHAPPED LIPS ( 1 FDA reports)
CHEILITIS ( 1 FDA reports)
CHEMICAL BURN OF SKIN ( 1 FDA reports)
CHEMOTHERAPY ( 1 FDA reports)
CHOLANGITIS SCLEROSING ( 1 FDA reports)
CHORIORETINAL ATROPHY ( 1 FDA reports)
CHROMOSOME ABNORMALITY ( 1 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 1 FDA reports)
CLONIC CONVULSION ( 1 FDA reports)
COGNITIVE DETERIORATION ( 1 FDA reports)
COGWHEEL RIGIDITY ( 1 FDA reports)
COLITIS VIRAL ( 1 FDA reports)
COLLATERAL CIRCULATION ( 1 FDA reports)
COLON CANCER METASTATIC ( 1 FDA reports)
COLONIC OBSTRUCTION ( 1 FDA reports)
COMA SCALE ABNORMAL ( 1 FDA reports)
COMPLEMENT FACTOR DECREASED ( 1 FDA reports)
CONDYLOMA ACUMINATUM ( 1 FDA reports)
CONGENITAL ATRIAL SEPTAL DEFECT ( 1 FDA reports)
CONGENITAL CORONARY ARTERY MALFORMATION ( 1 FDA reports)
CONGENITAL SCOLIOSIS ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
CONJUNCTIVITIS VIRAL ( 1 FDA reports)
CONSTRICTED AFFECT ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
CONTINUOUS POSITIVE AIRWAY PRESSURE ( 1 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 1 FDA reports)
CORNEAL DECOMPENSATION ( 1 FDA reports)
CORNEAL STRIAE ( 1 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 1 FDA reports)
CORONARY ARTERY PERFORATION ( 1 FDA reports)
CORONARY OSTIAL STENOSIS ( 1 FDA reports)
CORYNEBACTERIUM INFECTION ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CRYPTOCOCCOSIS ( 1 FDA reports)
CULTURE THROAT POSITIVE ( 1 FDA reports)
CULTURE WOUND POSITIVE ( 1 FDA reports)
CUTANEOUS VASCULITIS ( 1 FDA reports)
CYANOPSIA ( 1 FDA reports)
CYSTOSCOPY ( 1 FDA reports)
DEATH OF FRIEND ( 1 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 1 FDA reports)
DECREASED VIBRATORY SENSE ( 1 FDA reports)
DEFICIENCY ANAEMIA ( 1 FDA reports)
DELUSIONAL PERCEPTION ( 1 FDA reports)
DENTAL NECROSIS ( 1 FDA reports)
DEPENDENCE ON RESPIRATOR ( 1 FDA reports)
DEPRESSIVE SYMPTOM ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DERMATITIS PSORIASIFORM ( 1 FDA reports)
DETOXIFICATION ( 1 FDA reports)
DEVELOPMENTAL DELAY ( 1 FDA reports)
DEVICE BATTERY ISSUE ( 1 FDA reports)
DIABETIC BLINDNESS ( 1 FDA reports)
DIABETIC FOOT INFECTION ( 1 FDA reports)
DIABETIC RETINAL OEDEMA ( 1 FDA reports)
DIET REFUSAL ( 1 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA RECURRENT ( 1 FDA reports)
DISSEMINATED LARGE CELL LYMPHOMA ( 1 FDA reports)
DISSOCIATION ( 1 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DRUG CLEARANCE DECREASED ( 1 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 1 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 1 FDA reports)
DUODENAL NEOPLASM ( 1 FDA reports)
DYSPNOEA EXACERBATED ( 1 FDA reports)
DYSSOMNIA ( 1 FDA reports)
EAR INFECTION VIRAL ( 1 FDA reports)
EARLY MORNING AWAKENING ( 1 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
ECTOPIC PREGNANCY ( 1 FDA reports)
EDUCATIONAL PROBLEM ( 1 FDA reports)
EJACULATION FAILURE ( 1 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM QT INTERVAL ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT DEPRESSION ( 1 FDA reports)
ELEVATED MOOD ( 1 FDA reports)
EMPHYSEMATOUS BULLA ( 1 FDA reports)
ENDOMETRIAL CANCER ( 1 FDA reports)
ENDOMETRIAL DISORDER ( 1 FDA reports)
ENDOSCOPY ( 1 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ABNORMAL ( 1 FDA reports)
ENGRAFT FAILURE ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 1 FDA reports)
