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

PAIN ( 1271 FDA reports)
NAUSEA ( 1108 FDA reports)
HEADACHE ( 995 FDA reports)
DYSPNOEA ( 990 FDA reports)
DIZZINESS ( 953 FDA reports)
ANXIETY ( 908 FDA reports)
FATIGUE ( 901 FDA reports)
DEPRESSION ( 824 FDA reports)
VOMITING ( 815 FDA reports)
DIARRHOEA ( 770 FDA reports)
FALL ( 760 FDA reports)
ASTHENIA ( 753 FDA reports)
PYREXIA ( 707 FDA reports)
ARTHRALGIA ( 706 FDA reports)
DRUG INEFFECTIVE ( 663 FDA reports)
CONFUSIONAL STATE ( 662 FDA reports)
PNEUMONIA ( 629 FDA reports)
BACK PAIN ( 620 FDA reports)
COMPLETED SUICIDE ( 619 FDA reports)
DRUG INTERACTION ( 618 FDA reports)
PAIN IN EXTREMITY ( 594 FDA reports)
ABDOMINAL PAIN ( 581 FDA reports)
OEDEMA PERIPHERAL ( 581 FDA reports)
MALAISE ( 572 FDA reports)
WEIGHT DECREASED ( 569 FDA reports)
INSOMNIA ( 554 FDA reports)
CHEST PAIN ( 546 FDA reports)
TREMOR ( 531 FDA reports)
SOMNOLENCE ( 520 FDA reports)
ANAEMIA ( 501 FDA reports)
HYPOAESTHESIA ( 499 FDA reports)
HYPERTENSION ( 498 FDA reports)
HYPERHIDROSIS ( 474 FDA reports)
CARDIAC ARREST ( 473 FDA reports)
CONSTIPATION ( 456 FDA reports)
CONVULSION ( 449 FDA reports)
LOSS OF CONSCIOUSNESS ( 444 FDA reports)
DEHYDRATION ( 443 FDA reports)
PARAESTHESIA ( 427 FDA reports)
HYPOTENSION ( 425 FDA reports)
MUSCLE SPASMS ( 413 FDA reports)
WEIGHT INCREASED ( 402 FDA reports)
SUICIDAL IDEATION ( 399 FDA reports)
DEATH ( 398 FDA reports)
URINARY TRACT INFECTION ( 389 FDA reports)
OVERDOSE ( 380 FDA reports)
COUGH ( 368 FDA reports)
RENAL FAILURE ACUTE ( 361 FDA reports)
DECREASED APPETITE ( 356 FDA reports)
AGITATION ( 354 FDA reports)
SYNCOPE ( 347 FDA reports)
DRUG TOXICITY ( 345 FDA reports)
GAIT DISTURBANCE ( 345 FDA reports)
CONDITION AGGRAVATED ( 343 FDA reports)
RASH ( 343 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 335 FDA reports)
INJURY ( 329 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 328 FDA reports)
RESPIRATORY ARREST ( 325 FDA reports)
VISION BLURRED ( 318 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 313 FDA reports)
TACHYCARDIA ( 312 FDA reports)
NEUROPATHY PERIPHERAL ( 308 FDA reports)
PRURITUS ( 303 FDA reports)
RENAL FAILURE ( 298 FDA reports)
CEREBROVASCULAR ACCIDENT ( 293 FDA reports)
DYSPHAGIA ( 287 FDA reports)
OSTEOARTHRITIS ( 287 FDA reports)
ABDOMINAL PAIN UPPER ( 281 FDA reports)
DIABETES MELLITUS ( 277 FDA reports)
FEELING ABNORMAL ( 277 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 276 FDA reports)
PALPITATIONS ( 269 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 268 FDA reports)
PULMONARY EMBOLISM ( 268 FDA reports)
HALLUCINATION ( 258 FDA reports)
BLOOD GLUCOSE INCREASED ( 252 FDA reports)
OSTEONECROSIS OF JAW ( 249 FDA reports)
BLOOD PRESSURE INCREASED ( 248 FDA reports)
DEEP VEIN THROMBOSIS ( 248 FDA reports)
MYOCARDIAL INFARCTION ( 248 FDA reports)
BALANCE DISORDER ( 247 FDA reports)
MYALGIA ( 246 FDA reports)
SEPSIS ( 245 FDA reports)
RESPIRATORY FAILURE ( 242 FDA reports)
HAEMOGLOBIN DECREASED ( 239 FDA reports)
MULTIPLE DRUG OVERDOSE ( 236 FDA reports)
CARDIO-RESPIRATORY ARREST ( 234 FDA reports)
NECK PAIN ( 234 FDA reports)
ASTHMA ( 231 FDA reports)
MEMORY IMPAIRMENT ( 231 FDA reports)
EMOTIONAL DISTRESS ( 230 FDA reports)
SUICIDE ATTEMPT ( 230 FDA reports)
CELLULITIS ( 228 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 228 FDA reports)
COMA ( 227 FDA reports)
PLEURAL EFFUSION ( 224 FDA reports)
MIGRAINE ( 222 FDA reports)
HEART RATE INCREASED ( 216 FDA reports)
SEROTONIN SYNDROME ( 212 FDA reports)
AGGRESSION ( 210 FDA reports)
AMNESIA ( 210 FDA reports)
CHILLS ( 210 FDA reports)
DRY MOUTH ( 210 FDA reports)
LETHARGY ( 209 FDA reports)
CHOLELITHIASIS ( 208 FDA reports)
ERYTHEMA ( 208 FDA reports)
ATRIAL FIBRILLATION ( 207 FDA reports)
BRONCHITIS ( 206 FDA reports)
DELIRIUM ( 204 FDA reports)
PANCYTOPENIA ( 203 FDA reports)
DISTURBANCE IN ATTENTION ( 200 FDA reports)
INFECTION ( 193 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 192 FDA reports)
PANIC ATTACK ( 191 FDA reports)
SPEECH DISORDER ( 190 FDA reports)
MUSCULAR WEAKNESS ( 188 FDA reports)
CHEST DISCOMFORT ( 187 FDA reports)
BONE DISORDER ( 184 FDA reports)
MUSCULOSKELETAL PAIN ( 184 FDA reports)
BLOOD CREATININE INCREASED ( 183 FDA reports)
SLEEP DISORDER ( 183 FDA reports)
THROMBOCYTOPENIA ( 183 FDA reports)
CONTUSION ( 182 FDA reports)
DYSKINESIA ( 181 FDA reports)
SINUSITIS ( 181 FDA reports)
OSTEOMYELITIS ( 179 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 178 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 175 FDA reports)
OSTEOPOROSIS ( 174 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 172 FDA reports)
NEUTROPENIA ( 171 FDA reports)
INJECTION SITE PAIN ( 170 FDA reports)
BONE PAIN ( 169 FDA reports)
BRADYCARDIA ( 169 FDA reports)
IRRITABILITY ( 169 FDA reports)
PLATELET COUNT DECREASED ( 169 FDA reports)
SPINAL OSTEOARTHRITIS ( 169 FDA reports)
RHABDOMYOLYSIS ( 168 FDA reports)
INTENTIONAL OVERDOSE ( 167 FDA reports)
DISORIENTATION ( 166 FDA reports)
INFLUENZA LIKE ILLNESS ( 165 FDA reports)
HYPOKALAEMIA ( 164 FDA reports)
ABDOMINAL DISTENSION ( 162 FDA reports)
ATELECTASIS ( 161 FDA reports)
DEPRESSED MOOD ( 161 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 161 FDA reports)
SWELLING FACE ( 161 FDA reports)
URINARY RETENTION ( 161 FDA reports)
TYPE 2 DIABETES MELLITUS ( 160 FDA reports)
JOINT SWELLING ( 160 FDA reports)
DYSPEPSIA ( 158 FDA reports)
PAIN IN JAW ( 158 FDA reports)
ARTHRITIS ( 157 FDA reports)
DYSARTHRIA ( 156 FDA reports)
HYPONATRAEMIA ( 156 FDA reports)
SWELLING ( 155 FDA reports)
FIBROMYALGIA ( 154 FDA reports)
CARDIOMEGALY ( 153 FDA reports)
MENTAL DISORDER ( 153 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 151 FDA reports)
MENTAL STATUS CHANGES ( 151 FDA reports)
HYPERSENSITIVITY ( 150 FDA reports)
HYPOGLYCAEMIA ( 150 FDA reports)
DRUG DEPENDENCE ( 149 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 148 FDA reports)
CORONARY ARTERY DISEASE ( 147 FDA reports)
RESTLESSNESS ( 147 FDA reports)
NERVOUSNESS ( 146 FDA reports)
NIGHTMARE ( 145 FDA reports)
PULMONARY OEDEMA ( 145 FDA reports)
OSTEONECROSIS ( 142 FDA reports)
OEDEMA ( 141 FDA reports)
MOBILITY DECREASED ( 140 FDA reports)
RESTLESS LEGS SYNDROME ( 139 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 139 FDA reports)
HYPERKALAEMIA ( 138 FDA reports)
HIATUS HERNIA ( 137 FDA reports)
FLUSHING ( 135 FDA reports)
SLEEP APNOEA SYNDROME ( 134 FDA reports)
HERPES ZOSTER ( 133 FDA reports)
OBESITY ( 132 FDA reports)
ANOREXIA ( 131 FDA reports)
GASTRITIS ( 131 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 130 FDA reports)
MULTI-ORGAN FAILURE ( 130 FDA reports)
EMOTIONAL DISORDER ( 129 FDA reports)
DYSURIA ( 128 FDA reports)
RHEUMATOID ARTHRITIS ( 128 FDA reports)
SINUS TACHYCARDIA ( 127 FDA reports)
CATARACT ( 127 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 127 FDA reports)
HYPERLIPIDAEMIA ( 127 FDA reports)
INTERSTITIAL LUNG DISEASE ( 127 FDA reports)
OSTEOPENIA ( 127 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 126 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 124 FDA reports)
RENAL IMPAIRMENT ( 124 FDA reports)
ARRHYTHMIA ( 123 FDA reports)
DENTAL CARIES ( 123 FDA reports)
COLITIS ( 122 FDA reports)
METABOLIC ACIDOSIS ( 122 FDA reports)
MULTIPLE SCLEROSIS ( 122 FDA reports)
BLOOD PRESSURE DECREASED ( 121 FDA reports)
DEFORMITY ( 121 FDA reports)
LYMPHADENOPATHY ( 121 FDA reports)
MOOD SWINGS ( 120 FDA reports)
TOOTHACHE ( 120 FDA reports)
UNRESPONSIVE TO STIMULI ( 120 FDA reports)
BURNING SENSATION ( 119 FDA reports)
BLOOD SODIUM DECREASED ( 118 FDA reports)
CARDIAC DISORDER ( 118 FDA reports)
HEPATIC STEATOSIS ( 118 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 118 FDA reports)
HYPERGLYCAEMIA ( 117 FDA reports)
IMPAIRED HEALING ( 117 FDA reports)
ABNORMAL BEHAVIOUR ( 116 FDA reports)
OROPHARYNGEAL PAIN ( 116 FDA reports)
WITHDRAWAL SYNDROME ( 116 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 115 FDA reports)
HEPATIC ENZYME INCREASED ( 115 FDA reports)
NEURALGIA ( 115 FDA reports)
PARANOIA ( 115 FDA reports)
MITRAL VALVE INCOMPETENCE ( 114 FDA reports)
MOUTH ULCERATION ( 113 FDA reports)
SWOLLEN TONGUE ( 113 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 112 FDA reports)
PANCREATITIS ( 112 FDA reports)
PULMONARY CONGESTION ( 112 FDA reports)
CARDIAC FAILURE ( 111 FDA reports)
FEAR ( 111 FDA reports)
INFLUENZA ( 111 FDA reports)
PNEUMONIA ASPIRATION ( 110 FDA reports)
STOMATITIS ( 110 FDA reports)
VERTIGO ( 110 FDA reports)
VISUAL IMPAIRMENT ( 109 FDA reports)
ALOPECIA ( 109 FDA reports)
EYE PAIN ( 108 FDA reports)
ABDOMINAL DISCOMFORT ( 107 FDA reports)
CIRCULATORY COLLAPSE ( 107 FDA reports)
POLLAKIURIA ( 107 FDA reports)
HAEMORRHOIDS ( 106 FDA reports)
NEOPLASM MALIGNANT ( 106 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 106 FDA reports)
BLOOD UREA INCREASED ( 105 FDA reports)
RENAL FAILURE CHRONIC ( 105 FDA reports)
ANHEDONIA ( 104 FDA reports)
HEART RATE IRREGULAR ( 104 FDA reports)
INJECTION SITE ERYTHEMA ( 104 FDA reports)
INTENTIONAL DRUG MISUSE ( 104 FDA reports)
URTICARIA ( 104 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 103 FDA reports)
DRUG DOSE OMISSION ( 103 FDA reports)
PSYCHOTIC DISORDER ( 103 FDA reports)
DYSPHONIA ( 102 FDA reports)
PULMONARY HYPERTENSION ( 102 FDA reports)
RECTAL HAEMORRHAGE ( 102 FDA reports)
SKIN DISCOLOURATION ( 102 FDA reports)
STRESS ( 102 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 102 FDA reports)
TREATMENT NONCOMPLIANCE ( 101 FDA reports)
SKIN ULCER ( 100 FDA reports)
TINNITUS ( 100 FDA reports)
ACCIDENTAL OVERDOSE ( 100 FDA reports)
PALLOR ( 100 FDA reports)
ABASIA ( 99 FDA reports)
DECREASED INTEREST ( 99 FDA reports)
DRUG ABUSE ( 99 FDA reports)
LEUKOPENIA ( 99 FDA reports)
NEPHROLITHIASIS ( 99 FDA reports)
POISONING ( 99 FDA reports)
ROAD TRAFFIC ACCIDENT ( 99 FDA reports)
VISUAL ACUITY REDUCED ( 98 FDA reports)
DRUG HYPERSENSITIVITY ( 98 FDA reports)
DYSGEUSIA ( 98 FDA reports)
HOT FLUSH ( 98 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 98 FDA reports)
METASTASES TO BONE ( 98 FDA reports)
NASOPHARYNGITIS ( 98 FDA reports)
ECONOMIC PROBLEM ( 97 FDA reports)
GRAND MAL CONVULSION ( 97 FDA reports)
OFF LABEL USE ( 97 FDA reports)
FEELING HOT ( 96 FDA reports)
HYPOXIA ( 96 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 95 FDA reports)
CHOLECYSTITIS CHRONIC ( 94 FDA reports)
ANGER ( 93 FDA reports)
BLOOD GLUCOSE DECREASED ( 93 FDA reports)
GALLBLADDER DISORDER ( 93 FDA reports)
APHASIA ( 92 FDA reports)
DRUG EFFECT DECREASED ( 92 FDA reports)
MULTIPLE MYELOMA ( 92 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 91 FDA reports)
GASTROINTESTINAL DISORDER ( 91 FDA reports)
SEDATION ( 91 FDA reports)
TOOTH EXTRACTION ( 91 FDA reports)
FOOT FRACTURE ( 90 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 90 FDA reports)
RESPIRATORY DISTRESS ( 90 FDA reports)
BLINDNESS ( 89 FDA reports)
DIPLOPIA ( 89 FDA reports)
HEAD INJURY ( 89 FDA reports)
INCONTINENCE ( 89 FDA reports)
INFLAMMATION ( 89 FDA reports)
STAPHYLOCOCCAL INFECTION ( 89 FDA reports)
VENTRICULAR TACHYCARDIA ( 88 FDA reports)
BLOOD POTASSIUM DECREASED ( 88 FDA reports)
DYSPNOEA EXERTIONAL ( 88 FDA reports)
ORAL PAIN ( 88 FDA reports)
EPISTAXIS ( 87 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 87 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 86 FDA reports)
DYSSTASIA ( 85 FDA reports)
ERECTILE DYSFUNCTION ( 85 FDA reports)
MELAENA ( 85 FDA reports)
SENSORY DISTURBANCE ( 85 FDA reports)
DRY SKIN ( 84 FDA reports)
CRYING ( 83 FDA reports)
INCORRECT DOSE ADMINISTERED ( 83 FDA reports)
OESOPHAGITIS ( 83 FDA reports)
WHEEZING ( 83 FDA reports)
THROMBOSIS ( 82 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 82 FDA reports)
EATING DISORDER ( 82 FDA reports)
LIVER DISORDER ( 81 FDA reports)
FEBRILE NEUTROPENIA ( 80 FDA reports)
HEMIPARESIS ( 80 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 80 FDA reports)
MUSCLE TWITCHING ( 80 FDA reports)
HAEMOPTYSIS ( 79 FDA reports)
MYDRIASIS ( 78 FDA reports)
CARDIOMYOPATHY ( 77 FDA reports)
MEDICATION ERROR ( 77 FDA reports)
FEELING COLD ( 76 FDA reports)
LUNG INFILTRATION ( 76 FDA reports)
LUNG NEOPLASM ( 76 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 76 FDA reports)
DISEASE PROGRESSION ( 75 FDA reports)
EMPHYSEMA ( 75 FDA reports)
HAEMORRHAGE ( 75 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 75 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 74 FDA reports)
HIP FRACTURE ( 74 FDA reports)
MYOCARDIAL ISCHAEMIA ( 74 FDA reports)
TARDIVE DYSKINESIA ( 74 FDA reports)
BLISTER ( 73 FDA reports)
RESPIRATORY DEPRESSION ( 73 FDA reports)
CYANOSIS ( 72 FDA reports)
EAR PAIN ( 72 FDA reports)
HEPATIC FAILURE ( 72 FDA reports)
NIGHT SWEATS ( 72 FDA reports)
RASH ERYTHEMATOUS ( 72 FDA reports)
RIB FRACTURE ( 72 FDA reports)
TOOTH LOSS ( 71 FDA reports)
BODY TEMPERATURE INCREASED ( 71 FDA reports)
DRUG ABUSER ( 71 FDA reports)
LUNG DISORDER ( 71 FDA reports)
PRODUCT QUALITY ISSUE ( 71 FDA reports)
DYSTONIA ( 70 FDA reports)
PSORIASIS ( 70 FDA reports)
URINARY INCONTINENCE ( 70 FDA reports)
VIRAL INFECTION ( 70 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 69 FDA reports)
HAEMATOCRIT DECREASED ( 69 FDA reports)
MANIA ( 69 FDA reports)
OXYGEN SATURATION DECREASED ( 69 FDA reports)
DIVERTICULUM ( 68 FDA reports)
HAEMATEMESIS ( 68 FDA reports)
HAEMATOCHEZIA ( 68 FDA reports)
NERVOUS SYSTEM DISORDER ( 68 FDA reports)
UNEVALUABLE EVENT ( 68 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 67 FDA reports)
CEREBRAL INFARCTION ( 67 FDA reports)
ABNORMAL DREAMS ( 66 FDA reports)
ABSCESS ( 66 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 66 FDA reports)
LIMB INJURY ( 66 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 66 FDA reports)
EJECTION FRACTION DECREASED ( 65 FDA reports)
THINKING ABNORMAL ( 65 FDA reports)
HYPERSOMNIA ( 64 FDA reports)
INTESTINAL OBSTRUCTION ( 64 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 63 FDA reports)
CROHN'S DISEASE ( 63 FDA reports)
CYSTITIS ( 63 FDA reports)
DEAFNESS ( 63 FDA reports)
DIABETIC NEUROPATHY ( 63 FDA reports)
FLATULENCE ( 63 FDA reports)
HALLUCINATION, VISUAL ( 63 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 63 FDA reports)
HYPOTHYROIDISM ( 63 FDA reports)
JAUNDICE ( 63 FDA reports)
PREGNANCY ( 63 FDA reports)
PRODUCTIVE COUGH ( 63 FDA reports)
SCOLIOSIS ( 63 FDA reports)
TOOTH DISORDER ( 63 FDA reports)
DYSLIPIDAEMIA ( 62 FDA reports)
GASTRIC ULCER ( 62 FDA reports)
HYPERCHOLESTEROLAEMIA ( 62 FDA reports)
MALNUTRITION ( 62 FDA reports)
DRUG INTOLERANCE ( 61 FDA reports)
HAEMATURIA ( 61 FDA reports)
OVARIAN CYST ( 61 FDA reports)
SPINAL COLUMN STENOSIS ( 61 FDA reports)
SKIN EXFOLIATION ( 60 FDA reports)
SURGERY ( 60 FDA reports)
ANGINA PECTORIS ( 60 FDA reports)
HYPOPHAGIA ( 60 FDA reports)
PHARYNGITIS ( 60 FDA reports)
PRIMARY SEQUESTRUM ( 60 FDA reports)
COORDINATION ABNORMAL ( 59 FDA reports)
INJECTION SITE HAEMATOMA ( 59 FDA reports)
LOCALISED INFECTION ( 59 FDA reports)
MYOCLONUS ( 59 FDA reports)
POST PROCEDURAL COMPLICATION ( 59 FDA reports)
RASH MACULAR ( 59 FDA reports)
SCAR ( 59 FDA reports)
SCIATICA ( 59 FDA reports)
ENCEPHALOPATHY ( 58 FDA reports)
HEART RATE DECREASED ( 58 FDA reports)
INADEQUATE ANALGESIA ( 58 FDA reports)
PYELONEPHRITIS ( 58 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 58 FDA reports)
COAGULOPATHY ( 57 FDA reports)
COMPRESSION FRACTURE ( 57 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 57 FDA reports)
GENERALISED OEDEMA ( 57 FDA reports)
ILL-DEFINED DISORDER ( 57 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 57 FDA reports)
PANCREATITIS ACUTE ( 57 FDA reports)
PRESYNCOPE ( 57 FDA reports)
SEPTIC SHOCK ( 57 FDA reports)
TOOTH ABSCESS ( 57 FDA reports)
VISUAL DISTURBANCE ( 57 FDA reports)
ROTATOR CUFF SYNDROME ( 56 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 56 FDA reports)
ANKLE FRACTURE ( 56 FDA reports)
DEPENDENCE ( 56 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 56 FDA reports)
IRRITABLE BOWEL SYNDROME ( 56 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 56 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 56 FDA reports)
ABDOMINAL PAIN LOWER ( 55 FDA reports)
DEMENTIA ( 55 FDA reports)
FLUID RETENTION ( 55 FDA reports)
ILEUS ( 55 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 55 FDA reports)
SPINAL FRACTURE ( 55 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 54 FDA reports)
BRONCHOPNEUMONIA ( 54 FDA reports)
DIVERTICULITIS ( 54 FDA reports)
FEELING JITTERY ( 54 FDA reports)
PARALYSIS ( 54 FDA reports)
PERICARDIAL EFFUSION ( 54 FDA reports)
PULMONARY FIBROSIS ( 54 FDA reports)
ARTHROPATHY ( 53 FDA reports)
BREAST CANCER ( 53 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 53 FDA reports)
MENISCUS LESION ( 53 FDA reports)
PHOTOPHOBIA ( 53 FDA reports)
RENAL DISORDER ( 53 FDA reports)
SENSORY LOSS ( 53 FDA reports)
SKIN LESION ( 53 FDA reports)
SHOCK ( 52 FDA reports)
ADVERSE EVENT ( 52 FDA reports)
BLOOD ALBUMIN DECREASED ( 52 FDA reports)
DECUBITUS ULCER ( 52 FDA reports)
FEELING OF DESPAIR ( 52 FDA reports)
LOWER LIMB FRACTURE ( 52 FDA reports)
MUCOSAL INFLAMMATION ( 52 FDA reports)
ACCIDENTAL EXPOSURE ( 51 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 51 FDA reports)
ARTERIOSCLEROSIS ( 51 FDA reports)
HAEMATOMA ( 51 FDA reports)
IMPAIRED WORK ABILITY ( 51 FDA reports)
INJECTION SITE HAEMORRHAGE ( 51 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 51 FDA reports)
ORTHOSTATIC HYPOTENSION ( 51 FDA reports)
SKIN DISORDER ( 51 FDA reports)
TOOTH FRACTURE ( 51 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 51 FDA reports)
SINUS DISORDER ( 50 FDA reports)
GINGIVAL PAIN ( 50 FDA reports)
MAJOR DEPRESSION ( 50 FDA reports)
MUSCLE DISORDER ( 50 FDA reports)
POOR QUALITY SLEEP ( 50 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 49 FDA reports)
BURSITIS ( 49 FDA reports)
CEREBRAL ATROPHY ( 49 FDA reports)
COGNITIVE DISORDER ( 49 FDA reports)
DRUG LEVEL INCREASED ( 49 FDA reports)
FLANK PAIN ( 49 FDA reports)
GINGIVITIS ( 49 FDA reports)
RADICULOPATHY ( 49 FDA reports)
STEVENS-JOHNSON SYNDROME ( 49 FDA reports)
RHINORRHOEA ( 48 FDA reports)
TEARFULNESS ( 48 FDA reports)
DEVICE RELATED INFECTION ( 48 FDA reports)
EPILEPSY ( 48 FDA reports)
EXPOSED BONE IN JAW ( 48 FDA reports)
FLUID OVERLOAD ( 48 FDA reports)
HYPOAESTHESIA ORAL ( 48 FDA reports)
LUNG INFECTION ( 48 FDA reports)
MUSCLE RIGIDITY ( 48 FDA reports)
NEOPLASM PROGRESSION ( 48 FDA reports)
PERIODONTITIS ( 48 FDA reports)
ABORTION SPONTANEOUS ( 47 FDA reports)
AFFECTIVE DISORDER ( 47 FDA reports)
CANDIDIASIS ( 47 FDA reports)
CEREBRAL HAEMORRHAGE ( 47 FDA reports)
CHOLECYSTITIS ( 47 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 47 FDA reports)
DISCOMFORT ( 47 FDA reports)
DISSOCIATION ( 47 FDA reports)
FEMUR FRACTURE ( 47 FDA reports)
INCOHERENT ( 47 FDA reports)
SCHIZOPHRENIA ( 47 FDA reports)
TENDONITIS ( 47 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 47 FDA reports)
SINUS BRADYCARDIA ( 46 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 46 FDA reports)
URINE ODOUR ABNORMAL ( 46 FDA reports)
BREAST PAIN ( 46 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 46 FDA reports)
DIABETIC KETOACIDOSIS ( 46 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 46 FDA reports)
METASTASES TO LIVER ( 46 FDA reports)
METASTASES TO SPINE ( 46 FDA reports)
MOVEMENT DISORDER ( 46 FDA reports)
MULTIPLE INJURIES ( 46 FDA reports)
NASAL CONGESTION ( 46 FDA reports)
NEUTROPHIL COUNT DECREASED ( 46 FDA reports)
ASPIRATION ( 45 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 45 FDA reports)
EYE SWELLING ( 45 FDA reports)
FORMICATION ( 45 FDA reports)
GASTRIC DISORDER ( 45 FDA reports)
HEART VALVE INCOMPETENCE ( 45 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 45 FDA reports)
IMPAIRED DRIVING ABILITY ( 45 FDA reports)
JOINT EFFUSION ( 45 FDA reports)
LEUKOCYTOSIS ( 45 FDA reports)
MENTAL IMPAIRMENT ( 45 FDA reports)
PROTEINURIA ( 45 FDA reports)
SUDDEN DEATH ( 45 FDA reports)
TENDERNESS ( 44 FDA reports)
ANAPHYLACTIC REACTION ( 44 FDA reports)
BIPOLAR DISORDER ( 44 FDA reports)
COLD SWEAT ( 44 FDA reports)
DELUSION ( 44 FDA reports)
EXOSTOSIS ( 44 FDA reports)
HEPATITIS C ( 44 FDA reports)
LACTIC ACIDOSIS ( 44 FDA reports)
MASTICATION DISORDER ( 44 FDA reports)
RADIOTHERAPY ( 44 FDA reports)
ASCITES ( 43 FDA reports)
DISABILITY ( 43 FDA reports)
ECZEMA ( 43 FDA reports)
HEPATITIS ( 43 FDA reports)
KYPHOSIS ( 43 FDA reports)
METASTASES TO LUNG ( 43 FDA reports)
SPLENOMEGALY ( 43 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 42 FDA reports)
ULCER ( 42 FDA reports)
UPPER LIMB FRACTURE ( 42 FDA reports)
BLOOD BILIRUBIN INCREASED ( 42 FDA reports)
BONE LESION ( 42 FDA reports)
CARPAL TUNNEL SYNDROME ( 42 FDA reports)
CHROMATURIA ( 42 FDA reports)
CYST ( 42 FDA reports)
DRUG SCREEN POSITIVE ( 42 FDA reports)
GASTROENTERITIS ( 42 FDA reports)
INTENTIONAL MISUSE ( 42 FDA reports)
PAROSMIA ( 42 FDA reports)
PELVIC PAIN ( 42 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 42 FDA reports)
ACUTE SINUSITIS ( 41 FDA reports)
BRONCHOSPASM ( 41 FDA reports)
CARDIAC MURMUR ( 41 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 41 FDA reports)
DEVICE MALFUNCTION ( 41 FDA reports)
INFUSION RELATED REACTION ( 41 FDA reports)
MUSCLE TIGHTNESS ( 41 FDA reports)
RESPIRATORY DISORDER ( 41 FDA reports)
RHINITIS ALLERGIC ( 41 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 40 FDA reports)
SPINAL COMPRESSION FRACTURE ( 40 FDA reports)
BLOOD CALCIUM DECREASED ( 40 FDA reports)
DRUG ADMINISTRATION ERROR ( 40 FDA reports)
EXCORIATION ( 40 FDA reports)
FACE OEDEMA ( 40 FDA reports)
H1N1 INFLUENZA ( 40 FDA reports)
HUMERUS FRACTURE ( 40 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 40 FDA reports)
NO THERAPEUTIC RESPONSE ( 40 FDA reports)
ODYNOPHAGIA ( 40 FDA reports)
PATHOLOGICAL FRACTURE ( 40 FDA reports)
PEPTIC ULCER ( 40 FDA reports)
PHOTOSENSITIVITY REACTION ( 40 FDA reports)
RENAL PAIN ( 40 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 39 FDA reports)
FUNGAL INFECTION ( 39 FDA reports)
GLAUCOMA ( 39 FDA reports)
HYPOCALCAEMIA ( 39 FDA reports)
INCREASED APPETITE ( 39 FDA reports)
LABILE BLOOD PRESSURE ( 39 FDA reports)
PNEUMOTHORAX ( 39 FDA reports)
PSYCHIATRIC SYMPTOM ( 39 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 39 FDA reports)
RASH GENERALISED ( 39 FDA reports)
SPUTUM DISCOLOURED ( 39 FDA reports)
VAGINAL HAEMORRHAGE ( 39 FDA reports)
VIITH NERVE PARALYSIS ( 39 FDA reports)
AKATHISIA ( 38 FDA reports)
APNOEA ( 38 FDA reports)
BASAL CELL CARCINOMA ( 38 FDA reports)
COGWHEEL RIGIDITY ( 38 FDA reports)
FACIAL PAIN ( 38 FDA reports)
HEPATIC CYST ( 38 FDA reports)
LIP SWELLING ( 38 FDA reports)
PERICARDITIS ( 38 FDA reports)
PLATELET COUNT INCREASED ( 38 FDA reports)
BLOOD POTASSIUM INCREASED ( 37 FDA reports)
GINGIVAL DISORDER ( 37 FDA reports)
MENSTRUAL DISORDER ( 37 FDA reports)
NEUROPATHY ( 37 FDA reports)
PRURITUS GENERALISED ( 37 FDA reports)
RENAL CYST ( 37 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 36 FDA reports)
DROOLING ( 36 FDA reports)
DUODENAL ULCER ( 36 FDA reports)
EAR INFECTION ( 36 FDA reports)
HEART VALVE CALCIFICATION ( 36 FDA reports)
HYPERTHYROIDISM ( 36 FDA reports)
LIBIDO DECREASED ( 36 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 36 FDA reports)
ORAL DISORDER ( 36 FDA reports)
OSTEOLYSIS ( 36 FDA reports)
PERIPHERAL COLDNESS ( 36 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 36 FDA reports)
RASH PRURITIC ( 36 FDA reports)
SINUS HEADACHE ( 36 FDA reports)
THIRST ( 36 FDA reports)
SEXUAL DYSFUNCTION ( 35 FDA reports)
THROAT TIGHTNESS ( 35 FDA reports)
BRAIN OEDEMA ( 35 FDA reports)
