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

PAIN ( 381 FDA reports)
ANXIETY ( 309 FDA reports)
NAUSEA ( 293 FDA reports)
DYSPNOEA ( 286 FDA reports)
HEADACHE ( 275 FDA reports)
DEPRESSION ( 241 FDA reports)
DIZZINESS ( 240 FDA reports)
FALL ( 233 FDA reports)
FATIGUE ( 230 FDA reports)
VOMITING ( 214 FDA reports)
DRUG INEFFECTIVE ( 211 FDA reports)
ARTHRALGIA ( 205 FDA reports)
DIARRHOEA ( 194 FDA reports)
BACK PAIN ( 178 FDA reports)
INSOMNIA ( 178 FDA reports)
PAIN IN EXTREMITY ( 174 FDA reports)
COMPLETED SUICIDE ( 172 FDA reports)
OEDEMA PERIPHERAL ( 172 FDA reports)
WEIGHT DECREASED ( 172 FDA reports)
ASTHENIA ( 171 FDA reports)
ANAEMIA ( 168 FDA reports)
CHEST PAIN ( 161 FDA reports)
WEIGHT INCREASED ( 157 FDA reports)
PNEUMONIA ( 155 FDA reports)
DEATH ( 151 FDA reports)
CONFUSIONAL STATE ( 142 FDA reports)
LOSS OF CONSCIOUSNESS ( 141 FDA reports)
DIABETES MELLITUS ( 136 FDA reports)
DRUG INTERACTION ( 133 FDA reports)
PYREXIA ( 133 FDA reports)
MALAISE ( 132 FDA reports)
SUICIDAL IDEATION ( 132 FDA reports)
HYPERTENSION ( 131 FDA reports)
PARAESTHESIA ( 131 FDA reports)
NEUROPATHY PERIPHERAL ( 129 FDA reports)
CONSTIPATION ( 128 FDA reports)
ABDOMINAL PAIN ( 125 FDA reports)
HYPOAESTHESIA ( 122 FDA reports)
GAIT DISTURBANCE ( 117 FDA reports)
CONVULSION ( 109 FDA reports)
TREMOR ( 107 FDA reports)
DECREASED APPETITE ( 106 FDA reports)
SOMNOLENCE ( 102 FDA reports)
INJURY ( 100 FDA reports)
FEELING ABNORMAL ( 98 FDA reports)
OSTEONECROSIS OF JAW ( 98 FDA reports)
BLOOD GLUCOSE INCREASED ( 95 FDA reports)
BALANCE DISORDER ( 90 FDA reports)
RENAL FAILURE ACUTE ( 90 FDA reports)
RENAL FAILURE ( 89 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 88 FDA reports)
DEHYDRATION ( 88 FDA reports)
NECK PAIN ( 88 FDA reports)
RASH ( 88 FDA reports)
VISION BLURRED ( 86 FDA reports)
CARDIAC ARREST ( 85 FDA reports)
EMOTIONAL DISTRESS ( 85 FDA reports)
TYPE 2 DIABETES MELLITUS ( 85 FDA reports)
URINARY TRACT INFECTION ( 85 FDA reports)
CEREBROVASCULAR ACCIDENT ( 84 FDA reports)
OSTEOARTHRITIS ( 84 FDA reports)
PRURITUS ( 84 FDA reports)
COUGH ( 83 FDA reports)
MUSCULAR WEAKNESS ( 82 FDA reports)
MYOCARDIAL INFARCTION ( 82 FDA reports)
SUICIDE ATTEMPT ( 82 FDA reports)
PAIN IN JAW ( 81 FDA reports)
HYPERHIDROSIS ( 79 FDA reports)
ABDOMINAL PAIN UPPER ( 77 FDA reports)
BONE DISORDER ( 77 FDA reports)
HYPOTENSION ( 77 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 77 FDA reports)
OVERDOSE ( 77 FDA reports)
ATRIAL FIBRILLATION ( 76 FDA reports)
CONDITION AGGRAVATED ( 76 FDA reports)
MYALGIA ( 76 FDA reports)
MEMORY IMPAIRMENT ( 75 FDA reports)
MUSCLE SPASMS ( 74 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 73 FDA reports)
DYSPHAGIA ( 73 FDA reports)
BLOOD PRESSURE INCREASED ( 72 FDA reports)
DRUG TOXICITY ( 72 FDA reports)
PULMONARY EMBOLISM ( 70 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 68 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 67 FDA reports)
BRONCHITIS ( 66 FDA reports)
SYNCOPE ( 66 FDA reports)
AGGRESSION ( 65 FDA reports)
CARDIO-RESPIRATORY ARREST ( 65 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 65 FDA reports)
INFECTION ( 65 FDA reports)
ERYTHEMA ( 64 FDA reports)
MUSCULOSKELETAL PAIN ( 64 FDA reports)
RESPIRATORY FAILURE ( 63 FDA reports)
CELLULITIS ( 62 FDA reports)
DEEP VEIN THROMBOSIS ( 61 FDA reports)
FLUSHING ( 61 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 60 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 59 FDA reports)
NERVOUSNESS ( 59 FDA reports)
RESPIRATORY ARREST ( 59 FDA reports)
BONE PAIN ( 58 FDA reports)
PALPITATIONS ( 58 FDA reports)
CHILLS ( 57 FDA reports)
HEART RATE INCREASED ( 57 FDA reports)
PULMONARY OEDEMA ( 57 FDA reports)
SEPSIS ( 57 FDA reports)
TOOTH EXTRACTION ( 57 FDA reports)
DRY MOUTH ( 56 FDA reports)
INTENTIONAL OVERDOSE ( 56 FDA reports)
AMNESIA ( 55 FDA reports)
MIGRAINE ( 55 FDA reports)
OSTEOMYELITIS ( 55 FDA reports)
COLITIS ( 54 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 54 FDA reports)
IRRITABILITY ( 53 FDA reports)
DEPENDENCE ( 52 FDA reports)
AGITATION ( 51 FDA reports)
SPINAL OSTEOARTHRITIS ( 51 FDA reports)
ARTHRITIS ( 50 FDA reports)
IMPAIRED HEALING ( 50 FDA reports)
RECTAL HAEMORRHAGE ( 50 FDA reports)
MITRAL VALVE INCOMPETENCE ( 49 FDA reports)
MENTAL STATUS CHANGES ( 48 FDA reports)
PLEURAL EFFUSION ( 48 FDA reports)
SPEECH DISORDER ( 48 FDA reports)
SWELLING ( 48 FDA reports)
ABDOMINAL DISCOMFORT ( 47 FDA reports)
HYPERSENSITIVITY ( 47 FDA reports)
ANHEDONIA ( 46 FDA reports)
ASTHMA ( 46 FDA reports)
CORONARY ARTERY DISEASE ( 46 FDA reports)
DEFORMITY ( 46 FDA reports)
MENTAL DISORDER ( 46 FDA reports)
HYPERGLYCAEMIA ( 45 FDA reports)
HYPOGLYCAEMIA ( 45 FDA reports)
BRADYCARDIA ( 44 FDA reports)
MOUTH ULCERATION ( 44 FDA reports)
OSTEONECROSIS ( 44 FDA reports)
PANCYTOPENIA ( 44 FDA reports)
SINUSITIS ( 44 FDA reports)
PANCREATITIS ( 43 FDA reports)
PRIMARY SEQUESTRUM ( 43 FDA reports)
ABDOMINAL DISTENSION ( 42 FDA reports)
GASTRITIS ( 42 FDA reports)
HALLUCINATION ( 42 FDA reports)
BURNING SENSATION ( 41 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 41 FDA reports)
NEURALGIA ( 41 FDA reports)
URINARY RETENTION ( 41 FDA reports)
BLINDNESS ( 40 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 40 FDA reports)
DYSARTHRIA ( 40 FDA reports)
DYSKINESIA ( 40 FDA reports)
HYPERLIPIDAEMIA ( 40 FDA reports)
HYPONATRAEMIA ( 40 FDA reports)
SWELLING FACE ( 40 FDA reports)
UNRESPONSIVE TO STIMULI ( 40 FDA reports)
DIPLOPIA ( 39 FDA reports)
DYSPEPSIA ( 39 FDA reports)
HAEMOGLOBIN DECREASED ( 39 FDA reports)
INFLUENZA LIKE ILLNESS ( 39 FDA reports)
SKIN DISCOLOURATION ( 39 FDA reports)
SLEEP APNOEA SYNDROME ( 39 FDA reports)
SLEEP DISORDER ( 39 FDA reports)
THROMBOCYTOPENIA ( 39 FDA reports)
CATARACT ( 38 FDA reports)
DECREASED INTEREST ( 38 FDA reports)
DIABETIC NEUROPATHY ( 38 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 37 FDA reports)
INCORRECT DOSE ADMINISTERED ( 37 FDA reports)
SINUS TACHYCARDIA ( 37 FDA reports)
STOMATITIS ( 37 FDA reports)
CARDIOMEGALY ( 36 FDA reports)
CONTUSION ( 36 FDA reports)
FEELING HOT ( 36 FDA reports)
HAEMATOCHEZIA ( 36 FDA reports)
JOINT SWELLING ( 36 FDA reports)
MULTIPLE DRUG OVERDOSE ( 36 FDA reports)
ALOPECIA ( 35 FDA reports)
HYPOPHAGIA ( 35 FDA reports)
INJECTION SITE PAIN ( 35 FDA reports)
LYMPHADENOPATHY ( 35 FDA reports)
OEDEMA ( 35 FDA reports)
RENAL FAILURE CHRONIC ( 35 FDA reports)
STRESS ( 35 FDA reports)
ABASIA ( 34 FDA reports)
CHOLELITHIASIS ( 34 FDA reports)
DENTAL CARIES ( 34 FDA reports)
DRUG DOSE OMISSION ( 34 FDA reports)
HAEMORRHOIDS ( 34 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 34 FDA reports)
METASTASES TO BONE ( 34 FDA reports)
OSTEOPOROSIS ( 34 FDA reports)
TREATMENT NONCOMPLIANCE ( 34 FDA reports)
UNEVALUABLE EVENT ( 34 FDA reports)
VISUAL IMPAIRMENT ( 34 FDA reports)
WITHDRAWAL SYNDROME ( 34 FDA reports)
BONE LESION ( 33 FDA reports)
COMA ( 33 FDA reports)
DELIRIUM ( 33 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 33 FDA reports)
INJECTION SITE ERYTHEMA ( 33 FDA reports)
MOBILITY DECREASED ( 33 FDA reports)
RENAL IMPAIRMENT ( 33 FDA reports)
SURGERY ( 33 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 33 FDA reports)
VERTIGO ( 33 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 32 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 32 FDA reports)
HIATUS HERNIA ( 32 FDA reports)
LETHARGY ( 32 FDA reports)
NEPHROLITHIASIS ( 32 FDA reports)
OROPHARYNGEAL PAIN ( 32 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 32 FDA reports)
ROAD TRAFFIC ACCIDENT ( 32 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 32 FDA reports)
BLOOD PRESSURE DECREASED ( 31 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 31 FDA reports)
HYPOKALAEMIA ( 31 FDA reports)
INTESTINAL OBSTRUCTION ( 31 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 31 FDA reports)
OBESITY ( 31 FDA reports)