EPIGASTRIC DISCOMFORT ( 1 FDA reports)
ERYTHEMA NODOSUM ( 1 FDA reports)
EXPOSURE TO ALLERGEN ( 1 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 1 FDA reports)
EXTRADURAL HAEMATOMA ( 1 FDA reports)
EXTRAOCULAR MUSCLE PARESIS ( 1 FDA reports)
EXTREMITY NECROSIS ( 1 FDA reports)
EXTRUSION OF DEVICE ( 1 FDA reports)
EYE INFECTION VIRAL ( 1 FDA reports)
EYE OEDEMA ( 1 FDA reports)
EYELID DISORDER ( 1 FDA reports)
FACTOR VIII DEFICIENCY ( 1 FDA reports)
FANCONI SYNDROME ACQUIRED ( 1 FDA reports)
FAT NECROSIS ( 1 FDA reports)
FEAR OF DISEASE ( 1 FDA reports)
FEBRILE CONVULSION ( 1 FDA reports)
FEEDING DISORDER NEONATAL ( 1 FDA reports)
FEEDING TUBE COMPLICATION ( 1 FDA reports)
FINGER REPAIR OPERATION ( 1 FDA reports)
FLAT AFFECT ( 1 FDA reports)
FONTANELLE DEPRESSED ( 1 FDA reports)
FOOT AMPUTATION ( 1 FDA reports)
FOREIGN BODY IN EYE ( 1 FDA reports)
FRONTAL SINUS OPERATIONS ( 1 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 1 FDA reports)
FUNGAEMIA ( 1 FDA reports)
FUNGUS CULTURE POSITIVE ( 1 FDA reports)
FURUNCLE ( 1 FDA reports)
GALLBLADDER CANCER ( 1 FDA reports)
GALLBLADDER INJURY ( 1 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 1 FDA reports)
GALLOP RHYTHM PRESENT ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 1 FDA reports)
GAS GANGRENE ( 1 FDA reports)
GASTRIC BYPASS ( 1 FDA reports)
GASTRIC HYPOMOTILITY ( 1 FDA reports)
GASTRIC NEOPLASM ( 1 FDA reports)
GASTRIC OPERATION ( 1 FDA reports)
GASTRIC PERFORATION ( 1 FDA reports)
GASTRIC VARICES ( 1 FDA reports)
GASTROENTERITIS HELICOBACTER ( 1 FDA reports)
GASTROENTERITIS NONINFECTIOUS ( 1 FDA reports)
GASTROENTERITIS NOROVIRUS ( 1 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 1 FDA reports)
GASTROINTESTINAL INJURY ( 1 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 1 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 1 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 1 FDA reports)
GASTROINTESTINAL VIRAL INFECTION ( 1 FDA reports)
GASTROOESOPHAGEAL SPHINCTER INSUFFICIENCY ( 1 FDA reports)
GASTROSTOMY FAILURE ( 1 FDA reports)
GENITAL DISCOMFORT ( 1 FDA reports)
GENITAL PAIN ( 1 FDA reports)
GENITAL RASH ( 1 FDA reports)
GESTATIONAL DIABETES ( 1 FDA reports)
GINGIVAL HYPOPLASIA ( 1 FDA reports)
GLOMERULONEPHRITIS ( 1 FDA reports)
GLOMERULONEPHRITIS MINIMAL LESION ( 1 FDA reports)
GLOSSOPHARYNGEAL NERVE PARALYSIS ( 1 FDA reports)
GLUCOSE TOLERANCE DECREASED ( 1 FDA reports)
GRAM STAIN POSITIVE ( 1 FDA reports)
GRANULOCYTE COUNT INCREASED ( 1 FDA reports)
GYNAECOMASTIA ( 1 FDA reports)
H1N1 INFLUENZA ( 1 FDA reports)
HAEMATOLOGY TEST ABNORMAL ( 1 FDA reports)
HAEMOGLOBIN ( 1 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 1 FDA reports)
HAEMORRHAGIC DISORDER ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HAIR COLOUR CHANGES ( 1 FDA reports)
HEART VALVE CALCIFICATION ( 1 FDA reports)
HEAT STROKE ( 1 FDA reports)
HEAT THERAPY ( 1 FDA reports)
HELICOBACTER TEST POSITIVE ( 1 FDA reports)
HEMIVERTEBRA ( 1 FDA reports)
HEPATIC ATROPHY ( 1 FDA reports)
HEPATIC CALCIFICATION ( 1 FDA reports)
HEPATIC PAIN ( 1 FDA reports)
HEPATIC TRAUMA ( 1 FDA reports)
HEPATIC VEIN THROMBOSIS ( 1 FDA reports)
HEPATITIS B POSITIVE ( 1 FDA reports)
HEPATITIS C POSITIVE ( 1 FDA reports)
HEPATORENAL FAILURE ( 1 FDA reports)