CARDIOVASCULAR DISORDER ( 35 FDA reports)
CHOLECYSTECTOMY ( 35 FDA reports)
DRY EYE ( 35 FDA reports)
FIBROSIS ( 35 FDA reports)
FRACTURE ( 35 FDA reports)
GOUT ( 35 FDA reports)
INJECTION SITE REACTION ( 35 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 35 FDA reports)
MACULAR DEGENERATION ( 35 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 35 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 35 FDA reports)
RETCHING ( 35 FDA reports)
ADVERSE DRUG REACTION ( 34 FDA reports)
AZOTAEMIA ( 34 FDA reports)
CARDIAC VALVE DISEASE ( 34 FDA reports)
COLONIC POLYP ( 34 FDA reports)
GINGIVAL BLEEDING ( 34 FDA reports)
GOITRE ( 34 FDA reports)
HEPATOMEGALY ( 34 FDA reports)
HYPOTONIA ( 34 FDA reports)
KIDNEY INFECTION ( 34 FDA reports)
LUPUS-LIKE SYNDROME ( 34 FDA reports)
MOOD ALTERED ( 34 FDA reports)
MYOPATHY ( 34 FDA reports)
OSTEOSCLEROSIS ( 34 FDA reports)
PERONEAL NERVE PALSY ( 34 FDA reports)
PREMATURE LABOUR ( 34 FDA reports)
RESPIRATORY RATE INCREASED ( 34 FDA reports)
THROAT IRRITATION ( 34 FDA reports)
THERAPY NON-RESPONDER ( 33 FDA reports)
TORSADE DE POINTES ( 33 FDA reports)
ANEURYSM ( 33 FDA reports)
DERMATITIS ( 33 FDA reports)
DIVERTICULUM INTESTINAL ( 33 FDA reports)
GROIN PAIN ( 33 FDA reports)
HAEMODIALYSIS ( 33 FDA reports)
HYPOMAGNESAEMIA ( 33 FDA reports)
JOINT STIFFNESS ( 33 FDA reports)
CAESAREAN SECTION ( 32 FDA reports)
CYTOLYTIC HEPATITIS ( 32 FDA reports)
HEPATIC LESION ( 32 FDA reports)
HYPERAESTHESIA ( 32 FDA reports)
HYPERKERATOSIS ( 32 FDA reports)
INCREASED TENDENCY TO BRUISE ( 32 FDA reports)
IRON DEFICIENCY ANAEMIA ( 32 FDA reports)
PHARYNGEAL OEDEMA ( 32 FDA reports)
PLANTAR FASCIITIS ( 32 FDA reports)
PULSE ABSENT ( 32 FDA reports)
SOMNAMBULISM ( 32 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 32 FDA reports)
TONGUE ULCERATION ( 32 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 31 FDA reports)
AGRANULOCYTOSIS ( 31 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 31 FDA reports)
APATHY ( 31 FDA reports)
CORONARY ARTERY OCCLUSION ( 31 FDA reports)
FACIAL BONES FRACTURE ( 31 FDA reports)
FOOT DEFORMITY ( 31 FDA reports)
GASTRIC PH DECREASED ( 31 FDA reports)
HAND FRACTURE ( 31 FDA reports)
INTENTIONAL SELF-INJURY ( 31 FDA reports)
LYMPHADENITIS ( 31 FDA reports)
NEURITIS ( 31 FDA reports)
PATHOLOGICAL GAMBLING ( 31 FDA reports)
PNEUMONITIS ( 31 FDA reports)
AORTIC ANEURYSM ( 30 FDA reports)
ATAXIA ( 30 FDA reports)
BLOOD MAGNESIUM DECREASED ( 30 FDA reports)
DISEASE RECURRENCE ( 30 FDA reports)
HALLUCINATION, AUDITORY ( 30 FDA reports)
HOSPITALISATION ( 30 FDA reports)
HYPOKINESIA ( 30 FDA reports)
HYPOPHOSPHATAEMIA ( 30 FDA reports)
INJECTION SITE RASH ( 30 FDA reports)
LACERATION ( 30 FDA reports)
MENORRHAGIA ( 30 FDA reports)
METABOLIC SYNDROME ( 30 FDA reports)
NECROSIS ( 30 FDA reports)
RENAL INJURY ( 30 FDA reports)
SNORING ( 30 FDA reports)
STATUS EPILEPTICUS ( 30 FDA reports)
THERMAL BURN ( 30 FDA reports)
TRISMUS ( 30 FDA reports)
VASCULITIS ( 30 FDA reports)
WALKING AID USER ( 30 FDA reports)
SELF-INJURIOUS IDEATION ( 29 FDA reports)
SINUS CONGESTION ( 29 FDA reports)
SUBCUTANEOUS NODULE ( 29 FDA reports)
SYNOVIAL CYST ( 29 FDA reports)
TYPE 1 DIABETES MELLITUS ( 29 FDA reports)
AFFECT LABILITY ( 29 FDA reports)
CHOKING ( 29 FDA reports)
DYSPHEMIA ( 29 FDA reports)
FEELING DRUNK ( 29 FDA reports)
ILEUS PARALYTIC ( 29 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 29 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 29 FDA reports)
LARYNGEAL OEDEMA ( 29 FDA reports)
LUMBAR SPINAL STENOSIS ( 29 FDA reports)
NYSTAGMUS ( 29 FDA reports)
PLEURISY ( 29 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 29 FDA reports)
PROTHROMBIN TIME PROLONGED ( 29 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 29 FDA reports)
AGEUSIA ( 28 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 28 FDA reports)
BACK DISORDER ( 28 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 28 FDA reports)
BONE LOSS ( 28 FDA reports)
CACHEXIA ( 28 FDA reports)
CHONDROMALACIA ( 28 FDA reports)
COLITIS ISCHAEMIC ( 28 FDA reports)
DEREALISATION ( 28 FDA reports)
DRUG ERUPTION ( 28 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 28 FDA reports)
HALLUCINATIONS, MIXED ( 28 FDA reports)
HYPOTHERMIA ( 28 FDA reports)
JOINT DISLOCATION ( 28 FDA reports)
LABORATORY TEST ABNORMAL ( 28 FDA reports)
LARGE INTESTINAL ULCER ( 28 FDA reports)
MIDDLE INSOMNIA ( 28 FDA reports)
OCULAR HYPERAEMIA ( 28 FDA reports)
PARAESTHESIA ORAL ( 28 FDA reports)
POLYNEUROPATHY ( 28 FDA reports)
RASH PAPULAR ( 28 FDA reports)
SENSATION OF HEAVINESS ( 28 FDA reports)
URINE OUTPUT DECREASED ( 28 FDA reports)
VENTRICULAR FIBRILLATION ( 28 FDA reports)
TONGUE DISORDER ( 27 FDA reports)
ACUTE HEPATIC FAILURE ( 27 FDA reports)
ALCOHOL USE ( 27 FDA reports)
CARDIOGENIC SHOCK ( 27 FDA reports)
DERMATITIS CONTACT ( 27 FDA reports)
DIFFICULTY IN WALKING ( 27 FDA reports)
DUODENITIS ( 27 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 27 FDA reports)
ELECTROLYTE IMBALANCE ( 27 FDA reports)
FAECES DISCOLOURED ( 27 FDA reports)
HERNIA ( 27 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 27 FDA reports)
METASTASES TO LYMPH NODES ( 27 FDA reports)
MIOSIS ( 27 FDA reports)
MUSCLE STRAIN ( 27 FDA reports)
ORAL CANDIDIASIS ( 27 FDA reports)
PERIODONTAL DISEASE ( 27 FDA reports)
PERSECUTORY DELUSION ( 27 FDA reports)
PLEURITIC PAIN ( 27 FDA reports)
PSORIATIC ARTHROPATHY ( 27 FDA reports)
ACIDOSIS ( 26 FDA reports)
ANGIOEDEMA ( 26 FDA reports)
BILIARY DYSKINESIA ( 26 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 26 FDA reports)
BONE DEBRIDEMENT ( 26 FDA reports)
CEREBRAL ISCHAEMIA ( 26 FDA reports)
DIABETIC COMA ( 26 FDA reports)
ENDOCARDITIS ( 26 FDA reports)
HEMIPLEGIA ( 26 FDA reports)
HYPERTHERMIA ( 26 FDA reports)
MASS ( 26 FDA reports)
NEUTROPENIC SEPSIS ( 26 FDA reports)
OSTEITIS ( 26 FDA reports)
PANIC REACTION ( 26 FDA reports)
POLYSUBSTANCE ABUSE ( 26 FDA reports)
RESPIRATORY TRACT INFECTION ( 26 FDA reports)
SKIN BURNING SENSATION ( 26 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 26 FDA reports)
TACHYPNOEA ( 26 FDA reports)
TRANSAMINASES INCREASED ( 26 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 26 FDA reports)
VISUAL FIELD DEFECT ( 26 FDA reports)
RHINITIS ( 25 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 25 FDA reports)
SPINAL DISORDER ( 25 FDA reports)
THYROID DISORDER ( 25 FDA reports)
VITAMIN B12 DEFICIENCY ( 25 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL ABOVE THERAPEUTIC ( 25 FDA reports)
ARTHROPOD BITE ( 25 FDA reports)
BLINDNESS UNILATERAL ( 25 FDA reports)
BLOOD CALCIUM INCREASED ( 25 FDA reports)
BLOOD URINE PRESENT ( 25 FDA reports)
BREAST CANCER RECURRENT ( 25 FDA reports)
CHOLESTASIS ( 25 FDA reports)
CLOSTRIDIAL INFECTION ( 25 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 25 FDA reports)
DEPERSONALISATION ( 25 FDA reports)
ESSENTIAL HYPERTENSION ( 25 FDA reports)
HYPERVENTILATION ( 25 FDA reports)
IMMUNOSUPPRESSION ( 25 FDA reports)
INJECTION SITE SWELLING ( 25 FDA reports)
MICTURITION URGENCY ( 25 FDA reports)
NEPHROPATHY ( 25 FDA reports)
PULMONARY TOXICITY ( 25 FDA reports)
PURULENT DISCHARGE ( 25 FDA reports)
RESPIRATORY RATE DECREASED ( 25 FDA reports)
APHAGIA ( 24 FDA reports)
BEDRIDDEN ( 24 FDA reports)
BONE MARROW FAILURE ( 24 FDA reports)
CHOLECYSTITIS ACUTE ( 24 FDA reports)
COLITIS ULCERATIVE ( 24 FDA reports)
COLON CANCER ( 24 FDA reports)
DECREASED ACTIVITY ( 24 FDA reports)
DIABETIC RETINOPATHY ( 24 FDA reports)
DRUG TOLERANCE ( 24 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 24 FDA reports)
FACET JOINT SYNDROME ( 24 FDA reports)
FIBRIN D DIMER INCREASED ( 24 FDA reports)
HEPATIC CIRRHOSIS ( 24 FDA reports)
HYPOVOLAEMIA ( 24 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 24 FDA reports)
INTERMITTENT CLAUDICATION ( 24 FDA reports)
LIMB DISCOMFORT ( 24 FDA reports)
LIPOMA ( 24 FDA reports)
LUMBAR RADICULOPATHY ( 24 FDA reports)
ORTHOPNOEA ( 24 FDA reports)
PELVIC FRACTURE ( 24 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 24 FDA reports)
REFLUX OESOPHAGITIS ( 24 FDA reports)
SQUAMOUS CELL CARCINOMA ( 24 FDA reports)
URETHRAL STENOSIS ( 24 FDA reports)
VENTRICULAR HYPERTROPHY ( 24 FDA reports)
SUICIDAL BEHAVIOUR ( 23 FDA reports)
VENOUS THROMBOSIS ( 23 FDA reports)
VITAMIN D DEFICIENCY ( 23 FDA reports)
WHEELCHAIR USER ( 23 FDA reports)
ACUTE CORONARY SYNDROME ( 23 FDA reports)
AREFLEXIA ( 23 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 23 FDA reports)
BILIARY COLIC ( 23 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 23 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 23 FDA reports)
DERMATITIS EXFOLIATIVE ( 23 FDA reports)
DIABETIC NEPHROPATHY ( 23 FDA reports)
DILATATION ATRIAL ( 23 FDA reports)
ENDODONTIC PROCEDURE ( 23 FDA reports)
ENDOMETRIOSIS ( 23 FDA reports)
ERYTHEMA MULTIFORME ( 23 FDA reports)
FAECAL INCONTINENCE ( 23 FDA reports)
GINGIVAL SWELLING ( 23 FDA reports)
HOMICIDE ( 23 FDA reports)
HYPERTENSIVE HEART DISEASE ( 23 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 23 FDA reports)
JOINT INJURY ( 23 FDA reports)
METRORRHAGIA ( 23 FDA reports)
NOCTURIA ( 23 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 23 FDA reports)
OEDEMA MOUTH ( 23 FDA reports)
ORAL INTAKE REDUCED ( 23 FDA reports)
ACNE ( 22 FDA reports)
ALCOHOL POISONING ( 22 FDA reports)
ANXIETY DISORDER ( 22 FDA reports)
AORTIC VALVE INCOMPETENCE ( 22 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 22 FDA reports)
BLOOD PH DECREASED ( 22 FDA reports)
BRONCHITIS CHRONIC ( 22 FDA reports)
CAROTID ARTERY DISEASE ( 22 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 22 FDA reports)
EARLY SATIETY ( 22 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 22 FDA reports)
EYE HAEMORRHAGE ( 22 FDA reports)
EYE INFECTION ( 22 FDA reports)
HEPATIC ENCEPHALOPATHY ( 22 FDA reports)
HYDRONEPHROSIS ( 22 FDA reports)
HYPOVENTILATION ( 22 FDA reports)
INITIAL INSOMNIA ( 22 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 22 FDA reports)
INTRA-UTERINE DEATH ( 22 FDA reports)
KNEE ARTHROPLASTY ( 22 FDA reports)
LEFT ATRIAL DILATATION ( 22 FDA reports)
LOBAR PNEUMONIA ( 22 FDA reports)
MEDICAL DEVICE COMPLICATION ( 22 FDA reports)
MITRAL VALVE DISEASE ( 22 FDA reports)
MYOSITIS ( 22 FDA reports)
PARKINSONISM ( 22 FDA reports)
POISONING DELIBERATE ( 22 FDA reports)
RASH MACULO-PAPULAR ( 22 FDA reports)
SENSITIVITY OF TEETH ( 22 FDA reports)
SKIN IRRITATION ( 22 FDA reports)
TENDON DISORDER ( 22 FDA reports)
VAGINAL DISCHARGE ( 22 FDA reports)
WOUND ( 22 FDA reports)
SKIN LACERATION ( 21 FDA reports)
STUPOR ( 21 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 21 FDA reports)
TRIGEMINAL NEURALGIA ( 21 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 21 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 21 FDA reports)
ABNORMAL SENSATION IN EYE ( 21 FDA reports)
ABSCESS JAW ( 21 FDA reports)
ACCIDENT ( 21 FDA reports)
ACUTE RESPIRATORY FAILURE ( 21 FDA reports)
BODY TEMPERATURE DECREASED ( 21 FDA reports)
BONE DENSITY DECREASED ( 21 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 21 FDA reports)
CERVICAL DYSPLASIA ( 21 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 21 FDA reports)
EYE DISORDER ( 21 FDA reports)
FLAT AFFECT ( 21 FDA reports)
HYPERCALCAEMIA ( 21 FDA reports)
INJECTION SITE IRRITATION ( 21 FDA reports)
LACRIMATION INCREASED ( 21 FDA reports)
LYMPHOMA ( 21 FDA reports)
MENSTRUATION IRREGULAR ( 21 FDA reports)
MYELODYSPLASTIC SYNDROME ( 21 FDA reports)
NERVE INJURY ( 21 FDA reports)
ORAL CAVITY FISTULA ( 21 FDA reports)
ORAL HERPES ( 21 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 21 FDA reports)
ATRIOVENTRICULAR BLOCK ( 20 FDA reports)
BACK INJURY ( 20 FDA reports)
BIPOLAR I DISORDER ( 20 FDA reports)
BLADDER CANCER ( 20 FDA reports)
COLON ADENOMA ( 20 FDA reports)
ECCHYMOSIS ( 20 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 20 FDA reports)
GASTROENTERITIS VIRAL ( 20 FDA reports)
GINGIVAL ABSCESS ( 20 FDA reports)
GLOSSITIS ( 20 FDA reports)
GLOSSODYNIA ( 20 FDA reports)
GUN SHOT WOUND ( 20 FDA reports)
GYNAECOMASTIA ( 20 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 20 FDA reports)
HEPATOTOXICITY ( 20 FDA reports)
HIP ARTHROPLASTY ( 20 FDA reports)
HYPERURICAEMIA ( 20 FDA reports)
HYPOMANIA ( 20 FDA reports)
INJECTION SITE DISCOLOURATION ( 20 FDA reports)
LOCAL SWELLING ( 20 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 20 FDA reports)
LUNG CONSOLIDATION ( 20 FDA reports)
LUNG NEOPLASM MALIGNANT ( 20 FDA reports)
MIGRAINE WITH AURA ( 20 FDA reports)
MOTOR DYSFUNCTION ( 20 FDA reports)
MULTIPLE ALLERGIES ( 20 FDA reports)
PROCEDURAL PAIN ( 20 FDA reports)
SKIN CANCER ( 20 FDA reports)
SNEEZING ( 20 FDA reports)
TUBERCULOSIS ( 20 FDA reports)
UTERINE LEIOMYOMA ( 20 FDA reports)
WRIST FRACTURE ( 20 FDA reports)
STOMACH DISCOMFORT ( 19 FDA reports)
SYNOVIAL RUPTURE ( 19 FDA reports)
URINE ANALYSIS ABNORMAL ( 19 FDA reports)
ACCIDENTAL DEATH ( 19 FDA reports)
APPLICATION SITE ERYTHEMA ( 19 FDA reports)
CARDIOTOXICITY ( 19 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 19 FDA reports)
CHRONIC SINUSITIS ( 19 FDA reports)
DEVICE FAILURE ( 19 FDA reports)
DIASTOLIC DYSFUNCTION ( 19 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 19 FDA reports)
DRUG DISPENSING ERROR ( 19 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 19 FDA reports)
FACIAL PALSY ( 19 FDA reports)
FACIAL PARESIS ( 19 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 19 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 19 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 19 FDA reports)
GRANULOMA ( 19 FDA reports)
HYPERPHAGIA ( 19 FDA reports)
HYPERPLASIA ( 19 FDA reports)
JAW DISORDER ( 19 FDA reports)
LOOSE TOOTH ( 19 FDA reports)
NEUTROPHIL COUNT INCREASED ( 19 FDA reports)
NODULE ( 19 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 19 FDA reports)
PERIPHERAL ISCHAEMIA ( 19 FDA reports)
PERITONITIS ( 19 FDA reports)
PHLEBITIS ( 19 FDA reports)
PHYSICAL DISABILITY ( 19 FDA reports)
PNEUMONIA BACTERIAL ( 19 FDA reports)
RAYNAUD'S PHENOMENON ( 19 FDA reports)
RECTOCELE ( 19 FDA reports)
RETINAL DETACHMENT ( 19 FDA reports)
AEROMONA INFECTION ( 18 FDA reports)
ANGINA UNSTABLE ( 18 FDA reports)
ANURIA ( 18 FDA reports)
AORTIC CALCIFICATION ( 18 FDA reports)
APPENDICITIS ( 18 FDA reports)
ATRIAL FLUTTER ( 18 FDA reports)
BACTERIAL INFECTION ( 18 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 18 FDA reports)
CERVICAL SPINAL STENOSIS ( 18 FDA reports)
COMA SCALE ABNORMAL ( 18 FDA reports)
CYSTITIS INTERSTITIAL ( 18 FDA reports)
CYSTOCELE ( 18 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 18 FDA reports)
DRUG PRESCRIBING ERROR ( 18 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 18 FDA reports)
EOSINOPHILIA ( 18 FDA reports)
FAECALOMA ( 18 FDA reports)
FAMILY STRESS ( 18 FDA reports)
HAEMOLYTIC ANAEMIA ( 18 FDA reports)
HEPATIC MASS ( 18 FDA reports)
HYPERTENSIVE CRISIS ( 18 FDA reports)
ILEITIS ( 18 FDA reports)
MALIGNANT MELANOMA ( 18 FDA reports)
MASTOIDITIS ( 18 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 18 FDA reports)
ORAL INFECTION ( 18 FDA reports)
OTORRHOEA ( 18 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 18 FDA reports)
PETECHIAE ( 18 FDA reports)
PLEURAL FIBROSIS ( 18 FDA reports)
POLYURIA ( 18 FDA reports)
POOR PERIPHERAL CIRCULATION ( 18 FDA reports)
PROGRESSIVE SUPRANUCLEAR PALSY ( 18 FDA reports)
PROTEIN TOTAL INCREASED ( 18 FDA reports)
PULMONARY THROMBOSIS ( 18 FDA reports)
PULMONARY TUBERCULOSIS ( 18 FDA reports)
SKIN INDURATION ( 18 FDA reports)
SKIN REACTION ( 18 FDA reports)
SUBSTANCE ABUSE ( 18 FDA reports)
THROMBOPHLEBITIS ( 18 FDA reports)
TOOTH INFECTION ( 18 FDA reports)
VEIN DISORDER ( 18 FDA reports)
WOUND DECOMPOSITION ( 18 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 17 FDA reports)
SALIVARY HYPERSECRETION ( 17 FDA reports)
SUBCUTANEOUS ABSCESS ( 17 FDA reports)
TENDON RUPTURE ( 17 FDA reports)
TENSION HEADACHE ( 17 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 17 FDA reports)
VENTRICULAR ARRHYTHMIA ( 17 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 17 FDA reports)
ABDOMINAL TENDERNESS ( 17 FDA reports)
ACTINIC KERATOSIS ( 17 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 17 FDA reports)
BLADDER DISORDER ( 17 FDA reports)
BLOOD CHLORIDE DECREASED ( 17 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 17 FDA reports)
BODY MASS INDEX DECREASED ( 17 FDA reports)
BREAST MASS ( 17 FDA reports)
CERVICOBRACHIAL SYNDROME ( 17 FDA reports)
CHEILITIS ( 17 FDA reports)
CLUMSINESS ( 17 FDA reports)
CONCUSSION ( 17 FDA reports)
CONNECTIVE TISSUE DISORDER ( 17 FDA reports)
CORONARY ARTERY STENOSIS ( 17 FDA reports)
CREPITATIONS ( 17 FDA reports)
DIALYSIS ( 17 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 17 FDA reports)
ENCEPHALITIS ( 17 FDA reports)
ESCHERICHIA INFECTION ( 17 FDA reports)
EYE IRRITATION ( 17 FDA reports)
GENERALISED ANXIETY DISORDER ( 17 FDA reports)
GENITAL HERPES ( 17 FDA reports)
HEPATIC NECROSIS ( 17 FDA reports)
HYPOACUSIS ( 17 FDA reports)
HYPOAESTHESIA FACIAL ( 17 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 17 FDA reports)
INFARCTION ( 17 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 17 FDA reports)
INJECTION SITE NODULE ( 17 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 17 FDA reports)
MONONEURITIS ( 17 FDA reports)
MUSCLE INJURY ( 17 FDA reports)
NO ADVERSE EVENT ( 17 FDA reports)
OPTIC NEURITIS ( 17 FDA reports)
ORAL SURGERY ( 17 FDA reports)
PULMONARY MASS ( 17 FDA reports)
PYURIA ( 17 FDA reports)
RENAL ATROPHY ( 17 FDA reports)
RESPIRATORY TRACT CONGESTION ( 17 FDA reports)
ABSCESS LIMB ( 16 FDA reports)
ACUTE ABDOMEN ( 16 FDA reports)
ANGIOPATHY ( 16 FDA reports)
APRAXIA ( 16 FDA reports)
ARTHRITIS BACTERIAL ( 16 FDA reports)
BLOOD TEST ABNORMAL ( 16 FDA reports)
BRAIN NEOPLASM ( 16 FDA reports)
BREAST TENDERNESS ( 16 FDA reports)
CALCULUS URETERIC ( 16 FDA reports)
CHEST WALL MASS ( 16 FDA reports)
CLAVICLE FRACTURE ( 16 FDA reports)
CONJUNCTIVITIS ( 16 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 16 FDA reports)
EDENTULOUS ( 16 FDA reports)
EXTRASYSTOLES ( 16 FDA reports)
FEBRILE BONE MARROW APLASIA ( 16 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 16 FDA reports)
HELICOBACTER INFECTION ( 16 FDA reports)
INJECTION SITE PRURITUS ( 16 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 16 FDA reports)
JAW FRACTURE ( 16 FDA reports)
LARGE INTESTINE PERFORATION ( 16 FDA reports)
LEG AMPUTATION ( 16 FDA reports)
LOWER EXTREMITY MASS ( 16 FDA reports)
MELANOCYTIC NAEVUS ( 16 FDA reports)
MONOCYTE COUNT INCREASED ( 16 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 16 FDA reports)
MUSCULOSKELETAL DISORDER ( 16 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 16 FDA reports)
PROSTATITIS ( 16 FDA reports)
RALES ( 16 FDA reports)
RENAL TUBULAR NECROSIS ( 16 FDA reports)
RESPIRATORY ACIDOSIS ( 16 FDA reports)
SEASONAL ALLERGY ( 16 FDA reports)
SKIN HYPERTROPHY ( 16 FDA reports)
SKIN INFECTION ( 16 FDA reports)
SKIN TIGHTNESS ( 16 FDA reports)
STENT PLACEMENT ( 16 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 16 FDA reports)
TINEA PEDIS ( 16 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 16 FDA reports)
SHOULDER PAIN ( 15 FDA reports)
SOPOR ( 15 FDA reports)
TEMPERATURE INTOLERANCE ( 15 FDA reports)
THYROID NEOPLASM ( 15 FDA reports)
VITREOUS FLOATERS ( 15 FDA reports)
VITREOUS HAEMORRHAGE ( 15 FDA reports)
WOUND INFECTION ( 15 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 15 FDA reports)
ANAPHYLACTIC SHOCK ( 15 FDA reports)
ANGIONEUROTIC OEDEMA ( 15 FDA reports)
APPETITE DISORDER ( 15 FDA reports)
ATRIAL SEPTAL DEFECT ( 15 FDA reports)
AUTOIMMUNE DISORDER ( 15 FDA reports)
BARRETT'S OESOPHAGUS ( 15 FDA reports)
BLADDER MASS ( 15 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 15 FDA reports)
BONE FRAGMENTATION ( 15 FDA reports)
BREAST SWELLING ( 15 FDA reports)
BRUXISM ( 15 FDA reports)
CARDIAC FAILURE ACUTE ( 15 FDA reports)
CERVICAL CORD COMPRESSION ( 15 FDA reports)
CUSHING'S SYNDROME ( 15 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 15 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 15 FDA reports)
EYELID OEDEMA ( 15 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 15 FDA reports)
GASTRIC HAEMORRHAGE ( 15 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 15 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 15 FDA reports)
GRIP STRENGTH DECREASED ( 15 FDA reports)
HEPATITIS ACUTE ( 15 FDA reports)
HILAR LYMPHADENOPATHY ( 15 FDA reports)
HYPERTONIA ( 15 FDA reports)
HYPOREFLEXIA ( 15 FDA reports)
HYSTERECTOMY ( 15 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 15 FDA reports)
LIP HAEMORRHAGE ( 15 FDA reports)
LISTLESS ( 15 FDA reports)
LUNG HYPERINFLATION ( 15 FDA reports)
MITRAL VALVE PROLAPSE ( 15 FDA reports)
NEOPLASM ( 15 FDA reports)
NEPHROSCLEROSIS ( 15 FDA reports)
NERVE COMPRESSION ( 15 FDA reports)
OESOPHAGEAL DISORDER ( 15 FDA reports)
OESOPHAGEAL ULCER ( 15 FDA reports)
PAPILLOEDEMA ( 15 FDA reports)
PARKINSON'S DISEASE ( 15 FDA reports)
PERFORMANCE STATUS DECREASED ( 15 FDA reports)
PERSONALITY CHANGE ( 15 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 15 FDA reports)
PO2 DECREASED ( 15 FDA reports)
PROCEDURAL COMPLICATION ( 15 FDA reports)
PROCTALGIA ( 15 FDA reports)
APHONIA ( 14 FDA reports)
ARTERIAL STENOSIS ( 14 FDA reports)
BLOOD PRESSURE ABNORMAL ( 14 FDA reports)
BLOOD URIC ACID INCREASED ( 14 FDA reports)
BONE MARROW TRANSPLANT ( 14 FDA reports)
BREAST CANCER FEMALE ( 14 FDA reports)
BREAST CANCER IN SITU ( 14 FDA reports)
BRONCHITIS ACUTE ( 14 FDA reports)
CHEST X-RAY ABNORMAL ( 14 FDA reports)
COELIAC DISEASE ( 14 FDA reports)
COLLAPSE OF LUNG ( 14 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 14 FDA reports)
DIABETIC COMPLICATION ( 14 FDA reports)
DILATATION VENTRICULAR ( 14 FDA reports)
DIZZINESS POSTURAL ( 14 FDA reports)
FOOD CRAVING ( 14 FDA reports)
FRUSTRATION ( 14 FDA reports)
GASTRITIS EROSIVE ( 14 FDA reports)
GINGIVAL ULCERATION ( 14 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 14 FDA reports)
GOUTY ARTHRITIS ( 14 FDA reports)
GRAVITATIONAL OEDEMA ( 14 FDA reports)
HEARING IMPAIRED ( 14 FDA reports)
HEART INJURY ( 14 FDA reports)
HEPATIC CONGESTION ( 14 FDA reports)
HYPERREFLEXIA ( 14 FDA reports)
IMMUNE SYSTEM DISORDER ( 14 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 14 FDA reports)
INFECTIOUS PERITONITIS ( 14 FDA reports)
INJECTION SITE URTICARIA ( 14 FDA reports)
IRITIS ( 14 FDA reports)
LIPASE INCREASED ( 14 FDA reports)
LYMPHOCYTOSIS ( 14 FDA reports)
METABOLIC DISORDER ( 14 FDA reports)
METASTASIS ( 14 FDA reports)
MONOPLEGIA ( 14 FDA reports)
MUSCLE ATROPHY ( 14 FDA reports)
OROPHARYNGEAL BLISTERING ( 14 FDA reports)
PANIC DISORDER ( 14 FDA reports)
PCO2 INCREASED ( 14 FDA reports)
PHYSICAL ASSAULT ( 14 FDA reports)
PITUITARY TUMOUR BENIGN ( 14 FDA reports)
POLYDIPSIA ( 14 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 14 FDA reports)
PROTEIN URINE PRESENT ( 14 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 14 FDA reports)
SKIN WARM ( 14 FDA reports)
STRESS URINARY INCONTINENCE ( 14 FDA reports)
THYROID CANCER ( 14 FDA reports)
VARICOSE VEIN ( 14 FDA reports)
VENOUS THROMBOSIS LIMB ( 14 FDA reports)
VENTRICULAR DYSFUNCTION ( 14 FDA reports)
SELF ESTEEM DECREASED ( 13 FDA reports)
SENSATION OF FOREIGN BODY ( 13 FDA reports)
SKIN HAEMORRHAGE ( 13 FDA reports)
SPINAL FUSION ACQUIRED ( 13 FDA reports)
STEM CELL TRANSPLANT ( 13 FDA reports)
TIBIA FRACTURE ( 13 FDA reports)
TRANSPLANT FAILURE ( 13 FDA reports)
URINARY TRACT DISORDER ( 13 FDA reports)
UROSEPSIS ( 13 FDA reports)
VAGINAL INFECTION ( 13 FDA reports)