RADICULOPATHY ( 31 FDA reports)
RHABDOMYOLYSIS ( 31 FDA reports)
TACHYCARDIA ( 31 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 30 FDA reports)
ATELECTASIS ( 30 FDA reports)
CARDIAC FAILURE ( 30 FDA reports)
DEPRESSED MOOD ( 30 FDA reports)
DISORIENTATION ( 30 FDA reports)
HAEMATEMESIS ( 30 FDA reports)
HIP FRACTURE ( 30 FDA reports)
NASOPHARYNGITIS ( 30 FDA reports)
TENDERNESS ( 30 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 30 FDA reports)
ABNORMAL BEHAVIOUR ( 29 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 29 FDA reports)
FEAR ( 29 FDA reports)
HEPATIC ENZYME INCREASED ( 29 FDA reports)
INFLUENZA ( 29 FDA reports)
MULTI-ORGAN FAILURE ( 29 FDA reports)
RESPIRATORY DISTRESS ( 29 FDA reports)
THROMBOSIS ( 29 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 29 FDA reports)
ABNORMAL DREAMS ( 28 FDA reports)
CARDIAC DISORDER ( 28 FDA reports)
CHEST DISCOMFORT ( 28 FDA reports)
CYSTITIS ( 28 FDA reports)
DRUG ABUSE ( 28 FDA reports)
DYSURIA ( 28 FDA reports)
EATING DISORDER ( 28 FDA reports)
FEELING COLD ( 28 FDA reports)
OSTEOPENIA ( 28 FDA reports)
VISUAL ACUITY REDUCED ( 28 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 28 FDA reports)
BLOOD CREATININE INCREASED ( 27 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 27 FDA reports)
ECONOMIC PROBLEM ( 27 FDA reports)
EPISTAXIS ( 27 FDA reports)
HAEMORRHAGE ( 27 FDA reports)
HERPES ZOSTER ( 27 FDA reports)
OESOPHAGITIS ( 27 FDA reports)
PRODUCT QUALITY ISSUE ( 27 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 27 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 26 FDA reports)
ANGINA PECTORIS ( 26 FDA reports)
BASAL CELL CARCINOMA ( 26 FDA reports)
DYSPNOEA EXERTIONAL ( 26 FDA reports)
DYSSTASIA ( 26 FDA reports)
FIBROMYALGIA ( 26 FDA reports)
HEARING IMPAIRED ( 26 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 26 FDA reports)
MALNUTRITION ( 26 FDA reports)
MULTIPLE INJURIES ( 26 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 26 FDA reports)
PRODUCTIVE COUGH ( 26 FDA reports)
SCOLIOSIS ( 26 FDA reports)
TARDIVE DYSKINESIA ( 26 FDA reports)
URINARY INCONTINENCE ( 26 FDA reports)
ARRHYTHMIA ( 25 FDA reports)
ATAXIA ( 25 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 25 FDA reports)
BREAST CANCER ( 25 FDA reports)
CRYING ( 25 FDA reports)
DYSGEUSIA ( 25 FDA reports)
DYSPHONIA ( 25 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 25 FDA reports)
MAJOR DEPRESSION ( 25 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 25 FDA reports)
NERVOUS SYSTEM DISORDER ( 25 FDA reports)
SEDATION ( 25 FDA reports)
SKIN ULCER ( 25 FDA reports)
SOMNAMBULISM ( 25 FDA reports)
TOOTH LOSS ( 25 FDA reports)
TOOTHACHE ( 25 FDA reports)
BLISTER ( 24 FDA reports)
BURSITIS ( 24 FDA reports)
METASTASES TO LIVER ( 24 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 24 FDA reports)
NEUTROPENIA ( 24 FDA reports)
POLLAKIURIA ( 24 FDA reports)
RENAL CYST ( 24 FDA reports)
RESTLESS LEGS SYNDROME ( 24 FDA reports)
RESTLESSNESS ( 24 FDA reports)
ARTHROPATHY ( 23 FDA reports)
DISTURBANCE IN ATTENTION ( 23 FDA reports)
EXCORIATION ( 23 FDA reports)
HEPATIC CYST ( 23 FDA reports)
IRRITABLE BOWEL SYNDROME ( 23 FDA reports)
LEUKOPENIA ( 23 FDA reports)
LUMBAR SPINAL STENOSIS ( 23 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 23 FDA reports)
POISONING ( 23 FDA reports)
PSYCHOTIC DISORDER ( 23 FDA reports)
SEROTONIN SYNDROME ( 23 FDA reports)
BLOOD GLUCOSE DECREASED ( 22 FDA reports)
EYE PAIN ( 22 FDA reports)
GINGIVAL PAIN ( 22 FDA reports)
HEART RATE IRREGULAR ( 22 FDA reports)
HOT FLUSH ( 22 FDA reports)
INTENTIONAL DRUG MISUSE ( 22 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 22 FDA reports)
LUNG DISORDER ( 22 FDA reports)
OFF LABEL USE ( 22 FDA reports)
PANIC ATTACK ( 22 FDA reports)
PLATELET COUNT INCREASED ( 22 FDA reports)
PNEUMONITIS ( 22 FDA reports)
SKIN BURNING SENSATION ( 22 FDA reports)
SKIN DISORDER ( 22 FDA reports)
SKIN EXFOLIATION ( 22 FDA reports)
SKIN LESION ( 22 FDA reports)
STAPHYLOCOCCAL INFECTION ( 22 FDA reports)
DIVERTICULITIS ( 21 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 21 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 21 FDA reports)
FEBRILE NEUTROPENIA ( 21 FDA reports)
GINGIVAL DISORDER ( 21 FDA reports)
HEPATIC FAILURE ( 21 FDA reports)
HEPATIC STEATOSIS ( 21 FDA reports)
MASTICATION DISORDER ( 21 FDA reports)
MELAENA ( 21 FDA reports)
MENISCUS LESION ( 21 FDA reports)
MULTIPLE SCLEROSIS ( 21 FDA reports)
ORAL PAIN ( 21 FDA reports)
SPINAL COLUMN STENOSIS ( 21 FDA reports)
TINNITUS ( 21 FDA reports)
TOOTH FRACTURE ( 21 FDA reports)
VIRAL INFECTION ( 21 FDA reports)
ATRIAL FLUTTER ( 20 FDA reports)
BODY TEMPERATURE INCREASED ( 20 FDA reports)
CHOLECYSTITIS CHRONIC ( 20 FDA reports)
COAGULOPATHY ( 20 FDA reports)
COLONIC POLYP ( 20 FDA reports)
DISABILITY ( 20 FDA reports)
ECZEMA ( 20 FDA reports)
EMPHYSEMA ( 20 FDA reports)
FLUID RETENTION ( 20 FDA reports)
GRAND MAL CONVULSION ( 20 FDA reports)
HAEMATOMA ( 20 FDA reports)
HYPOTHYROIDISM ( 20 FDA reports)
HYPOXIA ( 20 FDA reports)
ILL-DEFINED DISORDER ( 20 FDA reports)
LIMB INJURY ( 20 FDA reports)
LUNG INFILTRATION ( 20 FDA reports)
MUSCLE TWITCHING ( 20 FDA reports)
MYOCARDIAL ISCHAEMIA ( 20 FDA reports)
PARANOIA ( 20 FDA reports)
POLYURIA ( 20 FDA reports)
PULMONARY CONGESTION ( 20 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 20 FDA reports)
BONE DENSITY DECREASED ( 19 FDA reports)
CARDIOMYOPATHY ( 19 FDA reports)
CHOLECYSTECTOMY ( 19 FDA reports)
DRUG DEPENDENCE ( 19 FDA reports)
FOOT FRACTURE ( 19 FDA reports)
HAEMATOCRIT DECREASED ( 19 FDA reports)
HAEMOPTYSIS ( 19 FDA reports)
HEMIPARESIS ( 19 FDA reports)
HYPERSOMNIA ( 19 FDA reports)
LUNG NEOPLASM ( 19 FDA reports)
MOOD SWINGS ( 19 FDA reports)
MULTIPLE MYELOMA ( 19 FDA reports)
PERICARDIAL EFFUSION ( 19 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 19 FDA reports)
RESPIRATORY DEPRESSION ( 19 FDA reports)
RHINITIS ALLERGIC ( 19 FDA reports)
THIRST ( 19 FDA reports)
TOOTH DISORDER ( 19 FDA reports)
WHEEZING ( 19 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 18 FDA reports)
ACUTE SINUSITIS ( 18 FDA reports)
BREAST CANCER FEMALE ( 18 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 18 FDA reports)
CEREBRAL ISCHAEMIA ( 18 FDA reports)
CHROMATURIA ( 18 FDA reports)
DIVERTICULUM INTESTINAL ( 18 FDA reports)
FISTULA ( 18 FDA reports)
FLANK PAIN ( 18 FDA reports)
GALLBLADDER DISORDER ( 18 FDA reports)
HALLUCINATION, VISUAL ( 18 FDA reports)
HEART RATE DECREASED ( 18 FDA reports)
HYPERKERATOSIS ( 18 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 18 FDA reports)
KNEE ARTHROPLASTY ( 18 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 18 FDA reports)
MUCOSAL INFLAMMATION ( 18 FDA reports)
NEURITIS ( 18 FDA reports)
NEUTROPHIL COUNT INCREASED ( 18 FDA reports)
PANCREATITIS ACUTE ( 18 FDA reports)
RHEUMATOID ARTHRITIS ( 18 FDA reports)
RIB FRACTURE ( 18 FDA reports)
SCAR ( 18 FDA reports)
SCIATICA ( 18 FDA reports)
ACCIDENTAL OVERDOSE ( 17 FDA reports)
AORTIC ANEURYSM ( 17 FDA reports)
BLOOD POTASSIUM DECREASED ( 17 FDA reports)
BLOOD UREA INCREASED ( 17 FDA reports)
CARDIAC MURMUR ( 17 FDA reports)
CAROTID ARTERY STENOSIS ( 17 FDA reports)
CHRONIC SINUSITIS ( 17 FDA reports)
EPILEPSY ( 17 FDA reports)
GINGIVITIS ( 17 FDA reports)
GOITRE ( 17 FDA reports)
HALLUCINATION, AUDITORY ( 17 FDA reports)
JOINT SPRAIN ( 17 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 17 FDA reports)
METASTASES TO LUNG ( 17 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 17 FDA reports)
NEOPLASM MALIGNANT ( 17 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 17 FDA reports)
NIGHTMARE ( 17 FDA reports)
OSTEOSCLEROSIS ( 17 FDA reports)
PERIPHERAL COLDNESS ( 17 FDA reports)
SINUS DISORDER ( 17 FDA reports)
TONGUE CYST ( 17 FDA reports)
TOOTH ABSCESS ( 17 FDA reports)
ACCIDENT ( 16 FDA reports)
ANKLE FRACTURE ( 16 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 16 FDA reports)