HEPATORENAL SYNDROME ( 1 FDA reports)
HEREDITARY ANGIOEDEMA ( 1 FDA reports)
HERNIA HIATUS REPAIR ( 1 FDA reports)
HETEROPHORIA ( 1 FDA reports)
HIGH FREQUENCY ABLATION ( 1 FDA reports)
HILAR LYMPHADENOPATHY ( 1 FDA reports)
HISTRIONIC PERSONALITY DISORDER ( 1 FDA reports)
HODGKIN'S DISEASE ( 1 FDA reports)
HODGKIN'S DISEASE STAGE IV ( 1 FDA reports)
HOMANS' SIGN POSITIVE ( 1 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 1 FDA reports)
HUNTINGTON'S DISEASE ( 1 FDA reports)
HYPEREMESIS GRAVIDARUM ( 1 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 1 FDA reports)
HYPERPLASTIC CHOLECYSTOPATHY ( 1 FDA reports)
HYPERSPLENISM ACQUIRED ( 1 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 1 FDA reports)
HYPERTHERMIA MALIGNANT ( 1 FDA reports)
HYPERTROPHIC SCAR ( 1 FDA reports)
HYPERTROPHY ( 1 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 1 FDA reports)
HYPOGONADISM MALE ( 1 FDA reports)
HYPOLIPIDAEMIA ( 1 FDA reports)
HYPOPERFUSION ( 1 FDA reports)
HYPOPHONESIS ( 1 FDA reports)
HYPOPHYSITIS ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
IGA NEPHROPATHY ( 1 FDA reports)
ILEOSTOMY ( 1 FDA reports)
ILLOGICAL THINKING ( 1 FDA reports)
IMMOBILIZATION PROLONGED ( 1 FDA reports)
IMMUNE TOLERANCE INDUCTION ( 1 FDA reports)
IMPAIRED FASTING GLUCOSE ( 1 FDA reports)
IMPLANT SITE ABSCESS ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR MALFUNCTION ( 1 FDA reports)
INAPPROPRIATE AFFECT ( 1 FDA reports)
INBORN ERROR OF METABOLISM ( 1 FDA reports)
INCISION SITE ERYTHEMA ( 1 FDA reports)
INCISIONAL HERNIA REPAIR ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 1 FDA reports)
INFANTILE APNOEIC ATTACK ( 1 FDA reports)
INFECTED CYST ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INFECTIVE MYOSITIS ( 1 FDA reports)
INFLUENZA IMMUNISATION ( 1 FDA reports)
INFUSION SITE BRUISING ( 1 FDA reports)
INFUSION SITE ERYTHEMA ( 1 FDA reports)
INFUSION SITE IRRITATION ( 1 FDA reports)
INFUSION SITE MASS ( 1 FDA reports)
INFUSION SITE PHLEBITIS ( 1 FDA reports)
INFUSION SITE PRURITUS ( 1 FDA reports)
INFUSION SITE RASH ( 1 FDA reports)
INGROWING NAIL ( 1 FDA reports)
INJECTION SITE BRUISING ( 1 FDA reports)
INJECTION SITE BURNING ( 1 FDA reports)
INJECTION SITE FIBROSIS ( 1 FDA reports)
INJECTION SITE PARAESTHESIA ( 1 FDA reports)
INJURY CORNEAL ( 1 FDA reports)
INSULIN-LIKE GROWTH FACTOR DECREASED ( 1 FDA reports)
INTENTION TREMOR ( 1 FDA reports)
INTERMITTENT EXPLOSIVE DISORDER ( 1 FDA reports)
INTERTRIGO ( 1 FDA reports)
INTERTRIGO CANDIDA ( 1 FDA reports)
INTERVERTEBRAL DISC INJURY ( 1 FDA reports)
INTESTINAL FISTULA ( 1 FDA reports)
INTESTINAL HAEMORRHAGE ( 1 FDA reports)
INTESTINAL HYPERMOTILITY ( 1 FDA reports)
INTESTINAL INFARCTION ( 1 FDA reports)
INTESTINAL ISCHAEMIA ( 1 FDA reports)
INTESTINAL SPASM ( 1 FDA reports)
INTESTINAL STOMA SITE BLEEDING ( 1 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 1 FDA reports)
INTRACARDIAC MASS ( 1 FDA reports)
INTRATHECAL PUMP INSERTION ( 1 FDA reports)
INVESTIGATION ABNORMAL ( 1 FDA reports)
IRITIS ( 1 FDA reports)
IRON OVERLOAD ( 1 FDA reports)
IRREGULAR SLEEP PHASE ( 1 FDA reports)
ISCHAEMIC NEUROPATHY ( 1 FDA reports)
IUCD COMPLICATION ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
JAW LESION EXCISION ( 1 FDA reports)
JOINT ARTHROPLASTY ( 1 FDA reports)
JUGULAR VEIN THROMBOSIS ( 1 FDA reports)