VASCULAR PSEUDOANEURYSM ( 13 FDA reports)
VENOUS INSUFFICIENCY ( 13 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 13 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 13 FDA reports)
AGORAPHOBIA ( 13 FDA reports)
ALVEOLOPLASTY ( 13 FDA reports)
AORTIC STENOSIS ( 13 FDA reports)
BLOOD AMYLASE INCREASED ( 13 FDA reports)
BLOOD CULTURE POSITIVE ( 13 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 13 FDA reports)
BREATH SOUNDS ABNORMAL ( 13 FDA reports)
BRONCHIAL SECRETION RETENTION ( 13 FDA reports)
CARDIAC ENZYMES INCREASED ( 13 FDA reports)
CATHETER RELATED INFECTION ( 13 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 13 FDA reports)
COSTOCHONDRITIS ( 13 FDA reports)
DENTURE WEARER ( 13 FDA reports)
DEPRESSIVE SYMPTOM ( 13 FDA reports)
DERMATITIS ALLERGIC ( 13 FDA reports)
DEVICE RELATED SEPSIS ( 13 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 13 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 13 FDA reports)
ENTEROCOCCAL INFECTION ( 13 FDA reports)
EUPHORIC MOOD ( 13 FDA reports)
EYE PRURITUS ( 13 FDA reports)
FISTULA ( 13 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 13 FDA reports)
GENERALISED ERYTHEMA ( 13 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 13 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 13 FDA reports)
HAEMOPHILUS INFECTION ( 13 FDA reports)
HEPATOCELLULAR DAMAGE ( 13 FDA reports)
HYPERAMYLASAEMIA ( 13 FDA reports)
HYPERTONIC BLADDER ( 13 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 13 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 13 FDA reports)
IMMOBILE ( 13 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 13 FDA reports)
INTESTINAL DILATATION ( 13 FDA reports)
ISCHAEMIA ( 13 FDA reports)
JAW OPERATION ( 13 FDA reports)
JOINT SPRAIN ( 13 FDA reports)
KNEE OPERATION ( 13 FDA reports)
LIVER INJURY ( 13 FDA reports)
MYASTHENIA GRAVIS ( 13 FDA reports)
MYOCARDITIS ( 13 FDA reports)
NECK INJURY ( 13 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 13 FDA reports)
OOPHORECTOMY ( 13 FDA reports)
PANCREATITIS CHRONIC ( 13 FDA reports)
PETIT MAL EPILEPSY ( 13 FDA reports)
PNEUMONIA VIRAL ( 13 FDA reports)
PREMATURE BABY ( 13 FDA reports)
PROSTATOMEGALY ( 13 FDA reports)
ACTINOMYCOSIS ( 12 FDA reports)
ALVEOLITIS ( 12 FDA reports)
ANTICHOLINERGIC SYNDROME ( 12 FDA reports)
ARTERIOVENOUS FISTULA OCCLUSION ( 12 FDA reports)
BILE DUCT OBSTRUCTION ( 12 FDA reports)
BLOOD CHLORIDE INCREASED ( 12 FDA reports)
BLOOD COUNT ABNORMAL ( 12 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 12 FDA reports)
BRAIN DEATH ( 12 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 12 FDA reports)
BREAKTHROUGH PAIN ( 12 FDA reports)
CARDIAC DEATH ( 12 FDA reports)
CATHETER SITE INFECTION ( 12 FDA reports)
CHOLESTEATOMA ( 12 FDA reports)
COMMUNICATION DISORDER ( 12 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 12 FDA reports)
DENTAL PULP DISORDER ( 12 FDA reports)
DERMAL CYST ( 12 FDA reports)
DYSMORPHISM ( 12 FDA reports)
DYSPAREUNIA ( 12 FDA reports)
DYSPHORIA ( 12 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 12 FDA reports)
EOSINOPHIL COUNT INCREASED ( 12 FDA reports)
EYE MOVEMENT DISORDER ( 12 FDA reports)
GANGRENE ( 12 FDA reports)
GASTRIC CANCER ( 12 FDA reports)
GASTRITIS HAEMORRHAGIC ( 12 FDA reports)
GESTATIONAL DIABETES ( 12 FDA reports)
GUILLAIN-BARRE SYNDROME ( 12 FDA reports)
HELLP SYNDROME ( 12 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 12 FDA reports)
INCISIONAL HERNIA ( 12 FDA reports)
INGUINAL HERNIA ( 12 FDA reports)
INTESTINAL ISCHAEMIA ( 12 FDA reports)
ISCHAEMIC STROKE ( 12 FDA reports)
JOINT CONTRACTURE ( 12 FDA reports)
LACUNAR INFARCTION ( 12 FDA reports)
LUDWIG ANGINA ( 12 FDA reports)
MENINGITIS VIRAL ( 12 FDA reports)
MENOPAUSAL SYMPTOMS ( 12 FDA reports)
MONOCLONAL GAMMOPATHY ( 12 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 12 FDA reports)
NAIL DISORDER ( 12 FDA reports)
NEUROSIS ( 12 FDA reports)
NON-CARDIAC CHEST PAIN ( 12 FDA reports)
OBSTRUCTIVE UROPATHY ( 12 FDA reports)
ONYCHOMYCOSIS ( 12 FDA reports)
OSTEOCHONDROSIS ( 12 FDA reports)
PAIN EXACERBATED ( 12 FDA reports)
PANCREATIC DISORDER ( 12 FDA reports)
PARTIAL SEIZURES ( 12 FDA reports)
POLYP COLORECTAL ( 12 FDA reports)
PRODUCT ADHESION ISSUE ( 12 FDA reports)
PUPIL FIXED ( 12 FDA reports)
RASH PUSTULAR ( 12 FDA reports)
RHONCHI ( 12 FDA reports)
SACROILIITIS ( 12 FDA reports)
SCRATCH ( 12 FDA reports)
SELF-MEDICATION ( 12 FDA reports)
SICK SINUS SYNDROME ( 12 FDA reports)
SPINAL CORD COMPRESSION ( 12 FDA reports)
STRABISMUS ( 12 FDA reports)
SYNOVITIS ( 12 FDA reports)
TOOTH DISCOLOURATION ( 12 FDA reports)
TRYPTASE INCREASED ( 12 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 12 FDA reports)
WOUND DEHISCENCE ( 12 FDA reports)
YELLOW SKIN ( 12 FDA reports)
RETINAL HAEMORRHAGE ( 11 FDA reports)
RHEUMATOID NODULE ( 11 FDA reports)
SEQUESTRECTOMY ( 11 FDA reports)
SINUS ARRHYTHMIA ( 11 FDA reports)
SKIN FIBROSIS ( 11 FDA reports)
SPINAL PAIN ( 11 FDA reports)
SPUTUM PURULENT ( 11 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 11 FDA reports)
STREPTOCOCCAL INFECTION ( 11 FDA reports)
STRESS FRACTURE ( 11 FDA reports)
SUDDEN CARDIAC DEATH ( 11 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 11 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 11 FDA reports)
TOBACCO ABUSE ( 11 FDA reports)
TROPONIN INCREASED ( 11 FDA reports)
UMBILICAL HERNIA ( 11 FDA reports)
UTERINE HAEMORRHAGE ( 11 FDA reports)
ABDOMINAL HERNIA ( 11 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 11 FDA reports)
ALCOHOLIC LIVER DISEASE ( 11 FDA reports)
BACTERAEMIA ( 11 FDA reports)
BONE EROSION ( 11 FDA reports)
BONE SARCOMA ( 11 FDA reports)
BRONCHIECTASIS ( 11 FDA reports)
BUTTOCK PAIN ( 11 FDA reports)
CARBON MONOXIDE POISONING ( 11 FDA reports)
CARDIAC TAMPONADE ( 11 FDA reports)
CARDIORENAL SYNDROME ( 11 FDA reports)
CAROTID ARTERY STENOSIS ( 11 FDA reports)
CERVIX CARCINOMA ( 11 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 11 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 11 FDA reports)
DENTAL PLAQUE ( 11 FDA reports)
DYSAESTHESIA ( 11 FDA reports)
FOOT OPERATION ( 11 FDA reports)
FURUNCLE ( 11 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 11 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 11 FDA reports)
GASTRIC POLYPS ( 11 FDA reports)
HEPATITIS CHOLESTATIC ( 11 FDA reports)
HERPES SIMPLEX ( 11 FDA reports)
HISTOPLASMOSIS ( 11 FDA reports)
HOMICIDAL IDEATION ( 11 FDA reports)
HUNGER ( 11 FDA reports)
HYPERNATRAEMIA ( 11 FDA reports)
HYPOALBUMINAEMIA ( 11 FDA reports)
JAUNDICE CHOLESTATIC ( 11 FDA reports)
JUGULAR VEIN THROMBOSIS ( 11 FDA reports)
LORDOSIS ( 11 FDA reports)
MACULAR HOLE ( 11 FDA reports)
MENINGIOMA ( 11 FDA reports)
MUSCLE CONTRACTURE ( 11 FDA reports)
MUSCLE CRAMP ( 11 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 11 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 11 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 11 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 11 FDA reports)
OPEN REDUCTION OF FRACTURE ( 11 FDA reports)
OPEN WOUND ( 11 FDA reports)
OPTIC NERVE INJURY ( 11 FDA reports)
ORAL DISCOMFORT ( 11 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 11 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 11 FDA reports)
PHOTOPSIA ( 11 FDA reports)
POLYMYALGIA RHEUMATICA ( 11 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 11 FDA reports)
PROTEIN TOTAL DECREASED ( 11 FDA reports)
QRS AXIS ABNORMAL ( 11 FDA reports)
ABDOMINAL WALL ABSCESS ( 10 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 10 FDA reports)
ACUTE PSYCHOSIS ( 10 FDA reports)
ADENOCARCINOMA ( 10 FDA reports)
ALLODYNIA ( 10 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 10 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 10 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 10 FDA reports)
APLASTIC ANAEMIA ( 10 FDA reports)
APPLICATION SITE PAIN ( 10 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 10 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 10 FDA reports)
BLEPHAROSPASM ( 10 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 10 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 10 FDA reports)
BLUE TOE SYNDROME ( 10 FDA reports)
CALCINOSIS ( 10 FDA reports)
CARDIAC PACEMAKER INSERTION ( 10 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 10 FDA reports)
CAROTID ARTERY OCCLUSION ( 10 FDA reports)
CATARACT OPERATION ( 10 FDA reports)
CATHETER RELATED COMPLICATION ( 10 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 10 FDA reports)
CEREBROVASCULAR DISORDER ( 10 FDA reports)
CHANGE OF BOWEL HABIT ( 10 FDA reports)
CHAPPED LIPS ( 10 FDA reports)
CONGO-CRIMEAN HAEMORRHAGIC FEVER ( 10 FDA reports)
DEMYELINATION ( 10 FDA reports)
EAR CONGESTION ( 10 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 10 FDA reports)
ENTHESOPATHY ( 10 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 10 FDA reports)
FEMORAL NECK FRACTURE ( 10 FDA reports)
FIBROADENOMA OF BREAST ( 10 FDA reports)
GALLBLADDER INJURY ( 10 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 10 FDA reports)
GINGIVAL EROSION ( 10 FDA reports)
HAEMODYNAMIC INSTABILITY ( 10 FDA reports)
HEMICEPHALALGIA ( 10 FDA reports)
HEPATIC PAIN ( 10 FDA reports)
HEPATITIS FULMINANT ( 10 FDA reports)
HYPERMETROPIA ( 10 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 10 FDA reports)
INJECTION SITE BRUISING ( 10 FDA reports)
INJECTION SITE INDURATION ( 10 FDA reports)
IRON DEFICIENCY ( 10 FDA reports)
JOINT INSTABILITY ( 10 FDA reports)
LEUKOENCEPHALOPATHY ( 10 FDA reports)
LIPIDS INCREASED ( 10 FDA reports)
LOSS OF LIBIDO ( 10 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 10 FDA reports)
MAMMOGRAM ABNORMAL ( 10 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 10 FDA reports)
MATERNAL EXPOSURE BEFORE PREGNANCY ( 10 FDA reports)
MENIERE'S DISEASE ( 10 FDA reports)
METAPLASIA ( 10 FDA reports)
MICTURITION DISORDER ( 10 FDA reports)
MOUTH HAEMORRHAGE ( 10 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 10 FDA reports)
NASAL SEPTUM DEVIATION ( 10 FDA reports)
NEUTROPHILIA ( 10 FDA reports)
OTITIS MEDIA CHRONIC ( 10 FDA reports)
PAIN OF SKIN ( 10 FDA reports)
PARAPROTEINAEMIA ( 10 FDA reports)
PAROTITIS ( 10 FDA reports)
PARTNER STRESS ( 10 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 10 FDA reports)
PROSTATE CANCER ( 10 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 10 FDA reports)
PSEUDOMONAS INFECTION ( 10 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 10 FDA reports)
PURULENCE ( 10 FDA reports)
RETINITIS ( 10 FDA reports)
RIGHT ATRIAL DILATATION ( 10 FDA reports)
SCIATIC NERVE INJURY ( 10 FDA reports)
SCREAMING ( 10 FDA reports)
SHOCK HAEMORRHAGIC ( 10 FDA reports)
SKIN NODULE ( 10 FDA reports)
STARING ( 10 FDA reports)
SUBDURAL HAEMATOMA ( 10 FDA reports)
TREATMENT FAILURE ( 10 FDA reports)
TRIGGER FINGER ( 10 FDA reports)
URINE SODIUM DECREASED ( 10 FDA reports)
VASCULITIC RASH ( 10 FDA reports)
VOMITING PROJECTILE ( 10 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 10 FDA reports)
RETINAL VASCULAR DISORDER ( 9 FDA reports)
RIGHT VENTRICULAR FAILURE ( 9 FDA reports)
SEBORRHOEIC DERMATITIS ( 9 FDA reports)
SEROMA ( 9 FDA reports)
SERUM FERRITIN INCREASED ( 9 FDA reports)
SKULL MALFORMATION ( 9 FDA reports)
SPLENIC INFARCTION ( 9 FDA reports)
SUDDEN ONSET OF SLEEP ( 9 FDA reports)
THROMBOSIS IN DEVICE ( 9 FDA reports)
TONGUE BITING ( 9 FDA reports)
UVEITIS ( 9 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 9 FDA reports)
WRONG DRUG ADMINISTERED ( 9 FDA reports)
ABORTION INDUCED ( 9 FDA reports)
ACCIDENTAL POISONING ( 9 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 9 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 9 FDA reports)
ALVEOLAR OSTEITIS ( 9 FDA reports)
AMMONIA INCREASED ( 9 FDA reports)
ANAEMIA POSTOPERATIVE ( 9 FDA reports)
ANGIOLIPOMA ( 9 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 9 FDA reports)
APHTHOUS STOMATITIS ( 9 FDA reports)
BILE DUCT STENOSIS ( 9 FDA reports)
BLADDER CYST ( 9 FDA reports)
BLADDER PROLAPSE ( 9 FDA reports)
BLOOD CREATINE INCREASED ( 9 FDA reports)
BLOOD IRON DECREASED ( 9 FDA reports)
BLOOD LACTIC ACID INCREASED ( 9 FDA reports)
BLOOD PH INCREASED ( 9 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 9 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 9 FDA reports)
BREAST ENLARGEMENT ( 9 FDA reports)
BRUGADA SYNDROME ( 9 FDA reports)
CARTILAGE ATROPHY ( 9 FDA reports)
CHOLANGITIS ( 9 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 9 FDA reports)
CLAUSTROPHOBIA ( 9 FDA reports)
CLONUS ( 9 FDA reports)
COLONOSCOPY ( 9 FDA reports)
CONGENITAL ANOMALY ( 9 FDA reports)
COR PULMONALE ( 9 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 9 FDA reports)
CORONARY ARTERY BYPASS ( 9 FDA reports)
CYSTITIS NONINFECTIVE ( 9 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 9 FDA reports)
DEAFNESS NEUROSENSORY ( 9 FDA reports)
DEAFNESS UNILATERAL ( 9 FDA reports)
DENTAL FISTULA ( 9 FDA reports)
DISSEMINATED TUBERCULOSIS ( 9 FDA reports)
DRUG LEVEL DECREASED ( 9 FDA reports)
DRUG THERAPY ( 9 FDA reports)
EAR DISORDER ( 9 FDA reports)
ECTOPIC PREGNANCY ( 9 FDA reports)
ELECTRIC SHOCK ( 9 FDA reports)
ERUCTATION ( 9 FDA reports)
EYELID PTOSIS ( 9 FDA reports)
FOAMING AT MOUTH ( 9 FDA reports)
FOETAL GROWTH RETARDATION ( 9 FDA reports)
GINGIVAL INFECTION ( 9 FDA reports)
GLUCOSE TOLERANCE DECREASED ( 9 FDA reports)
HAEMOLYSIS ( 9 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 9 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 9 FDA reports)
HAND DEFORMITY ( 9 FDA reports)
HEPATIC ENZYME ABNORMAL ( 9 FDA reports)
HEPATIC FIBROSIS ( 9 FDA reports)
HORDEOLUM ( 9 FDA reports)
HYPERACUSIS ( 9 FDA reports)
HYPERAMMONAEMIA ( 9 FDA reports)
HYPERBILIRUBINAEMIA ( 9 FDA reports)
HYPERMAGNESAEMIA ( 9 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 9 FDA reports)
ILIUM FRACTURE ( 9 FDA reports)
IMPLANT SITE INFECTION ( 9 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 9 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 9 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 9 FDA reports)
JOINT CREPITATION ( 9 FDA reports)
LEFT VENTRICULAR FAILURE ( 9 FDA reports)
LIGAMENT INJURY ( 9 FDA reports)
LIP PAIN ( 9 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 9 FDA reports)
METASTATIC NEOPLASM ( 9 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 9 FDA reports)
MONOCYTOSIS ( 9 FDA reports)
NARCOLEPSY ( 9 FDA reports)
NECK MASS ( 9 FDA reports)
NEPHROTIC SYNDROME ( 9 FDA reports)
NEUROLOGICAL SYMPTOM ( 9 FDA reports)
NODAL RHYTHM ( 9 FDA reports)
OESOPHAGEAL CARCINOMA ( 9 FDA reports)
OESOPHAGEAL SPASM ( 9 FDA reports)
OESOPHAGEAL STENOSIS ( 9 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 9 FDA reports)
ORGANISING PNEUMONIA ( 9 FDA reports)
ORTHOPEDIC PROCEDURE ( 9 FDA reports)
OSTEOMYELITIS CHRONIC ( 9 FDA reports)
PERICARDITIS CONSTRICTIVE ( 9 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 9 FDA reports)
PERSONALITY DISORDER ( 9 FDA reports)
POST HERPETIC NEURALGIA ( 9 FDA reports)
POST-TRAUMATIC NECK SYNDROME ( 9 FDA reports)
POSTURE ABNORMAL ( 9 FDA reports)
POTENTIATING DRUG INTERACTION ( 9 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 9 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 9 FDA reports)
PULSE ABNORMAL ( 9 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 9 FDA reports)
PUPILLARY DISORDER ( 9 FDA reports)
ABDOMINAL SEPSIS ( 8 FDA reports)
ABNORMAL FAECES ( 8 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 8 FDA reports)
ADJUSTMENT DISORDER ( 8 FDA reports)
ADRENAL MASS ( 8 FDA reports)
ALCOHOL ABUSE ( 8 FDA reports)
ALCOHOLISM ( 8 FDA reports)
ANAL STENOSIS ( 8 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 8 FDA reports)
APPARENT DEATH ( 8 FDA reports)
APPLICATION SITE PRURITUS ( 8 FDA reports)
ASTIGMATISM ( 8 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 8 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 8 FDA reports)
BILE DUCT STONE ( 8 FDA reports)
BIOPSY ( 8 FDA reports)
BIOPSY BONE MARROW ( 8 FDA reports)
BLADDER PAIN ( 8 FDA reports)
BLADDER SPASM ( 8 FDA reports)
BLEPHARITIS ( 8 FDA reports)
BLINDNESS TRANSIENT ( 8 FDA reports)
BLOOD BICARBONATE DECREASED ( 8 FDA reports)
BLOOD BICARBONATE INCREASED ( 8 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 8 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 8 FDA reports)
BREAST CALCIFICATIONS ( 8 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 8 FDA reports)
CATHETER PLACEMENT ( 8 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 8 FDA reports)
CEREBELLAR ATROPHY ( 8 FDA reports)
COLON CANCER RECURRENT ( 8 FDA reports)
CSF PROTEIN INCREASED ( 8 FDA reports)
DEBRIDEMENT ( 8 FDA reports)
DIABETIC FOOT ( 8 FDA reports)
DIAPHRAGMATIC HERNIA ( 8 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 8 FDA reports)
DUODENAL ULCER PERFORATION ( 8 FDA reports)
DYSENTERY ( 8 FDA reports)
DYSPHASIA ( 8 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 8 FDA reports)
EJACULATION FAILURE ( 8 FDA reports)
EMBOLISM ( 8 FDA reports)
ENURESIS ( 8 FDA reports)
EROSIVE OESOPHAGITIS ( 8 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 8 FDA reports)
EXERCISE TOLERANCE DECREASED ( 8 FDA reports)
FACE INJURY ( 8 FDA reports)
FAECES HARD ( 8 FDA reports)
FAT TISSUE INCREASED ( 8 FDA reports)
FOLLICULITIS ( 8 FDA reports)
FRACTURE NONUNION ( 8 FDA reports)
GAMBLING ( 8 FDA reports)
GASTROINTESTINAL PAIN ( 8 FDA reports)
GLYCOSURIA ( 8 FDA reports)
HAEMARTHROSIS ( 8 FDA reports)
HAEMORRHAGIC ANAEMIA ( 8 FDA reports)
HEART RATE ABNORMAL ( 8 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 8 FDA reports)
HOMOCYSTINAEMIA ( 8 FDA reports)
HUMAN PAPILLOMA VIRUS TEST POSITIVE ( 8 FDA reports)
HYPERCOAGULATION ( 8 FDA reports)
HYPERSEXUALITY ( 8 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 8 FDA reports)
ILLUSION ( 8 FDA reports)
IMPAIRED FASTING GLUCOSE ( 8 FDA reports)
INJECTION SITE BURNING ( 8 FDA reports)
INJECTION SITE NECROSIS ( 8 FDA reports)
INJECTION SITE WARMTH ( 8 FDA reports)
INTESTINAL PERFORATION ( 8 FDA reports)
INTESTINAL POLYP ( 8 FDA reports)
INTRACRANIAL ANEURYSM ( 8 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 8 FDA reports)
KLEBSIELLA INFECTION ( 8 FDA reports)
LARGE FOR DATES BABY ( 8 FDA reports)
LARYNGITIS ( 8 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 8 FDA reports)
LIFE EXPECTANCY SHORTENED ( 8 FDA reports)
LIVEDO RETICULARIS ( 8 FDA reports)
LYMPHOEDEMA ( 8 FDA reports)
MADAROSIS ( 8 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 8 FDA reports)
MASTECTOMY ( 8 FDA reports)
MESENTERIC VASCULAR INSUFFICIENCY ( 8 FDA reports)
METHAEMOGLOBINAEMIA ( 8 FDA reports)
MICROANGIOPATHY ( 8 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 8 FDA reports)
MUSCLE SPASTICITY ( 8 FDA reports)
OCCULT BLOOD POSITIVE ( 8 FDA reports)
ONYCHOCLASIS ( 8 FDA reports)
OPTIC NERVE DISORDER ( 8 FDA reports)
ORAL MUCOSAL BLISTERING ( 8 FDA reports)
OVERWEIGHT ( 8 FDA reports)
PANCREATIC CARCINOMA ( 8 FDA reports)
PARAPARESIS ( 8 FDA reports)
PARONYCHIA ( 8 FDA reports)
PCO2 DECREASED ( 8 FDA reports)
PERITONITIS BACTERIAL ( 8 FDA reports)
PICKWICKIAN SYNDROME ( 8 FDA reports)
PIGMENTATION DISORDER ( 8 FDA reports)
PLASMACYTOMA ( 8 FDA reports)
PLATELET DISORDER ( 8 FDA reports)
POLYP ( 8 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 8 FDA reports)
PRESBYOPIA ( 8 FDA reports)
PULMONARY INFARCTION ( 8 FDA reports)
QUALITY OF LIFE DECREASED ( 8 FDA reports)
RADIATION ASSOCIATED PAIN ( 8 FDA reports)
RADIATION PNEUMONITIS ( 8 FDA reports)
RADICULAR PAIN ( 8 FDA reports)
RECTAL CANCER ( 8 FDA reports)
RESUSCITATION ( 8 FDA reports)
RETROPERITONEAL ABSCESS ( 8 FDA reports)
SERUM FERRITIN DECREASED ( 8 FDA reports)
SKIN NECROSIS ( 8 FDA reports)
SLEEP TALKING ( 8 FDA reports)
SPLEEN CONGESTION ( 8 FDA reports)
SPLENIC LESION ( 8 FDA reports)
SPONDYLOLISTHESIS ( 8 FDA reports)
STOMATITIS NECROTISING ( 8 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 8 FDA reports)
THYROIDECTOMY ( 8 FDA reports)
TOE AMPUTATION ( 8 FDA reports)
TOXIC SKIN ERUPTION ( 8 FDA reports)
UNDERDOSE ( 8 FDA reports)
UTERINE CANCER ( 8 FDA reports)
VENTRICULAR HYPOKINESIA ( 8 FDA reports)
VERTEBROPLASTY ( 8 FDA reports)
VIRAL LOAD INCREASED ( 8 FDA reports)
VULVOVAGINAL PRURITUS ( 8 FDA reports)
WOUND DEBRIDEMENT ( 8 FDA reports)
WOUND SECRETION ( 8 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 7 FDA reports)
SARCOIDOSIS ( 7 FDA reports)
SEROSITIS ( 7 FDA reports)
SHOULDER ARTHROPLASTY ( 7 FDA reports)
SKIN GRAFT ( 7 FDA reports)
SKIN MASS ( 7 FDA reports)
SLEEP WALKING ( 7 FDA reports)
SLUGGISHNESS ( 7 FDA reports)
SOCIAL PHOBIA ( 7 FDA reports)
SPUTUM CULTURE POSITIVE ( 7 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 7 FDA reports)
STRESS SYMPTOMS ( 7 FDA reports)
SUFFOCATION FEELING ( 7 FDA reports)
TACHYCARDIA PAROXYSMAL ( 7 FDA reports)
TEETH BRITTLE ( 7 FDA reports)
TENSION ( 7 FDA reports)
TIC ( 7 FDA reports)
TONGUE DRY ( 7 FDA reports)
TONGUE PARALYSIS ( 7 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 7 FDA reports)
ULCER HAEMORRHAGE ( 7 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 7 FDA reports)
URINARY HESITATION ( 7 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 7 FDA reports)
VERTIGO POSITIONAL ( 7 FDA reports)
WEIGHT FLUCTUATION ( 7 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 7 FDA reports)
WOUND COMPLICATION ( 7 FDA reports)
WOUND DRAINAGE ( 7 FDA reports)
WOUND HAEMORRHAGE ( 7 FDA reports)
ABDOMINAL ADHESIONS ( 7 FDA reports)
ABDOMINAL INFECTION ( 7 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 7 FDA reports)
ACUTE PRERENAL FAILURE ( 7 FDA reports)
ADHESION ( 7 FDA reports)
ADRENAL INSUFFICIENCY ( 7 FDA reports)
ANOXIC ENCEPHALOPATHY ( 7 FDA reports)
AORTIC VALVE SCLEROSIS ( 7 FDA reports)
APPLICATION SITE VESICLES ( 7 FDA reports)
ARNOLD-CHIARI MALFORMATION ( 7 FDA reports)
ASTHENOPIA ( 7 FDA reports)
ATROPHY ( 7 FDA reports)
AUTOIMMUNE HEPATITIS ( 7 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 7 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 7 FDA reports)
BODY HEIGHT DECREASED ( 7 FDA reports)
BONE SCAN ABNORMAL ( 7 FDA reports)
BOWEL SOUNDS ABNORMAL ( 7 FDA reports)
BREAST CANCER METASTATIC ( 7 FDA reports)
CATHETER SEPSIS ( 7 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 7 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 7 FDA reports)
CHOLESTEROSIS ( 7 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 7 FDA reports)
COMPUTERISED TOMOGRAM ( 7 FDA reports)
CONVERSION DISORDER ( 7 FDA reports)
CRANIOTOMY ( 7 FDA reports)
DRUG CLEARANCE DECREASED ( 7 FDA reports)
DRUG RESISTANCE ( 7 FDA reports)
DRY THROAT ( 7 FDA reports)
DYSGRAPHIA ( 7 FDA reports)
EAR DISCOMFORT ( 7 FDA reports)
EMBOLIC STROKE ( 7 FDA reports)
ENCEPHALOMALACIA ( 7 FDA reports)
ENTERITIS ( 7 FDA reports)
EPICONDYLITIS ( 7 FDA reports)
EXCESSIVE EYE BLINKING ( 7 FDA reports)
EXTRAVASATION ( 7 FDA reports)
FAILURE TO THRIVE ( 7 FDA reports)
FEELING GUILTY ( 7 FDA reports)
FIBROMA ( 7 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 7 FDA reports)
FOREIGN BODY TRAUMA ( 7 FDA reports)
GALLBLADDER OPERATION ( 7 FDA reports)
GASTROINTESTINAL HYPERMOTILITY ( 7 FDA reports)
GINGIVAL RECESSION ( 7 FDA reports)
HAEMORRHAGE URINARY TRACT ( 7 FDA reports)
HAIR GROWTH ABNORMAL ( 7 FDA reports)
HELICOBACTER TEST POSITIVE ( 7 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 7 FDA reports)
HERNIA REPAIR ( 7 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 7 FDA reports)
HYDROCEPHALUS ( 7 FDA reports)
HYPOCHLORAEMIA ( 7 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 7 FDA reports)
INAPPROPRIATE AFFECT ( 7 FDA reports)