BONE DEBRIDEMENT ( 16 FDA reports)
CARPAL TUNNEL SYNDROME ( 16 FDA reports)
CORONARY ARTERY OCCLUSION ( 16 FDA reports)
CYST ( 16 FDA reports)
DIABETIC COMA ( 16 FDA reports)
DRUG LEVEL INCREASED ( 16 FDA reports)
DYSTONIA ( 16 FDA reports)
EMOTIONAL DISORDER ( 16 FDA reports)
GENERALISED OEDEMA ( 16 FDA reports)
JAW OPERATION ( 16 FDA reports)
LIVER DISORDER ( 16 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 16 FDA reports)
PLATELET COUNT DECREASED ( 16 FDA reports)
PNEUMONIA ASPIRATION ( 16 FDA reports)
PYELONEPHRITIS ( 16 FDA reports)
RENAL DISORDER ( 16 FDA reports)
ROTATOR CUFF SYNDROME ( 16 FDA reports)
THINKING ABNORMAL ( 16 FDA reports)
THYROID CANCER ( 16 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 16 FDA reports)
URTICARIA ( 16 FDA reports)
VIITH NERVE PARALYSIS ( 16 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 16 FDA reports)
ALVEOLOPLASTY ( 15 FDA reports)
ANGER ( 15 FDA reports)
APNOEA ( 15 FDA reports)
BLOOD CALCIUM INCREASED ( 15 FDA reports)
BONE EROSION ( 15 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 15 FDA reports)
CEREBRAL ATROPHY ( 15 FDA reports)
COLD SWEAT ( 15 FDA reports)
DEVICE RELATED INFECTION ( 15 FDA reports)
DISCOMFORT ( 15 FDA reports)
DIVERTICULUM ( 15 FDA reports)
DRUG EFFECT DECREASED ( 15 FDA reports)
EAR INJURY ( 15 FDA reports)
ENDODONTIC PROCEDURE ( 15 FDA reports)
FRACTURE ( 15 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 15 FDA reports)
HEPATITIS ( 15 FDA reports)
JOINT EFFUSION ( 15 FDA reports)
MOVEMENT DISORDER ( 15 FDA reports)
NIGHT SWEATS ( 15 FDA reports)
NOCTURIA ( 15 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 15 FDA reports)
OSTEITIS ( 15 FDA reports)
OXYGEN SATURATION DECREASED ( 15 FDA reports)
PARALYSIS ( 15 FDA reports)
PHARYNGEAL OEDEMA ( 15 FDA reports)
PULMONARY FIBROSIS ( 15 FDA reports)
PULMONARY HYPERTENSION ( 15 FDA reports)
PULMONARY THROMBOSIS ( 15 FDA reports)
SPINAL FRACTURE ( 15 FDA reports)
SYNOVIAL CYST ( 15 FDA reports)
TOOTH INFECTION ( 15 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 15 FDA reports)
ANGIOEDEMA ( 14 FDA reports)
APHASIA ( 14 FDA reports)
BIPOLAR DISORDER ( 14 FDA reports)
BLOOD BILIRUBIN INCREASED ( 14 FDA reports)
BLOOD SODIUM DECREASED ( 14 FDA reports)
CYANOSIS ( 14 FDA reports)
DELUSION ( 14 FDA reports)
DISEASE PROGRESSION ( 14 FDA reports)
EXOSTOSIS ( 14 FDA reports)
FLATULENCE ( 14 FDA reports)
FOOT DEFORMITY ( 14 FDA reports)
GASTRIC ULCER ( 14 FDA reports)
HAEMATURIA ( 14 FDA reports)
HEPATOMEGALY ( 14 FDA reports)
HYPERCHOLESTEROLAEMIA ( 14 FDA reports)
HYPERTONIC BLADDER ( 14 FDA reports)
LEUKOCYTOSIS ( 14 FDA reports)
ORAL CANDIDIASIS ( 14 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 14 FDA reports)
PURULENT DISCHARGE ( 14 FDA reports)
RASH MACULAR ( 14 FDA reports)
RASH PAPULAR ( 14 FDA reports)
RASH PRURITIC ( 14 FDA reports)
VENTRICULAR TACHYCARDIA ( 14 FDA reports)
AORTIC VALVE INCOMPETENCE ( 13 FDA reports)
BLINDNESS TRANSIENT ( 13 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 13 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 13 FDA reports)
CIRCULATORY COLLAPSE ( 13 FDA reports)
CONCUSSION ( 13 FDA reports)
DECUBITUS ULCER ( 13 FDA reports)
DEMENTIA ( 13 FDA reports)
DRY SKIN ( 13 FDA reports)
EAR PAIN ( 13 FDA reports)
EJECTION FRACTION DECREASED ( 13 FDA reports)
FACIAL PAIN ( 13 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 13 FDA reports)
HIP ARTHROPLASTY ( 13 FDA reports)
HYPERKALAEMIA ( 13 FDA reports)
HYPOCALCAEMIA ( 13 FDA reports)
IMPAIRED WORK ABILITY ( 13 FDA reports)
INFLAMMATION ( 13 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 13 FDA reports)
INTERSTITIAL LUNG DISEASE ( 13 FDA reports)
LARYNGITIS ( 13 FDA reports)
LYMPHOMA ( 13 FDA reports)
METABOLIC ENCEPHALOPATHY ( 13 FDA reports)
MYOPATHY ( 13 FDA reports)
NAIL DISORDER ( 13 FDA reports)
PATHOLOGICAL FRACTURE ( 13 FDA reports)
PRODUCT ADHESION ISSUE ( 13 FDA reports)
PSORIASIS ( 13 FDA reports)
RASH ERYTHEMATOUS ( 13 FDA reports)
SALIVARY HYPERSECRETION ( 13 FDA reports)
SEPTIC SHOCK ( 13 FDA reports)
SWOLLEN TONGUE ( 13 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 13 FDA reports)
ARTERIOSCLEROSIS ( 12 FDA reports)
ASPIRATION ( 12 FDA reports)
BRAIN NEOPLASM ( 12 FDA reports)
CROHN'S DISEASE ( 12 FDA reports)
DRUG HYPERSENSITIVITY ( 12 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 12 FDA reports)
FEMUR FRACTURE ( 12 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 12 FDA reports)
GINGIVAL BLEEDING ( 12 FDA reports)
GLAUCOMA ( 12 FDA reports)
GRANULOMA ( 12 FDA reports)
HYPOAESTHESIA FACIAL ( 12 FDA reports)
HYPOVENTILATION ( 12 FDA reports)
INCOHERENT ( 12 FDA reports)
INCONTINENCE ( 12 FDA reports)
INJECTION SITE HAEMATOMA ( 12 FDA reports)
LOCALISED INFECTION ( 12 FDA reports)
LOWER LIMB FRACTURE ( 12 FDA reports)
MEDICATION ERROR ( 12 FDA reports)
METASTASES TO SPINE ( 12 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 12 FDA reports)
PULMONARY VASCULITIS ( 12 FDA reports)
RENAL INJURY ( 12 FDA reports)
SENSATION OF HEAVINESS ( 12 FDA reports)
SENSORY LOSS ( 12 FDA reports)
SPLENOMEGALY ( 12 FDA reports)
ADVERSE DRUG REACTION ( 11 FDA reports)
BLOOD ALBUMIN DECREASED ( 11 FDA reports)
BLOOD CALCIUM DECREASED ( 11 FDA reports)
CAROTID ARTERY OCCLUSION ( 11 FDA reports)
CEREBRAL INFARCTION ( 11 FDA reports)
DEBRIDEMENT ( 11 FDA reports)
DENTAL FISTULA ( 11 FDA reports)
DIABETIC KETOACIDOSIS ( 11 FDA reports)
DUODENITIS ( 11 FDA reports)
ENCEPHALOPATHY ( 11 FDA reports)
EXTRASYSTOLES ( 11 FDA reports)
HYDRONEPHROSIS ( 11 FDA reports)
HYPERAESTHESIA ( 11 FDA reports)
IMMUNE SYSTEM DISORDER ( 11 FDA reports)
INCREASED TENDENCY TO BRUISE ( 11 FDA reports)
JAUNDICE ( 11 FDA reports)
JAW DISORDER ( 11 FDA reports)
KYPHOSIS ( 11 FDA reports)
LACERATION ( 11 FDA reports)
LARYNGEAL OEDEMA ( 11 FDA reports)
LUNG NEOPLASM MALIGNANT ( 11 FDA reports)
METABOLIC ACIDOSIS ( 11 FDA reports)
MOOD ALTERED ( 11 FDA reports)
MUSCLE TIGHTNESS ( 11 FDA reports)
NEOPLASM PROGRESSION ( 11 FDA reports)
ORTHOSTATIC HYPOTENSION ( 11 FDA reports)
PALLOR ( 11 FDA reports)
PERICARDITIS ( 11 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 11 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 11 FDA reports)
PROTHROMBIN TIME PROLONGED ( 11 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 11 FDA reports)
RETCHING ( 11 FDA reports)
SKIN HYPERTROPHY ( 11 FDA reports)
SKIN INDURATION ( 11 FDA reports)
SLEEP TALKING ( 11 FDA reports)
SPINAL DISORDER ( 11 FDA reports)
STEVENS-JOHNSON SYNDROME ( 11 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 11 FDA reports)
TENDONITIS ( 11 FDA reports)
THYROID NEOPLASM ( 11 FDA reports)
TONGUE ULCERATION ( 11 FDA reports)
TYPE 1 DIABETES MELLITUS ( 11 FDA reports)
VAGINAL HAEMORRHAGE ( 11 FDA reports)
ABDOMINAL PAIN LOWER ( 10 FDA reports)
ABORTION SPONTANEOUS ( 10 FDA reports)
ANOREXIA ( 10 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 10 FDA reports)
BACK DISORDER ( 10 FDA reports)
BREAST CANCER RECURRENT ( 10 FDA reports)
CACHEXIA ( 10 FDA reports)
CHANGE OF BOWEL HABIT ( 10 FDA reports)
CHONDROMALACIA ( 10 FDA reports)
COLITIS ULCERATIVE ( 10 FDA reports)
COMPRESSION FRACTURE ( 10 FDA reports)
DEVICE MALFUNCTION ( 10 FDA reports)
DIALYSIS ( 10 FDA reports)
DRUG SCREEN POSITIVE ( 10 FDA reports)
EYE SWELLING ( 10 FDA reports)
GASTROINTESTINAL DISORDER ( 10 FDA reports)
HEAD INJURY ( 10 FDA reports)
HEART RATE ABNORMAL ( 10 FDA reports)
HEPATIC LESION ( 10 FDA reports)
HOSPITALISATION ( 10 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 10 FDA reports)
HYSTERECTOMY ( 10 FDA reports)
INJECTION SITE PRURITUS ( 10 FDA reports)
INJECTION SITE SWELLING ( 10 FDA reports)
INTENTIONAL SELF-INJURY ( 10 FDA reports)
JOINT INJURY ( 10 FDA reports)
LACTIC ACIDOSIS ( 10 FDA reports)
LARGE INTESTINAL ULCER ( 10 FDA reports)
LIP SWELLING ( 10 FDA reports)