KERATORHEXIS ( 1 FDA reports)
KERATOSIS PILARIS ( 1 FDA reports)
KIDNEY MALROTATION ( 1 FDA reports)
LABILE BLOOD PRESSURE ( 1 FDA reports)
LAEVOCARDIA ( 1 FDA reports)
LANGERHANS' CELL GRANULOMATOSIS ( 1 FDA reports)
LARYNGOPHARYNGITIS ( 1 FDA reports)
LAXATIVE ABUSE ( 1 FDA reports)
LAZINESS ( 1 FDA reports)
LEARNING DISORDER ( 1 FDA reports)
LEPROSY ( 1 FDA reports)
LICE INFESTATION ( 1 FDA reports)
LIFE SUPPORT ( 1 FDA reports)
LIMB DEFORMITY ( 1 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 1 FDA reports)
LIPASE DECREASED ( 1 FDA reports)
LIPOMA EXCISION ( 1 FDA reports)
LISTERIOSIS ( 1 FDA reports)
LIVER FUNCTION TEST ( 1 FDA reports)
LONG QT SYNDROME ( 1 FDA reports)
LOOSE BODY IN JOINT ( 1 FDA reports)
LOSS OF CONTROL OF LEGS ( 1 FDA reports)
LOWER LIMB DEFORMITY ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION FUNGAL ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
LUMBAR HERNIA ( 1 FDA reports)
LUNG LOBECTOMY ( 1 FDA reports)
LUPUS PNEUMONITIS ( 1 FDA reports)
LYMPH NODE PAIN ( 1 FDA reports)
LYMPHADENECTOMY ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
LYMPHOID TISSUE OPERATION ( 1 FDA reports)
MACROGLOSSIA ( 1 FDA reports)
MACULAR HOLE ( 1 FDA reports)
MACULOPATHY ( 1 FDA reports)
MADAROSIS ( 1 FDA reports)
MAGNESIUM METABOLISM DISORDER ( 1 FDA reports)
MALE SEXUAL DYSFUNCTION ( 1 FDA reports)
MALIGNANT ASCITES ( 1 FDA reports)
MAMMOPLASTY ( 1 FDA reports)
MASKED FACIES ( 1 FDA reports)
MASS EXCISION ( 1 FDA reports)
MAY-THURNER SYNDROME ( 1 FDA reports)
MECHANICAL URTICARIA ( 1 FDA reports)
MEGAKARYOCYTES DECREASED ( 1 FDA reports)
MEIGE'S SYNDROME ( 1 FDA reports)
MENINGIOMA BENIGN ( 1 FDA reports)
MENOMETRORRHAGIA ( 1 FDA reports)
MENOPAUSAL DISORDER ( 1 FDA reports)
MENOPAUSAL SYMPTOMS ( 1 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 1 FDA reports)
METAL POISONING ( 1 FDA reports)
METASTASES TO BLADDER ( 1 FDA reports)
METASTASES TO CHEST WALL ( 1 FDA reports)
METASTASES TO MENINGES ( 1 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 1 FDA reports)
METHAEMOGLOBINAEMIA ( 1 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST ( 1 FDA reports)
MICROALBUMINURIA ( 1 FDA reports)
MICROCOCCUS INFECTION ( 1 FDA reports)
MICROCYTOSIS ( 1 FDA reports)
MICROVASCULAR ANGINA ( 1 FDA reports)
MILD MENTAL RETARDATION ( 1 FDA reports)
MITRAL VALVE DISEASE MIXED ( 1 FDA reports)
MIXED INCONTINENCE ( 1 FDA reports)
MONOCLONAL GAMMOPATHY ( 1 FDA reports)
MONONEUROPATHY ( 1 FDA reports)
MONONEUROPATHY MULTIPLEX ( 1 FDA reports)
MUCOSAL ULCERATION ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MUCOUS STOOLS ( 1 FDA reports)
MULTIPLE SYSTEM ATROPHY ( 1 FDA reports)
MUSCLE ENZYME INCREASED ( 1 FDA reports)
MYELITIS ( 1 FDA reports)
MYELITIS TRANSVERSE ( 1 FDA reports)
MYELOPATHY ( 1 FDA reports)
MYOCARDIAL FIBROSIS ( 1 FDA reports)
MYOCARDITIS ( 1 FDA reports)
MYOGLOBIN URINE ( 1 FDA reports)
MYOPATHY STEROID ( 1 FDA reports)
MYOSCLEROSIS ( 1 FDA reports)
MYOSITIS OSSIFICANS ( 1 FDA reports)
NAEVUS CELL NAEVUS ( 1 FDA reports)
NAIL DISCOLOURATION ( 1 FDA reports)
NAIL OPERATION ( 1 FDA reports)
NASAL INFLAMMATION ( 1 FDA reports)
NASAL ODOUR ( 1 FDA reports)
NASAL SEPTUM ULCERATION ( 1 FDA reports)
NEAR DROWNING ( 1 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 1 FDA reports)
NEOPLASM SKIN ( 1 FDA reports)