INCISION SITE INFECTION ( 7 FDA reports)
INJECTION SITE OEDEMA ( 7 FDA reports)
INNER EAR DISORDER ( 7 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 7 FDA reports)
INTESTINAL HAEMORRHAGE ( 7 FDA reports)
INTESTINAL INFARCTION ( 7 FDA reports)
JUGULAR VEIN DISTENSION ( 7 FDA reports)
KETOACIDOSIS ( 7 FDA reports)
LACTOSE INTOLERANCE ( 7 FDA reports)
LERICHE SYNDROME ( 7 FDA reports)
LEUKAEMIA ( 7 FDA reports)
LIMB OPERATION ( 7 FDA reports)
LIP INJURY ( 7 FDA reports)
LONG QT SYNDROME ( 7 FDA reports)
LYMPH GLAND INFECTION ( 7 FDA reports)
MAGNESIUM DEFICIENCY ( 7 FDA reports)
MASKED FACIES ( 7 FDA reports)
MENOPAUSE ( 7 FDA reports)
METABOLIC ENCEPHALOPATHY ( 7 FDA reports)
METASTASES TO MENINGES ( 7 FDA reports)
MYOCARDIAL FIBROSIS ( 7 FDA reports)
NASAL MUCOSAL DISORDER ( 7 FDA reports)
NASAL ULCER ( 7 FDA reports)
NEUROTOXICITY ( 7 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 7 FDA reports)
NON-SMALL CELL LUNG CANCER ( 7 FDA reports)
OCULAR ICTERUS ( 7 FDA reports)
ONYCHOMADESIS ( 7 FDA reports)
OPTIC NEUROPATHY ( 7 FDA reports)
ORGAN FAILURE ( 7 FDA reports)
OSTEORADIONECROSIS ( 7 FDA reports)
OVARIAN MASS ( 7 FDA reports)
PAPILLOMA ( 7 FDA reports)
PIRIFORMIS SYNDROME ( 7 FDA reports)
PITTING OEDEMA ( 7 FDA reports)
PLEURAL DISORDER ( 7 FDA reports)
PNEUMONIA MYCOPLASMAL ( 7 FDA reports)
POLYCYSTIC OVARIES ( 7 FDA reports)
POLYDACTYLY ( 7 FDA reports)
POST PROCEDURAL INFECTION ( 7 FDA reports)
PSYCHOMOTOR RETARDATION ( 7 FDA reports)
PURPURA ( 7 FDA reports)
PYELOCALIECTASIS ( 7 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 7 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 7 FDA reports)
ADENOMA BENIGN ( 6 FDA reports)
AGITATION NEONATAL ( 6 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 6 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 6 FDA reports)
AMENORRHOEA ( 6 FDA reports)
ANOSMIA ( 6 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 6 FDA reports)
AORTIC BRUIT ( 6 FDA reports)
AORTIC VALVE REPLACEMENT ( 6 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 6 FDA reports)
ASBESTOSIS ( 6 FDA reports)
ASPIRATION PLEURAL CAVITY ( 6 FDA reports)
BACTERIAL TEST POSITIVE ( 6 FDA reports)
BLADDER OPERATION ( 6 FDA reports)
BLOOD DISORDER ( 6 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 6 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 6 FDA reports)
BLOOD SODIUM INCREASED ( 6 FDA reports)
BRADYKINESIA ( 6 FDA reports)
BRAIN INJURY ( 6 FDA reports)
BREAST CYST ( 6 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 6 FDA reports)
BURNS SECOND DEGREE ( 6 FDA reports)
CARDIAC ANEURYSM ( 6 FDA reports)
CARDIAC HYPERTROPHY ( 6 FDA reports)
CATHETERISATION CARDIAC ( 6 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 6 FDA reports)
CEREBRAL HAEMATOMA ( 6 FDA reports)
CHOREA ( 6 FDA reports)
CLEFT PALATE ( 6 FDA reports)
CLOSTRIDIUM COLITIS ( 6 FDA reports)
COMPARTMENT SYNDROME ( 6 FDA reports)
COMPULSIVE SHOPPING ( 6 FDA reports)
CONDUCTION DISORDER ( 6 FDA reports)
CUSHINGOID ( 6 FDA reports)
CYSTITIS HAEMORRHAGIC ( 6 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 6 FDA reports)
DENTAL OPERATION ( 6 FDA reports)
DEPRESSION SUICIDAL ( 6 FDA reports)
DEVELOPMENTAL DELAY ( 6 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 6 FDA reports)
DIABETES WITH HYPEROSMOLARITY ( 6 FDA reports)
DROP ATTACKS ( 6 FDA reports)
DRUG EFFECT INCREASED ( 6 FDA reports)
DRUG EFFECT PROLONGED ( 6 FDA reports)
DYSKINESIA OESOPHAGEAL ( 6 FDA reports)
DYSMENORRHOEA ( 6 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 6 FDA reports)
ELECTROCARDIOGRAM QT SHORTENED ( 6 FDA reports)
ENDOMETRIAL CANCER STAGE II ( 6 FDA reports)
ENERGY INCREASED ( 6 FDA reports)
EPIDIDYMITIS ( 6 FDA reports)
ESCHERICHIA BACTERAEMIA ( 6 FDA reports)
EXPIRED DRUG ADMINISTERED ( 6 FDA reports)
EXTREMITY CONTRACTURE ( 6 FDA reports)
FASCIITIS ( 6 FDA reports)
FEAR OF DEATH ( 6 FDA reports)
FEEDING DISORDER ( 6 FDA reports)
FLASHBACK ( 6 FDA reports)
FOOD INTOLERANCE ( 6 FDA reports)
FOOD POISONING ( 6 FDA reports)
FUNGAEMIA ( 6 FDA reports)
FUNGAL SKIN INFECTION ( 6 FDA reports)
GASTRIC ULCER PERFORATION ( 6 FDA reports)
GASTROINTESTINAL INFECTION ( 6 FDA reports)
GINGIVAL ATROPHY ( 6 FDA reports)
GINGIVAL ERYTHEMA ( 6 FDA reports)
GRANULOMA ANNULARE ( 6 FDA reports)
HAEMORRHAGIC STROKE ( 6 FDA reports)
HAIR COLOUR CHANGES ( 6 FDA reports)
HAIR DISORDER ( 6 FDA reports)
HALLUCINATION, TACTILE ( 6 FDA reports)
HEAD TITUBATION ( 6 FDA reports)
HELICOBACTER GASTRITIS ( 6 FDA reports)
HEPATITIS A ( 6 FDA reports)
HEPATITIS TOXIC ( 6 FDA reports)
HICCUPS ( 6 FDA reports)
HODGKIN'S DISEASE STAGE IV ( 6 FDA reports)
HOSTILITY ( 6 FDA reports)
HYPOGONADISM ( 6 FDA reports)
ILEAL STENOSIS ( 6 FDA reports)
IMPULSIVE BEHAVIOUR ( 6 FDA reports)
INFECTED SKIN ULCER ( 6 FDA reports)
INJECTION SITE MASS ( 6 FDA reports)
INTESTINAL RESECTION ( 6 FDA reports)
INTRACARDIAC THROMBUS ( 6 FDA reports)
ISCHAEMIC HEPATITIS ( 6 FDA reports)
IVTH NERVE PARESIS ( 6 FDA reports)
KIDNEY ENLARGEMENT ( 6 FDA reports)
KLEBSIELLA TEST POSITIVE ( 6 FDA reports)
LIGAMENT SPRAIN ( 6 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 6 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 6 FDA reports)
LYMPH NODE TUBERCULOSIS ( 6 FDA reports)
LYMPHOPENIA ( 6 FDA reports)
MALIGNANT HYPERTENSION ( 6 FDA reports)
MEDIASTINAL DISORDER ( 6 FDA reports)
MEGACOLON ( 6 FDA reports)
MENINGITIS ASEPTIC ( 6 FDA reports)
METABOLIC ALKALOSIS ( 6 FDA reports)
METASTATIC SQUAMOUS CELL CARCINOMA ( 6 FDA reports)
MICROCEPHALY ( 6 FDA reports)
MOANING ( 6 FDA reports)
MUCOUS MEMBRANE DISORDER ( 6 FDA reports)
MULTI-ORGAN DISORDER ( 6 FDA reports)
MUSCLE ABSCESS ( 6 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 6 FDA reports)
NEUROGENIC BLADDER ( 6 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 6 FDA reports)
OBSTRUCTION ( 6 FDA reports)
OCULAR VASCULAR DISORDER ( 6 FDA reports)
OPPORTUNISTIC INFECTION ( 6 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 6 FDA reports)
OSTEOMA ( 6 FDA reports)
OSTEOMALACIA ( 6 FDA reports)
OTITIS MEDIA ACUTE ( 6 FDA reports)
OVARIAN ABSCESS ( 6 FDA reports)
PANCREATIC ATROPHY ( 6 FDA reports)
PARAPLEGIA ( 6 FDA reports)
PATELLA FRACTURE ( 6 FDA reports)
PEAU D'ORANGE ( 6 FDA reports)
PERIPHERAL NERVE LESION ( 6 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 6 FDA reports)
PO2 INCREASED ( 6 FDA reports)
POOR DENTAL CONDITION ( 6 FDA reports)
PRE-ECLAMPSIA ( 6 FDA reports)
PROTEUS INFECTION ( 6 FDA reports)
PROTHROMBIN TIME SHORTENED ( 6 FDA reports)
PSEUDOPOLYPOSIS ( 6 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 6 FDA reports)
PTERYGIUM ( 6 FDA reports)
PULMONARY GRANULOMA ( 6 FDA reports)
RECTAL DISCHARGE ( 6 FDA reports)
RECTAL POLYP ( 6 FDA reports)
RECURRENT CANCER ( 6 FDA reports)
RENAL CANCER METASTATIC ( 6 FDA reports)
RESPIRATION ABNORMAL ( 6 FDA reports)
RHINALGIA ( 6 FDA reports)
ROSACEA ( 6 FDA reports)
ROTATOR CUFF REPAIR ( 6 FDA reports)
SCAB ( 6 FDA reports)
SCLERODERMA ( 6 FDA reports)
SENILE DEMENTIA ( 6 FDA reports)
SINUS ARREST ( 6 FDA reports)
SOCIAL PROBLEM ( 6 FDA reports)
SPINAL FUSION SURGERY ( 6 FDA reports)
SPINAL X-RAY ABNORMAL ( 6 FDA reports)
TACHYARRHYTHMIA ( 6 FDA reports)
TENOSYNOVITIS ( 6 FDA reports)
TESTICULAR MASS ( 6 FDA reports)
THROMBOCYTOPENIC PURPURA ( 6 FDA reports)
TINEL'S SIGN ( 6 FDA reports)
TONGUE BLISTERING ( 6 FDA reports)
TONGUE COATED ( 6 FDA reports)
TONIC CLONIC MOVEMENTS ( 6 FDA reports)
TONSILLAR DISORDER ( 6 FDA reports)
TONSILLITIS ( 6 FDA reports)
TOOTH REPAIR ( 6 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 6 FDA reports)
TRANSFUSION REACTION ( 6 FDA reports)
TUMOUR HAEMORRHAGE ( 6 FDA reports)
TUMOUR LYSIS SYNDROME ( 6 FDA reports)
UHTHOFF'S PHENOMENON ( 6 FDA reports)
ULCERATIVE KERATITIS ( 6 FDA reports)
ULNA FRACTURE ( 6 FDA reports)
UTERINE DISORDER ( 6 FDA reports)
VASCULAR OCCLUSION ( 6 FDA reports)
VERTEBRAL COLUMN MASS ( 6 FDA reports)
VESTIBULAR DISORDER ( 6 FDA reports)
VOCAL CORD POLYP ( 6 FDA reports)
XEROSIS ( 6 FDA reports)
RHINOVIRUS INFECTION ( 5 FDA reports)
SACRALISATION ( 5 FDA reports)
SALIVA ALTERED ( 5 FDA reports)
SCLERITIS ( 5 FDA reports)
SEBORRHOEIC KERATOSIS ( 5 FDA reports)
SENSATION OF PRESSURE ( 5 FDA reports)
SERONEGATIVE ARTHRITIS ( 5 FDA reports)
SHIFT TO THE LEFT ( 5 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 5 FDA reports)
SINOATRIAL BLOCK ( 5 FDA reports)
SINUS TARSI SYNDROME ( 5 FDA reports)
SKIN EROSION ( 5 FDA reports)
SKIN HYPERPIGMENTATION ( 5 FDA reports)
SKIN HYPOPIGMENTATION ( 5 FDA reports)
SKIN INJURY ( 5 FDA reports)
SKIN NEOPLASM EXCISION ( 5 FDA reports)
SKIN PLAQUE ( 5 FDA reports)
SKIN TURGOR DECREASED ( 5 FDA reports)
SLEEP TERROR ( 5 FDA reports)
SOFT TISSUE INFLAMMATION ( 5 FDA reports)
SPINAL LAMINECTOMY ( 5 FDA reports)
SPINAL OPERATION ( 5 FDA reports)
SPONDYLITIC MYELOPATHY ( 5 FDA reports)
SUBILEUS ( 5 FDA reports)
TANDEM GAIT TEST ABNORMAL ( 5 FDA reports)
TENDON INJURY ( 5 FDA reports)
TENDON PAIN ( 5 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 5 FDA reports)
THROMBOCYTOSIS ( 5 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 5 FDA reports)
TUBERCULIN TEST POSITIVE ( 5 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 5 FDA reports)
URETHRITIS ( 5 FDA reports)
URINE KETONE BODY PRESENT ( 5 FDA reports)
VAGINAL CANDIDIASIS ( 5 FDA reports)
VAGINAL CYST ( 5 FDA reports)
VAGINITIS GARDNERELLA ( 5 FDA reports)
VENOUS OCCLUSION ( 5 FDA reports)
VENTRICULAR SEPTAL DEFECT REPAIR ( 5 FDA reports)
VIBRATION TEST ABNORMAL ( 5 FDA reports)
VITAMIN D DECREASED ( 5 FDA reports)
VITH NERVE PARALYSIS ( 5 FDA reports)
VITREOUS DETACHMENT ( 5 FDA reports)
VULVOVAGINAL DISCOMFORT ( 5 FDA reports)
ABDOMINAL RIGIDITY ( 5 FDA reports)
ABSCESS DRAINAGE ( 5 FDA reports)
ADRENAL ADENOMA ( 5 FDA reports)
ADRENAL DISORDER ( 5 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 5 FDA reports)
ANAL HAEMORRHAGE ( 5 FDA reports)
ANION GAP INCREASED ( 5 FDA reports)
ANOGENITAL WARTS ( 5 FDA reports)
ANOXIA ( 5 FDA reports)
ANTIDEPRESSANT DRUG LEVEL INCREASED ( 5 FDA reports)
AORTIC VALVE CALCIFICATION ( 5 FDA reports)
APLASIA PURE RED CELL ( 5 FDA reports)
APPLICATION SITE DERMATITIS ( 5 FDA reports)
APPLICATION SITE IRRITATION ( 5 FDA reports)
ARTERIAL HAEMORRHAGE ( 5 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 5 FDA reports)
ASPERGILLOSIS ( 5 FDA reports)
ATHEROSCLEROSIS ( 5 FDA reports)
AUTOMATISM ( 5 FDA reports)
BACTERIAL SEPSIS ( 5 FDA reports)
BENCE JONES PROTEINURIA ( 5 FDA reports)
BILE DUCT CANCER ( 5 FDA reports)
BILIARY TRACT DISORDER ( 5 FDA reports)
BLOOD ALCOHOL INCREASED ( 5 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 5 FDA reports)
BLOOD PRESSURE ORTHOSTATIC DECREASED ( 5 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 5 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 5 FDA reports)
BLOOD UREA DECREASED ( 5 FDA reports)
BLOODY DISCHARGE ( 5 FDA reports)
BODY MASS INDEX INCREASED ( 5 FDA reports)
BONE FISTULA ( 5 FDA reports)
BONE MARROW DEPRESSION ( 5 FDA reports)
BONE MARROW DISORDER ( 5 FDA reports)
BONE OPERATION ( 5 FDA reports)
BRAIN OPERATION ( 5 FDA reports)
BRAIN SCAN ABNORMAL ( 5 FDA reports)
BREAST RECONSTRUCTION ( 5 FDA reports)
BRONCHIOLITIS ( 5 FDA reports)
CARDIAC FLUTTER ( 5 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 5 FDA reports)
CARDIOPULMONARY FAILURE ( 5 FDA reports)
CATHETER REMOVAL ( 5 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 5 FDA reports)
CEREBELLAR HAEMORRHAGE ( 5 FDA reports)
CEREBRAL CYST ( 5 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 5 FDA reports)
CHEST WALL PAIN ( 5 FDA reports)
CHLAMYDIAL INFECTION ( 5 FDA reports)
CHOLECYSTITIS INFECTIVE ( 5 FDA reports)
CONVULSIVE THRESHOLD LOWERED ( 5 FDA reports)
CRYPTOCOCCOSIS ( 5 FDA reports)
CUTANEOUS VASCULITIS ( 5 FDA reports)
DEFAECATION URGENCY ( 5 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 5 FDA reports)
DERMATITIS BULLOUS ( 5 FDA reports)
DETOXIFICATION ( 5 FDA reports)
DIABETIC AUTONOMIC NEUROPATHY ( 5 FDA reports)
DIABETIC GASTROPARESIS ( 5 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 5 FDA reports)
DISSOCIATIVE FUGUE ( 5 FDA reports)
DOPAMINE DYSREGULATION SYNDROME ( 5 FDA reports)
DRUG TOLERANCE INCREASED ( 5 FDA reports)
DYSTHYMIC DISORDER ( 5 FDA reports)
EAR ABRASION ( 5 FDA reports)
EARLY MORNING AWAKENING ( 5 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 5 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 5 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 5 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 5 FDA reports)
ENDOTRACHEAL INTUBATION ( 5 FDA reports)
ENTEROVIRUS INFECTION ( 5 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 5 FDA reports)
EXOPHTHALMOS ( 5 FDA reports)
EYE INJURY ( 5 FDA reports)
FEELINGS OF WORTHLESSNESS ( 5 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 5 FDA reports)
FLUID INTAKE REDUCED ( 5 FDA reports)
FLUID INTAKE RESTRICTION ( 5 FDA reports)
FRACTURED COCCYX ( 5 FDA reports)
FRACTURED SACRUM ( 5 FDA reports)
GASTRIC BYPASS ( 5 FDA reports)
GASTRIC DILATATION ( 5 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 5 FDA reports)
GINGIVAL HYPERPLASIA ( 5 FDA reports)
GLOMERULONEPHRITIS ( 5 FDA reports)
GRIMACING ( 5 FDA reports)
HAEMANGIOMA OF LIVER ( 5 FDA reports)
HAEMATOSPERMIA ( 5 FDA reports)
HAIR TEXTURE ABNORMAL ( 5 FDA reports)
HANGOVER ( 5 FDA reports)
HEAD DISCOMFORT ( 5 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 5 FDA reports)
HEPATIC NEOPLASM ( 5 FDA reports)
HEPATOBILIARY SCAN ABNORMAL ( 5 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 5 FDA reports)
HYPERAEMIA ( 5 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 5 FDA reports)
HYPERBILIRUBINAEMIA NEONATAL ( 5 FDA reports)
HYPERCHLORHYDRIA ( 5 FDA reports)
HYPERPROLACTINAEMIA ( 5 FDA reports)
HYPERVIGILANCE ( 5 FDA reports)
ILEOSTOMY ( 5 FDA reports)
INCISION SITE HAEMORRHAGE ( 5 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 5 FDA reports)
INFUSION SITE PAIN ( 5 FDA reports)
INJECTION SITE INFECTION ( 5 FDA reports)
INJECTION SITE PAPULE ( 5 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 5 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 5 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 5 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 5 FDA reports)
INTUBATION ( 5 FDA reports)
IRREGULAR SLEEP PHASE ( 5 FDA reports)
JUDGEMENT IMPAIRED ( 5 FDA reports)
LEPROSY ( 5 FDA reports)
LHERMITTE'S SIGN ( 5 FDA reports)
LIGAMENT RUPTURE ( 5 FDA reports)
LIP DISORDER ( 5 FDA reports)
LOSS OF EMPLOYMENT ( 5 FDA reports)
LOW TURNOVER OSTEOPATHY ( 5 FDA reports)
LYME DISEASE ( 5 FDA reports)
LYMPHANGITIS ( 5 FDA reports)
MALABSORPTION ( 5 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 5 FDA reports)
MEAN CELL VOLUME INCREASED ( 5 FDA reports)
MECHANICAL VENTILATION ( 5 FDA reports)
MEDICATION RESIDUE ( 5 FDA reports)
MENSTRUATION DELAYED ( 5 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 5 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 5 FDA reports)
MICROSCOPIC POLYANGIITIS ( 5 FDA reports)
MITRAL VALVE CALCIFICATION ( 5 FDA reports)
MUSCLE FATIGUE ( 5 FDA reports)
MUSCLE HAEMORRHAGE ( 5 FDA reports)
MYELITIS ( 5 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 5 FDA reports)
MYOGLOBINAEMIA ( 5 FDA reports)
MYOPIA ( 5 FDA reports)
NAIL INFECTION ( 5 FDA reports)
NASAL DISCOMFORT ( 5 FDA reports)
NEGATIVE THOUGHTS ( 5 FDA reports)
NEONATAL DISORDER ( 5 FDA reports)
NEONATAL RESPIRATORY DEPRESSION ( 5 FDA reports)
NEOPLASM SKIN ( 5 FDA reports)
NEPHRITIS INTERSTITIAL ( 5 FDA reports)
NEUROMYELITIS OPTICA ( 5 FDA reports)
NIKOLSKY'S SIGN ( 5 FDA reports)
NOSOCOMIAL INFECTION ( 5 FDA reports)
OESOPHAGEAL OPERATION ( 5 FDA reports)
OESOPHAGITIS ULCERATIVE ( 5 FDA reports)
OLIGOHYDRAMNIOS ( 5 FDA reports)
ORAL DISCHARGE ( 5 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 5 FDA reports)
OSTECTOMY ( 5 FDA reports)
OTITIS MEDIA ( 5 FDA reports)
OXYGEN SUPPLEMENTATION ( 5 FDA reports)
PAINFUL RESPIRATION ( 5 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 5 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 5 FDA reports)
PERIODONTAL INFECTION ( 5 FDA reports)
PERIORBITAL OEDEMA ( 5 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 5 FDA reports)
PHARYNGEAL ERYTHEMA ( 5 FDA reports)
PLATELET TRANSFUSION ( 5 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 5 FDA reports)
POLYPECTOMY ( 5 FDA reports)
POST CONCUSSION SYNDROME ( 5 FDA reports)
POST THROMBOTIC SYNDROME ( 5 FDA reports)
POSTICTAL STATE ( 5 FDA reports)
POUCHITIS ( 5 FDA reports)
PREMATURE DELIVERY ( 5 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 5 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 5 FDA reports)
QUADRIPARESIS ( 5 FDA reports)
RECTAL FISSURE ( 5 FDA reports)
REGURGITATION ( 5 FDA reports)
RENAL ANEURYSM ( 5 FDA reports)
RENAL ARTERY STENOSIS ( 5 FDA reports)
RENAL CELL CARCINOMA ( 5 FDA reports)
RESORPTION BONE INCREASED ( 5 FDA reports)
RETAINED PLACENTA OR MEMBRANES ( 5 FDA reports)
ABDOMINAL MASS ( 4 FDA reports)
ABDOMINAL SYMPTOM ( 4 FDA reports)
ABDOMINAL WALL INFECTION ( 4 FDA reports)
ABNORMAL CLOTTING FACTOR ( 4 FDA reports)
ABNORMAL WEIGHT GAIN ( 4 FDA reports)
ABULIA ( 4 FDA reports)
ACUTE LUNG INJURY ( 4 FDA reports)
ACUTE PULMONARY OEDEMA ( 4 FDA reports)
ADENOTONSILLECTOMY ( 4 FDA reports)
ALVEOLITIS ALLERGIC ( 4 FDA reports)
AMPUTATION ( 4 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 4 FDA reports)
ANAEMIA MACROCYTIC ( 4 FDA reports)
ANORECTAL DISORDER ( 4 FDA reports)
ANORGASMIA ( 4 FDA reports)
ANTIDEPRESSANT DRUG LEVEL ABOVE THERAPEUTIC ( 4 FDA reports)
AORTIC ANEURYSM REPAIR ( 4 FDA reports)
AORTIC ATHEROSCLEROSIS ( 4 FDA reports)
AORTIC DISORDER ( 4 FDA reports)
AORTIC VALVE DISEASE ( 4 FDA reports)
APNOEIC ATTACK ( 4 FDA reports)
ARTERIAL INSUFFICIENCY ( 4 FDA reports)
ARTERIOGRAM CORONARY ( 4 FDA reports)
ARTHRITIS INFECTIVE ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 4 FDA reports)
ATROPHIC VULVOVAGINITIS ( 4 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 4 FDA reports)
AXILLARY PAIN ( 4 FDA reports)
AXONAL NEUROPATHY ( 4 FDA reports)
BASEDOW'S DISEASE ( 4 FDA reports)
BEHCET'S SYNDROME ( 4 FDA reports)
BENIGN MUSCLE NEOPLASM ( 4 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 4 FDA reports)
BINGE EATING ( 4 FDA reports)
BLADDER DYSFUNCTION ( 4 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 4 FDA reports)
BLOOD GASES ABNORMAL ( 4 FDA reports)
BLOOD MAGNESIUM INCREASED ( 4 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 4 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 4 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 4 FDA reports)
BLOOD UREA ABNORMAL ( 4 FDA reports)
BONE CYST ( 4 FDA reports)
BONE DECALCIFICATION ( 4 FDA reports)
BONE GRAFT ( 4 FDA reports)
BONE NEOPLASM MALIGNANT ( 4 FDA reports)
BOTULISM ( 4 FDA reports)
BRADYPNOEA ( 4 FDA reports)
BRAIN HERNIATION ( 4 FDA reports)
BRAIN NATRIURETIC PEPTIDE DECREASED ( 4 FDA reports)
BREAST DISCOMFORT ( 4 FDA reports)
BREAST LUMP REMOVAL ( 4 FDA reports)
BREAST OPERATION ( 4 FDA reports)
BRONCHOPLEURAL FISTULA ( 4 FDA reports)
CARDIAC ASTHMA ( 4 FDA reports)
CARDIAC FAILURE CHRONIC ( 4 FDA reports)
CARDIAC OPERATION ( 4 FDA reports)
CARDIAC PERFORATION ( 4 FDA reports)
CARDIAC SEPTAL DEFECT ( 4 FDA reports)
CARDIAC STRESS TEST ( 4 FDA reports)
CEREBELLAR ATAXIA ( 4 FDA reports)
CEREBRAL THROMBOSIS ( 4 FDA reports)
CERUMEN IMPACTION ( 4 FDA reports)
CERVICAL POLYP ( 4 FDA reports)
CHONDROPATHY ( 4 FDA reports)
CHORIORETINAL ATROPHY ( 4 FDA reports)
CHRONIC HEPATITIS ( 4 FDA reports)
COARCTATION OF THE AORTA ( 4 FDA reports)
COLON INJURY ( 4 FDA reports)
COLON POLYPECTOMY ( 4 FDA reports)
COMPLEX PARTIAL SEIZURES ( 4 FDA reports)
CONGENITAL NYSTAGMUS ( 4 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 4 FDA reports)
CONSTRICTED AFFECT ( 4 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 4 FDA reports)
CORNEAL REFLEX DECREASED ( 4 FDA reports)
CORONARY ANGIOPLASTY ( 4 FDA reports)
CORONARY ARTERY THROMBOSIS ( 4 FDA reports)
CRANIOSYNOSTOSIS ( 4 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 4 FDA reports)
CULTURE URINE POSITIVE ( 4 FDA reports)
DEAFNESS BILATERAL ( 4 FDA reports)
DECREASED EYE CONTACT ( 4 FDA reports)
DELIRIUM TREMENS ( 4 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 4 FDA reports)
DERMATITIS PSORIASIFORM ( 4 FDA reports)
DEVICE BREAKAGE ( 4 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 4 FDA reports)
DIPLEGIA ( 4 FDA reports)
DISSOCIATIVE DISORDER ( 4 FDA reports)
DRUG INTERACTION POTENTIATION ( 4 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 4 FDA reports)
DRUG TOLERANCE DECREASED ( 4 FDA reports)
DRUG-INDUCED LIVER INJURY ( 4 FDA reports)
DUODENAL POLYP ( 4 FDA reports)
DYSLALIA ( 4 FDA reports)
DYSPLASIA ( 4 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 4 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX SHORTENED ( 4 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 4 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 4 FDA reports)
ELEVATED MOOD ( 4 FDA reports)
EMPYEMA ( 4 FDA reports)
ENDOMETRIAL ABLATION ( 4 FDA reports)
ENDOMETRIAL CANCER ( 4 FDA reports)
ENTEROCUTANEOUS FISTULA ( 4 FDA reports)
ERYSIPELAS ( 4 FDA reports)
ESCHERICHIA VAGINITIS ( 4 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 4 FDA reports)
EXFOLIATIVE RASH ( 4 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 4 FDA reports)
EYE DISCHARGE ( 4 FDA reports)
EYE INFLAMMATION ( 4 FDA reports)
EYES SUNKEN ( 4 FDA reports)
FACIAL NERVE DISORDER ( 4 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 4 FDA reports)
FINGER AMPUTATION ( 4 FDA reports)
FOREARM FRACTURE ( 4 FDA reports)
GALLBLADDER POLYP ( 4 FDA reports)
GASTRIC PERFORATION ( 4 FDA reports)
GASTROINTESTINAL NEOPLASM ( 4 FDA reports)
GASTROINTESTINAL ULCER ( 4 FDA reports)
GLIOSIS ( 4 FDA reports)
GRANULOCYTE COUNT INCREASED ( 4 FDA reports)
HAEMATOMA INFECTION ( 4 FDA reports)
HAEMORRHOID OPERATION ( 4 FDA reports)
HEART DISEASE CONGENITAL ( 4 FDA reports)
HEAT STROKE ( 4 FDA reports)
HEMIANOPIA HOMONYMOUS ( 4 FDA reports)
HEPATITIS B ( 4 FDA reports)
HEPATITIS C RNA POSITIVE ( 4 FDA reports)
HEPATOCELLULAR INJURY ( 4 FDA reports)
HERNIA OBSTRUCTIVE ( 4 FDA reports)
HERPES VIRUS INFECTION ( 4 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 4 FDA reports)
HODGKIN'S DISEASE ( 4 FDA reports)
HYPERALBUMINAEMIA ( 4 FDA reports)
HYPERGAMMAGLOBULINAEMIA BENIGN MONOCLONAL ( 4 FDA reports)
HYPERPARATHYROIDISM ( 4 FDA reports)
HYPOCHROMIC ANAEMIA ( 4 FDA reports)
HYPOPERFUSION ( 4 FDA reports)
HYPOPROTEINAEMIA ( 4 FDA reports)
HYPOVITAMINOSIS ( 4 FDA reports)
ILIAC ARTERY THROMBOSIS ( 4 FDA reports)
IMPATIENCE ( 4 FDA reports)
IMPETIGO ( 4 FDA reports)
IMPRISONMENT ( 4 FDA reports)
IMPULSE-CONTROL DISORDER ( 4 FDA reports)
INADEQUATE DIET ( 4 FDA reports)
INCISION SITE COMPLICATION ( 4 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 4 FDA reports)
INCORRECT STORAGE OF DRUG ( 4 FDA reports)
INDURATION ( 4 FDA reports)
INFECTIVE ANEURYSM ( 4 FDA reports)
INFLAMMATORY MARKER INCREASED ( 4 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 4 FDA reports)
INFUSION SITE ERYTHEMA ( 4 FDA reports)
INJECTION SITE VESICLES ( 4 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 4 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 4 FDA reports)
JAUNDICE NEONATAL ( 4 FDA reports)
JEJUNITIS ( 4 FDA reports)
KERATOACANTHOMA ( 4 FDA reports)
KIDNEY FIBROSIS ( 4 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 4 FDA reports)
LASER THERAPY ( 4 FDA reports)
LEGAL PROBLEM ( 4 FDA reports)
LICHENIFICATION ( 4 FDA reports)
LIPOPROTEIN (A) INCREASED ( 4 FDA reports)