LIPOMA ( 10 FDA reports)
LOOSE TOOTH ( 10 FDA reports)
MELANOCYTIC NAEVUS ( 10 FDA reports)
NECK MASS ( 10 FDA reports)
OCULAR HYPERAEMIA ( 10 FDA reports)
ORAL DISCOMFORT ( 10 FDA reports)
ORAL INFECTION ( 10 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 10 FDA reports)
PEPTIC ULCER ( 10 FDA reports)
POSTNASAL DRIP ( 10 FDA reports)
PRURITUS GENERALISED ( 10 FDA reports)
RENAL PAIN ( 10 FDA reports)
SENSATION OF FOREIGN BODY ( 10 FDA reports)
SENSORY DISTURBANCE ( 10 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 10 FDA reports)
SPINAL COMPRESSION FRACTURE ( 10 FDA reports)
THYROID DISORDER ( 10 FDA reports)
UTERINE LEIOMYOMA ( 10 FDA reports)
VASCULITIS ( 10 FDA reports)
WOUND DEHISCENCE ( 10 FDA reports)
ABSCESS ( 9 FDA reports)
ACIDOSIS ( 9 FDA reports)
ACTINIC KERATOSIS ( 9 FDA reports)
ACTINOMYCOSIS ( 9 FDA reports)
ACUTE RESPIRATORY FAILURE ( 9 FDA reports)
AGEUSIA ( 9 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 9 FDA reports)
ANEURYSM ( 9 FDA reports)
ANGINA UNSTABLE ( 9 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 9 FDA reports)
AORTIC STENOSIS ( 9 FDA reports)
ASCITES ( 9 FDA reports)
ATRIAL SEPTAL DEFECT ( 9 FDA reports)
AUTOIMMUNE DISORDER ( 9 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 9 FDA reports)
BACTERAEMIA ( 9 FDA reports)
BLOOD URINE PRESENT ( 9 FDA reports)
BRONCHITIS CHRONIC ( 9 FDA reports)
CARDIOVASCULAR DISORDER ( 9 FDA reports)
CEREBRAL HAEMORRHAGE ( 9 FDA reports)
COLON POLYPECTOMY ( 9 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 9 FDA reports)
COORDINATION ABNORMAL ( 9 FDA reports)
CYSTOCELE ( 9 FDA reports)
DEAFNESS ( 9 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 9 FDA reports)
DENTURE WEARER ( 9 FDA reports)
DERMAL CYST ( 9 FDA reports)
ESSENTIAL HYPERTENSION ( 9 FDA reports)
FACIAL BONES FRACTURE ( 9 FDA reports)
FUNGAL INFECTION ( 9 FDA reports)
GROIN PAIN ( 9 FDA reports)
HEPATIC MASS ( 9 FDA reports)
HEPATITIS C ( 9 FDA reports)
HOMICIDAL IDEATION ( 9 FDA reports)
HYPERCALCAEMIA ( 9 FDA reports)
HYPERTENSIVE HEART DISEASE ( 9 FDA reports)
HYPOTHERMIA ( 9 FDA reports)
ILEUS ( 9 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 9 FDA reports)
IMPAIRED DRIVING ABILITY ( 9 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 9 FDA reports)
INFUSION RELATED REACTION ( 9 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 9 FDA reports)
LIMB DISCOMFORT ( 9 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 9 FDA reports)
MENORRHAGIA ( 9 FDA reports)
METAMORPHOPSIA ( 9 FDA reports)
MOTOR DYSFUNCTION ( 9 FDA reports)
MYASTHENIA GRAVIS ( 9 FDA reports)
NASAL CONGESTION ( 9 FDA reports)
ORAL DISORDER ( 9 FDA reports)
OSTEOLYSIS ( 9 FDA reports)
OVARIAN CYST ( 9 FDA reports)
PELVIC PAIN ( 9 FDA reports)
PHARYNGITIS ( 9 FDA reports)
POST PROCEDURAL COMPLICATION ( 9 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 9 FDA reports)
PREGNANCY ( 9 FDA reports)
PSEUDOMONAS INFECTION ( 9 FDA reports)
RADIOTHERAPY ( 9 FDA reports)
RASH GENERALISED ( 9 FDA reports)
RECTOCELE ( 9 FDA reports)
RESPIRATORY TRACT INFECTION ( 9 FDA reports)
RHINALGIA ( 9 FDA reports)
SINUS HEADACHE ( 9 FDA reports)
SKIN LACERATION ( 9 FDA reports)
SPINAL FUSION SURGERY ( 9 FDA reports)
SQUAMOUS CELL CARCINOMA ( 9 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 9 FDA reports)
TORSADE DE POINTES ( 9 FDA reports)
ULCER HAEMORRHAGE ( 9 FDA reports)
UPPER LIMB FRACTURE ( 9 FDA reports)
WRIST FRACTURE ( 9 FDA reports)
AFFECTIVE DISORDER ( 8 FDA reports)
ANAPHYLACTIC REACTION ( 8 FDA reports)
APATHY ( 8 FDA reports)
APPETITE DISORDER ( 8 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 8 FDA reports)
BILE DUCT STENOSIS ( 8 FDA reports)
BLINDNESS UNILATERAL ( 8 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 8 FDA reports)
BONE MARROW TRANSPLANT ( 8 FDA reports)
BREAST PAIN ( 8 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 8 FDA reports)
BRONCHOSPASM ( 8 FDA reports)
BRUXISM ( 8 FDA reports)
CARDIAC ENZYMES INCREASED ( 8 FDA reports)
CERVICAL CORD COMPRESSION ( 8 FDA reports)
CHOLECYSTITIS ( 8 FDA reports)
COGNITIVE DISORDER ( 8 FDA reports)
COLON ADENOMA ( 8 FDA reports)
DERMATITIS ( 8 FDA reports)
DERMATITIS CONTACT ( 8 FDA reports)
DIABETIC RETINOPATHY ( 8 FDA reports)
DRUG LEVEL DECREASED ( 8 FDA reports)
DRY EYE ( 8 FDA reports)
EAR DISCOMFORT ( 8 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 8 FDA reports)
EYE DISORDER ( 8 FDA reports)
FASCIITIS ( 8 FDA reports)
FIBROSIS ( 8 FDA reports)
FLUID OVERLOAD ( 8 FDA reports)
FORMICATION ( 8 FDA reports)
GASTROENTERITIS VIRAL ( 8 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 8 FDA reports)
HAEMORRHAGIC ANAEMIA ( 8 FDA reports)
HEMICEPHALALGIA ( 8 FDA reports)
HEMIPLEGIA ( 8 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 8 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 8 FDA reports)
HYPOACUSIS ( 8 FDA reports)
IMMUNOSUPPRESSION ( 8 FDA reports)
INADEQUATE ANALGESIA ( 8 FDA reports)
INTENTIONAL MISUSE ( 8 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 8 FDA reports)
INTESTINAL PERFORATION ( 8 FDA reports)
INTESTINAL RESECTION ( 8 FDA reports)
KETOACIDOSIS ( 8 FDA reports)
KNEE OPERATION ( 8 FDA reports)
LIBIDO DECREASED ( 8 FDA reports)
LUNG INFECTION ( 8 FDA reports)
LYMPHOCYTOSIS ( 8 FDA reports)
MACULAR DEGENERATION ( 8 FDA reports)
MASS ( 8 FDA reports)
MENINGIOMA ( 8 FDA reports)
MUSCLE INJURY ( 8 FDA reports)
MUSCLE STRAIN ( 8 FDA reports)
MYDRIASIS ( 8 FDA reports)
ORAL SURGERY ( 8 FDA reports)
OTORRHOEA ( 8 FDA reports)
PAIN OF SKIN ( 8 FDA reports)
POOR QUALITY SLEEP ( 8 FDA reports)
POST CONCUSSION SYNDROME ( 8 FDA reports)
POST THROMBOTIC SYNDROME ( 8 FDA reports)
PRESYNCOPE ( 8 FDA reports)
RASH MACULO-PAPULAR ( 8 FDA reports)
RESORPTION BONE INCREASED ( 8 FDA reports)
RESPIRATORY DISORDER ( 8 FDA reports)
RHINORRHOEA ( 8 FDA reports)
SEXUAL DYSFUNCTION ( 8 FDA reports)
SINUS BRADYCARDIA ( 8 FDA reports)
SINUS TARSI SYNDROME ( 8 FDA reports)
SKIN CANCER ( 8 FDA reports)
SKIN TIGHTNESS ( 8 FDA reports)
STEM CELL TRANSPLANT ( 8 FDA reports)
STOMATITIS NECROTISING ( 8 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 8 FDA reports)
THROAT TIGHTNESS ( 8 FDA reports)
TOOTH REPAIR ( 8 FDA reports)
TOXIC NODULAR GOITRE ( 8 FDA reports)
TRISMUS ( 8 FDA reports)
TUBERCULOSIS ( 8 FDA reports)
URETHRAL STENOSIS ( 8 FDA reports)
VAGINAL INFECTION ( 8 FDA reports)
WOUND ( 8 FDA reports)
ABDOMINAL HERNIA ( 7 FDA reports)
ACUTE PRERENAL FAILURE ( 7 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 7 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 7 FDA reports)
BACTERIAL INFECTION ( 7 FDA reports)
BLOOD CHLORIDE DECREASED ( 7 FDA reports)
BLOOD COUNT ABNORMAL ( 7 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 7 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 7 FDA reports)
BONE NEOPLASM MALIGNANT ( 7 FDA reports)
BRAIN OEDEMA ( 7 FDA reports)
CARDIAC VALVE DISEASE ( 7 FDA reports)
CATHETERISATION CARDIAC ( 7 FDA reports)
CEREBROVASCULAR DISORDER ( 7 FDA reports)
CLUMSINESS ( 7 FDA reports)
CORONARY ARTERY STENOSIS ( 7 FDA reports)
CRANIOTOMY ( 7 FDA reports)
DISEASE RECURRENCE ( 7 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 7 FDA reports)
DRUG INTOLERANCE ( 7 FDA reports)
EAR CONGESTION ( 7 FDA reports)
EAR DISORDER ( 7 FDA reports)
ENTEROCOCCAL INFECTION ( 7 FDA reports)
EYE IRRITATION ( 7 FDA reports)
FOOD CRAVING ( 7 FDA reports)
GASTROENTERITIS ( 7 FDA reports)
GENITAL HERPES ( 7 FDA reports)
GINGIVAL ULCERATION ( 7 FDA reports)
GLOSSODYNIA ( 7 FDA reports)
GOUT ( 7 FDA reports)
HAEMOLYTIC ANAEMIA ( 7 FDA reports)
HAND DEFORMITY ( 7 FDA reports)
HEART VALVE INCOMPETENCE ( 7 FDA reports)
HORDEOLUM ( 7 FDA reports)
LIVER INJURY ( 7 FDA reports)
MENTAL IMPAIRMENT ( 7 FDA reports)
METASTASES TO LYMPH NODES ( 7 FDA reports)
METASTATIC NEOPLASM ( 7 FDA reports)
MYOMECTOMY ( 7 FDA reports)
MYOSITIS ( 7 FDA reports)