NEPHRECTOMY ( 1 FDA reports)
NEPHROPATHY TOXIC ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NERVE ROOT COMPRESSION ( 1 FDA reports)
NEUROGENIC BOWEL ( 1 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
NEUROMYELITIS OPTICA ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
NIGHT BLINDNESS ( 1 FDA reports)
NIPPLE DISORDER ( 1 FDA reports)
NO ADVERSE EFFECT ( 1 FDA reports)
NO ADVERSE REACTION ( 1 FDA reports)
NOCTURNAL DYSPNOEA ( 1 FDA reports)
NODAL RHYTHM ( 1 FDA reports)
NON-ALCOHOLIC STEATOHEPATITIS ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE III ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IIIB ( 1 FDA reports)
OBSTRUCTION GASTRIC ( 1 FDA reports)
OCCIPITAL NEURALGIA ( 1 FDA reports)
OCCUPATIONAL PROBLEM ENVIRONMENTAL ( 1 FDA reports)
OCULAR VASCULAR DISORDER ( 1 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 1 FDA reports)
OESOPHAGEAL CARCINOMA ( 1 FDA reports)
OESOPHAGEAL HYPOMOTILITY ( 1 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 1 FDA reports)
OESOPHAGEAL PERFORATION ( 1 FDA reports)
OESOPHAGEAL SPASM ( 1 FDA reports)
OMENTECTOMY ( 1 FDA reports)
ONYCHOCLASIS ( 1 FDA reports)
ONYCHOPHAGIA ( 1 FDA reports)
OPTIC ATROPHY ( 1 FDA reports)
ORAL MUCOSAL BLISTERING ( 1 FDA reports)
ORAL PRURITUS ( 1 FDA reports)
ORGANIC ERECTILE DYSFUNCTION ( 1 FDA reports)
OROPHARYNGEAL SWELLING ( 1 FDA reports)
ORTHOSTATIC INTOLERANCE ( 1 FDA reports)
OSTEOARTHROPATHY ( 1 FDA reports)
OSTEOCHONDROSIS ( 1 FDA reports)
OSTEOMALACIA ( 1 FDA reports)
OSTEOMYELITIS BACTERIAL ( 1 FDA reports)
OSTEOPOROSIS POSTMENOPAUSAL ( 1 FDA reports)
OSTEOPOROTIC FRACTURE ( 1 FDA reports)
OVARIAN ENLARGEMENT ( 1 FDA reports)
OVARIAN FAILURE ( 1 FDA reports)
OXYGEN SATURATION ABNORMAL ( 1 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 1 FDA reports)
PALATAL OEDEMA ( 1 FDA reports)
PANCREAS TRANSPLANT ( 1 FDA reports)
PANCREATIC ATROPHY ( 1 FDA reports)
PANCREATIC CYST ( 1 FDA reports)
PANCREATIC DUCT DILATATION ( 1 FDA reports)
PANCREATIC ENLARGEMENT ( 1 FDA reports)
PANCREATIC NEOPLASM ( 1 FDA reports)
PAPILLA OF VATER STENOSIS ( 1 FDA reports)
PAPILLARY MUSCLE DISORDER ( 1 FDA reports)
PAPILLOMA EXCISION ( 1 FDA reports)
PARADOXICAL DRUG REACTION ( 1 FDA reports)
PARAPARESIS ( 1 FDA reports)
PARAPSORIASIS ( 1 FDA reports)
PARATHYROID DISORDER ( 1 FDA reports)
PARENT-CHILD PROBLEM ( 1 FDA reports)
PATELLA FRACTURE ( 1 FDA reports)
PEAK EXPIRATORY FLOW RATE DECREASED ( 1 FDA reports)
PELVIC FLOOR MUSCLE WEAKNESS ( 1 FDA reports)
PELVIC INFECTION ( 1 FDA reports)
PELVIC MASS ( 1 FDA reports)
PENILE WART ( 1 FDA reports)
PENIS DISORDER ( 1 FDA reports)
PERFORMANCE STATUS DECREASED ( 1 FDA reports)
PERICARDIAL DISEASE ( 1 FDA reports)
PERICARDIAL FIBROSIS ( 1 FDA reports)
PERIODIC LIMB MOVEMENT DISORDER ( 1 FDA reports)
PERITONEAL DIALYSIS ( 1 FDA reports)
PERITONEAL EFFUSION ( 1 FDA reports)
PERITONITIS BACTERIAL ( 1 FDA reports)
PERITONITIS SCLEROSING ( 1 FDA reports)
PERIVASCULAR DERMATITIS ( 1 FDA reports)
PHARYNGEAL ABSCESS ( 1 FDA reports)
PHARYNGEAL HYPOAESTHESIA ( 1 FDA reports)
PHARYNGEAL NEOPLASM ( 1 FDA reports)
PHLEBOLITH ( 1 FDA reports)
PHOBIA OF DRIVING ( 1 FDA reports)
PLAGIOCEPHALY ( 1 FDA reports)
PLASMA CELLS INCREASED ( 1 FDA reports)
PLASMA VISCOSITY DECREASED ( 1 FDA reports)
PLATELET AGGREGATION ABNORMAL ( 1 FDA reports)