LISTERIOSIS ( 4 FDA reports)
LOSS OF CONTROL OF LEGS ( 4 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 4 FDA reports)
LUNG ADENOCARCINOMA ( 4 FDA reports)
LUNG CANCER METASTATIC ( 4 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE 0 ( 4 FDA reports)
MACULAR OEDEMA ( 4 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 4 FDA reports)
MAMMOGRAM ( 4 FDA reports)
MASS EXCISION ( 4 FDA reports)
MEAN CELL HAEMOGLOBIN ( 4 FDA reports)
MECONIUM STAIN ( 4 FDA reports)
MEDICAL DEVICE IMPLANTATION ( 4 FDA reports)
MENINGITIS BACTERIAL ( 4 FDA reports)
MENINGITIS HERPES ( 4 FDA reports)
MENINGITIS TUBERCULOUS ( 4 FDA reports)
MERALGIA PARAESTHETICA ( 4 FDA reports)
MONONUCLEOSIS SYNDROME ( 4 FDA reports)
MORBID THOUGHTS ( 4 FDA reports)
MUCOSAL EROSION ( 4 FDA reports)
MULTIPLE FRACTURES ( 4 FDA reports)
MUSCLE HYPERTROPHY ( 4 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX IMMUNE RESTORATION DISEASE ( 4 FDA reports)
MYODESOPSIA ( 4 FDA reports)
MYOGLOBIN BLOOD PRESENT ( 4 FDA reports)
MYOGLOBIN URINE PRESENT ( 4 FDA reports)
NARCOTIC INTOXICATION ( 4 FDA reports)
NASAL SEPTUM PERFORATION ( 4 FDA reports)
NERVE ROOT COMPRESSION ( 4 FDA reports)
NERVE ROOT LESION ( 4 FDA reports)
NEURODERMATITIS ( 4 FDA reports)
NEUROMA ( 4 FDA reports)
NEUTROPHIL COUNT ( 4 FDA reports)
NICOTINE DEPENDENCE ( 4 FDA reports)
OESOPHAGOSCOPY ABNORMAL ( 4 FDA reports)
OPEN FRACTURE ( 4 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 4 FDA reports)
ORTHOSTATIC INTOLERANCE ( 4 FDA reports)
OTITIS EXTERNA ( 4 FDA reports)
OXYGEN SATURATION ABNORMAL ( 4 FDA reports)
PACHYMENINGITIS ( 4 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 4 FDA reports)
PANCREATIC ENZYMES INCREASED ( 4 FDA reports)
PANCREATIC NEOPLASM ( 4 FDA reports)
PAPILLOMA VIRAL INFECTION ( 4 FDA reports)
PARADOXICAL EMBOLISM ( 4 FDA reports)
PELVIC ABSCESS ( 4 FDA reports)
PERIARTHRITIS ( 4 FDA reports)
PERICARDIAL DISEASE ( 4 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 4 FDA reports)
PERITONEAL DIALYSIS ( 4 FDA reports)
PERITONEAL HAEMORRHAGE ( 4 FDA reports)
PERSISTENT FOETAL CIRCULATION ( 4 FDA reports)
PHANTOM PAIN ( 4 FDA reports)
PHONOPHOBIA ( 4 FDA reports)
PNEUMONIA LEGIONELLA ( 4 FDA reports)
POLYTRAUMATISM ( 4 FDA reports)
PORCELAIN GALLBLADDER ( 4 FDA reports)
POST PROCEDURAL PAIN ( 4 FDA reports)
POSTNASAL DRIP ( 4 FDA reports)
POSTURAL ORTHOSTATIC TACHYCARDIA SYNDROME ( 4 FDA reports)
POSTURING ( 4 FDA reports)
PRESCRIBED OVERDOSE ( 4 FDA reports)
PROCTITIS ( 4 FDA reports)
PROTEUS TEST POSITIVE ( 4 FDA reports)
PROTRUSION TONGUE ( 4 FDA reports)
PULMONARY HYPOPLASIA ( 4 FDA reports)
PULMONARY MYCOSIS ( 4 FDA reports)
RADIUS FRACTURE ( 4 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 4 FDA reports)
RENAL COLIC ( 4 FDA reports)
RENAL TUBULAR ACIDOSIS ( 4 FDA reports)
RETINAL TEAR ( 4 FDA reports)
RETINAL VEIN OCCLUSION ( 4 FDA reports)
RHEUMATOID FACTOR INCREASED ( 4 FDA reports)
ROCKY MOUNTAIN SPOTTED FEVER ( 4 FDA reports)
SCAN MYOCARDIAL PERFUSION ( 4 FDA reports)
SECONDARY HYPOGONADISM ( 4 FDA reports)
SHUNT MALFUNCTION ( 4 FDA reports)
SICCA SYNDROME ( 4 FDA reports)
SICKLE CELL TRAIT ( 4 FDA reports)
SINUS POLYP ( 4 FDA reports)
SKIN ATROPHY ( 4 FDA reports)
SKIN CHAPPED ( 4 FDA reports)
SKIN PAPILLOMA ( 4 FDA reports)
SKULL FRACTURE ( 4 FDA reports)
SPINAL COLUMN INJURY ( 4 FDA reports)
SPINAL CORD DISORDER ( 4 FDA reports)
SPINAL CORD INJURY ( 4 FDA reports)
SPLEEN DISORDER ( 4 FDA reports)
SPLENIC GRANULOMA ( 4 FDA reports)
STASIS DERMATITIS ( 4 FDA reports)
STILLBIRTH ( 4 FDA reports)
STREPTOCOCCAL SEPSIS ( 4 FDA reports)
SUBDURAL HAEMORRHAGE ( 4 FDA reports)
SUBENDOCARDIAL ISCHAEMIA ( 4 FDA reports)
SUDDEN HEARING LOSS ( 4 FDA reports)
SUNBURN ( 4 FDA reports)
SURGICAL FAILURE ( 4 FDA reports)
SWEAT GLAND DISORDER ( 4 FDA reports)
TEMPORAL LOBE EPILEPSY ( 4 FDA reports)
TEMPOROMANDIBULAR JOINT SURGERY ( 4 FDA reports)
TENDON OPERATION ( 4 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 4 FDA reports)
TOE OPERATION ( 4 FDA reports)
TONGUE INJURY ( 4 FDA reports)
TOOTH INJURY ( 4 FDA reports)
TOOTH MALFORMATION ( 4 FDA reports)
TOXIC ENCEPHALOPATHY ( 4 FDA reports)
TRANSPLANT REJECTION ( 4 FDA reports)
TRAUMATIC BRAIN INJURY ( 4 FDA reports)
TUNNEL VISION ( 4 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 4 FDA reports)
URGE INCONTINENCE ( 4 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 4 FDA reports)
URINARY TRACT OBSTRUCTION ( 4 FDA reports)
URINE CYTOLOGY ABNORMAL ( 4 FDA reports)
URINE FLOW DECREASED ( 4 FDA reports)
VARICELLA ( 4 FDA reports)
VARICES OESOPHAGEAL ( 4 FDA reports)
VEIN PAIN ( 4 FDA reports)
VENOUS STASIS ( 4 FDA reports)
VENTRICULAR DYSKINESIA ( 4 FDA reports)
VERBAL ABUSE ( 4 FDA reports)
VIRAL PHARYNGITIS ( 4 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 4 FDA reports)
VULVOVAGINAL PAIN ( 4 FDA reports)
VULVOVAGINAL SWELLING ( 4 FDA reports)
WISDOM TEETH REMOVAL ( 4 FDA reports)
WITHDRAWAL BLEEDING IRREGULAR ( 4 FDA reports)
WRIST DEFORMITY ( 4 FDA reports)
YAWNING ( 4 FDA reports)
RETROPERITONEAL HAEMATOMA ( 3 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 3 FDA reports)
RETROPERITONEAL NEOPLASM ( 3 FDA reports)
RHYTHM IDIOVENTRICULAR ( 3 FDA reports)
RIB DEFORMITY ( 3 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 3 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 3 FDA reports)
SCINTILLATING SCOTOMA ( 3 FDA reports)
SCOTOMA ( 3 FDA reports)
SECRETION DISCHARGE ( 3 FDA reports)
SERUM SICKNESS ( 3 FDA reports)
SIMPLE PARTIAL SEIZURES ( 3 FDA reports)
SINUS OPERATION ( 3 FDA reports)
SKELETAL INJURY ( 3 FDA reports)
SKIN BACTERIAL INFECTION ( 3 FDA reports)
SKIN FISSURES ( 3 FDA reports)
SKIN OEDEMA ( 3 FDA reports)
SKIN TEST POSITIVE ( 3 FDA reports)
SKULL FRACTURED BASE ( 3 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 3 FDA reports)
SLOW RESPONSE TO STIMULI ( 3 FDA reports)
SPECIFIC GRAVITY URINE INCREASED ( 3 FDA reports)
SPINAL DECOMPRESSION ( 3 FDA reports)
SPONDYLOLYSIS ( 3 FDA reports)
SPONDYLOSIS ( 3 FDA reports)
SPUTUM INCREASED ( 3 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 3 FDA reports)
STRESS CARDIOMYOPATHY ( 3 FDA reports)
STRIDOR ( 3 FDA reports)
TELANGIECTASIA ( 3 FDA reports)
TEMPERATURE REGULATION DISORDER ( 3 FDA reports)
TESTIS CANCER ( 3 FDA reports)
THEFT ( 3 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 3 FDA reports)
THERAPEUTIC RESPONSE INCREASED ( 3 FDA reports)
THYROIDITIS ( 3 FDA reports)
THYROXINE FREE INCREASED ( 3 FDA reports)
TINEA CRURIS ( 3 FDA reports)
TOE DEFORMITY ( 3 FDA reports)
TONGUE SPASM ( 3 FDA reports)
TOXIC SHOCK SYNDROME ( 3 FDA reports)
TRACHEOBRONCHITIS ( 3 FDA reports)
TRANSFUSION ( 3 FDA reports)
TRAUMATIC LUNG INJURY ( 3 FDA reports)
TREMOR NEONATAL ( 3 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 3 FDA reports)
TUMOUR MARKER INCREASED ( 3 FDA reports)
TUMOUR NECROSIS ( 3 FDA reports)
UNINTENDED PREGNANCY ( 3 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 3 FDA reports)
URINE COLOUR ABNORMAL ( 3 FDA reports)
URINE OUTPUT INCREASED ( 3 FDA reports)
URTICARIA GENERALISED ( 3 FDA reports)
VAGINITIS BACTERIAL ( 3 FDA reports)
VASCULAR CALCIFICATION ( 3 FDA reports)
VASCULAR INSUFFICIENCY ( 3 FDA reports)
VASCULAR OPERATION ( 3 FDA reports)
VASODILATATION ( 3 FDA reports)
VASOMOTOR RHINITIS ( 3 FDA reports)
VASOSPASM ( 3 FDA reports)
VENA CAVA THROMBOSIS ( 3 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 3 FDA reports)
VENOUS INJURY ( 3 FDA reports)
VENTRICULAR FLUTTER ( 3 FDA reports)
VERTEBRAL WEDGING ( 3 FDA reports)
VISCERAL CONGESTION ( 3 FDA reports)
VOCAL CORD PARESIS ( 3 FDA reports)
VULVAL OEDEMA ( 3 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 3 FDA reports)
WATER INTOXICATION ( 3 FDA reports)
WEIGHT LOSS POOR ( 3 FDA reports)
WHIPLASH INJURY ( 3 FDA reports)
WHITE BLOOD CELL COUNT ( 3 FDA reports)
WHOLE BLOOD TRANSFUSION ( 3 FDA reports)
WOLFF-PARKINSON-WHITE SYNDROME ( 3 FDA reports)
WOUND TREATMENT ( 3 FDA reports)
WRIST SURGERY ( 3 FDA reports)
ABDOMINAL COMPARTMENT SYNDROME ( 3 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 3 FDA reports)
ACCIDENTAL NEEDLE STICK ( 3 FDA reports)
ACUTE LEFT VENTRICULAR FAILURE ( 3 FDA reports)
ACUTE POLYNEUROPATHY ( 3 FDA reports)
ADNEXA UTERI PAIN ( 3 FDA reports)
ADVERSE REACTION ( 3 FDA reports)
AGITATED DEPRESSION ( 3 FDA reports)
AGNOSIA ( 3 FDA reports)
AIDS ENCEPHALOPATHY ( 3 FDA reports)
ALOPECIA AREATA ( 3 FDA reports)
ANAESTHETIC COMPLICATION NEUROLOGICAL ( 3 FDA reports)
ANAL ABSCESS ( 3 FDA reports)
ANAL FISSURE ( 3 FDA reports)
ANAL SKIN TAGS ( 3 FDA reports)
ANIMAL SCRATCH ( 3 FDA reports)
ANOREXIA NERVOSA ( 3 FDA reports)
ANTIANDROGEN THERAPY ( 3 FDA reports)
ANTIBODY TEST POSITIVE ( 3 FDA reports)
ANTICOAGULATION DRUG LEVEL BELOW THERAPEUTIC ( 3 FDA reports)
ANTIDEPRESSANT DRUG CLEARANCE DECREASED ( 3 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 3 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL BELOW THERAPEUTIC ( 3 FDA reports)
AORTIC VALVE STENOSIS ( 3 FDA reports)
APLASIA ( 3 FDA reports)
APPENDICECTOMY ( 3 FDA reports)
APPLICATION SITE BLEEDING ( 3 FDA reports)
APPLICATION SITE REACTION ( 3 FDA reports)
ARTERIAL DISORDER ( 3 FDA reports)
ARTERIAL THROMBOSIS ( 3 FDA reports)
ARTERIOSPASM CORONARY ( 3 FDA reports)
ASEPTIC NECROSIS BONE ( 3 FDA reports)
ASPIRATION TRACHEAL ( 3 FDA reports)
ASTHMA LATE ONSET ( 3 FDA reports)
AURICULAR SWELLING ( 3 FDA reports)
AUTOIMMUNE THYROIDITIS ( 3 FDA reports)
BACTERIAL DISEASE CARRIER ( 3 FDA reports)
BALLOON ATRIAL SEPTOSTOMY ( 3 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 3 FDA reports)
BARTHOLIN'S ABSCESS ( 3 FDA reports)
BARTHOLIN'S CYST ( 3 FDA reports)
BED REST ( 3 FDA reports)
BENIGN BREAST NEOPLASM ( 3 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 3 FDA reports)
BIOPSY SKIN ABNORMAL ( 3 FDA reports)
BLADDER NEOPLASM ( 3 FDA reports)
BLINDNESS CORTICAL ( 3 FDA reports)
BLISTER INFECTED ( 3 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE DECREASED ( 3 FDA reports)
BLOOD CREATININE ( 3 FDA reports)
BLOOD CREATININE DECREASED ( 3 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 3 FDA reports)
BLOOD KETONE BODY INCREASED ( 3 FDA reports)
BLOOD OESTROGEN ABNORMAL ( 3 FDA reports)
BORDERLINE PERSONALITY DISORDER ( 3 FDA reports)
BRADYARRHYTHMIA ( 3 FDA reports)
BRAIN ABSCESS ( 3 FDA reports)
BRAIN STEM HAEMORRHAGE ( 3 FDA reports)
BRAIN STEM INFARCTION ( 3 FDA reports)
BREAST DISCHARGE ( 3 FDA reports)
BREAST DISORDER ( 3 FDA reports)
BREAST FIBROSIS ( 3 FDA reports)
BREAST NECROSIS ( 3 FDA reports)
BRONCHIAL OBSTRUCTION ( 3 FDA reports)
BRONCHITIS VIRAL ( 3 FDA reports)
BULLOUS LUNG DISEASE ( 3 FDA reports)
BUNDLE BRANCH BLOCK ( 3 FDA reports)
BUNION ( 3 FDA reports)
BURSA DISORDER ( 3 FDA reports)
BURSITIS INFECTIVE ( 3 FDA reports)
CALCIFICATION OF MUSCLE ( 3 FDA reports)
CAMPYLOBACTER INFECTION ( 3 FDA reports)
CARDIAC VALVE VEGETATION ( 3 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 3 FDA reports)
CARDIOVASCULAR DECONDITIONING ( 3 FDA reports)
CARDIOVERSION ( 3 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 3 FDA reports)
CENTRAL LINE INFECTION ( 3 FDA reports)
CEREBELLAR INFARCTION ( 3 FDA reports)
CEREBELLAR SYNDROME ( 3 FDA reports)
CEREBRAL CALCIFICATION ( 3 FDA reports)
CEREBRAL DISORDER ( 3 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 3 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 3 FDA reports)
CERVIX CARCINOMA STAGE 0 ( 3 FDA reports)
CERVIX INFLAMMATION ( 3 FDA reports)
CHEST WALL OPERATION ( 3 FDA reports)
CHOKING SENSATION ( 3 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 3 FDA reports)
CHRONIC RESPIRATORY DISEASE ( 3 FDA reports)
CLEFT LIP ( 3 FDA reports)
CLUBBING ( 3 FDA reports)
COCCIDIOIDOMYCOSIS ( 3 FDA reports)
COLLAGEN DISORDER ( 3 FDA reports)
COLON CANCER METASTATIC ( 3 FDA reports)
COLON OPERATION ( 3 FDA reports)
COLORECTAL CANCER METASTATIC ( 3 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 3 FDA reports)
CONGENITAL BLADDER ANOMALY ( 3 FDA reports)
CONGENITAL CENTRAL NERVOUS SYSTEM ANOMALY ( 3 FDA reports)
CONGENITAL CHOROID PLEXUS CYST ( 3 FDA reports)
CONGENITAL HAIR DISORDER ( 3 FDA reports)
CONGENITAL NAIL DISORDER ( 3 FDA reports)
CONTRAST MEDIA REACTION ( 3 FDA reports)
CONVULSION NEONATAL ( 3 FDA reports)
CORNEAL ABRASION ( 3 FDA reports)
CORNEAL DEPOSITS ( 3 FDA reports)
CORNEAL DYSTROPHY ( 3 FDA reports)
CRANIAL NERVE DISORDER ( 3 FDA reports)
CRYOTHERAPY ( 3 FDA reports)
CSF TEST ABNORMAL ( 3 FDA reports)
CSF WHITE BLOOD CELL COUNT INCREASED ( 3 FDA reports)
CYSTITIS BACTERIAL ( 3 FDA reports)
DARK CIRCLES UNDER EYES ( 3 FDA reports)
DENTAL CARE ( 3 FDA reports)
DERMATITIS ACNEIFORM ( 3 FDA reports)
DEVICE DIFFICULT TO USE ( 3 FDA reports)
DIABETES INSIPIDUS ( 3 FDA reports)
DIAPHRAGMALGIA ( 3 FDA reports)
DROWNING ( 3 FDA reports)
DYSHIDROSIS ( 3 FDA reports)
DYSPLASTIC NAEVUS SYNDROME ( 3 FDA reports)
EAR HAEMORRHAGE ( 3 FDA reports)
EFFUSION ( 3 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 3 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 3 FDA reports)
EMBOLISM ARTERIAL ( 3 FDA reports)
ENAMEL ANOMALY ( 3 FDA reports)
ENDOCARDIAL FIBROSIS ( 3 FDA reports)
ENDOCARDITIS BACTERIAL ( 3 FDA reports)
ENTERITIS INFECTIOUS ( 3 FDA reports)
ENTEROCOLITIS ( 3 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 3 FDA reports)
EPIGASTRIC DISCOMFORT ( 3 FDA reports)
ERYTHEMA NODOSUM ( 3 FDA reports)
ESCHAR ( 3 FDA reports)
EXPOSURE TO TOXIC AGENT ( 3 FDA reports)
EXTRANODAL MARGINAL ZONE B-CELL LYMPHOMA (MALT TYPE) ( 3 FDA reports)
EXTRAVASATION BLOOD ( 3 FDA reports)
EYE OEDEMA ( 3 FDA reports)
EYE ROLLING ( 3 FDA reports)
FACIAL ASYMMETRY ( 3 FDA reports)
FACIAL DYSMORPHISM ( 3 FDA reports)
FACIAL SPASM ( 3 FDA reports)
FEEDING DISORDER NEONATAL ( 3 FDA reports)
FEMALE GENITAL OPERATION ( 3 FDA reports)
FEMORAL ARTERY OCCLUSION ( 3 FDA reports)
FLAT FEET ( 3 FDA reports)
FLIGHT OF IDEAS ( 3 FDA reports)
FOOD ALLERGY ( 3 FDA reports)
FOOD AVERSION ( 3 FDA reports)
FOOD INTERACTION ( 3 FDA reports)
FORCED EXPIRATORY VOLUME DECREASED ( 3 FDA reports)
FOREIGN BODY ASPIRATION ( 3 FDA reports)
GASTRIC CYST ( 3 FDA reports)
GASTRODUODENAL ULCER ( 3 FDA reports)
GASTROINTESTINAL CARCINOMA ( 3 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 3 FDA reports)
GASTROINTESTINAL PERFORATION ( 3 FDA reports)
GASTROINTESTINAL TRACT IRRITATION ( 3 FDA reports)
GAZE PALSY ( 3 FDA reports)
GENITAL NEOPLASM MALIGNANT FEMALE ( 3 FDA reports)
GENITAL ULCERATION ( 3 FDA reports)
GLOBULINS DECREASED ( 3 FDA reports)
GLOMERULOSCLEROSIS ( 3 FDA reports)
GRAFT VERSUS HOST DISEASE ( 3 FDA reports)
GRANULOCYTES MATURATION ARREST ( 3 FDA reports)
GROWTH RETARDATION ( 3 FDA reports)
HAEMOCONCENTRATION ( 3 FDA reports)
HAEMOGLOBIN ( 3 FDA reports)
HAEMOGLOBIN ABNORMAL ( 3 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 3 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 3 FDA reports)
HAEMORRHAGIC DIATHESIS ( 3 FDA reports)
HEPATIC TRAUMA ( 3 FDA reports)
HEPATORENAL SYNDROME ( 3 FDA reports)
HETEROTAXIA ( 3 FDA reports)
HIDRADENITIS ( 3 FDA reports)
HIP DYSPLASIA ( 3 FDA reports)
HIP SURGERY ( 3 FDA reports)
HIRSUTISM ( 3 FDA reports)
HISTAMINE LEVEL INCREASED ( 3 FDA reports)
HISTONE ANTIBODY POSITIVE ( 3 FDA reports)
HUMAN EHRLICHIOSIS ( 3 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 3 FDA reports)
HYDROTHORAX ( 3 FDA reports)
HYPERCAPNIA ( 3 FDA reports)
HYPERGLOBULINAEMIA ( 3 FDA reports)
HYPEROSMOLAR STATE ( 3 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 3 FDA reports)
HYPERPHOSPHATAEMIA ( 3 FDA reports)
HYPERTONIA NEONATAL ( 3 FDA reports)
HYPOCHONDRIASIS ( 3 FDA reports)
HYPOGLYCAEMIC COMA ( 3 FDA reports)
HYPOGLYCAEMIC ENCEPHALOPATHY ( 3 FDA reports)
HYPOMENORRHOEA ( 3 FDA reports)
HYPOPLASTIC LEFT HEART SYNDROME ( 3 FDA reports)
HYPOTRICHOSIS ( 3 FDA reports)
HYPOVOLAEMIC SHOCK ( 3 FDA reports)
IMMINENT ABORTION ( 3 FDA reports)
IMMUNODEFICIENCY ( 3 FDA reports)
IMMUNOGLOBULINS INCREASED ( 3 FDA reports)
INCISION SITE PAIN ( 3 FDA reports)
INCISIONAL DRAINAGE ( 3 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 3 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 3 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 3 FDA reports)
INFUSION SITE EXTRAVASATION ( 3 FDA reports)
INGROWING NAIL ( 3 FDA reports)
INJECTION SITE ABSCESS ( 3 FDA reports)
INJECTION SITE CELLULITIS ( 3 FDA reports)
INJECTION SITE CYST ( 3 FDA reports)
INJECTION SITE DISCHARGE ( 3 FDA reports)
INJECTION SITE DISCOMFORT ( 3 FDA reports)
INJECTION SITE SCAB ( 3 FDA reports)
INJECTION SITE SCAR ( 3 FDA reports)
INJECTION SITE ULCER ( 3 FDA reports)
INJURY ASPHYXIATION ( 3 FDA reports)
INSULIN RESISTANCE ( 3 FDA reports)
INTERCOSTAL RETRACTION ( 3 FDA reports)
INTERNAL HERNIA ( 3 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 3 FDA reports)
INVESTIGATION ABNORMAL ( 3 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 3 FDA reports)
IRON BINDING CAPACITY TOTAL INCREASED ( 3 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 3 FDA reports)
IVTH NERVE PARALYSIS ( 3 FDA reports)
JAW CYST ( 3 FDA reports)
KARYOTYPE ANALYSIS ABNORMAL ( 3 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 3 FDA reports)
KLEBSIELLA BACTERAEMIA ( 3 FDA reports)
LABYRINTHITIS ( 3 FDA reports)
LAPAROTOMY ( 3 FDA reports)
LEIOMYOMA ( 3 FDA reports)
LEUKAEMIA PLASMACYTIC ( 3 FDA reports)
LICHEN PLANUS ( 3 FDA reports)
LIMB ASYMMETRY ( 3 FDA reports)
LIMB CRUSHING INJURY ( 3 FDA reports)
LIMB DEFORMITY ( 3 FDA reports)
LIP BLISTER ( 3 FDA reports)
LIPOHYPERTROPHY ( 3 FDA reports)
LIVER ABSCESS ( 3 FDA reports)
LOCALISED OEDEMA ( 3 FDA reports)
LOGORRHOEA ( 3 FDA reports)
LOOSE STOOLS ( 3 FDA reports)
LYMPH NODE ABSCESS ( 3 FDA reports)
LYMPH NODE PAIN ( 3 FDA reports)
LYMPHADENECTOMY ( 3 FDA reports)
LYMPHANGIOMA ( 3 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 3 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 3 FDA reports)
MACULOPATHY ( 3 FDA reports)
MALIGNANT ANORECTAL NEOPLASM ( 3 FDA reports)
MALIGNANT FIBROUS HISTIOCYTOMA ( 3 FDA reports)
MALLORY-WEISS SYNDROME ( 3 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 3 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 3 FDA reports)
MEDICAL DIET ( 3 FDA reports)
MELANOSIS COLI ( 3 FDA reports)
MENINGITIS ( 3 FDA reports)
METASTASES TO ADRENALS ( 3 FDA reports)
METASTASES TO PERITONEUM ( 3 FDA reports)
METASTATIC GASTRIC CANCER ( 3 FDA reports)
METASTATIC PAIN ( 3 FDA reports)
MICROGRAPHIC SKIN SURGERY ( 3 FDA reports)
MITOCHONDRIAL TOXICITY ( 3 FDA reports)
MONOCYTE COUNT DECREASED ( 3 FDA reports)
MONONEUROPATHY ( 3 FDA reports)
MOTION SICKNESS ( 3 FDA reports)
MYELOFIBROSIS ( 3 FDA reports)
MYELOID LEUKAEMIA ( 3 FDA reports)
MYELOPATHY ( 3 FDA reports)
MYOGLOBIN URINE ( 3 FDA reports)
MYOKYMIA ( 3 FDA reports)
MYOSCLEROSIS ( 3 FDA reports)
NASAL DRYNESS ( 3 FDA reports)
NASAL POLYPS ( 3 FDA reports)
NEGATIVISM ( 3 FDA reports)
NEPHROCALCINOSIS ( 3 FDA reports)
NEUROPATHIC ARTHROPATHY ( 3 FDA reports)
NEUTROPENIC COLITIS ( 3 FDA reports)
NO ADVERSE DRUG EFFECT ( 3 FDA reports)
NODAL ARRHYTHMIA ( 3 FDA reports)
NODULE ON EXTREMITY ( 3 FDA reports)
NONSPECIFIC REACTION ( 3 FDA reports)
OBTURATOR HERNIA ( 3 FDA reports)
OESOPHAGEAL CANCER METASTATIC ( 3 FDA reports)
OILY SKIN ( 3 FDA reports)
ORAL SOFT TISSUE DISORDER ( 3 FDA reports)
ORTHOSIS USER ( 3 FDA reports)
OSTEOMYELITIS ACUTE ( 3 FDA reports)
OSTEOPOROTIC FRACTURE ( 3 FDA reports)
PALATAL OEDEMA ( 3 FDA reports)
PANCREATITIS RELAPSING ( 3 FDA reports)
PARACENTESIS ( 3 FDA reports)
PARACHUTE MITRAL VALVE ( 3 FDA reports)
PARADOXICAL DRUG REACTION ( 3 FDA reports)
PARATHYROID TUMOUR BENIGN ( 3 FDA reports)
PARESIS ( 3 FDA reports)
PAROTID GLAND ENLARGEMENT ( 3 FDA reports)
PAST-POINTING ( 3 FDA reports)
PEAK EXPIRATORY FLOW RATE DECREASED ( 3 FDA reports)
PEMPHIGOID ( 3 FDA reports)
PERFORATED ULCER ( 3 FDA reports)
PERICARDITIS INFECTIVE ( 3 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 3 FDA reports)
PERNICIOUS ANAEMIA ( 3 FDA reports)
PHARMACEUTICAL PRODUCT COUNTERFEIT ( 3 FDA reports)
PHLEBITIS SUPERFICIAL ( 3 FDA reports)
PHOBIA OF DRIVING ( 3 FDA reports)
PILOERECTION ( 3 FDA reports)
PLATELET COUNT ( 3 FDA reports)
PLEURAL ADHESION ( 3 FDA reports)
PLEURAL NEOPLASM ( 3 FDA reports)
PNEUMOCEPHALUS ( 3 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 3 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 3 FDA reports)
PNEUMOPERITONEUM ( 3 FDA reports)
POLYCYTHAEMIA ( 3 FDA reports)
POLYMENORRHOEA ( 3 FDA reports)
PORPHYRIA ( 3 FDA reports)
POST PROCEDURAL PNEUMONIA ( 3 FDA reports)
POST-TRAUMATIC HEADACHE ( 3 FDA reports)
POST-TRAUMATIC PAIN ( 3 FDA reports)
POSTOPERATIVE ADHESION ( 3 FDA reports)
POSTOPERATIVE INFECTION ( 3 FDA reports)
PRINZMETAL ANGINA ( 3 FDA reports)
PROCEDURAL NAUSEA ( 3 FDA reports)
PRODUCT PACKAGING ISSUE ( 3 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 3 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 3 FDA reports)
PROSTATISM ( 3 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 3 FDA reports)
PSEUDOPOLYP ( 3 FDA reports)
PSYCHOLOGICAL TRAUMA ( 3 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 3 FDA reports)
PULMONARY SARCOIDOSIS ( 3 FDA reports)
PULMONARY SEPSIS ( 3 FDA reports)
PULSE PRESSURE DECREASED ( 3 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 3 FDA reports)
PYELONEPHRITIS ACUTE ( 3 FDA reports)
PYELONEPHRITIS CHRONIC ( 3 FDA reports)
PYOTHORAX ( 3 FDA reports)
QUADRIPLEGIA ( 3 FDA reports)
RADIATION SKIN INJURY ( 3 FDA reports)
RASH VESICULAR ( 3 FDA reports)
RECTAL PROLAPSE ( 3 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 3 FDA reports)
REFLEXES ABNORMAL ( 3 FDA reports)
REFLUX GASTRITIS ( 3 FDA reports)
REFRACTION DISORDER ( 3 FDA reports)
RENAL APLASIA ( 3 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 3 FDA reports)
RENAL HYPERTENSION ( 3 FDA reports)
RESPIRATORY ALKALOSIS ( 3 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS BRONCHIOLITIS ( 3 FDA reports)
ABDOMINAL ABSCESS ( 2 FDA reports)
ABDOMINAL NEOPLASM ( 2 FDA reports)
ABDOMINAL OPERATION ( 2 FDA reports)
ABDOMINAL REBOUND TENDERNESS ( 2 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 2 FDA reports)
ABORTION ( 2 FDA reports)
ABORTION THREATENED ( 2 FDA reports)
ABSCESS NECK ( 2 FDA reports)
ACARODERMATITIS ( 2 FDA reports)
ACCELERATED HYPERTENSION ( 2 FDA reports)
ACUTE LEUKAEMIA ( 2 FDA reports)
ADJUSTMENT DISORDER WITH MIXED ANXIETY AND DEPRESSED MOOD ( 2 FDA reports)
ADNEXA UTERI MASS ( 2 FDA reports)
ADRENOCORTICAL INSUFFICIENCY CHRONIC ( 2 FDA reports)
AEROPHAGIA ( 2 FDA reports)
ALCOHOL INTERACTION ( 2 FDA reports)
ALCOHOL INTOLERANCE ( 2 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 2 FDA reports)
ALKALOSIS ( 2 FDA reports)
ALPHA 1 GLOBULIN INCREASED ( 2 FDA reports)
ANALGESIC DRUG LEVEL INCREASED ( 2 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 2 FDA reports)
ANKLE OPERATION ( 2 FDA reports)
ANKYLOSING SPONDYLITIS ( 2 FDA reports)
ANORECTAL DISCOMFORT ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 2 FDA reports)
ANTISOCIAL BEHAVIOUR ( 2 FDA reports)
ANTISOCIAL PERSONALITY DISORDER ( 2 FDA reports)
AORTIC ANEURYSM RUPTURE ( 2 FDA reports)
AORTIC DISSECTION ( 2 FDA reports)
APPENDICITIS PERFORATED ( 2 FDA reports)
APPENDIX DISORDER ( 2 FDA reports)
APPLICATION SITE EXCORIATION ( 2 FDA reports)
APPLICATION SITE NECROSIS ( 2 FDA reports)
APPLICATION SITE RASH ( 2 FDA reports)
APPLICATION SITE SWELLING ( 2 FDA reports)
APTYALISM ( 2 FDA reports)
ARACHNOIDITIS ( 2 FDA reports)
ARTERIOVENOUS GRAFT SITE INFECTION ( 2 FDA reports)
ARTERY DISSECTION ( 2 FDA reports)
ARTHRITIS ENTEROPATHIC ( 2 FDA reports)