NERVE INJURY ( 7 FDA reports)
NEUTROPENIC SEPSIS ( 7 FDA reports)
OPEN REDUCTION OF FRACTURE ( 7 FDA reports)
PANCREATIC DISORDER ( 7 FDA reports)
PARAESTHESIA ORAL ( 7 FDA reports)
PERICARDITIS CONSTRICTIVE ( 7 FDA reports)
PERONEAL NERVE PALSY ( 7 FDA reports)
PHOTOPSIA ( 7 FDA reports)
PHYSICAL DISABILITY ( 7 FDA reports)
PILOERECTION ( 7 FDA reports)
PNEUMOTHORAX ( 7 FDA reports)
POLYMYALGIA RHEUMATICA ( 7 FDA reports)
POLYPECTOMY ( 7 FDA reports)
PSORIATIC ARTHROPATHY ( 7 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 7 FDA reports)
PURULENCE ( 7 FDA reports)
RALES ( 7 FDA reports)
SACROILIITIS ( 7 FDA reports)
SELF-INJURIOUS IDEATION ( 7 FDA reports)
SEQUESTRECTOMY ( 7 FDA reports)
SHOCK ( 7 FDA reports)
SHOULDER ARTHROPLASTY ( 7 FDA reports)
SKIN SWELLING ( 7 FDA reports)
SKULL MALFORMATION ( 7 FDA reports)
SOCIAL PROBLEM ( 7 FDA reports)
SPONDYLOLISTHESIS ( 7 FDA reports)
SPUTUM DISCOLOURED ( 7 FDA reports)
STERNOTOMY ( 7 FDA reports)
STRESS FRACTURE ( 7 FDA reports)
SUDDEN DEATH ( 7 FDA reports)
THYROIDECTOMY ( 7 FDA reports)
TRANSAMINASES INCREASED ( 7 FDA reports)
VENTRICULAR SEPTAL DEFECT REPAIR ( 7 FDA reports)
VOMITING PROJECTILE ( 7 FDA reports)
WOUND SECRETION ( 7 FDA reports)
ABDOMINAL TENDERNESS ( 6 FDA reports)
ADHESION ( 6 FDA reports)
ANTISOCIAL BEHAVIOUR ( 6 FDA reports)
AORTIC CALCIFICATION ( 6 FDA reports)
APPLICATION SITE RASH ( 6 FDA reports)
AURICULAR PERICHONDRITIS ( 6 FDA reports)
AZOTAEMIA ( 6 FDA reports)
BILIARY COLIC ( 6 FDA reports)
BILIARY DYSKINESIA ( 6 FDA reports)
BLADDER PROLAPSE ( 6 FDA reports)
BLADDER SPASM ( 6 FDA reports)
BLOOD CREATINE INCREASED ( 6 FDA reports)
BLOOD PH DECREASED ( 6 FDA reports)
BODY HEIGHT DECREASED ( 6 FDA reports)
BODY TEMPERATURE DECREASED ( 6 FDA reports)
BREAST CALCIFICATIONS ( 6 FDA reports)
BRONCHOPNEUMONIA ( 6 FDA reports)
CHOROIDAL NEOVASCULARISATION ( 6 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 6 FDA reports)
COLLAPSE OF LUNG ( 6 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 6 FDA reports)
CREPITATIONS ( 6 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 6 FDA reports)
DEMYELINATION ( 6 FDA reports)
DROOLING ( 6 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 6 FDA reports)
ELECTROLYTE IMBALANCE ( 6 FDA reports)
ERECTILE DYSFUNCTION ( 6 FDA reports)
EROSIVE OESOPHAGITIS ( 6 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 6 FDA reports)
EXTREMITY CONTRACTURE ( 6 FDA reports)
EYE INFECTION ( 6 FDA reports)
EYE INFLAMMATION ( 6 FDA reports)
FAMILY STRESS ( 6 FDA reports)
GANGRENE ( 6 FDA reports)
GASTRITIS EROSIVE ( 6 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 6 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 6 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 6 FDA reports)
GINGIVAL ABSCESS ( 6 FDA reports)
HAEMODIALYSIS ( 6 FDA reports)
HAND FRACTURE ( 6 FDA reports)
HEPATIC CIRRHOSIS ( 6 FDA reports)
HEPATIC PAIN ( 6 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 6 FDA reports)
HOSTILITY ( 6 FDA reports)
ILEUS PARALYTIC ( 6 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 6 FDA reports)
INITIAL INSOMNIA ( 6 FDA reports)
INJECTION SITE HAEMORRHAGE ( 6 FDA reports)
INJECTION SITE IRRITATION ( 6 FDA reports)
LACTOSE INTOLERANCE ( 6 FDA reports)
LEFT ATRIAL DILATATION ( 6 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 6 FDA reports)
LEG AMPUTATION ( 6 FDA reports)
LOCAL SWELLING ( 6 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED RECURRENT ( 6 FDA reports)
MACULOPATHY ( 6 FDA reports)
MENSTRUAL DISORDER ( 6 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 6 FDA reports)
METASTATIC PAIN ( 6 FDA reports)
MIOSIS ( 6 FDA reports)
MONOCYTOSIS ( 6 FDA reports)
MOUTH HAEMORRHAGE ( 6 FDA reports)
MYOCLONUS ( 6 FDA reports)
NASAL MUCOSAL DISORDER ( 6 FDA reports)
NECROSIS ( 6 FDA reports)
NON-CARDIAC CHEST PAIN ( 6 FDA reports)
ODYNOPHAGIA ( 6 FDA reports)
OOPHORECTOMY ( 6 FDA reports)
OPEN WOUND ( 6 FDA reports)
OPTIC ATROPHY ( 6 FDA reports)
ORTHOSIS USER ( 6 FDA reports)
OSTEOMYELITIS CHRONIC ( 6 FDA reports)
PANCREATITIS RELAPSING ( 6 FDA reports)
PANIC REACTION ( 6 FDA reports)
PARATHYROIDECTOMY ( 6 FDA reports)
PERIODONTAL INFECTION ( 6 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 6 FDA reports)
PHARYNGEAL ERYTHEMA ( 6 FDA reports)
PHOTOPHOBIA ( 6 FDA reports)
PLEURITIC PAIN ( 6 FDA reports)
PROTEINURIA ( 6 FDA reports)
QUALITY OF LIFE DECREASED ( 6 FDA reports)
RESPIRATORY ACIDOSIS ( 6 FDA reports)
RESPIRATORY RATE DECREASED ( 6 FDA reports)
RESPIRATORY RATE INCREASED ( 6 FDA reports)
RETINAL DETACHMENT ( 6 FDA reports)
SCHIZOPHRENIA ( 6 FDA reports)
SCREAMING ( 6 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 6 FDA reports)
SKIN INFECTION ( 6 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 6 FDA reports)
SNORING ( 6 FDA reports)
SOCIAL PHOBIA ( 6 FDA reports)
SUBCUTANEOUS ABSCESS ( 6 FDA reports)
TEARFULNESS ( 6 FDA reports)
THERMAL BURN ( 6 FDA reports)
TIC ( 6 FDA reports)
ULCER ( 6 FDA reports)
VAGINAL DISCHARGE ( 6 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 6 FDA reports)
VERTEBRAL WEDGING ( 6 FDA reports)
VISUAL FIELD DEFECT ( 6 FDA reports)
WALKING AID USER ( 6 FDA reports)
WHEELCHAIR USER ( 6 FDA reports)
ABDOMINAL SEPSIS ( 5 FDA reports)
ACCIDENTAL POISONING ( 5 FDA reports)
ADRENAL ADENOMA ( 5 FDA reports)
ADRENAL INSUFFICIENCY ( 5 FDA reports)
ADVERSE EVENT ( 5 FDA reports)
AFFECT LABILITY ( 5 FDA reports)
ANGIONEUROTIC OEDEMA ( 5 FDA reports)
APHAGIA ( 5 FDA reports)
APPENDICITIS ( 5 FDA reports)
ARTHROPOD BITE ( 5 FDA reports)
ASPIRATION PLEURAL CAVITY ( 5 FDA reports)
ATRIOVENTRICULAR BLOCK ( 5 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 5 FDA reports)
BEDRIDDEN ( 5 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 5 FDA reports)
BLADDER DISCOMFORT ( 5 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 5 FDA reports)
BLOOD POTASSIUM INCREASED ( 5 FDA reports)
BLOOD PRESSURE ABNORMAL ( 5 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 5 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 5 FDA reports)
BLOOD TEST ABNORMAL ( 5 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 5 FDA reports)
BONE FRAGMENTATION ( 5 FDA reports)
BONE SCAN ABNORMAL ( 5 FDA reports)
BREAST CANCER IN SITU ( 5 FDA reports)
BREAST FIBROSIS ( 5 FDA reports)
BREAST NECROSIS ( 5 FDA reports)
BREAST SWELLING ( 5 FDA reports)
CARDIAC ANEURYSM ( 5 FDA reports)
CATHETER PLACEMENT ( 5 FDA reports)
CATHETER SITE HAEMORRHAGE ( 5 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 5 FDA reports)
CERVIX CARCINOMA ( 5 FDA reports)
COLON CANCER ( 5 FDA reports)
COLOUR BLINDNESS ACQUIRED ( 5 FDA reports)
CONNECTIVE TISSUE DISORDER ( 5 FDA reports)
COR PULMONALE ( 5 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 5 FDA reports)
DENTAL PROSTHESIS USER ( 5 FDA reports)
DEPRESSIVE SYMPTOM ( 5 FDA reports)
DIFFICULTY IN WALKING ( 5 FDA reports)
DRUG ADMINISTRATION ERROR ( 5 FDA reports)
DRUG ERUPTION ( 5 FDA reports)
DRUG PRESCRIBING ERROR ( 5 FDA reports)
DUODENAL ULCER ( 5 FDA reports)
DYSLIPIDAEMIA ( 5 FDA reports)
EARLY SATIETY ( 5 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 5 FDA reports)
FACE OEDEMA ( 5 FDA reports)
FACIAL NERVE DISORDER ( 5 FDA reports)
FACIAL PARESIS ( 5 FDA reports)
FAECES DISCOLOURED ( 5 FDA reports)
FEELING JITTERY ( 5 FDA reports)
FIBULA FRACTURE ( 5 FDA reports)
FOAMING AT MOUTH ( 5 FDA reports)
FOLLICULITIS ( 5 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 5 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 5 FDA reports)
GASTRIC DISORDER ( 5 FDA reports)
GINGIVAL SWELLING ( 5 FDA reports)
GLOSSITIS ( 5 FDA reports)
HAEMORRHAGIC STROKE ( 5 FDA reports)
HAEMOTHORAX ( 5 FDA reports)
HELICOBACTER INFECTION ( 5 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 5 FDA reports)
HERNIA ( 5 FDA reports)
HERPES SIMPLEX ( 5 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 5 FDA reports)