PLATELET FUNCTION TEST ABNORMAL ( 1 FDA reports)
PLATELET MORPHOLOGY ABNORMAL ( 1 FDA reports)
PLEURAL ADHESION ( 1 FDA reports)
PLEURODESIS ( 1 FDA reports)
PLEUROPERICARDITIS ( 1 FDA reports)
PNEUMOCOCCAL SEPSIS ( 1 FDA reports)
PNEUMONIA MYCOPLASMAL ( 1 FDA reports)
PNEUMONIA NECROTISING ( 1 FDA reports)
PO2 INCREASED ( 1 FDA reports)
POIKILOCYTOSIS ( 1 FDA reports)
POLYMEDICATION ( 1 FDA reports)
POLYMENORRHOEA ( 1 FDA reports)
PORPHYRIA NON-ACUTE ( 1 FDA reports)
PORTAL HYPERTENSION ( 1 FDA reports)
PORTAL VEIN THROMBOSIS ( 1 FDA reports)
POST PROCEDURAL DIARRHOEA ( 1 FDA reports)
POST PROCEDURAL SEPSIS ( 1 FDA reports)
POST-THORACOTOMY PAIN SYNDROME ( 1 FDA reports)
POST-TRAUMATIC HEADACHE ( 1 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 1 FDA reports)
POSTOPERATIVE CONSTIPATION ( 1 FDA reports)
POSTOPERATIVE FEVER ( 1 FDA reports)
POSTOPERATIVE ILEUS ( 1 FDA reports)
POSTURING ( 1 FDA reports)
POTENTIATING DRUG INTERACTION ( 1 FDA reports)
PRE-EXISTING DISEASE ( 1 FDA reports)
PRECANCEROUS CELLS PRESENT ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
PREMATURE LABOUR ( 1 FDA reports)
PREMATURE RECOVERY FROM ANAESTHESIA ( 1 FDA reports)
PREMENSTRUAL SYNDROME ( 1 FDA reports)
PRESBYOESOPHAGUS ( 1 FDA reports)
PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
PROCEDURAL HYPERTENSION ( 1 FDA reports)
PROCEDURAL HYPOTENSION ( 1 FDA reports)
PROCEDURAL SITE REACTION ( 1 FDA reports)
PROCTOCOLECTOMY ( 1 FDA reports)
PRODUCT COATING ISSUE ( 1 FDA reports)
PRODUCT TASTE ABNORMAL ( 1 FDA reports)
PROGESTERONE DECREASED ( 1 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 1 FDA reports)
PROSTATIC DISORDER ( 1 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 1 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PRURITUS GENITAL ( 1 FDA reports)
PSEUDOMYXOMA PERITONEI ( 1 FDA reports)
PSYCHOGENIC ERECTILE DYSFUNCTION ( 1 FDA reports)
PSYCHOLOGICAL ABUSE ( 1 FDA reports)
PSYCHOMOTOR RETARDATION ( 1 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 1 FDA reports)
PSYCHOSOMATIC DISEASE ( 1 FDA reports)
PSYCHOTIC BEHAVIOUR ( 1 FDA reports)
PULMONARY ARTERY STENOSIS CONGENITAL ( 1 FDA reports)
PULMONARY CALCIFICATION ( 1 FDA reports)
PULMONARY MALFORMATION ( 1 FDA reports)
PULMONARY MICROEMBOLI ( 1 FDA reports)
PULMONARY VENO-OCCLUSIVE DISEASE ( 1 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 1 FDA reports)
PUPILS UNEQUAL ( 1 FDA reports)
PYELONEPHRITIS ACUTE ( 1 FDA reports)
QRS AXIS ABNORMAL ( 1 FDA reports)
RADIAL NERVE INJURY ( 1 FDA reports)
RADIATION INJURY ( 1 FDA reports)
RADIATION RETINOPATHY ( 1 FDA reports)
RADICULITIS CERVICAL ( 1 FDA reports)
RATHKE'S CLEFT CYST ( 1 FDA reports)
REACTION TO AZO-DYES ( 1 FDA reports)
REBOUND EFFECT ( 1 FDA reports)
RECTAL DISCHARGE ( 1 FDA reports)
RECTAL FISSURE ( 1 FDA reports)
RED BLOOD CELL ABNORMALITY ( 1 FDA reports)
RED BLOOD CELLS SEMEN ( 1 FDA reports)
REGURGITATION ( 1 FDA reports)
REGURGITATION OF FOOD ( 1 FDA reports)
RELATIONSHIP BREAKDOWN ( 1 FDA reports)
RENAL ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL CANCER ( 1 FDA reports)
RENAL CELL CARCINOMA ( 1 FDA reports)
RENAL CELL CARCINOMA RECURRENT ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE III ( 1 FDA reports)
RENAL CYST HAEMORRHAGE ( 1 FDA reports)
RESPIRATORY ACIDOSIS ( 1 FDA reports)