ARTHRODESIS ( 2 FDA reports)
ARTHROSCOPIC SURGERY ( 2 FDA reports)
ASPHYXIA ( 2 FDA reports)
ASTERIXIS ( 2 FDA reports)
ASTHMATIC CRISIS ( 2 FDA reports)
ATRIAL HYPERTROPHY ( 2 FDA reports)
ATRIAL TACHYCARDIA ( 2 FDA reports)
ATRIAL THROMBOSIS ( 2 FDA reports)
AUTONOMIC NEUROPATHY ( 2 FDA reports)
B-CELL LYMPHOMA ( 2 FDA reports)
B-CELL LYMPHOMA STAGE IV ( 2 FDA reports)
BABINSKI REFLEX TEST ( 2 FDA reports)
BACILLUS INFECTION ( 2 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 2 FDA reports)
BENIGN LYMPH NODE NEOPLASM ( 2 FDA reports)
BENIGN NEOPLASM ( 2 FDA reports)
BENIGN NEOPLASM OF SPINAL CORD ( 2 FDA reports)
BENIGN UTERINE NEOPLASM ( 2 FDA reports)
BILIARY DILATATION ( 2 FDA reports)
BILIARY SEPSIS ( 2 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 2 FDA reports)
BIOPSY BLADDER ABNORMAL ( 2 FDA reports)
BIOPSY SITE UNSPECIFIED ABNORMAL ( 2 FDA reports)
BIOPSY SKIN ( 2 FDA reports)
BLADDER NECK OBSTRUCTION ( 2 FDA reports)
BLADDER PAPILLOMA ( 2 FDA reports)
BLADDER TAMPONADE ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE NORMAL ( 2 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 2 FDA reports)
BLOOD CORTISOL ABNORMAL ( 2 FDA reports)
BLOOD CORTISOL INCREASED ( 2 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 2 FDA reports)
BLOOD ETHANOL INCREASED ( 2 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE ABNORMAL ( 2 FDA reports)
BLOOD PROLACTIN INCREASED ( 2 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 2 FDA reports)
BLOOD URIC ACID DECREASED ( 2 FDA reports)
BLUNTED AFFECT ( 2 FDA reports)
BODY DYSMORPHIC DISORDER ( 2 FDA reports)
BODY TINEA ( 2 FDA reports)
BONE DEVELOPMENT ABNORMAL ( 2 FDA reports)
BONE FORMATION DECREASED ( 2 FDA reports)
BONE METABOLISM DISORDER ( 2 FDA reports)
BONE SWELLING ( 2 FDA reports)
BOWEN'S DISEASE ( 2 FDA reports)
BRAIN COMPRESSION ( 2 FDA reports)
BREATH ODOUR ( 2 FDA reports)
BREATH SOUNDS ABSENT ( 2 FDA reports)
BRONCHIAL WALL THICKENING ( 2 FDA reports)
BULIMIA NERVOSA ( 2 FDA reports)
CALCIUM IONISED DECREASED ( 2 FDA reports)
CALCIUM IONISED INCREASED ( 2 FDA reports)
CANDIDA PNEUMONIA ( 2 FDA reports)
CARBON DIOXIDE DECREASED ( 2 FDA reports)
CARCINOID TUMOUR ( 2 FDA reports)
CARCINOID TUMOUR OF THE APPENDIX ( 2 FDA reports)
CARCINOMA IN SITU OF SKIN ( 2 FDA reports)
CARDIAC MYXOMA ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 2 FDA reports)
CARNITINE PALMITOYLTRANSFERASE DEFICIENCY ( 2 FDA reports)
CAROTID ARTERIAL EMBOLUS ( 2 FDA reports)
CARTILAGE INJURY ( 2 FDA reports)
CATATONIA ( 2 FDA reports)
CATHETER SITE HAEMORRHAGE ( 2 FDA reports)
CELL DEATH ( 2 FDA reports)
CENTRAL OBESITY ( 2 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 2 FDA reports)
CEREBRAL ATROPHY CONGENITAL ( 2 FDA reports)
CEREBRAL HYGROMA ( 2 FDA reports)
CEREBROSPINAL FLUID LEAKAGE ( 2 FDA reports)
CERVIX CARCINOMA RECURRENT ( 2 FDA reports)
CERVIX DISORDER ( 2 FDA reports)
CHARLES BONNET SYNDROME ( 2 FDA reports)
CHEST EXPANSION DECREASED ( 2 FDA reports)
CHONDROPLASTY ( 2 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 2 FDA reports)
CITROBACTER INFECTION ( 2 FDA reports)
CLONIC CONVULSION ( 2 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 2 FDA reports)
COLECTOMY ( 2 FDA reports)
COLON NEOPLASM ( 2 FDA reports)
COLONIC STENOSIS ( 2 FDA reports)
COMA HEPATIC ( 2 FDA reports)
COMMINUTED FRACTURE ( 2 FDA reports)
COMPLICATION OF PREGNANCY ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 2 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 2 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 2 FDA reports)
COOMBS TEST NEGATIVE ( 2 FDA reports)
COOMBS TEST POSITIVE ( 2 FDA reports)
COPPER DEFICIENCY ( 2 FDA reports)
CORNEAL TRANSPLANT ( 2 FDA reports)
CRANIOCEREBRAL INJURY ( 2 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 2 FDA reports)
CRYPTORCHISM ( 2 FDA reports)
CSF GLUCOSE ABNORMAL ( 2 FDA reports)
CSF PRESSURE INCREASED ( 2 FDA reports)
CSF PROTEIN ABNORMAL ( 2 FDA reports)
CSF WHITE BLOOD CELL COUNT POSITIVE ( 2 FDA reports)
CULTURE POSITIVE ( 2 FDA reports)
CULTURE STOOL POSITIVE ( 2 FDA reports)
CULTURE WOUND POSITIVE ( 2 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 2 FDA reports)
CYANOSIS CENTRAL ( 2 FDA reports)
CYCLIC VOMITING SYNDROME ( 2 FDA reports)
CYST RUPTURE ( 2 FDA reports)
CYTOMEGALOVIRUS GASTRITIS ( 2 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 2 FDA reports)
DEJA VU ( 2 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 2 FDA reports)
DENTAL TREATMENT ( 2 FDA reports)
DEVICE DISLOCATION ( 2 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 2 FDA reports)
DIALYSIS DEVICE COMPLICATION ( 2 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 2 FDA reports)
DIASTOLIC HYPERTENSION ( 2 FDA reports)
DISLOCATION OF JOINT PROSTHESIS ( 2 FDA reports)
DISSOCIATIVE IDENTITY DISORDER ( 2 FDA reports)
DISTRACTIBILITY ( 2 FDA reports)
DIVERTICULAR PERFORATION ( 2 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 2 FDA reports)
DRUG ADMINISTERED IN WRONG DEVICE ( 2 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 2 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 2 FDA reports)
DRUG LEVEL ( 2 FDA reports)
DRUG LEVEL FLUCTUATING ( 2 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 2 FDA reports)
DRY GANGRENE ( 2 FDA reports)
DUODENAL STENOSIS ( 2 FDA reports)
DYSPLASTIC NAEVUS ( 2 FDA reports)
EAR INJURY ( 2 FDA reports)
EAR NEOPLASM ( 2 FDA reports)
EJECTION FRACTION ( 2 FDA reports)
ELBOW OPERATION ( 2 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ( 2 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 2 FDA reports)
ELECTROMYOGRAM ABNORMAL ( 2 FDA reports)
ENCEPHALITIC INFECTION ( 2 FDA reports)
ENCEPHALITIS VIRAL ( 2 FDA reports)
ENDOMETRIAL CANCER STAGE I ( 2 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ABNORMAL ( 2 FDA reports)
ENLARGED UVULA ( 2 FDA reports)
ENTEROBACTER INFECTION ( 2 FDA reports)
ENTEROBACTER TEST POSITIVE ( 2 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 2 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 2 FDA reports)
EOSINOPHILIC PNEUMONIA CHRONIC ( 2 FDA reports)
EPIDERMAL NAEVUS ( 2 FDA reports)
EPIDURAL LIPOMATOSIS ( 2 FDA reports)
ERYTHEMA INFECTIOSUM ( 2 FDA reports)
ERYTHEMA OF EYELID ( 2 FDA reports)
ERYTHROMELALGIA ( 2 FDA reports)
ERYTHROPENIA ( 2 FDA reports)
EUTHANASIA ( 2 FDA reports)
EXANTHEM ( 2 FDA reports)
EXPLORATIVE LAPAROTOMY ( 2 FDA reports)
EXPOSURE TO EXTREME TEMPERATURE ( 2 FDA reports)
FAECAL VOMITING ( 2 FDA reports)
FAILURE OF IMPLANT ( 2 FDA reports)
FANCONI SYNDROME ACQUIRED ( 2 FDA reports)
FAT EMBOLISM ( 2 FDA reports)
FEELING HOT AND COLD ( 2 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 2 FDA reports)
FINGER REPAIR OPERATION ( 2 FDA reports)
FISTULA DISCHARGE ( 2 FDA reports)
FLUID REPLACEMENT ( 2 FDA reports)
FOETAL DISTRESS SYNDROME ( 2 FDA reports)
FOLLICLE CENTRE LYMPHOMA, FOLLICULAR GRADE I, II, III STAGE IV ( 2 FDA reports)
FOREIGN BODY IN EYE ( 2 FDA reports)
FRACTURE DISPLACEMENT ( 2 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 2 FDA reports)
FUNGAL PERITONITIS ( 2 FDA reports)
GALACTORRHOEA ( 2 FDA reports)
GALLBLADDER NECROSIS ( 2 FDA reports)
GALLBLADDER PERFORATION ( 2 FDA reports)
GASTRIC INFECTION ( 2 FDA reports)
GASTRIC STENOSIS ( 2 FDA reports)
GASTROENTERITIS SALMONELLA ( 2 FDA reports)
GASTROINTESTINAL ANASTOMOTIC LEAK ( 2 FDA reports)
GASTROINTESTINAL DYSPLASIA ( 2 FDA reports)
GASTROINTESTINAL INJURY ( 2 FDA reports)
GASTROINTESTINAL NECROSIS ( 2 FDA reports)
GASTROINTESTINAL OEDEMA ( 2 FDA reports)
GASTROINTESTINAL STENOSIS ( 2 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 2 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 2 FDA reports)
GASTROINTESTINAL VIRAL INFECTION ( 2 FDA reports)
GASTROSTOMY TUBE INSERTION ( 2 FDA reports)
GENERAL SYMPTOM ( 2 FDA reports)
GENITAL BURNING SENSATION ( 2 FDA reports)
GENITAL DISCOMFORT ( 2 FDA reports)
GENITAL PAIN ( 2 FDA reports)
GLARE ( 2 FDA reports)
GLASGOW COMA SCALE ( 2 FDA reports)
GLIOBLASTOMA ( 2 FDA reports)
GLOBULINS INCREASED ( 2 FDA reports)
GRANULOCYTOPENIA ( 2 FDA reports)
HAEMATOLOGICAL MALIGNANCY ( 2 FDA reports)
HAEMATOTOXICITY ( 2 FDA reports)
HAEMOBILIA ( 2 FDA reports)
HAEMOCHROMATOSIS ( 2 FDA reports)
HAEMORRHAGIC CYST ( 2 FDA reports)
HAEMORRHAGIC DISORDER ( 2 FDA reports)
HAEMOSTASIS ( 2 FDA reports)
HAEMOTHORAX ( 2 FDA reports)
HALLUCINATION, OLFACTORY ( 2 FDA reports)
HALO VISION ( 2 FDA reports)
HEART SOUNDS ABNORMAL ( 2 FDA reports)
HEAT RASH ( 2 FDA reports)
HELMINTHIC INFECTION ( 2 FDA reports)
HEPATIC ARTERY THROMBOSIS ( 2 FDA reports)
HEPATIC INFARCTION ( 2 FDA reports)
HEPATIC INFECTION BACTERIAL ( 2 FDA reports)
HEPATITIS VIRAL ( 2 FDA reports)
HEPATOJUGULAR REFLUX ( 2 FDA reports)
HEPATOSPLENIC CANDIDIASIS ( 2 FDA reports)
HEPATOSPLENOMEGALY ( 2 FDA reports)
HEREDITARY ANGIOEDEMA ( 2 FDA reports)
HERNIA CONGENITAL ( 2 FDA reports)
HERNIAL EVENTRATION ( 2 FDA reports)
HIP SWELLING ( 2 FDA reports)
HISTOPLASMOSIS DISSEMINATED ( 2 FDA reports)
HIV INFECTION ( 2 FDA reports)
HOMANS' SIGN ( 2 FDA reports)
HUNGRY BONE SYNDROME ( 2 FDA reports)
HYPEREMESIS GRAVIDARUM ( 2 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 2 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 2 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 2 FDA reports)
HYPERTHERMIA MALIGNANT ( 2 FDA reports)
HYPERTRICHOSIS ( 2 FDA reports)
HYPERTROPHY ( 2 FDA reports)
HYPERVISCOSITY SYNDROME ( 2 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 2 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 2 FDA reports)
HYPOLIPIDAEMIA ( 2 FDA reports)
HYPOSMIA ( 2 FDA reports)
HYPOTHALAMO-PITUITARY DISORDERS ( 2 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 2 FDA reports)
IATROGENIC INJURY ( 2 FDA reports)
IIIRD NERVE PARESIS ( 2 FDA reports)
IMPAIRED SELF-CARE ( 2 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 2 FDA reports)
INCORRECT DRUG DOSAGE FORM ADMINISTERED ( 2 FDA reports)
INCREASED BRONCHIAL SECRETION ( 2 FDA reports)
INDUCED LABOUR ( 2 FDA reports)
INFECTIVE PULMONARY EXACERBATION OF CYSTIC FIBROSIS ( 2 FDA reports)
INFERTILITY FEMALE ( 2 FDA reports)
INFLAMMATORY PSEUDOTUMOUR ( 2 FDA reports)
INFUSION SITE HAEMATOMA ( 2 FDA reports)
INFUSION SITE PRURITUS ( 2 FDA reports)
INHALATION THERAPY ( 2 FDA reports)
INJECTION SITE ATROPHY ( 2 FDA reports)
INJECTION SITE STREAKING ( 2 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 2 FDA reports)
INTERTRIGO ( 2 FDA reports)
INTERVERTEBRAL DISC INJURY ( 2 FDA reports)
INTESTINAL HYPOMOTILITY ( 2 FDA reports)
INTRACRANIAL HYPOTENSION ( 2 FDA reports)
IRON OVERLOAD ( 2 FDA reports)
JC VIRUS INFECTION ( 2 FDA reports)
JOB DISSATISFACTION ( 2 FDA reports)
JOINT ABSCESS ( 2 FDA reports)
JOINT LOCK ( 2 FDA reports)
JUVENILE ARTHRITIS ( 2 FDA reports)
KERATITIS ( 2 FDA reports)
KLEBSIELLA SEPSIS ( 2 FDA reports)
LABELLED DRUG-FOOD INTERACTION MEDICATION ERROR ( 2 FDA reports)
LARYNGEAL DISORDER ( 2 FDA reports)
LATEX ALLERGY ( 2 FDA reports)
LEUKOPLAKIA ( 2 FDA reports)
LIBIDO INCREASED ( 2 FDA reports)
LIP OEDEMA ( 2 FDA reports)
LIPIDS ABNORMAL ( 2 FDA reports)
LIPIDS DECREASED ( 2 FDA reports)
LIPODYSTROPHY ACQUIRED ( 2 FDA reports)
LIQUID PRODUCT PHYSICAL ISSUE ( 2 FDA reports)
LIVER SCAN ABNORMAL ( 2 FDA reports)
LOCALISED OSTEOARTHRITIS ( 2 FDA reports)
LUMBAR PUNCTURE HEADACHE ( 2 FDA reports)
LUNG ABSCESS ( 2 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 2 FDA reports)
LYMPHOCYTIC INFILTRATION ( 2 FDA reports)
MALABSORPTION FROM INJECTION SITE ( 2 FDA reports)
MALARIA ( 2 FDA reports)
MALIGNANT ASCITES ( 2 FDA reports)
MALIGNANT MELANOMA STAGE I ( 2 FDA reports)
MALIGNANT OVARIAN CYST ( 2 FDA reports)
MARASMUS ( 2 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 2 FDA reports)
MEAN CELL VOLUME DECREASED ( 2 FDA reports)
MEDICAL DEVICE REMOVAL ( 2 FDA reports)
MENDELSON'S SYNDROME ( 2 FDA reports)
MENINGEAL DISORDER ( 2 FDA reports)
MENINGIOMA BENIGN ( 2 FDA reports)
MENINGITIS CHEMICAL ( 2 FDA reports)
MENINGITIS PNEUMOCOCCAL ( 2 FDA reports)
MENINGOCOCCAL INFECTION ( 2 FDA reports)
MENISCUS REMOVAL ( 2 FDA reports)
MERYCISM ( 2 FDA reports)
MESENTERIC ARTERY THROMBOSIS ( 2 FDA reports)
METASTASES TO BLADDER ( 2 FDA reports)
METASTASES TO CHEST WALL ( 2 FDA reports)
METASTASES TO MUSCLE ( 2 FDA reports)
METASTASES TO OVARY ( 2 FDA reports)
METASTASES TO PELVIS ( 2 FDA reports)
METASTASES TO PLEURA ( 2 FDA reports)
MICROCYTIC ANAEMIA ( 2 FDA reports)
MIDDLE EAR EFFUSION ( 2 FDA reports)
MITOCHONDRIAL MYOPATHY ( 2 FDA reports)
MIXED LIVER INJURY ( 2 FDA reports)
MONOPARESIS ( 2 FDA reports)
MORPHOEA ( 2 FDA reports)
MORTON'S NEUROMA ( 2 FDA reports)
MOTOR NEURONE DISEASE ( 2 FDA reports)
MUCOSAL DRYNESS ( 2 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 2 FDA reports)
MUSCLE ENZYME INCREASED ( 2 FDA reports)
MUSCLE MASS ( 2 FDA reports)
MUSCLE NECROSIS ( 2 FDA reports)
MUSCLE RUPTURE ( 2 FDA reports)
MUTISM ( 2 FDA reports)
MYCOSIS FUNGOIDES ( 2 FDA reports)
MYOCLONIC EPILEPSY ( 2 FDA reports)
MYOMECTOMY ( 2 FDA reports)
MYOPERICARDITIS ( 2 FDA reports)
NAIL OPERATION ( 2 FDA reports)
NARCISSISTIC PERSONALITY DISORDER ( 2 FDA reports)
NASAL DISORDER ( 2 FDA reports)
NASAL SINUS DRAINAGE ( 2 FDA reports)
NASOPHARYNGEAL DISORDER ( 2 FDA reports)
NECROTISING FASCIITIS ( 2 FDA reports)
NEEDLE TRACK MARKS ( 2 FDA reports)
NEPHRITIS ( 2 FDA reports)
NEPHROGENIC ANAEMIA ( 2 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 2 FDA reports)
NEPHROPATHY TOXIC ( 2 FDA reports)
NERVE BLOCK ( 2 FDA reports)
NERVE DEGENERATION ( 2 FDA reports)
NEUROGENIC BOWEL ( 2 FDA reports)
NEUROMYOPATHY ( 2 FDA reports)
NEUROTRANSMITTER LEVEL ALTERED ( 2 FDA reports)
NEUTROPHIL TOXIC GRANULATION PRESENT ( 2 FDA reports)
NIEMANN-PICK DISEASE ( 2 FDA reports)
NIGHT BLINDNESS ( 2 FDA reports)
NO ADVERSE EFFECT ( 2 FDA reports)
NOCTURNAL DYSPNOEA ( 2 FDA reports)
OBSESSIVE THOUGHTS ( 2 FDA reports)
OBSTRUCTIVE CHRONIC BRONCHITIS WITH ACUTE EXACERBATION ( 2 FDA reports)
OCCIPITAL NEURALGIA ( 2 FDA reports)
OEDEMA GENITAL ( 2 FDA reports)
OESOPHAGEAL FOOD IMPACTION ( 2 FDA reports)
OESOPHAGEAL OEDEMA ( 2 FDA reports)
OESOPHAGEAL PAIN ( 2 FDA reports)
OESOPHAGEAL POLYP ( 2 FDA reports)
OLIGOMENORRHOEA ( 2 FDA reports)
OLIGURIA ( 2 FDA reports)
ON AND OFF PHENOMENON ( 2 FDA reports)
OPERATIVE HAEMORRHAGE ( 2 FDA reports)
OPTIC ATROPHY ( 2 FDA reports)
ORAL MUCOSAL DISCOLOURATION ( 2 FDA reports)
ORAL MUCOSAL ERUPTION ( 2 FDA reports)
ORBITAL OEDEMA ( 2 FDA reports)
OROANTRAL FISTULA ( 2 FDA reports)
OROPHARYNGEAL SWELLING ( 2 FDA reports)
OSTEOCHONDROMA ( 2 FDA reports)
OVARIAN CANCER ( 2 FDA reports)
OVARIAN CANCER RECURRENT ( 2 FDA reports)
OVARIAN ENLARGEMENT ( 2 FDA reports)
OVARIAN INFECTION ( 2 FDA reports)
PANCREATIC CYST ( 2 FDA reports)
PANCREATIC DUCT DILATATION ( 2 FDA reports)
PANCREATIC DUCT STENOSIS ( 2 FDA reports)
PANCREATIC ENLARGEMENT ( 2 FDA reports)
PANCREATIC INJURY ( 2 FDA reports)
PANCREATIC MASS ( 2 FDA reports)
PANIC DISORDER WITHOUT AGORAPHOBIA ( 2 FDA reports)
PANOPHTHALMITIS ( 2 FDA reports)
PAPULE ( 2 FDA reports)
PARALYSIS FLACCID ( 2 FDA reports)
PARASITE URINE TEST POSITIVE ( 2 FDA reports)
PARATHYROID TUMOUR ( 2 FDA reports)
PATHOGEN RESISTANCE ( 2 FDA reports)
PELVIC MASS ( 2 FDA reports)
PELVIC VENOUS THROMBOSIS ( 2 FDA reports)
PENILE PROSTHESIS INSERTION ( 2 FDA reports)
PENIS CARCINOMA ( 2 FDA reports)
PEPTIC ULCER PERFORATION ( 2 FDA reports)
PERINEPHRIC COLLECTION ( 2 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 2 FDA reports)
PERIPHERAL EMBOLISM ( 2 FDA reports)
PERIRECTAL ABSCESS ( 2 FDA reports)
PERIVASCULAR DERMATITIS ( 2 FDA reports)
PHAGOPHOBIA ( 2 FDA reports)
PHALANGEAL HYPOPLASIA ( 2 FDA reports)
PHARYNGEAL HYPOAESTHESIA ( 2 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 2 FDA reports)
PHYSIOTHERAPY ( 2 FDA reports)
PLASMACYTOSIS ( 2 FDA reports)
PLASMODIUM FALCIPARUM INFECTION ( 2 FDA reports)
PLATELET COUNT ABNORMAL ( 2 FDA reports)
PLEURAL HAEMORRHAGE ( 2 FDA reports)
PLEUROTHOTONUS ( 2 FDA reports)
PNEUMONIA FUNGAL ( 2 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 2 FDA reports)
POOR PERSONAL HYGIENE ( 2 FDA reports)
POOR WEIGHT GAIN NEONATAL ( 2 FDA reports)
PORIOMANIA ( 2 FDA reports)
PORPHYRIA ACUTE ( 2 FDA reports)
PORTAL HYPERTENSION ( 2 FDA reports)
PORTAL VEIN THROMBOSIS ( 2 FDA reports)
POST LAMINECTOMY SYNDROME ( 2 FDA reports)
POST PROCEDURAL FISTULA ( 2 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 2 FDA reports)
POSTOPERATIVE FEVER ( 2 FDA reports)
POSTOPERATIVE ILEUS ( 2 FDA reports)
PRECANCEROUS SKIN LESION ( 2 FDA reports)
PREGNANCY WITH CONTRACEPTIVE DEVICE ( 2 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 2 FDA reports)
PRESSURE OF SPEECH ( 2 FDA reports)
PRIAPISM ( 2 FDA reports)
PROCEDURAL HYPOTENSION ( 2 FDA reports)
PROCEDURAL VOMITING ( 2 FDA reports)
PRODUCT FORMULATION ISSUE ( 2 FDA reports)
PROPIONIBACTERIUM INFECTION ( 2 FDA reports)
PROSTHESIS USER ( 2 FDA reports)
PROSTRATION ( 2 FDA reports)
PROTEIN S DEFICIENCY ( 2 FDA reports)
PROTHROMBIN TIME ( 2 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 2 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 2 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 2 FDA reports)
PUBIS FRACTURE ( 2 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 2 FDA reports)
PULMONARY ARTERY ANEURYSM ( 2 FDA reports)
PULMONARY CAVITATION ( 2 FDA reports)
PULMONARY EOSINOPHILIA ( 2 FDA reports)
PULMONARY HAEMORRHAGE ( 2 FDA reports)
PULMONARY MALFORMATION ( 2 FDA reports)
PULPITIS DENTAL ( 2 FDA reports)
PUSTULAR PSORIASIS ( 2 FDA reports)
PYLORIC STENOSIS ( 2 FDA reports)
PYODERMA ( 2 FDA reports)
PYODERMA GANGRENOSUM ( 2 FDA reports)
PYOGENIC GRANULOMA ( 2 FDA reports)
RADIAL NERVE PALSY ( 2 FDA reports)
RADIATION OESOPHAGITIS ( 2 FDA reports)
RASH MORBILLIFORM ( 2 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 2 FDA reports)
READING DISORDER ( 2 FDA reports)
REBOUND EFFECT ( 2 FDA reports)
RED BLOOD CELLS CSF POSITIVE ( 2 FDA reports)
REFRACTORY ANAEMIA WITH AN EXCESS OF BLASTS ( 2 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 2 FDA reports)
RELAPSING-REMITTING MULTIPLE SCLEROSIS ( 2 FDA reports)
RENAL HAEMORRHAGE ( 2 FDA reports)
RENAL HYPOPLASIA ( 2 FDA reports)
RENAL NECROSIS ( 2 FDA reports)
RENAL OSTEODYSTROPHY ( 2 FDA reports)
RENAL TRANSPLANT ( 2 FDA reports)
RENAL TUBULAR DISORDER ( 2 FDA reports)
RENAL VASCULITIS ( 2 FDA reports)
REPETITIVE SPEECH ( 2 FDA reports)
RESIDUAL URINE VOLUME INCREASED ( 2 FDA reports)
RESPIRATORY PARALYSIS ( 2 FDA reports)
RESTING TREMOR ( 2 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 2 FDA reports)
RETICULOCYTOSIS ( 2 FDA reports)
RETINOPATHY ( 2 FDA reports)
RETROGRADE AMNESIA ( 2 FDA reports)
RHABDOMYOMA ( 2 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 2 FDA reports)
RHEUMATOID VASCULITIS ( 2 FDA reports)
RIFT VALLEY FEVER ( 2 FDA reports)
SACRAL PAIN ( 2 FDA reports)
SALIVARY GLAND CALCULUS ( 2 FDA reports)
SALPINGITIS ( 2 FDA reports)
SARCOMA ( 2 FDA reports)
SCAN ABNORMAL ( 2 FDA reports)
SCAR PAIN ( 2 FDA reports)
SCROTAL OEDEMA ( 2 FDA reports)
SCROTAL SWELLING ( 2 FDA reports)
SEPSIS SYNDROME ( 2 FDA reports)
SERRATIA SEPSIS ( 2 FDA reports)
SHORT-BOWEL SYNDROME ( 2 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 2 FDA reports)
SJOGREN'S SYNDROME ( 2 FDA reports)
SKIN CANDIDA ( 2 FDA reports)
SKIN DEPIGMENTATION ( 2 FDA reports)
SKIN MACERATION ( 2 FDA reports)
SKIN MALFORMATION ( 2 FDA reports)
SLEEP ATTACKS ( 2 FDA reports)
SMALL INTESTINAL PERFORATION ( 2 FDA reports)
SMEAR CERVIX ABNORMAL ( 2 FDA reports)
SMOKER ( 2 FDA reports)
SOMATISATION DISORDER ( 2 FDA reports)
SOMATOFORM DISORDER ( 2 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 2 FDA reports)
SPEECH REHABILITATION ( 2 FDA reports)
SPHINCTER OF ODDI DYSFUNCTION ( 2 FDA reports)
SPINAL CORPECTOMY ( 2 FDA reports)
SPINAL NERVE STIMULATOR IMPLANTATION ( 2 FDA reports)
SPLEEN SCAN ABNORMAL ( 2 FDA reports)
SPLENIC VEIN THROMBOSIS ( 2 FDA reports)
SPUTUM ABNORMAL ( 2 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 2 FDA reports)
STATUS MIGRAINOSUS ( 2 FDA reports)
STERNOTOMY ( 2 FDA reports)
STOMACH MASS ( 2 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 2 FDA reports)
STRESS INCONTINENCE ( 2 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 2 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 2 FDA reports)
SUPERFICIAL SPREADING MELANOMA STAGE UNSPECIFIED ( 2 FDA reports)
SUPERINFECTION ( 2 FDA reports)
SUSPICIOUSNESS ( 2 FDA reports)
SWEAT DISCOLOURATION ( 2 FDA reports)
SYNCOPE VASOVAGAL ( 2 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 2 FDA reports)
T-LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
TABLET PHYSICAL ISSUE ( 2 FDA reports)
TARSAL TUNNEL SYNDROME ( 2 FDA reports)
TERMINAL STATE ( 2 FDA reports)
TESTICULAR SWELLING ( 2 FDA reports)
TETANY ( 2 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 2 FDA reports)
THERAPY CESSATION ( 2 FDA reports)
THERAPY REGIMEN CHANGED ( 2 FDA reports)
THOUGHT INSERTION ( 2 FDA reports)
THROMBOANGIITIS OBLITERANS ( 2 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 2 FDA reports)
THYMUS ENLARGEMENT ( 2 FDA reports)
THYROID CYST ( 2 FDA reports)
TOBACCO USER ( 2 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 2 FDA reports)
TOOTH EROSION ( 2 FDA reports)
TORTICOLLIS ( 2 FDA reports)
TOTAL LUNG CAPACITY INCREASED ( 2 FDA reports)
TRACHEAL DISORDER ( 2 FDA reports)
TRANCE ( 2 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 2 FDA reports)
TRANSPOSITION OF THE GREAT VESSELS ( 2 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 2 FDA reports)
TRI-IODOTHYRONINE INCREASED ( 2 FDA reports)
TRICHOTILLOMANIA ( 2 FDA reports)
TRIGEMINAL NERVE DISORDER ( 2 FDA reports)
TUBERCULOSIS OF PERIPHERAL LYMPH NODES ( 2 FDA reports)
TUBEROUS SCLEROSIS ( 2 FDA reports)
TYPE I HYPERSENSITIVITY ( 2 FDA reports)
UNEMPLOYMENT ( 2 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 2 FDA reports)
UPPER AIRWAY RESISTANCE SYNDROME ( 2 FDA reports)
UPPER EXTREMITY MASS ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 2 FDA reports)
URETHRAL PAIN ( 2 FDA reports)
URETHRAL POLYP ( 2 FDA reports)
URINE ABNORMALITY ( 2 FDA reports)
UTERINE ENLARGEMENT ( 2 FDA reports)
UTERINE INFECTION ( 2 FDA reports)
VAGINAL PAIN ( 2 FDA reports)
VASCULAR ACCESS COMPLICATION ( 2 FDA reports)
VASCULAR DEMENTIA ( 2 FDA reports)
VASCULAR ENCEPHALOPATHY ( 2 FDA reports)
VASCULAR GRAFT OCCLUSION ( 2 FDA reports)
VASCULAR INJURY ( 2 FDA reports)
VASCULAR RUPTURE ( 2 FDA reports)
VASCULAR SKIN DISORDER ( 2 FDA reports)
VASCULITIS NECROTISING ( 2 FDA reports)
VASOCONSTRICTION ( 2 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 2 FDA reports)
VESTIBULITIS ( 2 FDA reports)
VICTIM OF SEXUAL ABUSE ( 2 FDA reports)
VIRAL LOAD DECREASED ( 2 FDA reports)
VIRAL MYOCARDITIS ( 2 FDA reports)
VISCERAL PAIN ( 2 FDA reports)
VISUAL PATHWAY DISORDER ( 2 FDA reports)
VITAMIN B1 DEFICIENCY ( 2 FDA reports)
VITAMIN B12 INCREASED ( 2 FDA reports)
VOCAL CORD DISORDER ( 2 FDA reports)
VOCAL CORD POLYPECTOMY ( 2 FDA reports)
VOLVULUS ( 2 FDA reports)
VOLVULUS OF BOWEL ( 2 FDA reports)
VULVAL DISORDER ( 2 FDA reports)
VULVOVAGINAL ERYTHEMA ( 2 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 2 FDA reports)
WALDENSTROM'S MACROGLOBULINAEMIA ( 2 FDA reports)
WALKING DISTANCE TEST ABNORMAL ( 2 FDA reports)
WEANING FAILURE ( 2 FDA reports)
WEIGHT GAIN POOR ( 2 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 2 FDA reports)
WOUND NECROSIS ( 2 FDA reports)
XANTHOPSIA ( 2 FDA reports)
ZINC DEFICIENCY ( 2 FDA reports)
RETINAL FUNCTION TEST ABNORMAL ( 1 FDA reports)
RETINAL PIGMENT EPITHELIAL TEAR ( 1 FDA reports)