HODGKIN'S DISEASE ( 5 FDA reports)
HYPERCOAGULATION ( 5 FDA reports)
HYPOAESTHESIA ORAL ( 5 FDA reports)
HYPOMANIA ( 5 FDA reports)
HYPOPHOSPHATAEMIA ( 5 FDA reports)
ILEOSTOMY ( 5 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 5 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 5 FDA reports)
INFARCTION ( 5 FDA reports)
INJECTION SITE REACTION ( 5 FDA reports)
INJECTION SITE WARMTH ( 5 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 5 FDA reports)
IRON DEFICIENCY ( 5 FDA reports)
LABORATORY TEST ABNORMAL ( 5 FDA reports)
LACRIMATION INCREASED ( 5 FDA reports)
LERICHE SYNDROME ( 5 FDA reports)
LEUKOPLAKIA ( 5 FDA reports)
LINEAR IGA DISEASE ( 5 FDA reports)
MAMMOGRAM ABNORMAL ( 5 FDA reports)
MANDIBULAR PROSTHESIS USER ( 5 FDA reports)
MASTECTOMY ( 5 FDA reports)
MESENTERIC VASCULAR INSUFFICIENCY ( 5 FDA reports)
METASTASES TO MOUTH ( 5 FDA reports)
MIGRAINE WITH AURA ( 5 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 5 FDA reports)
MYOCARDIAL FIBROSIS ( 5 FDA reports)
NECK INJURY ( 5 FDA reports)
NEOPLASM ( 5 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 5 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 5 FDA reports)
NYSTAGMUS ( 5 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 5 FDA reports)
OCCULT BLOOD POSITIVE ( 5 FDA reports)
OEDEMA MOUTH ( 5 FDA reports)
ONYCHOCLASIS ( 5 FDA reports)
ONYCHOMYCOSIS ( 5 FDA reports)
ORGAN FAILURE ( 5 FDA reports)
OROANTRAL FISTULA ( 5 FDA reports)
ORTHOPNOEA ( 5 FDA reports)
OSTECTOMY ( 5 FDA reports)
OSTEOCHONDROSIS ( 5 FDA reports)
OVARIAN CANCER ( 5 FDA reports)
PANCREATITIS CHRONIC ( 5 FDA reports)
PARAPLEGIA ( 5 FDA reports)
PARKINSONISM ( 5 FDA reports)
PELVIC FRACTURE ( 5 FDA reports)
PERIODONTAL DISEASE ( 5 FDA reports)
PERIODONTITIS ( 5 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 5 FDA reports)
PHLEBITIS ( 5 FDA reports)
PLASMACYTOMA ( 5 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 5 FDA reports)
POLYP ( 5 FDA reports)
PREMATURE LABOUR ( 5 FDA reports)
PROCTALGIA ( 5 FDA reports)
PULMONARY GRANULOMA ( 5 FDA reports)
REFLUX OESOPHAGITIS ( 5 FDA reports)
RENAL TUBULAR NECROSIS ( 5 FDA reports)
RESPIRATORY ALKALOSIS ( 5 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 5 FDA reports)
RHINITIS ( 5 FDA reports)
RIB DEFORMITY ( 5 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 5 FDA reports)
SEROMA ( 5 FDA reports)
SICK SINUS SYNDROME ( 5 FDA reports)
SKIN IRRITATION ( 5 FDA reports)
SKIN NEOPLASM EXCISION ( 5 FDA reports)
STILL'S DISEASE ADULT ONSET ( 5 FDA reports)
TACHYPNOEA ( 5 FDA reports)
TENDON DISORDER ( 5 FDA reports)
THROAT IRRITATION ( 5 FDA reports)
TIBIA FRACTURE ( 5 FDA reports)
TINEA PEDIS ( 5 FDA reports)
TONGUE DISORDER ( 5 FDA reports)
UMBILICAL HERNIA ( 5 FDA reports)
URINARY HESITATION ( 5 FDA reports)
VEIN DISORDER ( 5 FDA reports)
VENTRICULAR DYSKINESIA ( 5 FDA reports)
VENTRICULAR HYPERTROPHY ( 5 FDA reports)
VENTRICULAR HYPOKINESIA ( 5 FDA reports)
WOUND HAEMORRHAGE ( 5 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 5 FDA reports)
ABDOMINAL RIGIDITY ( 4 FDA reports)
ABNORMAL FAECES ( 4 FDA reports)
ABNORMAL SENSATION IN EYE ( 4 FDA reports)
ABSCESS DRAINAGE ( 4 FDA reports)
ABSCESS LIMB ( 4 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 4 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 4 FDA reports)
ADDISON'S DISEASE ( 4 FDA reports)
ANOXIC ENCEPHALOPATHY ( 4 FDA reports)
AORTIC DISORDER ( 4 FDA reports)
APHONIA ( 4 FDA reports)
APHTHOUS STOMATITIS ( 4 FDA reports)
APPLICATION SITE ERYTHEMA ( 4 FDA reports)
AREFLEXIA ( 4 FDA reports)
ARTERIAL INSUFFICIENCY ( 4 FDA reports)
ARTHRODESIS ( 4 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 4 FDA reports)
ATROPHY ( 4 FDA reports)
BACK INJURY ( 4 FDA reports)
BARRETT'S OESOPHAGUS ( 4 FDA reports)
BIOPSY BONE MARROW ( 4 FDA reports)
BLADDER CYST ( 4 FDA reports)
BLADDER DISORDER ( 4 FDA reports)
BLADDER DYSFUNCTION ( 4 FDA reports)
BLOOD MAGNESIUM DECREASED ( 4 FDA reports)
BLOOD OSMOLARITY DECREASED ( 4 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 4 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 4 FDA reports)
BRAIN DEATH ( 4 FDA reports)
BREAST OPERATION ( 4 FDA reports)
BRONCHIAL SECRETION RETENTION ( 4 FDA reports)
BRONCHIECTASIS ( 4 FDA reports)
BRONCHITIS ACUTE ( 4 FDA reports)
CARDIOGENIC SHOCK ( 4 FDA reports)
CATARACT NUCLEAR ( 4 FDA reports)
CERVICAL DYSPLASIA ( 4 FDA reports)
CERVICAL SPINAL STENOSIS ( 4 FDA reports)
CHEILITIS ( 4 FDA reports)
CHEST WALL MASS ( 4 FDA reports)
CHLAMYDIAL INFECTION ( 4 FDA reports)
CHOROIDAL EFFUSION ( 4 FDA reports)
CLOSTRIDIAL INFECTION ( 4 FDA reports)
COLITIS ISCHAEMIC ( 4 FDA reports)
COLON CANCER RECURRENT ( 4 FDA reports)
COLONOSCOPY ( 4 FDA reports)
COLOUR BLINDNESS ( 4 FDA reports)
CONDUCTION DISORDER ( 4 FDA reports)
CULTURE URINE POSITIVE ( 4 FDA reports)
DEAFNESS NEUROSENSORY ( 4 FDA reports)
DENTAL OPERATION ( 4 FDA reports)
DRUG ABUSER ( 4 FDA reports)
DRUG ADDICT ( 4 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 4 FDA reports)
DYSPAREUNIA ( 4 FDA reports)
DYSPHEMIA ( 4 FDA reports)
DYSPLASIA ( 4 FDA reports)
ECCHYMOSIS ( 4 FDA reports)
EDENTULOUS ( 4 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 4 FDA reports)
ENDOTRACHEAL INTUBATION ( 4 FDA reports)
EUPHORIC MOOD ( 4 FDA reports)
EYE INJURY ( 4 FDA reports)
EYELID OEDEMA ( 4 FDA reports)
FACET JOINT SYNDROME ( 4 FDA reports)
FACIAL PALSY ( 4 FDA reports)
FAECALOMA ( 4 FDA reports)
FIBROADENOMA OF BREAST ( 4 FDA reports)
FRUSTRATION ( 4 FDA reports)
FUNGAEMIA ( 4 FDA reports)
GINGIVAL INFECTION ( 4 FDA reports)
GOUTY ARTHRITIS ( 4 FDA reports)
GYNAECOMASTIA ( 4 FDA reports)
HAEMANGIOMA ( 4 FDA reports)
HALLUCINATIONS, MIXED ( 4 FDA reports)
HEAD DISCOMFORT ( 4 FDA reports)
HEPATIC ENZYME ABNORMAL ( 4 FDA reports)
HUMAN PAPILLOMA VIRUS TEST POSITIVE ( 4 FDA reports)
HYPERNATRAEMIA ( 4 FDA reports)
HYPERPHAGIA ( 4 FDA reports)
HYPERVENTILATION ( 4 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 4 FDA reports)
HYPOTONIA ( 4 FDA reports)
ILIAC ARTERY THROMBOSIS ( 4 FDA reports)
IMMOBILE ( 4 FDA reports)
IMPLANT SITE INFECTION ( 4 FDA reports)
INCISION SITE COMPLICATION ( 4 FDA reports)
INCREASED APPETITE ( 4 FDA reports)
INFANTILE APNOEIC ATTACK ( 4 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 4 FDA reports)
INJECTION SITE OEDEMA ( 4 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 4 FDA reports)
IRON DEFICIENCY ANAEMIA ( 4 FDA reports)
JAW FRACTURE ( 4 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 4 FDA reports)
KLEBSIELLA INFECTION ( 4 FDA reports)
LACUNAR INFARCTION ( 4 FDA reports)
LIP PAIN ( 4 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 4 FDA reports)
LYMPHADENECTOMY ( 4 FDA reports)
LYMPHOEDEMA ( 4 FDA reports)
MANIA ( 4 FDA reports)
MENINGITIS HERPES ( 4 FDA reports)
MENINGITIS VIRAL ( 4 FDA reports)
MIDDLE INSOMNIA ( 4 FDA reports)
MITRAL VALVE PROLAPSE ( 4 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 4 FDA reports)
MONOPLEGIA ( 4 FDA reports)
MULTI-ORGAN DISORDER ( 4 FDA reports)
MULTIPLE ALLERGIES ( 4 FDA reports)
MUSCLE ATROPHY ( 4 FDA reports)
MUSCLE RIGIDITY ( 4 FDA reports)
NEPHROGENIC ANAEMIA ( 4 FDA reports)
NERVE COMPRESSION ( 4 FDA reports)
NEUROTOXICITY ( 4 FDA reports)
NO ADVERSE EVENT ( 4 FDA reports)
NODAL RHYTHM ( 4 FDA reports)
NODULE ( 4 FDA reports)
NOSOCOMIAL INFECTION ( 4 FDA reports)
OESOPHAGEAL ULCER ( 4 FDA reports)
ORAL LICHEN PLANUS ( 4 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 4 FDA reports)
OTITIS MEDIA ( 4 FDA reports)
PANIC DISORDER ( 4 FDA reports)
PARAPARESIS ( 4 FDA reports)
PEAK EXPIRATORY FLOW RATE DECREASED ( 4 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 4 FDA reports)
PHOTOSENSITIVITY REACTION ( 4 FDA reports)
PLEURAL DISORDER ( 4 FDA reports)
PLEURAL FIBROSIS ( 4 FDA reports)
PLEURISY ( 4 FDA reports)
PNEUMONIA VIRAL ( 4 FDA reports)
POLYNEUROPATHY ( 4 FDA reports)