RESPIRATORY ALKALOSIS ( 1 FDA reports)
RESPIRATORY RATE DECREASED ( 1 FDA reports)
RESPIRATORY TRACT INFECTION BACTERIAL ( 1 FDA reports)
RETICULOCYTOPENIA ( 1 FDA reports)
RETINAL ARTERY OCCLUSION ( 1 FDA reports)
RETINAL DISORDER ( 1 FDA reports)
RETINAL OEDEMA ( 1 FDA reports)
REVERSIBLE ISCHAEMIC NEUROLOGICAL DEFICIT ( 1 FDA reports)
RHEUMATIC HEART DISEASE ( 1 FDA reports)
RHINALGIA ( 1 FDA reports)
RIGHT ATRIAL DILATATION ( 1 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
SALIVARY GLAND CYST ( 1 FDA reports)
SALMONELLOSIS ( 1 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 1 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 1 FDA reports)
SCROTAL IRRITATION ( 1 FDA reports)
SCROTAL MASS ( 1 FDA reports)
SCROTAL OEDEMA ( 1 FDA reports)
SCROTAL PAIN ( 1 FDA reports)
SECONDARY ADRENOCORTICAL INSUFFICIENCY ( 1 FDA reports)
SEMEN VISCOSITY ABNORMAL ( 1 FDA reports)
SEPSIS NEONATAL ( 1 FDA reports)
SEPTIC EMBOLUS ( 1 FDA reports)
SERONEGATIVE ARTHRITIS ( 1 FDA reports)
SEROSITIS ( 1 FDA reports)
SERUM SEROTONIN INCREASED ( 1 FDA reports)
SIALOADENITIS ( 1 FDA reports)
SIALOMETAPLASIA ( 1 FDA reports)
SINUSITIS FUNGAL ( 1 FDA reports)
SKIN HAEMORRHAGE ( 1 FDA reports)
SKIN INFLAMMATION ( 1 FDA reports)
SKIN NODULE ( 1 FDA reports)
SKIN TOXICITY ( 1 FDA reports)
SKIN TURGOR DECREASED ( 1 FDA reports)
SLEEP PHASE RHYTHM DISTURBANCE ( 1 FDA reports)
SLEEP TALKING ( 1 FDA reports)
SLUGGISHNESS ( 1 FDA reports)
SMALL BOWEL ANGIOEDEMA ( 1 FDA reports)
SMALL CELL CARCINOMA ( 1 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
SMALL INTESTINE CARCINOMA ( 1 FDA reports)
SMOOTH MUSCLE ANTIBODY POSITIVE ( 1 FDA reports)
SOCIAL PHOBIA ( 1 FDA reports)
SOFT TISSUE HAEMORRHAGE ( 1 FDA reports)
SOFT TISSUE INFLAMMATION ( 1 FDA reports)
SOMATIC DELUSION ( 1 FDA reports)
SPERMATOCELE ( 1 FDA reports)
SPLENIC ABSCESS ( 1 FDA reports)
SPLENIC VEIN THROMBOSIS ( 1 FDA reports)
SPONDYLITIC MYELOPATHY ( 1 FDA reports)
SPUTUM ABNORMAL ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
SPUTUM INCREASED ( 1 FDA reports)
STENOTROPHOMONAS INFECTION ( 1 FDA reports)
STERNAL FRACTURE ( 1 FDA reports)
STILLBIRTH ( 1 FDA reports)
STOMA SITE REACTION ( 1 FDA reports)
STOMACH MASS ( 1 FDA reports)
STREPTOCOCCAL SEPSIS ( 1 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 1 FDA reports)
STRESS CARDIOMYOPATHY ( 1 FDA reports)
STRIDOR ( 1 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 1 FDA reports)
SUDDEN VISUAL LOSS ( 1 FDA reports)
SULPHAEMOGLOBINAEMIA ( 1 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 1 FDA reports)
SUPPRESSED LACTATION ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
SUTURE RUPTURE ( 1 FDA reports)
SYSTEMIC CANDIDA ( 1 FDA reports)
SYSTOLIC DYSFUNCTION ( 1 FDA reports)
SYSTOLIC HYPERTENSION ( 1 FDA reports)
TEMPERATURE PERCEPTION TEST DECREASED ( 1 FDA reports)
TERMINAL STATE ( 1 FDA reports)
TETANY ( 1 FDA reports)
THEFT ( 1 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE FOR UNAPPROVED INDICATION ( 1 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 1 FDA reports)
THOUGHT BLOCKING ( 1 FDA reports)
THROMBOEMBOLIC STROKE ( 1 FDA reports)
THROMBOSIS IN DEVICE ( 1 FDA reports)
THROMBOTIC STROKE ( 1 FDA reports)
THYROTOXIC CRISIS ( 1 FDA reports)
THYROXINE FREE DECREASED ( 1 FDA reports)
THYROXINE INCREASED ( 1 FDA reports)