RETINAL VEIN THROMBOSIS ( 1 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 1 FDA reports)
RETROVIRAL INFECTION ( 1 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 1 FDA reports)
REVISION OF INTERNAL FIXATION ( 1 FDA reports)
RHEUMATIC HEART DISEASE ( 1 FDA reports)
RHEUMATOID LUNG ( 1 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
ROSAI-DORFMAN SYNDROME ( 1 FDA reports)
RUPTURED DIVERTICULUM OF COLON ( 1 FDA reports)
SALIVARY GLAND DISORDER ( 1 FDA reports)
SALIVARY GLAND MASS ( 1 FDA reports)
SALIVARY GLAND NEOPLASM ( 1 FDA reports)
SALIVARY GLAND PAIN ( 1 FDA reports)
SALMONELLOSIS ( 1 FDA reports)
SCAN ABDOMEN ABNORMAL ( 1 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 1 FDA reports)
SCAPULA FRACTURE ( 1 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 1 FDA reports)
SCHIZOTYPAL PERSONALITY DISORDER ( 1 FDA reports)
SCIATIC NERVE NEUROPATHY ( 1 FDA reports)
SCROTAL INFECTION ( 1 FDA reports)
SCROTAL IRRITATION ( 1 FDA reports)
SCROTAL PAIN ( 1 FDA reports)
SEASONAL AFFECTIVE DISORDER ( 1 FDA reports)
SECONDARY ADRENOCORTICAL INSUFFICIENCY ( 1 FDA reports)
SEDATIVE THERAPY ( 1 FDA reports)
SELF ESTEEM INFLATED ( 1 FDA reports)
SENSORY INTEGRATIVE DYSFUNCTION ( 1 FDA reports)
SEPSIS NEONATAL ( 1 FDA reports)
SEPTIC EMBOLUS ( 1 FDA reports)
SEPTOPLASTY ( 1 FDA reports)
SERRATIA INFECTION ( 1 FDA reports)
SEX HORMONE BINDING GLOBULIN DECREASED ( 1 FDA reports)
SEXUALLY TRANSMITTED DISEASE ( 1 FDA reports)
SHOCK HYPOGLYCAEMIC ( 1 FDA reports)
SHOULDER OPERATION ( 1 FDA reports)
SIALOADENITIS ( 1 FDA reports)
SICKLE CELL ANAEMIA ( 1 FDA reports)
SIGNET-RING CELL CARCINOMA ( 1 FDA reports)
SINUS PAIN ( 1 FDA reports)
SINUSITIS ASPERGILLUS ( 1 FDA reports)
SKIN DISCOMFORT ( 1 FDA reports)
SKIN HYPOPLASIA ( 1 FDA reports)
SKIN INFLAMMATION ( 1 FDA reports)
SKIN ODOUR ABNORMAL ( 1 FDA reports)
SKIN STRIAE ( 1 FDA reports)
SKIN SWELLING ( 1 FDA reports)
SKIN TOXICITY ( 1 FDA reports)
SKIN WRINKLING ( 1 FDA reports)
SLEEP DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
SLEEP STUDY ABNORMAL ( 1 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 1 FDA reports)
SMALL FOR DATES BABY ( 1 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 1 FDA reports)
SMALL INTESTINE CARCINOMA ( 1 FDA reports)
SMEAR SITE UNSPECIFIED ABNORMAL ( 1 FDA reports)
SOFT TISSUE DISORDER ( 1 FDA reports)
SOFT TISSUE MASS ( 1 FDA reports)
SOLILOQUY ( 1 FDA reports)
SOMATIC DELUSION ( 1 FDA reports)
SPIDER VEIN ( 1 FDA reports)
SPINAL CLAUDICATION ( 1 FDA reports)
SPINAL CORD INFARCTION ( 1 FDA reports)
SPINAL CORD ISCHAEMIA ( 1 FDA reports)
SPINAL HAEMANGIOMA ( 1 FDA reports)
SPIROMETRY ABNORMAL ( 1 FDA reports)
SPLENIC CANDIDIASIS ( 1 FDA reports)
SPLENIC NEOPLASM MALIGNANCY UNSPECIFIED ( 1 FDA reports)
SPONDYLITIS ( 1 FDA reports)
SPONDYLOARTHROPATHY ( 1 FDA reports)
SPONTANEOUS PENILE ERECTION ( 1 FDA reports)
STAPHYLOCOCCAL SCALDED SKIN SYNDROME ( 1 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
STEAL SYNDROME ( 1 FDA reports)
STENT OCCLUSION ( 1 FDA reports)
STEREOTYPY ( 1 FDA reports)
STERNAL FRACTURE ( 1 FDA reports)
STILL'S DISEASE ADULT ONSET ( 1 FDA reports)
STOMA SITE REACTION ( 1 FDA reports)
STOOLS WATERY ( 1 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 1 FDA reports)
STRESS AT WORK ( 1 FDA reports)
SUDDEN VISUAL LOSS ( 1 FDA reports)
SULPHAEMOGLOBINAEMIA ( 1 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 1 FDA reports)
SUPRAPUBIC PAIN ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
SUTURE INSERTION ( 1 FDA reports)
SUTURE RELATED COMPLICATION ( 1 FDA reports)
SUTURE RUPTURE ( 1 FDA reports)
SYNOVIAL DISORDER ( 1 FDA reports)
SYNOVIAL FLUID ANALYSIS ABNORMAL ( 1 FDA reports)
SYSTOLIC HYPERTENSION ( 1 FDA reports)
T-CELL TYPE ACUTE LEUKAEMIA ( 1 FDA reports)
TALIPES ( 1 FDA reports)
TARSAL TUNNEL DECOMPRESSION ( 1 FDA reports)
TEAR DISCOLOURATION ( 1 FDA reports)
TEMPORAL ARTERITIS ( 1 FDA reports)
TENOSYNOVITIS STENOSANS ( 1 FDA reports)
TERMINAL INSOMNIA ( 1 FDA reports)
TERTIARY SYPHILIS ( 1 FDA reports)
TESTICULAR DISORDER ( 1 FDA reports)
THALAMIC INFARCTION ( 1 FDA reports)
THALAMUS HAEMORRHAGE ( 1 FDA reports)
THERAPEUTIC EMBOLISATION ( 1 FDA reports)
THORACIC HAEMORRHAGE ( 1 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 1 FDA reports)
THORACOTOMY ( 1 FDA reports)
THROAT CANCER ( 1 FDA reports)
THROMBOCYTHAEMIA ( 1 FDA reports)
THYROID OPERATION ( 1 FDA reports)
THYROXINE FREE DECREASED ( 1 FDA reports)
TICK-BORNE FEVER ( 1 FDA reports)
TINEA INFECTION ( 1 FDA reports)
TINEA VERSICOLOUR ( 1 FDA reports)
TONGUE DISCOLOURATION ( 1 FDA reports)
TONGUE ERUPTION ( 1 FDA reports)
TONGUE OEDEMA ( 1 FDA reports)
TOOTH IMPACTED ( 1 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO DECREASED ( 1 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO INCREASED ( 1 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 1 FDA reports)
TOXOPLASMOSIS ( 1 FDA reports)
TRACHEAL MASS ( 1 FDA reports)
TRACHEAL STENOSIS ( 1 FDA reports)
TRACHEITIS ( 1 FDA reports)
TRACHEOSTOMY ( 1 FDA reports)
TRACHEOSTOMY MALFUNCTION ( 1 FDA reports)
TRANSAMINASES ABNORMAL ( 1 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 1 FDA reports)
TRANSPLANT ( 1 FDA reports)
TRAUMATIC ARTHRITIS ( 1 FDA reports)
TRAUMATIC FRACTURE ( 1 FDA reports)
TRAUMATIC LIVER INJURY ( 1 FDA reports)
TRENDELENBURG'S SYMPTOM ( 1 FDA reports)
TRI-IODOTHYRONINE DECREASED ( 1 FDA reports)
TRI-IODOTHYRONINE FREE ABNORMAL ( 1 FDA reports)
TRICHOMONIASIS ( 1 FDA reports)
TRICUSPID VALVE DISEASE ( 1 FDA reports)
TROPONIN ( 1 FDA reports)
TULARAEMIA ( 1 FDA reports)
TUMOUR ULCERATION ( 1 FDA reports)
TURNER'S SYNDROME ( 1 FDA reports)
TWIN PREGNANCY ( 1 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 1 FDA reports)
ULNAR NERVE PALSY ( 1 FDA reports)
ULNAR NEURITIS ( 1 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 1 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 1 FDA reports)
UMBILICAL HAEMORRHAGE ( 1 FDA reports)
UMBILICAL HERNIA REPAIR ( 1 FDA reports)
UNDERWEIGHT ( 1 FDA reports)
UNEQUAL LIMB LENGTH ( 1 FDA reports)
UNEXPECTED THERAPEUTIC DRUG EFFECT ( 1 FDA reports)
UPPER MOTOR NEURONE LESION ( 1 FDA reports)
URAEMIC ENCEPHALOPATHY ( 1 FDA reports)
URETERAL STENT INSERTION ( 1 FDA reports)
URETHRAL CARUNCLE ( 1 FDA reports)
URETHRAL DISCHARGE ( 1 FDA reports)
URETHRAL DISORDER ( 1 FDA reports)
URINARY CASTS ( 1 FDA reports)
URINARY CASTS PRESENT ( 1 FDA reports)
URINARY RETENTION POSTOPERATIVE ( 1 FDA reports)
URINARY SYSTEM X-RAY ABNORMAL ( 1 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 1 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
URINE ARSENIC DECREASED ( 1 FDA reports)
URINE CALCIUM ( 1 FDA reports)
URINE OSMOLARITY INCREASED ( 1 FDA reports)
URINE POTASSIUM INCREASED ( 1 FDA reports)
UROGENITAL HAEMORRHAGE ( 1 FDA reports)
UROGRAM ABNORMAL ( 1 FDA reports)
URTICARIA PIGMENTOSA ( 1 FDA reports)
USE OF ACCESSORY RESPIRATORY MUSCLES ( 1 FDA reports)
UTERINE CERVIX STENOSIS ( 1 FDA reports)
VACCINATION COMPLICATION ( 1 FDA reports)
VAGAL NERVE STIMULATOR IMPLANTATION ( 1 FDA reports)
VAGINAL BURNING SENSATION ( 1 FDA reports)
VAGINAL FISTULA ( 1 FDA reports)
VAGINAL INFLAMMATION ( 1 FDA reports)
VAGINAL MYCOSIS ( 1 FDA reports)
VAGINAL ODOUR ( 1 FDA reports)
VAGINAL ULCERATION ( 1 FDA reports)
VARICOSE VEIN RUPTURED ( 1 FDA reports)
VASCULAR BYPASS GRAFT ( 1 FDA reports)
VASCULAR MALFORMATION PERIPHERAL ( 1 FDA reports)
VASCULAR NEOPLASM ( 1 FDA reports)
VASCULAR STENOSIS ( 1 FDA reports)
VASCULITIS CEREBRAL ( 1 FDA reports)
VENA CAVA FILTER INSERTION ( 1 FDA reports)
VENOUS HAEMORRHAGE ( 1 FDA reports)
VENOUS PRESSURE INCREASED ( 1 FDA reports)
VENTRICULAR ASYSTOLE ( 1 FDA reports)
VENTRICULAR TACHYARRHYTHMIA ( 1 FDA reports)
VERTEBRAL INJURY ( 1 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 1 FDA reports)
VESTIBULAR NEURONITIS ( 1 FDA reports)
VICTIM OF CHILD ABUSE ( 1 FDA reports)
VICTIM OF CRIME ( 1 FDA reports)
VIRAEMIA ( 1 FDA reports)
VIRAL RASH ( 1 FDA reports)
VIRUS SEROLOGY TEST POSITIVE ( 1 FDA reports)
VISION ABNORMAL NEONATAL ( 1 FDA reports)
VISUAL ACUITY TESTS ABNORMAL ( 1 FDA reports)
VISUAL BRIGHTNESS ( 1 FDA reports)
VITAMIN B COMPLEX DEFICIENCY ( 1 FDA reports)
VITAMIN B1 DECREASED ( 1 FDA reports)
VITAMIN K DEFICIENCY ( 1 FDA reports)
VITH NERVE DISORDER ( 1 FDA reports)
VITILIGO ( 1 FDA reports)
VITREOUS OPACITIES ( 1 FDA reports)
VOCAL CORD INFLAMMATION ( 1 FDA reports)
VOCAL CORD PARALYSIS ( 1 FDA reports)
VOLVULUS OF SMALL BOWEL ( 1 FDA reports)
VULVAL ULCERATION ( 1 FDA reports)
VULVOVAGINAL DRYNESS ( 1 FDA reports)
WALKING DISABILITY ( 1 FDA reports)
WATER POLLUTION ( 1 FDA reports)
WEGENER'S GRANULOMATOSIS ( 1 FDA reports)
WEIGHT ABNORMAL ( 1 FDA reports)
WEST NILE VIRAL INFECTION ( 1 FDA reports)
WHITE BLOOD CELL ANALYSIS INCREASED ( 1 FDA reports)
WOUND CLOSURE ( 1 FDA reports)
WOUND INFECTION BACTERIAL ( 1 FDA reports)
X-RAY DENTAL ( 1 FDA reports)
XANTHOGRANULOMA ( 1 FDA reports)
XANTHOMA ( 1 FDA reports)
YERSINIA INFECTION ( 1 FDA reports)
ABDOMINAL INJURY ( 1 FDA reports)
ABDOMINAL WALL MASS ( 1 FDA reports)
ABNORMAL CHEST SOUND ( 1 FDA reports)
ABORTION INCOMPLETE ( 1 FDA reports)
ABSCESS INTESTINAL ( 1 FDA reports)
ABSCESS SOFT TISSUE ( 1 FDA reports)
ACCELERATED IDIOVENTRICULAR RHYTHM ( 1 FDA reports)
ACCOMMODATION DISORDER ( 1 FDA reports)
ACID BASE BALANCE ABNORMAL ( 1 FDA reports)
ACINETOBACTER INFECTION ( 1 FDA reports)
ACNE CYSTIC ( 1 FDA reports)
ACQUIRED PYLORIC STENOSIS ( 1 FDA reports)
ACTH STIMULATION TEST ABNORMAL ( 1 FDA reports)
ACUTE CHEST SYNDROME ( 1 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA (IN REMISSION) ( 1 FDA reports)
ACUTE MYELOMONOCYTIC LEUKAEMIA ( 1 FDA reports)
ADDISON'S DISEASE ( 1 FDA reports)
ADENOMATOUS POLYPOSIS COLI ( 1 FDA reports)
ADENOMYOSIS ( 1 FDA reports)
ADJUSTMENT DISORDER WITH ANXIETY ( 1 FDA reports)
ADMINISTRATION SITE REACTION ( 1 FDA reports)
ADRENAL SUPPRESSION ( 1 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 1 FDA reports)
AKINESIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ( 1 FDA reports)
ALBUMIN GLOBULIN RATIO ABNORMAL ( 1 FDA reports)
ALBUMINURIA ( 1 FDA reports)
ALCOHOL PROBLEM ( 1 FDA reports)
ALLERGENIC DESENSITISATION PROCEDURE ( 1 FDA reports)
ALLERGIC BRONCHITIS ( 1 FDA reports)
ALLERGY TO CHEMICALS ( 1 FDA reports)
ALLOGENIC BONE MARROW TRANSPLANTATION THERAPY ( 1 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 1 FDA reports)
ALVEOLITIS FIBROSING ( 1 FDA reports)
AMPHETAMINES POSITIVE ( 1 FDA reports)
AMYLOIDOSIS ( 1 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 1 FDA reports)
AMYOTROPHY ( 1 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 1 FDA reports)
ANAL FISTULA ( 1 FDA reports)
ANAL PRURITUS ( 1 FDA reports)
ANAL SPHINCTER ATONY ( 1 FDA reports)
ANALGESIA ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
ANAPLASTIC ASTROCYTOMA ( 1 FDA reports)
ANASTOMOTIC STENOSIS ( 1 FDA reports)
ANDROGEN DEFICIENCY ( 1 FDA reports)
ANDROGENS DECREASED ( 1 FDA reports)
ANEURYSM RUPTURED ( 1 FDA reports)
ANGIOGRAM ABNORMAL ( 1 FDA reports)
ANGIOMYOLIPOMA ( 1 FDA reports)
ANORECTAL OPERATION ( 1 FDA reports)
ANOSOGNOSIA ( 1 FDA reports)
ANTEPARTUM HAEMORRHAGE ( 1 FDA reports)
ANTERIOR CHAMBER INFLAMMATION ( 1 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-THYROID ANTIBODY POSITIVE ( 1 FDA reports)
ANTIBIOTIC PROPHYLAXIS ( 1 FDA reports)
ANTIBODY TEST ABNORMAL ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL ABNORMAL ( 1 FDA reports)
ANTICONVULSANT TOXICITY ( 1 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 1 FDA reports)
ANTINUCLEAR ANTIBODY ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL ( 1 FDA reports)
ANXIETY DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
AORTIC INJURY ( 1 FDA reports)
AORTIC VALVE ATRESIA ( 1 FDA reports)
AORTITIS ( 1 FDA reports)
APPARENT LIFE THREATENING EVENT ( 1 FDA reports)
APPLICATION SITE DISCOLOURATION ( 1 FDA reports)
APPLICATION SITE EXFOLIATION ( 1 FDA reports)
APPLICATION SITE HYPERAESTHESIA ( 1 FDA reports)
APPLICATION SITE HYPERSENSITIVITY ( 1 FDA reports)
APPLICATION SITE INFLAMMATION ( 1 FDA reports)
APPLICATION SITE URTICARIA ( 1 FDA reports)
ARTERIAL RUPTURE ( 1 FDA reports)
ARTERIAL STENT INSERTION ( 1 FDA reports)
ARTERIOSCLEROSIS OBLITERANS ( 1 FDA reports)
ARTERIOVENOUS GRAFT SITE HAEMATOMA ( 1 FDA reports)
ARTERITIS OBLITERANS ( 1 FDA reports)
ARTIFICIAL MENOPAUSE ( 1 FDA reports)
ASPIRATION JOINT ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK THIRD DEGREE ( 1 FDA reports)
ATRIOVENTRICULAR SEPTAL DEFECT ( 1 FDA reports)
ATTENTION-SEEKING BEHAVIOUR ( 1 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 1 FDA reports)
AUTISM ( 1 FDA reports)
AUTOIMMUNE NEUROPATHY ( 1 FDA reports)
AXILLARY MASS ( 1 FDA reports)
AXILLARY VEIN THROMBOSIS ( 1 FDA reports)
B-LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
BABESIOSIS ( 1 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 1 FDA reports)
BACTERIA STOOL IDENTIFIED ( 1 FDA reports)
BACTERIA URINE IDENTIFIED ( 1 FDA reports)
BACTERIAL ANTIGEN POSITIVE ( 1 FDA reports)
BACTERIAL CULTURE POSITIVE ( 1 FDA reports)
BASAL GANGLIA HAEMORRHAGE ( 1 FDA reports)
BASAL GANGLIA STROKE ( 1 FDA reports)
BASE EXCESS ABNORMAL ( 1 FDA reports)
BASE EXCESS NEGATIVE ( 1 FDA reports)
BASE EXCESS POSITIVE ( 1 FDA reports)
BASOSQUAMOUS CARCINOMA OF SKIN ( 1 FDA reports)
BENIGN CARDIAC NEOPLASM ( 1 FDA reports)
BENIGN GASTRIC NEOPLASM ( 1 FDA reports)
BENIGN NEOPLASM OF BLADDER ( 1 FDA reports)
BENIGN SOFT TISSUE NEOPLASM ( 1 FDA reports)
BENIGN TUMOUR EXCISION ( 1 FDA reports)
BEREAVEMENT REACTION ( 1 FDA reports)
BICUSPID AORTIC VALVE ( 1 FDA reports)
BICYTOPENIA ( 1 FDA reports)
BILIARY CIRRHOSIS ( 1 FDA reports)
BILIARY NEOPLASM ( 1 FDA reports)
BIOPSY BRAIN ABNORMAL ( 1 FDA reports)
BIOPSY LIVER ABNORMAL ( 1 FDA reports)
BIOPSY LUNG ( 1 FDA reports)
BIOPSY LYMPH GLAND ( 1 FDA reports)
BIPOLAR II DISORDER ( 1 FDA reports)
BLADDER DISCOMFORT ( 1 FDA reports)
BLADDER DISTENSION ( 1 FDA reports)
BLADDER OBSTRUCTION ( 1 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 1 FDA reports)
BLAST CELLS PRESENT ( 1 FDA reports)
BLAST CRISIS IN MYELOGENOUS LEUKAEMIA ( 1 FDA reports)
BLEEDING TIME PROLONGED ( 1 FDA reports)
BLINDNESS CONGENITAL ( 1 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 1 FDA reports)
BLOOD AMYLASE DECREASED ( 1 FDA reports)
BLOOD BICARBONATE ABNORMAL ( 1 FDA reports)
BLOOD BILIRUBIN ( 1 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 1 FDA reports)
BLOOD CALCIUM ABNORMAL ( 1 FDA reports)
BLOOD CANNABINOIDS INCREASED ( 1 FDA reports)
BLOOD CORTISOL DECREASED ( 1 FDA reports)
BLOOD COUNT ( 1 FDA reports)
BLOOD CREATINE DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD HOMOCYSTEINE DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 1 FDA reports)
BLOOD KETONE BODY PRESENT ( 1 FDA reports)
BLOOD LACTIC ACID DECREASED ( 1 FDA reports)
BLOOD LUTEINISING HORMONE DECREASED ( 1 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 1 FDA reports)
BLOOD OSMOLARITY DECREASED ( 1 FDA reports)
BLOOD PRESSURE ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ( 1 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 1 FDA reports)
BLOOD TESTOSTERONE ABNORMAL ( 1 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 1 FDA reports)
BLOOD URINE ( 1 FDA reports)
BLOOD ZINC DECREASED ( 1 FDA reports)
BONE CANCER METASTATIC ( 1 FDA reports)
BONE GIANT CELL TUMOUR ( 1 FDA reports)
BONE INFARCTION ( 1 FDA reports)
BORDERLINE MENTAL IMPAIRMENT ( 1 FDA reports)
BRACHIAL PLEXOPATHY ( 1 FDA reports)
BRACHIAL PLEXUS INJURY ( 1 FDA reports)
BRADYPHRENIA ( 1 FDA reports)
BRAIN CANCER METASTATIC ( 1 FDA reports)
BRAIN CONTUSION ( 1 FDA reports)
BRAIN HYPOXIA ( 1 FDA reports)
BRAIN MIDLINE SHIFT ( 1 FDA reports)
BRAIN SCAN NORMAL ( 1 FDA reports)
BRAIN STEM SYNDROME ( 1 FDA reports)
BREAST ADENOMA ( 1 FDA reports)
BREAST CANCER STAGE IV ( 1 FDA reports)
BREAST HYPERPLASIA ( 1 FDA reports)
BREAST MICROCALCIFICATION ( 1 FDA reports)
BREAST NEOPLASM ( 1 FDA reports)
BREATH SOUNDS ( 1 FDA reports)
BREATHING-RELATED SLEEP DISORDER ( 1 FDA reports)
BRONCHIAL CARCINOMA ( 1 FDA reports)
BRONCHIAL HYPERACTIVITY ( 1 FDA reports)
BRONCHITIS BACTERIAL ( 1 FDA reports)
BRONCHOPNEUMOPATHY ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 1 FDA reports)
BRONCHOSPASM PARADOXICAL ( 1 FDA reports)
BUNION OPERATION ( 1 FDA reports)
BURGLARY VICTIM ( 1 FDA reports)
BURKITT'S LYMPHOMA ( 1 FDA reports)
BURN OESOPHAGEAL ( 1 FDA reports)
BURNING MOUTH SYNDROME ( 1 FDA reports)
BURNS THIRD DEGREE ( 1 FDA reports)
BURSA INJURY ( 1 FDA reports)
BUTTERFLY RASH ( 1 FDA reports)
CAFE AU LAIT SPOTS ( 1 FDA reports)
CALCIFICATION METASTATIC ( 1 FDA reports)
CALCIPHYLAXIS ( 1 FDA reports)
CALCULUS URINARY ( 1 FDA reports)
CANCER PAIN ( 1 FDA reports)
CANDIDA SEPSIS ( 1 FDA reports)
CAPILLARY DISORDER ( 1 FDA reports)
CAPILLARY LEAK SYNDROME ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 125 INCREASED ( 1 FDA reports)
CARBOHYDRATE METABOLISM DISORDER ( 1 FDA reports)
CARBON DIOXIDE INCREASED ( 1 FDA reports)
CARBON MONOXIDE DIFFUSING CAPACITY DECREASED ( 1 FDA reports)
CARBOXYHAEMOGLOBIN INCREASED ( 1 FDA reports)
CARDIAC ABLATION ( 1 FDA reports)
CARDIAC MURMUR FUNCTIONAL ( 1 FDA reports)
CARDIAC NEOPLASM UNSPECIFIED ( 1 FDA reports)
CARDIAC PACEMAKER REPLACEMENT ( 1 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 1 FDA reports)
CARDIO-RESPIRATORY DISTRESS ( 1 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 1 FDA reports)
CARDITIS ( 1 FDA reports)
CARNITINE DECREASED ( 1 FDA reports)
CAROTID ARTERY THROMBOSIS ( 1 FDA reports)
CAROTID BRUIT ( 1 FDA reports)
CAROTID ENDARTERECTOMY ( 1 FDA reports)
CARTILAGE NEOPLASM ( 1 FDA reports)
CATAPLEXY ( 1 FDA reports)
CATECHOLAMINES URINE INCREASED ( 1 FDA reports)
CATHETER SITE PAIN ( 1 FDA reports)
CATHETER SITE PRURITUS ( 1 FDA reports)
CAUDA EQUINA SYNDROME ( 1 FDA reports)
CD4 LYMPHOCYTES ABNORMAL ( 1 FDA reports)
CD8 LYMPHOCYTES DECREASED ( 1 FDA reports)
CELLULITIS ENTEROCOCCAL ( 1 FDA reports)
CELLULITIS STREPTOCOCCAL ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM ABSCESS ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 1 FDA reports)
CENTRAL VENOUS PRESSURE INCREASED ( 1 FDA reports)
CENTRAL-ALVEOLAR HYPOVENTILATION ( 1 FDA reports)
CEREBELLAR ARTERY OCCLUSION ( 1 FDA reports)
CEREBELLAR HAEMATOMA ( 1 FDA reports)
CEREBRAL PALSY ( 1 FDA reports)
CEREBROVASCULAR SPASM ( 1 FDA reports)
CERVICAL MYELOPATHY ( 1 FDA reports)
CERVICAL SPINE FLATTENING ( 1 FDA reports)
CERVICITIS ( 1 FDA reports)
CERVIX CANCER METASTATIC ( 1 FDA reports)
CHEMICAL INJURY ( 1 FDA reports)
CHEMOTHERAPY ( 1 FDA reports)
CHEYNE-STOKES RESPIRATION ( 1 FDA reports)
CHILLBLAINS ( 1 FDA reports)
CHOLANGITIS SCLEROSING ( 1 FDA reports)
CHOLESTASIS OF PREGNANCY ( 1 FDA reports)
CHOLURIA ( 1 FDA reports)
CHORIOAMNIONITIS ( 1 FDA reports)
CHOROIDAL NEOVASCULARISATION ( 1 FDA reports)
CHOROIDITIS ( 1 FDA reports)
CHROMATOPSIA ( 1 FDA reports)
CHROMOSOME ANALYSIS ABNORMAL ( 1 FDA reports)
CHRONIC FATIGUE SYNDROME ( 1 FDA reports)
CHRONIC INFLAMMATORY DEMYELINATING POLYRADICULONEUROPATHY ( 1 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 1 FDA reports)
CHRONIC MYELOID LEUKAEMIA TRANSFORMATION ( 1 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 1 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 1 FDA reports)
CIRCUMORAL OEDEMA ( 1 FDA reports)
CLEFT LIP AND PALATE ( 1 FDA reports)
CLINODACTYLY ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST ( 1 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 1 FDA reports)
COAGULATION FACTOR DECREASED ( 1 FDA reports)
COAGULATION FACTOR X LEVEL INCREASED ( 1 FDA reports)
COAGULATION TEST ABNORMAL ( 1 FDA reports)
COAGULATION TIME PROLONGED ( 1 FDA reports)
COLITIS COLLAGENOUS ( 1 FDA reports)
COLITIS PSEUDOMEMBRANOUS ( 1 FDA reports)
COLON GANGRENE ( 1 FDA reports)
COLONIC PSEUDO-OBSTRUCTION ( 1 FDA reports)
COLORECTAL CANCER STAGE IV ( 1 FDA reports)
COLOSTOMY ( 1 FDA reports)
COLOUR BLINDNESS ( 1 FDA reports)
COLOUR VISION TESTS ABNORMAL ( 1 FDA reports)
COMA BLISTER ( 1 FDA reports)
COMPLEMENT FACTOR DECREASED ( 1 FDA reports)
COMPLICATION OF DELIVERY ( 1 FDA reports)
CONDUCTIVE DEAFNESS ( 1 FDA reports)
CONGENITAL ANOMALY IN OFFSPRING ( 1 FDA reports)
CONGENITAL HYDRONEPHROSIS ( 1 FDA reports)
CONJUNCTIVAL OEDEMA ( 1 FDA reports)
CONTINUOUS POSITIVE AIRWAY PRESSURE ( 1 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 1 FDA reports)
CONTRAST MEDIA ALLERGY ( 1 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 1 FDA reports)
CORONARY ARTERY DISSECTION ( 1 FDA reports)
CORONARY ARTERY EMBOLISM ( 1 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 1 FDA reports)
CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
CORONARY ARTERY SURGERY ( 1 FDA reports)
CRANIOPHARYNGIOMA ( 1 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
CREATINE URINE INCREASED ( 1 FDA reports)
CRUSH INJURY ( 1 FDA reports)
CRYOGLOBULINAEMIA ( 1 FDA reports)
CRYPTOGENIC CIRRHOSIS ( 1 FDA reports)
CSF CELL COUNT ABNORMAL ( 1 FDA reports)
CSF CELL COUNT INCREASED ( 1 FDA reports)
CYSTOCELE REPAIR ( 1 FDA reports)
CYSTOSCOPY ABNORMAL ( 1 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 1 FDA reports)
CYTOMEGALOVIRUS GASTROINTESTINAL INFECTION ( 1 FDA reports)
CYTOMEGALOVIRUS OESOPHAGITIS ( 1 FDA reports)
DACRYOADENITIS ACQUIRED ( 1 FDA reports)
DAYDREAMING ( 1 FDA reports)
DEAFNESS TRANSITORY ( 1 FDA reports)
DEATH NEONATAL ( 1 FDA reports)
DEATH OF CHILD ( 1 FDA reports)
DEATH OF PARENT ( 1 FDA reports)
DECEREBRATION ( 1 FDA reports)
DELINQUENCY ( 1 FDA reports)
DELIVERY ( 1 FDA reports)
DENGUE FEVER ( 1 FDA reports)
DENTAL EXAMINATION ABNORMAL ( 1 FDA reports)
DENTAL IMPLANTATION ( 1 FDA reports)
DENTAL NECROSIS ( 1 FDA reports)
DEPENDENT RUBOR ( 1 FDA reports)
DERMATITIS ATOPIC ( 1 FDA reports)
DERMATITIS DIAPER ( 1 FDA reports)
DERMATOPHYTOSIS ( 1 FDA reports)
DERMOGRAPHISM ( 1 FDA reports)
DEVELOPMENTAL COORDINATION DISORDER ( 1 FDA reports)
DEVICE ADHESION ISSUE ( 1 FDA reports)
DEVICE DAMAGE ( 1 FDA reports)
DEVICE INEFFECTIVE ( 1 FDA reports)
DEVICE ISSUE ( 1 FDA reports)
DEVICE LEAKAGE ( 1 FDA reports)
DEVICE OCCLUSION ( 1 FDA reports)
DEVICE PACING ISSUE ( 1 FDA reports)
DEXAMETHASONE SUPPRESSION TEST POSITIVE ( 1 FDA reports)
DIABETIC ENTEROPATHY ( 1 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 1 FDA reports)
DIABETIC KETOACIDOTIC HYPERGLYCAEMIC COMA ( 1 FDA reports)
DIABETIC ULCER ( 1 FDA reports)
DIABETIC VASCULAR DISORDER ( 1 FDA reports)
DIAPHRAGMATIC DISORDER ( 1 FDA reports)
DIARRHOEA NEONATAL ( 1 FDA reports)
DIASTOLIC HYPOTENSION ( 1 FDA reports)
DIEULAFOY'S VASCULAR MALFORMATION ( 1 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 1 FDA reports)
DIRECTIONAL DOPPLER FLOW TESTS ABNORMAL ( 1 FDA reports)
DISEASE COMPLICATION ( 1 FDA reports)
DISINHIBITION ( 1 FDA reports)
DISLOCATION OF VERTEBRA ( 1 FDA reports)
DISSEMINATED LARGE CELL LYMPHOMA ( 1 FDA reports)
DISTAL INTESTINAL OBSTRUCTION SYNDROME ( 1 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 1 FDA reports)
DOUBLE STRANDED DNA ANTIBODY POSITIVE ( 1 FDA reports)
DRUG DIVERSION ( 1 FDA reports)
DRUG HALF-LIFE INCREASED ( 1 FDA reports)
DRUG INTERACTION INHIBITION ( 1 FDA reports)
DRUG LEVEL CHANGED ( 1 FDA reports)
DRUG SCREEN NEGATIVE ( 1 FDA reports)
DRUG THERAPEUTIC INCOMPATIBILITY ( 1 FDA reports)
DRUG WITHDRAWAL HEADACHE ( 1 FDA reports)
DUODENAL SCARRING ( 1 FDA reports)
DURAL TEAR ( 1 FDA reports)
DYSACUSIS ( 1 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 1 FDA reports)
DYSKINESIA NEONATAL ( 1 FDA reports)
DYSPNOEA EXACERBATED ( 1 FDA reports)