POOR PERIPHERAL CIRCULATION ( 4 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 4 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 4 FDA reports)
POSTURE ABNORMAL ( 4 FDA reports)
PROSTATE CANCER ( 4 FDA reports)
PROSTATOMEGALY ( 4 FDA reports)
PROTEUS INFECTION ( 4 FDA reports)
PSYCHOMOTOR RETARDATION ( 4 FDA reports)
PULMONARY MASS ( 4 FDA reports)
PULSE PRESSURE DECREASED ( 4 FDA reports)
PUPILLARY DISORDER ( 4 FDA reports)
PUSTULAR PSORIASIS ( 4 FDA reports)
PYURIA ( 4 FDA reports)
RADIATION ASSOCIATED PAIN ( 4 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 4 FDA reports)
RENAL ARTERY STENOSIS ( 4 FDA reports)
RIGHT VENTRICULAR FAILURE ( 4 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 4 FDA reports)
SARCOIDOSIS ( 4 FDA reports)
SEASONAL ALLERGY ( 4 FDA reports)
SELF ESTEEM DECREASED ( 4 FDA reports)
SELF-MEDICATION ( 4 FDA reports)
SERUM SICKNESS ( 4 FDA reports)
SKIN GRAFT ( 4 FDA reports)
SKIN NECROSIS ( 4 FDA reports)
SPINAL LAMINECTOMY ( 4 FDA reports)
STENT PLACEMENT ( 4 FDA reports)
STRESS URINARY INCONTINENCE ( 4 FDA reports)
SUFFOCATION FEELING ( 4 FDA reports)
TACHYCARDIA PAROXYSMAL ( 4 FDA reports)
TENDON PAIN ( 4 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 4 FDA reports)
THERAPY NON-RESPONDER ( 4 FDA reports)
THROMBOSIS IN DEVICE ( 4 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 4 FDA reports)
TOBACCO ABUSE ( 4 FDA reports)
TOXIC ENCEPHALOPATHY ( 4 FDA reports)
TRACHEAL STENOSIS ( 4 FDA reports)
TREATMENT FAILURE ( 4 FDA reports)
TRIGEMINAL NEURALGIA ( 4 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 4 FDA reports)
URINE FLOW DECREASED ( 4 FDA reports)
VASCULITIS CEREBRAL ( 4 FDA reports)
VITAMIN B12 DEFICIENCY ( 4 FDA reports)
VITH NERVE PARALYSIS ( 4 FDA reports)
VITREOUS HAEMORRHAGE ( 4 FDA reports)
VOCAL CORD DISORDER ( 4 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 4 FDA reports)
ABDOMINAL MASS ( 3 FDA reports)
ABSCESS JAW ( 3 FDA reports)
ACCIDENTAL DEATH ( 3 FDA reports)
ACNE ( 3 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 3 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 3 FDA reports)
ACUTE ABDOMEN ( 3 FDA reports)
ACUTE PSYCHOSIS ( 3 FDA reports)
ADENOIDECTOMY ( 3 FDA reports)
AMMONIA INCREASED ( 3 FDA reports)
AMYLOIDOSIS ( 3 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 3 FDA reports)
ANAL FISSURE ( 3 FDA reports)
ANGIOPATHY ( 3 FDA reports)
ANGIOPLASTY ( 3 FDA reports)
ANOSMIA ( 3 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 3 FDA reports)
AORTIC VALVE CALCIFICATION ( 3 FDA reports)
APLASTIC ANAEMIA ( 3 FDA reports)
APPLICATION SITE IRRITATION ( 3 FDA reports)
ARTERIAL STENOSIS ( 3 FDA reports)
ARTERIAL THROMBOSIS ( 3 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 3 FDA reports)
ARTERIOSPASM CORONARY ( 3 FDA reports)
ASBESTOSIS ( 3 FDA reports)
ASTIGMATISM ( 3 FDA reports)
AUTOIMMUNE HEPATITIS ( 3 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 3 FDA reports)
AUTOMATISM ( 3 FDA reports)
BED REST ( 3 FDA reports)
BENIGN NEOPLASM ( 3 FDA reports)
BILE DUCT OBSTRUCTION ( 3 FDA reports)
BILE DUCT STONE ( 3 FDA reports)
BIOPSY ( 3 FDA reports)
BIOPSY BLADDER ABNORMAL ( 3 FDA reports)
BIOPSY SKIN ABNORMAL ( 3 FDA reports)
BLADDER CANCER ( 3 FDA reports)
BLADDER OBSTRUCTION ( 3 FDA reports)
BLADDER OPERATION ( 3 FDA reports)
BLADDER PAIN ( 3 FDA reports)
BLOOD AMYLASE INCREASED ( 3 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 3 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 3 FDA reports)
BLOOD CULTURE POSITIVE ( 3 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 3 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 3 FDA reports)
BLOOD UREA ABNORMAL ( 3 FDA reports)
BLOODY DISCHARGE ( 3 FDA reports)
BONE DENSITY ABNORMAL ( 3 FDA reports)
BONE FISTULA ( 3 FDA reports)
BONE SWELLING ( 3 FDA reports)
BRAIN CANCER METASTATIC ( 3 FDA reports)
BREAST CANCER METASTATIC ( 3 FDA reports)
BREAST ENLARGEMENT ( 3 FDA reports)
BREAST LUMP REMOVAL ( 3 FDA reports)
BREAST TENDERNESS ( 3 FDA reports)
BRUGADA SYNDROME ( 3 FDA reports)
CANDIDIASIS ( 3 FDA reports)
CARDIAC FLUTTER ( 3 FDA reports)
CARDIAC PERFORATION ( 3 FDA reports)
CARDIAC VALVE VEGETATION ( 3 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 3 FDA reports)
CARDIOPULMONARY BYPASS ( 3 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 3 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 3 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 3 FDA reports)
CERVICOBRACHIAL SYNDROME ( 3 FDA reports)
CHOLECYSTITIS ACUTE ( 3 FDA reports)
CHONDROPLASTY ( 3 FDA reports)
COAGULATION FACTOR X LEVEL INCREASED ( 3 FDA reports)
COARCTATION OF THE AORTA ( 3 FDA reports)
COELIAC DISEASE ( 3 FDA reports)
COGNITIVE DETERIORATION ( 3 FDA reports)
COMMUNICATION DISORDER ( 3 FDA reports)
COMPUTERISED TOMOGRAM ( 3 FDA reports)
CONGENITAL ANOMALY ( 3 FDA reports)
CONJUNCTIVITIS ( 3 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 3 FDA reports)
CONVERSION DISORDER ( 3 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 3 FDA reports)
DECREASED ACTIVITY ( 3 FDA reports)
DEVICE ADHESION ISSUE ( 3 FDA reports)
DIABETIC NEPHROPATHY ( 3 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 3 FDA reports)
DILATATION VENTRICULAR ( 3 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 3 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 3 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 3 FDA reports)
DYSPHORIA ( 3 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 3 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 3 FDA reports)
EMBOLISM VENOUS ( 3 FDA reports)
ENCEPHALITIS ( 3 FDA reports)
ENCEPHALITIS HERPES ( 3 FDA reports)
ENDOCARDITIS BACTERIAL ( 3 FDA reports)
ENDOPHTHALMITIS ( 3 FDA reports)
ENTEROCOCCAL SEPSIS ( 3 FDA reports)
EOSINOPHILIA ( 3 FDA reports)
ERUCTATION ( 3 FDA reports)
ERYTHEMA MULTIFORME ( 3 FDA reports)
EYELID DISORDER ( 3 FDA reports)
FAECES HARD ( 3 FDA reports)
FEAR OF DEATH ( 3 FDA reports)
FEELING GUILTY ( 3 FDA reports)
FEELING OF DESPAIR ( 3 FDA reports)
FEELINGS OF WORTHLESSNESS ( 3 FDA reports)
FEMORAL NECK FRACTURE ( 3 FDA reports)
FOREIGN BODY TRAUMA ( 3 FDA reports)
FURUNCLE ( 3 FDA reports)
GALLBLADDER POLYP ( 3 FDA reports)
GASTRIC BYPASS ( 3 FDA reports)
GASTRIC HAEMORRHAGE ( 3 FDA reports)
GASTRIC HYPOMOTILITY ( 3 FDA reports)
GASTROENTERITIS NOROVIRUS ( 3 FDA reports)
GASTROINTESTINAL PERFORATION ( 3 FDA reports)
GASTROSTOMY FAILURE ( 3 FDA reports)
GENERALISED ERYTHEMA ( 3 FDA reports)
GINGIVAL EROSION ( 3 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 3 FDA reports)
GRAVITATIONAL OEDEMA ( 3 FDA reports)
GRIMACING ( 3 FDA reports)
HAEMORRHOID OPERATION ( 3 FDA reports)
HEART DISEASE CONGENITAL ( 3 FDA reports)
HEAT RASH ( 3 FDA reports)
HELICOBACTER GASTRITIS ( 3 FDA reports)
HEPATITIS A ( 3 FDA reports)
HEPATITIS ACUTE ( 3 FDA reports)
HEPATOTOXICITY ( 3 FDA reports)
HERPES VIRUS INFECTION ( 3 FDA reports)
HIDRADENITIS ( 3 FDA reports)
HILAR LYMPHADENOPATHY ( 3 FDA reports)
HIP SURGERY ( 3 FDA reports)
HUNGER ( 3 FDA reports)
HYPERCAPNIA ( 3 FDA reports)
HYPERCHLORHYDRIA ( 3 FDA reports)
HYPERVIGILANCE ( 3 FDA reports)
HYPOALBUMINAEMIA ( 3 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 3 FDA reports)
IMPULSIVE BEHAVIOUR ( 3 FDA reports)
INJECTION SITE DISCOLOURATION ( 3 FDA reports)
INJECTION SITE RASH ( 3 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 3 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 3 FDA reports)
INTERMITTENT CLAUDICATION ( 3 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 3 FDA reports)
INTESTINAL HAEMORRHAGE ( 3 FDA reports)
INTESTINAL POLYP ( 3 FDA reports)
INTESTINAL PROLAPSE ( 3 FDA reports)
ISCHAEMIA ( 3 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 3 FDA reports)
ISCHAEMIC STROKE ( 3 FDA reports)
JAUNDICE CHOLESTATIC ( 3 FDA reports)
JOINT DISLOCATION ( 3 FDA reports)
LEFT VENTRICULAR FAILURE ( 3 FDA reports)