TINEA VERSICOLOUR ( 1 FDA reports)
TOE DEFORMITY ( 1 FDA reports)
TONGUE DRY ( 1 FDA reports)
TONSILLAR HYPERTROPHY ( 1 FDA reports)
TONSILLECTOMY ( 1 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO INCREASED ( 1 FDA reports)
TOTAL HYSTERECTOMY ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TOXIC SHOCK SYNDROME ( 1 FDA reports)
TOXOPLASMA SEROLOGY ( 1 FDA reports)
TRACHEAL OEDEMA ( 1 FDA reports)
TRACHEAL STENOSIS ( 1 FDA reports)
TRACHEOBRONCHITIS ( 1 FDA reports)
TRACHEOSTOMY ( 1 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 1 FDA reports)
TRANSFUSION REACTION ( 1 FDA reports)
TRI-IODOTHYRONINE INCREASED ( 1 FDA reports)
TRICUSPID VALVE DISEASE ( 1 FDA reports)
TUBAL LIGATION ( 1 FDA reports)
TYPE I HYPERSENSITIVITY ( 1 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 1 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 1 FDA reports)
UNEXPECTED THERAPEUTIC DRUG EFFECT ( 1 FDA reports)
UNWANTED AWARENESS DURING ANAESTHESIA ( 1 FDA reports)
UPPER EXTREMITY MASS ( 1 FDA reports)
UPPER MOTOR NEURONE LESION ( 1 FDA reports)
URETERAL DISORDER ( 1 FDA reports)
URETERAL SPASM ( 1 FDA reports)
URETERIC CANCER ( 1 FDA reports)
URETHRAL DILATATION ( 1 FDA reports)
URETHRAL PAIN ( 1 FDA reports)
URETHRAL SYNDROME ( 1 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 1 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 1 FDA reports)
URINE BILIRUBIN INCREASED ( 1 FDA reports)
URINE OSMOLARITY INCREASED ( 1 FDA reports)
URINE OUTPUT INCREASED ( 1 FDA reports)
UROBILIN URINE ( 1 FDA reports)
UROBILIN URINE PRESENT ( 1 FDA reports)
UROGRAM ( 1 FDA reports)
USE OF ACCESSORY RESPIRATORY MUSCLES ( 1 FDA reports)
UTERINE CANCER ( 1 FDA reports)
UTERINE CONTRACTIONS ABNORMAL ( 1 FDA reports)
UTERINE ENLARGEMENT ( 1 FDA reports)
UTERINE MASS ( 1 FDA reports)
VAGINAL CANDIDIASIS ( 1 FDA reports)
VAGINAL CYST ( 1 FDA reports)
VAGINAL HYSTERECTOMY ( 1 FDA reports)
VAGINAL LEUKOPLAKIA ( 1 FDA reports)
VAGINAL ODOUR ( 1 FDA reports)
VAGINAL PAIN ( 1 FDA reports)
VAGINITIS ATROPHIC ( 1 FDA reports)
VAGUS NERVE DISORDER ( 1 FDA reports)
VARICELLA ( 1 FDA reports)
VASCULAR HEADACHE ( 1 FDA reports)
VASCULAR PSEUDOANEURYSM ( 1 FDA reports)
VASCULITIC RASH ( 1 FDA reports)
VASOSPASM ( 1 FDA reports)
VENOUS INJURY ( 1 FDA reports)
VERBAL ABUSE ( 1 FDA reports)
VERTEBRAL INJURY ( 1 FDA reports)
VERY LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
VESTIBULITIS ( 1 FDA reports)
VIRAL MYOSITIS ( 1 FDA reports)
VISUAL BRIGHTNESS ( 1 FDA reports)
VITAMIN B12 DECREASED ( 1 FDA reports)
VITAMIN B12 INCREASED ( 1 FDA reports)
VITILIGO ( 1 FDA reports)
VOCAL CORD NEOPLASM ( 1 FDA reports)
VOCAL CORD THICKENING ( 1 FDA reports)
VOLUME BLOOD DECREASED ( 1 FDA reports)
VOLUME BLOOD INCREASED ( 1 FDA reports)
VULVOVAGINAL DRYNESS ( 1 FDA reports)
VULVOVAGINAL PAIN ( 1 FDA reports)
WALKING DISABILITY ( 1 FDA reports)
WART EXCISION ( 1 FDA reports)
WEANING FAILURE ( 1 FDA reports)
WEGENER'S GRANULOMATOSIS ( 1 FDA reports)
WEIGHT GAIN POOR ( 1 FDA reports)
WEIGHT LOSS DIET ( 1 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
WHITE BLOOD CELLS URINE ( 1 FDA reports)
WHITE CLOT SYNDROME ( 1 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 1 FDA reports)
WOUND NECROSIS ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)
X-RAY ABNORMAL ( 1 FDA reports)