DYSTROPHIC CALCIFICATION ( 1 FDA reports)
EAR PRURITUS ( 1 FDA reports)
ECTOPIC PREGNANCY WITH INTRAUTERINE DEVICE ( 1 FDA reports)
ECZEMA ASTEATOTIC ( 1 FDA reports)
ECZEMA NUMMULAR ( 1 FDA reports)
EJACULATION DISORDER ( 1 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM QT INTERVAL ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROCONVULSIVE THERAPY ( 1 FDA reports)
ELECTROLYTE DEPLETION ( 1 FDA reports)
ELECTROPHORESIS ABNORMAL ( 1 FDA reports)
EMBOLISM VENOUS ( 1 FDA reports)
EMPHYSEMATOUS BULLA ( 1 FDA reports)
ENANTHEMA ( 1 FDA reports)
ENCEPHALITIS BRAIN STEM ( 1 FDA reports)
ENDOCARDITIS STAPHYLOCOCCAL ( 1 FDA reports)
ENDOCRINE DISORDER ( 1 FDA reports)
ENDOLYMPHATIC HYDROPS ( 1 FDA reports)
ENDOMETRIAL ADENOMA ( 1 FDA reports)
ENDOMETRIAL DISORDER ( 1 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 1 FDA reports)
ENDOPHTHALMITIS ( 1 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 1 FDA reports)
ENGRAFT FAILURE ( 1 FDA reports)
ENTERAL NUTRITION ( 1 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 1 FDA reports)
ENTEROVESICAL FISTULA ( 1 FDA reports)
ENZYME ABNORMALITY ( 1 FDA reports)
ENZYME INHIBITION ( 1 FDA reports)
ENZYME LEVEL INCREASED ( 1 FDA reports)
EOSINOPHIL COUNT DECREASED ( 1 FDA reports)
EOSINOPHIL PERCENTAGE ABNORMAL ( 1 FDA reports)
EPHELIDES ( 1 FDA reports)
EPIDERMAL NECROSIS ( 1 FDA reports)
EPIDERMOLYSIS ( 1 FDA reports)
EPIDERMOLYSIS BULLOSA ( 1 FDA reports)
EPIGLOTTITIS ( 1 FDA reports)
EPILEPSY CONGENITAL ( 1 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY ( 1 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 1 FDA reports)
EROSIVE DUODENITIS ( 1 FDA reports)
ERYTHEMA INDURATUM ( 1 FDA reports)
ERYTHEMA MIGRANS ( 1 FDA reports)
ESCHERICHIA SEPSIS ( 1 FDA reports)
ESCHERICHIA TEST POSITIVE ( 1 FDA reports)
ESSENTIAL TREMOR ( 1 FDA reports)
EXAGGERATED STARTLE RESPONSE ( 1 FDA reports)
EXERCISE ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
EXSANGUINATION ( 1 FDA reports)
EXTRADURAL ABSCESS ( 1 FDA reports)
EXTRASKELETAL OSSIFICATION ( 1 FDA reports)
EXTRASKELETAL OSTEOSARCOMA ( 1 FDA reports)
EXTREMITY NECROSIS ( 1 FDA reports)
EXTRINSIC VASCULAR COMPRESSION ( 1 FDA reports)
EYE ABSCESS ( 1 FDA reports)
EYE INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
EYE INFECTION VIRAL ( 1 FDA reports)
EYE OPERATION ( 1 FDA reports)
EYELASH THICKENING ( 1 FDA reports)
EYELID FUNCTION DISORDER ( 1 FDA reports)
FABRY'S DISEASE ( 1 FDA reports)
FACTITIOUS DISORDER ( 1 FDA reports)
FACTOR X DEFICIENCY ( 1 FDA reports)
FAECALITH ( 1 FDA reports)
FAECES PALE ( 1 FDA reports)
FALLOPIAN TUBE CYST ( 1 FDA reports)
FAMILIAL HYPOCALCIURIC HYPERCALCAEMIA ( 1 FDA reports)
FEAR OF DISEASE ( 1 FDA reports)
FEEDING TUBE COMPLICATION ( 1 FDA reports)
FEMALE ORGASMIC DISORDER ( 1 FDA reports)
FEMALE SEXUAL AROUSAL DISORDER ( 1 FDA reports)
FEMALE SEXUAL DYSFUNCTION ( 1 FDA reports)
FEMORAL HERNIA ( 1 FDA reports)
FEMORAL HERNIA, OBSTRUCTIVE ( 1 FDA reports)
FIBRINOLYSIS INCREASED ( 1 FDA reports)
FIBRINOUS BRONCHITIS ( 1 FDA reports)
FIBROUS HISTIOCYTOMA ( 1 FDA reports)
FIBULA FRACTURE ( 1 FDA reports)
FLOODING ( 1 FDA reports)
FOETAL ANTICONVULSANT SYNDROME ( 1 FDA reports)
FOETAL CARDIAC DISORDER ( 1 FDA reports)
FOETAL GROWTH RESTRICTION ( 1 FDA reports)
FORCEPS DELIVERY ( 1 FDA reports)
FOREIGN BODY ( 1 FDA reports)
FRACTURE DELAYED UNION ( 1 FDA reports)
FRACTURE MALUNION ( 1 FDA reports)
FRONTOTEMPORAL DEMENTIA ( 1 FDA reports)
FULL BLOOD COUNT DECREASED ( 1 FDA reports)
FUNCTIONAL RESIDUAL CAPACITY DECREASED ( 1 FDA reports)
FUNGAL OESOPHAGITIS ( 1 FDA reports)
FUNGAL RASH ( 1 FDA reports)
FUNGUS SPUTUM TEST POSITIVE ( 1 FDA reports)
FUNGUS STOOL IDENTIFIED ( 1 FDA reports)
GALLBLADDER CANCER ( 1 FDA reports)
GALLOP RHYTHM PRESENT ( 1 FDA reports)
GASTRIC CANCER STAGE III ( 1 FDA reports)
GASTRIC LAVAGE ( 1 FDA reports)
GASTRIC OUTLET OBSTRUCTION ( 1 FDA reports)
GASTRITIS ATROPHIC ( 1 FDA reports)
GASTROENTERITIS BACTERIAL ( 1 FDA reports)
GASTROENTERITIS ESCHERICHIA COLI ( 1 FDA reports)
GASTROENTERITIS NORWALK VIRUS ( 1 FDA reports)
GASTROENTERITIS RADIATION ( 1 FDA reports)
GASTROENTERITIS ROTAVIRUS ( 1 FDA reports)
GASTROINTESTINAL BACTERIAL INFECTION ( 1 FDA reports)
GASTROINTESTINAL MUCOSAL NECROSIS ( 1 FDA reports)
GASTROSTOMY ( 1 FDA reports)
GENE MUTATION ( 1 FDA reports)
GENE MUTATION IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
GENITAL DISORDER FEMALE ( 1 FDA reports)
GENITAL SWELLING ( 1 FDA reports)
GILBERT'S SYNDROME ( 1 FDA reports)
GINGIVAL DISCOLOURATION ( 1 FDA reports)
GINGIVAL PRURITUS ( 1 FDA reports)
GLAUCOMA SURGERY ( 1 FDA reports)
GLIOMA ( 1 FDA reports)
GLOMERULONEPHRITIS MEMBRANOPROLIFERATIVE ( 1 FDA reports)
GLOSSOPTOSIS ( 1 FDA reports)
GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY ( 1 FDA reports)
GLYCOPEPTIDE ANTIBIOTIC RESISTANT ENTEROCOCCAL INFECTION ( 1 FDA reports)
GONORRHOEA ( 1 FDA reports)
GRAFT INFECTION ( 1 FDA reports)
GRAFT THROMBOSIS ( 1 FDA reports)
GRANULOCYTE COUNT DECREASED ( 1 FDA reports)
GRANULOCYTES ABNORMAL ( 1 FDA reports)
HABITUAL ABORTION ( 1 FDA reports)
HAEMANGIOMA ( 1 FDA reports)
HAEMATOCRIT ABNORMAL ( 1 FDA reports)
HAEMATOCRIT INCREASED ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMORRHAGIC ASCITES ( 1 FDA reports)
HAEMOSIDEROSIS ( 1 FDA reports)
HAIR PLUCKING ( 1 FDA reports)
HAPTOGLOBIN DECREASED ( 1 FDA reports)
HAPTOGLOBIN INCREASED ( 1 FDA reports)
HEART RATE ( 1 FDA reports)
HEART VALVE REPLACEMENT ( 1 FDA reports)
HEAT EXHAUSTION ( 1 FDA reports)
HEAT ILLNESS ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA TEST ( 1 FDA reports)
HEPATIC CANCER METASTATIC ( 1 FDA reports)
HEPATIC CANDIDIASIS ( 1 FDA reports)
HEPATIC SIDEROSIS ( 1 FDA reports)
HEPATITIS ALCOHOLIC ( 1 FDA reports)
HEPATITIS C POSITIVE ( 1 FDA reports)
HEPATITIS C VIRUS ( 1 FDA reports)
HEPATITIS CHRONIC ACTIVE ( 1 FDA reports)
HERPES DERMATITIS ( 1 FDA reports)
HISTRIONIC PERSONALITY DISORDER ( 1 FDA reports)
HOARSENESS ( 1 FDA reports)
HOLMES-ADIE PUPIL ( 1 FDA reports)
HOMANS' SIGN POSITIVE ( 1 FDA reports)
HORMONE LEVEL ABNORMAL ( 1 FDA reports)
HORNER'S SYNDROME ( 1 FDA reports)
HOSPICE CARE ( 1 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 1 FDA reports)
HUNTINGTON'S DISEASE ( 1 FDA reports)
HYPERCHLORAEMIA ( 1 FDA reports)
HYPERDYNAMIC LEFT VENTRICLE ( 1 FDA reports)
HYPERPARATHYROIDISM PRIMARY ( 1 FDA reports)
HYPERPLASTIC CHOLECYSTOPATHY ( 1 FDA reports)
HYPERPYREXIA ( 1 FDA reports)
HYPERTENSIVE CARDIOMEGALY ( 1 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 1 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 1 FDA reports)
HYPERTROPHIC SCAR ( 1 FDA reports)
HYPERTROPHY BREAST ( 1 FDA reports)
HYPERTROPHY OF TONGUE PAPILLAE ( 1 FDA reports)
HYPERVOLAEMIA ( 1 FDA reports)
HYPOGEUSIA ( 1 FDA reports)
HYPOPHYSECTOMY ( 1 FDA reports)
HYPOPHYSITIS ( 1 FDA reports)
HYPOPITUITARISM ( 1 FDA reports)
HYPOTHALAMO-PITUITARY DISORDER ( 1 FDA reports)
HYPOTONIA NEONATAL ( 1 FDA reports)
HYPOURICAEMIA ( 1 FDA reports)
HYSTEROSALPINGO-OOPHORECTOMY ( 1 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 1 FDA reports)
IGA NEPHROPATHY ( 1 FDA reports)
IIIRD NERVE PARALYSIS ( 1 FDA reports)
ILEECTOMY ( 1 FDA reports)
ILEUS SPASTIC ( 1 FDA reports)
ILIAC ARTERY OCCLUSION ( 1 FDA reports)
ILIAC ARTERY STENOSIS ( 1 FDA reports)
IMMUNOGLOBULINS DECREASED ( 1 FDA reports)
IMMUNOLOGY TEST ABNORMAL ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG THERAPY ( 1 FDA reports)
IMPLANT SITE REACTION ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR REPLACEMENT ( 1 FDA reports)
INABILITY TO CRAWL ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED BY DEVICE ( 1 FDA reports)
INCORRECT PRODUCT STORAGE ( 1 FDA reports)
INDIFFERENCE ( 1 FDA reports)
INFECTED CYST ( 1 FDA reports)
INFECTION PROPHYLAXIS ( 1 FDA reports)
INFLAMMATION OF WOUND ( 1 FDA reports)
INFLUENZA VIRUS TEST POSITIVE ( 1 FDA reports)
INFUSION ( 1 FDA reports)
INFUSION SITE HAEMORRHAGE ( 1 FDA reports)
INFUSION SITE IRRITATION ( 1 FDA reports)
INFUSION SITE PARAESTHESIA ( 1 FDA reports)
INFUSION SITE PHLEBITIS ( 1 FDA reports)
INFUSION SITE RASH ( 1 FDA reports)
INFUSION SITE REACTION ( 1 FDA reports)
INFUSION SITE SWELLING ( 1 FDA reports)
INFUSION SITE URTICARIA ( 1 FDA reports)
INHIBITORY DRUG INTERACTION ( 1 FDA reports)
INJECTION SITE COLDNESS ( 1 FDA reports)
INJECTION SITE EXFOLIATION ( 1 FDA reports)
INJECTION SITE EXTRAVASATION ( 1 FDA reports)
INJECTION SITE INFLAMMATION ( 1 FDA reports)
INSTILLATION SITE ERYTHEMA ( 1 FDA reports)
INSTILLATION SITE PAIN ( 1 FDA reports)
INSULIN C-PEPTIDE DECREASED ( 1 FDA reports)
INSULIN C-PEPTIDE INCREASED ( 1 FDA reports)
INSULIN RESISTANT DIABETES ( 1 FDA reports)
INSULIN-REQUIRING TYPE II DIABETES MELLITUS ( 1 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 1 FDA reports)
INTERNAL INJURY ( 1 FDA reports)
INTESTINAL GANGRENE ( 1 FDA reports)
INTESTINAL PROLAPSE ( 1 FDA reports)
INTESTINAL STENOSIS ( 1 FDA reports)
INTESTINAL ULCER ( 1 FDA reports)
INTRACRANIAL INJURY ( 1 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 1 FDA reports)
INTRAMEDULLARY ROD INSERTION ( 1 FDA reports)
INTRASPINAL ABSCESS ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE NEONATAL ( 1 FDA reports)
INTUSSUSCEPTION ( 1 FDA reports)
INVESTIGATION ( 1 FDA reports)
IRIDOCYCLITIS ( 1 FDA reports)
IRIS INJURY ( 1 FDA reports)
JAW LESION EXCISION ( 1 FDA reports)
JOINT ARTHROPLASTY ( 1 FDA reports)
JOINT DESTRUCTION ( 1 FDA reports)
KELOID SCAR ( 1 FDA reports)
KERATOPATHY ( 1 FDA reports)
KERATORHEXIS ( 1 FDA reports)
KETOSIS ( 1 FDA reports)
KIDNEY SMALL ( 1 FDA reports)
KNEE DEFORMITY ( 1 FDA reports)
KUSSMAUL RESPIRATION ( 1 FDA reports)
KYPHOSCOLIOSIS ( 1 FDA reports)
LABORATORY TEST INTERFERENCE ( 1 FDA reports)
LABOUR COMPLICATION ( 1 FDA reports)
LACTATION DISORDER ( 1 FDA reports)
LARGE INTESTINAL STRICTURE ( 1 FDA reports)
LARYNGEAL CANCER ( 1 FDA reports)
LARYNGOMALACIA ( 1 FDA reports)
LARYNGOPHARYNGITIS ( 1 FDA reports)
LARYNGOTRACHEAL OEDEMA ( 1 FDA reports)
LATE DEVELOPER ( 1 FDA reports)
LATE METABOLIC ACIDOSIS OF NEWBORN ( 1 FDA reports)
LATENT TUBERCULOSIS ( 1 FDA reports)
LEARNING DISABILITY ( 1 FDA reports)
LEUKAEMIA RECURRENT ( 1 FDA reports)
LEUKOERYTHROBLASTIC ANAEMIA ( 1 FDA reports)
LIBIDO DISORDER ( 1 FDA reports)
LIGAMENT CALCIFICATION ( 1 FDA reports)
LIGAMENT DISORDER ( 1 FDA reports)
LIGAMENT OPERATION ( 1 FDA reports)
LIGAMENT PAIN ( 1 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 1 FDA reports)
LIP DRY ( 1 FDA reports)
LIP EXFOLIATION ( 1 FDA reports)
LIP INFECTION ( 1 FDA reports)
LIP NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 1 FDA reports)
LIPASE URINE INCREASED ( 1 FDA reports)
LIPOATROPHY ( 1 FDA reports)
LIPOMATOSIS ( 1 FDA reports)
LITHOTRIPSY ( 1 FDA reports)
LIVE BIRTH ( 1 FDA reports)
LIVER TRANSPLANT ( 1 FDA reports)
LIVER TRANSPLANT REJECTION ( 1 FDA reports)
LOCKED-IN SYNDROME ( 1 FDA reports)
LOSS OF PROPRIOCEPTION ( 1 FDA reports)
LOWER LIMB DEFORMITY ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION BACTERIAL ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION VIRAL ( 1 FDA reports)
LUMBAR PUNCTURE ( 1 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 1 FDA reports)
LUNG ADENOCARCINOMA STAGE I ( 1 FDA reports)
LUNG ADENOCARCINOMA STAGE IV ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED RECURRENT ( 1 FDA reports)
LUNG CYST BENIGN ( 1 FDA reports)
LUNG INJURY ( 1 FDA reports)
LUNG LOBECTOMY ( 1 FDA reports)
LUNG OPERATION ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE III ( 1 FDA reports)
LYMPHADENITIS BACTERIAL ( 1 FDA reports)
LYMPHATIC DISORDER ( 1 FDA reports)
LYMPHOID TISSUE HYPERPLASIA ( 1 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
LYMPHOSTASIS ( 1 FDA reports)
MACROCYTOSIS ( 1 FDA reports)
MACULE ( 1 FDA reports)
MALE SEXUAL DYSFUNCTION ( 1 FDA reports)
MALIGNANT MELANOMA IN SITU ( 1 FDA reports)
MALIGNANT OMENTUM NEOPLASM ( 1 FDA reports)
MALIGNANT PALATE NEOPLASM ( 1 FDA reports)
MALIGNANT RENAL HYPERTENSION ( 1 FDA reports)
MALIGNANT SOFT TISSUE NEOPLASM ( 1 FDA reports)
MAMMOPLASTY ( 1 FDA reports)
MANDIBULECTOMY ( 1 FDA reports)
MARITAL PROBLEM ( 1 FDA reports)
MARROW HYPERPLASIA ( 1 FDA reports)
MATRIX METALLOPROTEINASE-3 ( 1 FDA reports)
MEAN ARTERIAL PRESSURE DECREASED ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 1 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 1 FDA reports)
MEAN PLATELET VOLUME INCREASED ( 1 FDA reports)
MEASLES ( 1 FDA reports)
MECHANICAL VENTILATION COMPLICATION ( 1 FDA reports)
MEDIASTINAL OPERATION ( 1 FDA reports)
MEDIASTINOSCOPY ( 1 FDA reports)
MEIGE'S SYNDROME ( 1 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 1 FDA reports)
MENINGORADICULITIS ( 1 FDA reports)
METAMORPHOPSIA ( 1 FDA reports)
METASTASES TO PERINEUM ( 1 FDA reports)
METASTASES TO SOFT TISSUE ( 1 FDA reports)
METASTASES TO SPLEEN ( 1 FDA reports)
METASTATIC CARCINOMA OF THE BLADDER ( 1 FDA reports)
METATARSALGIA ( 1 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST POSITIVE ( 1 FDA reports)
MICROALBUMINURIA ( 1 FDA reports)
MICROANGIOPATHIC HAEMOLYTIC ANAEMIA ( 1 FDA reports)
MICROGNATHIA ( 1 FDA reports)
MICROSOMIA ( 1 FDA reports)
MICROVASCULAR ANGINA ( 1 FDA reports)
MICTURITION FREQUENCY DECREASED ( 1 FDA reports)
MILK ALLERGY ( 1 FDA reports)
MINI MENTAL STATUS EXAMINATION ABNORMAL ( 1 FDA reports)
MITOCHONDRIAL CYTOPATHY ( 1 FDA reports)
MITRAL VALVE REPAIR ( 1 FDA reports)
MITRAL VALVE STENOSIS ( 1 FDA reports)
MIXED RECEPTIVE-EXPRESSIVE LANGUAGE DISORDER ( 1 FDA reports)
MONONEUROPATHY MULTIPLEX ( 1 FDA reports)
MOUTH CYST ( 1 FDA reports)
MOUTH INJURY ( 1 FDA reports)
MULTIPLE PREGNANCY ( 1 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 1 FDA reports)
MUMPS ( 1 FDA reports)
MUSCLE SWELLING ( 1 FDA reports)
MYCOBACTERIA SPUTUM TEST POSITIVE ( 1 FDA reports)
MYCOBACTERIA TEST ( 1 FDA reports)
MYCOBACTERIAL INFECTION ( 1 FDA reports)
MYCOBACTERIUM TUBERCULOSIS COMPLEX TEST POSITIVE ( 1 FDA reports)
MYCOTIC ANEURYSM ( 1 FDA reports)
MYELITIS TRANSVERSE ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 1 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 1 FDA reports)
MYOCARDIAL RUPTURE ( 1 FDA reports)
MYOGLOBINURIA ( 1 FDA reports)
MYOPATHY STEROID ( 1 FDA reports)
N-TELOPEPTIDE URINE DECREASED ( 1 FDA reports)
NAIL DISCOLOURATION ( 1 FDA reports)
NAIL GROWTH ABNORMAL ( 1 FDA reports)
NAIL PICKING ( 1 FDA reports)
NAIL TINEA ( 1 FDA reports)
NASAL CYST ( 1 FDA reports)
NASAL OBSTRUCTION ( 1 FDA reports)
NASAL SEPTAL OPERATION ( 1 FDA reports)
NECROBIOSIS ( 1 FDA reports)
NECROSIS ISCHAEMIC ( 1 FDA reports)
NECROTISING RETINITIS ( 1 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 1 FDA reports)
NEONATAL OVERSEDATION ( 1 FDA reports)
NEONATAL TACHYPNOEA ( 1 FDA reports)
NEOPLASM PROSTATE ( 1 FDA reports)
NEPHRECTOMY ( 1 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 1 FDA reports)
NERVOUS SYSTEM SURGERY ( 1 FDA reports)
NEURODEGENERATIVE DISORDER ( 1 FDA reports)
NEUROENDOCRINE CARCINOMA ( 1 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
NEUROMUSCULAR BLOCK PROLONGED ( 1 FDA reports)
NEUROPATHIC PAIN ( 1 FDA reports)
NEUROPSYCHOLOGICAL TEST ABNORMAL ( 1 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 1 FDA reports)
NIPPLE DISORDER ( 1 FDA reports)
NIPPLE PAIN ( 1 FDA reports)
NITRITE URINE ABSENT ( 1 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
NODAL MARGINAL ZONE B-CELL LYMPHOMA ( 1 FDA reports)
NON-ALCOHOLIC STEATOHEPATITIS ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE I ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IIIB ( 1 FDA reports)
NOREPINEPHRINE INCREASED ( 1 FDA reports)
NORMAL NEWBORN ( 1 FDA reports)
NUTRITIONAL SUPPORT ( 1 FDA reports)
OBSESSIVE-COMPULSIVE PERSONALITY DISORDER ( 1 FDA reports)
OBSTRUCTED LABOUR ( 1 FDA reports)
OEDEMA DUE TO CARDIAC DISEASE ( 1 FDA reports)
OESOPHAGEAL ACHALASIA ( 1 FDA reports)
OESOPHAGEAL ADENOCARCINOMA ( 1 FDA reports)
OESOPHAGEAL DYSPLASIA ( 1 FDA reports)
OESOPHAGEAL IRRITATION ( 1 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 1 FDA reports)
OESOPHAGITIS HAEMORRHAGIC ( 1 FDA reports)
ONYCHALGIA ( 1 FDA reports)
ONYCHOPHAGIA ( 1 FDA reports)
OPHTHALMOPLEGIA ( 1 FDA reports)
OPIATES ( 1 FDA reports)
OPIATES POSITIVE ( 1 FDA reports)
OPTIC DISC DISORDER ( 1 FDA reports)
OPTIC NERVE HYPOPLASIA ( 1 FDA reports)
OPTIC NEURITIS RETROBULBAR ( 1 FDA reports)
ORAL MUCOSAL PETECHIAE ( 1 FDA reports)
ORAL PRURITUS ( 1 FDA reports)
ORAL TORUS ( 1 FDA reports)
ORGASM ABNORMAL ( 1 FDA reports)
OROPHARYNGEAL SPASM ( 1 FDA reports)
ORTHOPEDIC EXAMINATION ABNORMAL ( 1 FDA reports)
OSTEITIS DEFORMANS ( 1 FDA reports)
OSTEOTOMY ( 1 FDA reports)
OVARIAN ATROPHY ( 1 FDA reports)
OVARIAN CANCER METASTATIC ( 1 FDA reports)
OVARIAN CYST RUPTURED ( 1 FDA reports)
OVARIAN DISORDER ( 1 FDA reports)
OXYGEN SATURATION ( 1 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 1 FDA reports)
PAIN MANAGEMENT ( 1 FDA reports)
PAINFUL DEFAECATION ( 1 FDA reports)
PALATAL DYSPLASIA ( 1 FDA reports)
PANCREAS INFECTION ( 1 FDA reports)
PANCREAS LIPOMATOSIS ( 1 FDA reports)
PANCREATECTOMY ( 1 FDA reports)
PANCREATIC CALCIFICATION ( 1 FDA reports)
PANCREATIC INSUFFICIENCY ( 1 FDA reports)
PANCREATIC NECROSIS ( 1 FDA reports)
PANCREATIC OPERATION ( 1 FDA reports)
PARACENTESIS ABDOMEN ( 1 FDA reports)
PARANASAL CYST ( 1 FDA reports)
PARAPSORIASIS ( 1 FDA reports)
PARASOMNIA ( 1 FDA reports)
PARATHYROIDECTOMY ( 1 FDA reports)
PARKINSONIAN GAIT ( 1 FDA reports)
PAROPHTHALMIA ( 1 FDA reports)
PARTIAL SEIZURES WITH SECONDARY GENERALISATION ( 1 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 1 FDA reports)
PCO2 ABNORMAL ( 1 FDA reports)
PEDAL PULSE DECREASED ( 1 FDA reports)
PELVIC CONGESTION ( 1 FDA reports)
PELVIC DISCOMFORT ( 1 FDA reports)
PELVIC HAEMATOMA ( 1 FDA reports)
PEMPHIGUS ( 1 FDA reports)
PENIS DISORDER ( 1 FDA reports)
PERCUSSION TEST ABNORMAL ( 1 FDA reports)
PERCUTANEOUS CORONARY INTERVENTION ( 1 FDA reports)
PERIANAL ABSCESS ( 1 FDA reports)
PERIANAL ERYTHEMA ( 1 FDA reports)
PERICARDIAL FIBROSIS ( 1 FDA reports)
PERINEAL CYST ( 1 FDA reports)
PERIODIC LIMB MOVEMENT DISORDER ( 1 FDA reports)
PERIORBITAL HAEMATOMA ( 1 FDA reports)
PERIPHERAL ARTERY ANGIOPLASTY ( 1 FDA reports)
PERIPHERAL NERVE OPERATION ( 1 FDA reports)
PERIPHERAL OCCLUSIVE DISEASE ( 1 FDA reports)
PERIPHERAL PARALYSIS ( 1 FDA reports)
PERIPROCTITIS ( 1 FDA reports)
PERIRENAL HAEMATOMA ( 1 FDA reports)
PERITONEAL ABSCESS ( 1 FDA reports)
PERITONEAL DISORDER ( 1 FDA reports)
PERITONEAL FLUID ANALYSIS ABNORMAL ( 1 FDA reports)
PERIUMBILICAL ABSCESS ( 1 FDA reports)
PERTUSSIS ( 1 FDA reports)
PH BODY FLUID DECREASED ( 1 FDA reports)
PH BODY FLUID INCREASED ( 1 FDA reports)
PHAEOCHROMOCYTOMA ( 1 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 1 FDA reports)
PHENYLKETONURIA ( 1 FDA reports)
PHLEBOSCLEROSIS ( 1 FDA reports)
PHOBIA ( 1 FDA reports)
PHONOLOGICAL DISORDER ( 1 FDA reports)
PHRENIC NERVE PARALYSIS ( 1 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 1 FDA reports)
PIGMENTED NAEVUS ( 1 FDA reports)
PILONIDAL CYST ( 1 FDA reports)
PINGUECULA ( 1 FDA reports)
PLASMAPHERESIS ( 1 FDA reports)
PLATELET AGGREGATION INCREASED ( 1 FDA reports)
PLEURODESIS ( 1 FDA reports)
PNEUMATOSIS INTESTINALIS ( 1 FDA reports)
PNEUMOCOCCAL INFECTION ( 1 FDA reports)
PNEUMOCONIOSIS ( 1 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 1 FDA reports)
PNEUMONIA KLEBSIELLA ( 1 FDA reports)
PO2 ABNORMAL ( 1 FDA reports)
POLYARTHRITIS ( 1 FDA reports)
POLYMYALGIA ( 1 FDA reports)
POLYMYOSITIS ( 1 FDA reports)
PORTAL HYPERTENSIVE GASTROPATHY ( 1 FDA reports)
POSITIVE ROMBERGISM ( 1 FDA reports)
POST CHOLECYSTECTOMY SYNDROME ( 1 FDA reports)
POST GASTRIC SURGERY SYNDROME ( 1 FDA reports)
POST LUMBAR PUNCTURE SYNDROME ( 1 FDA reports)
POST POLIO SYNDROME ( 1 FDA reports)
POST PROCEDURAL BILE LEAK ( 1 FDA reports)
POST PROCEDURAL DISCOMFORT ( 1 FDA reports)
POST PROCEDURAL HAEMATOMA ( 1 FDA reports)
POST PROCEDURAL OEDEMA ( 1 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 1 FDA reports)
POSTMENOPAUSE ( 1 FDA reports)
POSTOPERATIVE ABSCESS ( 1 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 1 FDA reports)
POSTRENAL FAILURE ( 1 FDA reports)
POVERTY OF SPEECH ( 1 FDA reports)
PRADER-WILLI SYNDROME ( 1 FDA reports)
PRE-EXISTING DISEASE ( 1 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 1 FDA reports)
PREMENSTRUAL SYNDROME ( 1 FDA reports)
PRESBYACUSIS ( 1 FDA reports)
PROCEDURAL SITE REACTION ( 1 FDA reports)
PROCTOCOLITIS ( 1 FDA reports)
PRODUCT OUTER PACKAGING ISSUE ( 1 FDA reports)
PRODUCT PACKAGING QUANTITY ISSUE ( 1 FDA reports)
PRODUCT PHYSICAL ISSUE ( 1 FDA reports)
PROGRESSIVE RELAPSING MULTIPLE SCLEROSIS ( 1 FDA reports)
PROLAPSE REPAIR ( 1 FDA reports)
PROLONGED EXPIRATION ( 1 FDA reports)
PROSTATE CANCER METASTATIC ( 1 FDA reports)
PROSTATE CANCER STAGE 0 ( 1 FDA reports)
PROSTATE CANCER STAGE I ( 1 FDA reports)
PROSTATE INFECTION ( 1 FDA reports)
PROSTATIC DISORDER ( 1 FDA reports)
PROSTATIC OBSTRUCTION ( 1 FDA reports)
PROSTATIC OPERATION ( 1 FDA reports)
PROSTHESIS IMPLANTATION ( 1 FDA reports)
PROTEIN C DECREASED ( 1 FDA reports)
PROTEIN C DEFICIENCY ( 1 FDA reports)
PROTEIN C INCREASED ( 1 FDA reports)
PROTEIN S DECREASED ( 1 FDA reports)
PROTEIN URINE ( 1 FDA reports)
PROTEIN-LOSING GASTROENTEROPATHY ( 1 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 1 FDA reports)
PRURIGO ( 1 FDA reports)
PSEUDOCYST ( 1 FDA reports)
PSEUDODEMENTIA ( 1 FDA reports)
PSEUDOPAPILLOEDEMA ( 1 FDA reports)
PSEUDOPHAEOCHROMOCYTOMA ( 1 FDA reports)
PSEUDOPORPHYRIA ( 1 FDA reports)
PSYCHOGENIC PAIN DISORDER ( 1 FDA reports)
PSYCHOMOTOR SEIZURES ( 1 FDA reports)
PSYCHOSOMATIC DISEASE ( 1 FDA reports)
PUBIC PAIN ( 1 FDA reports)
PUBIC RAMI FRACTURE ( 1 FDA reports)
PULMONARY ARTERIAL WEDGE PRESSURE INCREASED ( 1 FDA reports)
PULMONARY ARTERY DILATATION ( 1 FDA reports)
PULMONARY ARTERY STENOSIS CONGENITAL ( 1 FDA reports)
PULMONARY NECROSIS ( 1 FDA reports)
PULMONARY VALVE STENOSIS ( 1 FDA reports)
PUNCTATE KERATITIS ( 1 FDA reports)
PUPILLARY LIGHT REFLEX TESTS NORMAL ( 1 FDA reports)
PUPILS UNEQUAL ( 1 FDA reports)
PYELECTASIA ( 1 FDA reports)
PYOMYOSITIS ( 1 FDA reports)
PYOPNEUMOTHORAX ( 1 FDA reports)
Q FEVER ( 1 FDA reports)
RADIAL PULSE ABNORMAL ( 1 FDA reports)
RADIATION INJURY ( 1 FDA reports)
RADICAL HYSTERECTOMY ( 1 FDA reports)
RADICULAR SYNDROME ( 1 FDA reports)
RADICULITIS CERVICAL ( 1 FDA reports)
RADICULITIS LUMBOSACRAL ( 1 FDA reports)
RAPID EYE MOVEMENTS SLEEP ABNORMAL ( 1 FDA reports)
RATHKE'S CLEFT CYST ( 1 FDA reports)
REACTION TO AZO-DYES ( 1 FDA reports)
REACTION TO COLOURING ( 1 FDA reports)
REACTIVE PSYCHOSIS ( 1 FDA reports)
RECTAL ABSCESS ( 1 FDA reports)
RECTAL LESION ( 1 FDA reports)
RED BLOOD CELL ABNORMALITY ( 1 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
REFLUX LARYNGITIS ( 1 FDA reports)
REFRACTORY ANAEMIA ( 1 FDA reports)
RENAL CANCER ( 1 FDA reports)
RENAL INFARCT ( 1 FDA reports)
RENAL MASS ( 1 FDA reports)
RENOVASCULAR HYPERTENSION ( 1 FDA reports)
REPETITIVE STRAIN INJURY ( 1 FDA reports)
RESPIRATORY FATIGUE ( 1 FDA reports)
RESPIRATORY FUME INHALATION DISORDER ( 1 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 1 FDA reports)
RESPIRATORY TRACT INFECTION BACTERIAL ( 1 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 1 FDA reports)
RESPIRATORY TRACT IRRITATION ( 1 FDA reports)
RESPIRATORY TRACT OEDEMA ( 1 FDA reports)
RETICULOCYTE COUNT ABNORMAL ( 1 FDA reports)
RETICULOCYTE COUNT DECREASED ( 1 FDA reports)
RETICULOCYTE COUNT INCREASED ( 1 FDA reports)
RETINAL ARTERY OCCLUSION ( 1 FDA reports)

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