LIFE EXPECTANCY SHORTENED ( 3 FDA reports)
LIP DRY ( 3 FDA reports)
LOBAR PNEUMONIA ( 3 FDA reports)
LOSS OF LIBIDO ( 3 FDA reports)
LUMBAR RADICULOPATHY ( 3 FDA reports)
LUNG HYPERINFLATION ( 3 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 3 FDA reports)
MALIGNANT MELANOMA ( 3 FDA reports)
MASS EXCISION ( 3 FDA reports)
MASTITIS ( 3 FDA reports)
MEDICAL DEVICE COMPLICATION ( 3 FDA reports)
MEGACOLON ( 3 FDA reports)
MENISCUS REMOVAL ( 3 FDA reports)
METABOLIC SYNDROME ( 3 FDA reports)
METASTASES TO BLADDER ( 3 FDA reports)
METASTASIS ( 3 FDA reports)
METRORRHAGIA ( 3 FDA reports)
MICTURITION URGENCY ( 3 FDA reports)
MITRAL VALVE CALCIFICATION ( 3 FDA reports)
MOANING ( 3 FDA reports)
NAIL INFECTION ( 3 FDA reports)
NEPHROPATHY ( 3 FDA reports)
NEPHROSCLEROSIS ( 3 FDA reports)
NEUROMA ( 3 FDA reports)
NEUTROPHIL COUNT DECREASED ( 3 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 3 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 3 FDA reports)
NON-SMALL CELL LUNG CANCER ( 3 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 3 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 3 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 3 FDA reports)
OBSTRUCTIVE UROPATHY ( 3 FDA reports)
OESOPHAGEAL ACHALASIA ( 3 FDA reports)
OESOPHAGEAL PAIN ( 3 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 3 FDA reports)
ONYCHOMADESIS ( 3 FDA reports)
ORAL HERPES ( 3 FDA reports)
OROPHARYNGEAL BLISTERING ( 3 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 3 FDA reports)
OSTEITIS DEFORMANS ( 3 FDA reports)
OSTEORADIONECROSIS ( 3 FDA reports)
PAPILLOEDEMA ( 3 FDA reports)
PAPILLOMA ( 3 FDA reports)
PARAESTHESIA OF GENITAL MALE ( 3 FDA reports)
PARANOID PERSONALITY DISORDER ( 3 FDA reports)
PARKINSON'S DISEASE ( 3 FDA reports)
PARONYCHIA ( 3 FDA reports)
PCO2 INCREASED ( 3 FDA reports)
PERIPHERAL ISCHAEMIA ( 3 FDA reports)
PERITONEAL ADHESIONS ( 3 FDA reports)
PERSECUTORY DELUSION ( 3 FDA reports)
PERSONALITY CHANGE ( 3 FDA reports)
PERSONALITY DISORDER ( 3 FDA reports)
PHANTOM PAIN ( 3 FDA reports)
PIGMENTATION DISORDER ( 3 FDA reports)
PNEUMONIA BACTERIAL ( 3 FDA reports)
PO2 INCREASED ( 3 FDA reports)
POLYDIPSIA ( 3 FDA reports)
PORPHYRIA ( 3 FDA reports)
POST HERPETIC NEURALGIA ( 3 FDA reports)
POST PROCEDURAL FISTULA ( 3 FDA reports)
POSTOPERATIVE ILEUS ( 3 FDA reports)
POSTOPERATIVE INFECTION ( 3 FDA reports)
POTENTIATING DRUG INTERACTION ( 3 FDA reports)
PREMATURE BABY ( 3 FDA reports)
PROCEDURAL COMPLICATION ( 3 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 3 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 3 FDA reports)
PROSTHESIS USER ( 3 FDA reports)
PSYCHIATRIC SYMPTOM ( 3 FDA reports)
PULMONARY INFARCTION ( 3 FDA reports)
PUPIL FIXED ( 3 FDA reports)
PURPURA ( 3 FDA reports)
PYOGENIC GRANULOMA ( 3 FDA reports)
RASH PUSTULAR ( 3 FDA reports)
RASH VESICULAR ( 3 FDA reports)
RECTAL FISSURE ( 3 FDA reports)
RENAL ATROPHY ( 3 FDA reports)
RENAL HYPERTENSION ( 3 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 3 FDA reports)
RETINOPATHY ( 3 FDA reports)
SCHIZOAFFECTIVE DISORDER BIPOLAR TYPE ( 3 FDA reports)
SCHIZOID PERSONALITY DISORDER ( 3 FDA reports)
SCINTILLATING SCOTOMA ( 3 FDA reports)
SCROTAL INFECTION ( 3 FDA reports)
SEPTIC ARTHRITIS STAPHYLOCOCCAL ( 3 FDA reports)
SERUM FERRITIN INCREASED ( 3 FDA reports)
SKIN CHAPPED ( 3 FDA reports)
SKIN FIBROSIS ( 3 FDA reports)
SKULL FRACTURE ( 3 FDA reports)
SPINAL CORPECTOMY ( 3 FDA reports)
SPINAL DECOMPRESSION ( 3 FDA reports)
SPONDYLITIC MYELOPATHY ( 3 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 3 FDA reports)
STATUS EPILEPTICUS ( 3 FDA reports)
STERNAL FRACTURE ( 3 FDA reports)
STOMACH DISCOMFORT ( 3 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 3 FDA reports)
SUBCUTANEOUS NODULE ( 3 FDA reports)
SUBDURAL HAEMATOMA ( 3 FDA reports)
SUICIDAL BEHAVIOUR ( 3 FDA reports)
SUPRAPUBIC PAIN ( 3 FDA reports)
SYNOVITIS ( 3 FDA reports)
TELANGIECTASIA ( 3 FDA reports)
TEMPORAL ARTERITIS ( 3 FDA reports)
TONSILLECTOMY ( 3 FDA reports)
TOXOPLASMOSIS ( 3 FDA reports)
TROPONIN INCREASED ( 3 FDA reports)
UMBILICAL HERNIA REPAIR ( 3 FDA reports)
UNDERDOSE ( 3 FDA reports)
URINARY TRACT DISORDER ( 3 FDA reports)
URINE ODOUR ABNORMAL ( 3 FDA reports)
UTERINE PROLAPSE ( 3 FDA reports)
VASCULAR CALCIFICATION ( 3 FDA reports)
VASCULAR GRAFT OCCLUSION ( 3 FDA reports)
VASCULAR OCCLUSION ( 3 FDA reports)
VENOUS INSUFFICIENCY ( 3 FDA reports)
VENOUS THROMBOSIS LIMB ( 3 FDA reports)
VENTRICULAR ARRHYTHMIA ( 3 FDA reports)
VENTRICULAR FIBRILLATION ( 3 FDA reports)
VERTEBRAL COLUMN MASS ( 3 FDA reports)
VIBRATION TEST ABNORMAL ( 3 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 3 FDA reports)
VITAMIN D DECREASED ( 3 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 3 FDA reports)
WOLFF-PARKINSON-WHITE SYNDROME ( 3 FDA reports)
WOUND COMPLICATION ( 3 FDA reports)
WOUND DRAINAGE ( 3 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 2 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 2 FDA reports)
ACCOMMODATION DISORDER ( 2 FDA reports)
ACUTE CORONARY SYNDROME ( 2 FDA reports)
ACUTE INTERSTITIAL PNEUMONITIS ( 2 FDA reports)
ACUTE LUNG INJURY ( 2 FDA reports)
ADENOMYOSIS ( 2 FDA reports)
ADJUSTMENT DISORDER ( 2 FDA reports)
ADVANCED SLEEP PHASE ( 2 FDA reports)
AKATHISIA ( 2 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 2 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 2 FDA reports)
ALCOHOL POISONING ( 2 FDA reports)
ALCOHOL USE ( 2 FDA reports)
ALCOHOLIC ( 2 FDA reports)
ALCOHOLIC SEIZURE ( 2 FDA reports)
ALCOHOLISM ( 2 FDA reports)
ALLERGIC RESPIRATORY SYMPTOM ( 2 FDA reports)
ALLODYNIA ( 2 FDA reports)
ALVEOLITIS ( 2 FDA reports)
AMENORRHOEA ( 2 FDA reports)
AMPUTATION ( 2 FDA reports)
ANAEMIA POSTOPERATIVE ( 2 FDA reports)
ANAL FISTULA ( 2 FDA reports)
ANALGESIA ( 2 FDA reports)
ANAPHYLACTIC SHOCK ( 2 FDA reports)
ANION GAP DECREASED ( 2 FDA reports)
ANOGENITAL WARTS ( 2 FDA reports)
ANORECTAL DISCOMFORT ( 2 FDA reports)
ANOSOGNOSIA ( 2 FDA reports)
ANTICHOLINERGIC SYNDROME ( 2 FDA reports)
ANTIDEPRESSANT DRUG LEVEL INCREASED ( 2 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 2 FDA reports)
AORTIC ANEURYSM REPAIR ( 2 FDA reports)
AORTIC ELONGATION ( 2 FDA reports)
AORTIC VALVE REPLACEMENT ( 2 FDA reports)
AORTIC VALVE SCLEROSIS ( 2 FDA reports)
AORTIC VALVE STENOSIS ( 2 FDA reports)
APLASIA ( 2 FDA reports)
APPLICATION SITE DISCOLOURATION ( 2 FDA reports)
APPLICATION SITE EROSION ( 2 FDA reports)
APPLICATION SITE REACTION ( 2 FDA reports)
APPLICATION SITE SCAB ( 2 FDA reports)
ARTERIAL DISORDER ( 2 FDA reports)
ASPERGILLOSIS ( 2 FDA reports)
ASTERIXIS ( 2 FDA reports)
ATHEROSCLEROSIS ( 2 FDA reports)
ATRIAL TACHYCARDIA ( 2 FDA reports)
AUTONOMIC NEUROPATHY ( 2 FDA reports)
BACTERIAL DISEASE CARRIER ( 2 FDA reports)
BENIGN NEOPLASM OF BLADDER ( 2 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 2 FDA reports)
BILIARY TRACT DISORDER ( 2 FDA reports)
BIOPSY BONE ABNORMAL ( 2 FDA reports)
BLINDNESS CORTICAL ( 2 FDA reports)
BLOOD BICARBONATE INCREASED ( 2 FDA reports)
BLOOD BLISTER ( 2 FDA reports)
BLOOD CREATININE ABNORMAL ( 2 FDA reports)
BLOOD GASES ABNORMAL ( 2 FDA reports)
BLOOD MAGNESIUM INCREASED ( 2 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 2 FDA reports)
BLOOD UREA DECREASED ( 2 FDA reports)
BLOOD URIC ACID INCREASED ( 2 FDA reports)
BONE MARROW FAILURE ( 2 FDA reports)
BORDERLINE PERSONALITY DISORDER ( 2 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 2 FDA reports)
BRADYARRHYTHMIA ( 2 FDA reports)
BRAIN CONTUSION ( 2 FDA reports)
BRAIN INJURY ( 2 FDA reports)
BRAIN OPERATION ( 2 FDA reports)
BREAKTHROUGH PAIN ( 2 FDA reports)
BREAST DISORDER ( 2 FDA reports)
BREAST NEOPLASM ( 2 FDA reports)
BRONCHIOLITIS ( 2 FDA reports)
BURNING SENSATION MUCOSAL ( 2 FDA reports)
CALCINOSIS ( 2 FDA reports)
CARBUNCLE ( 2 FDA reports)
CARDIAC PACEMAKER INSERTION ( 2 FDA reports)
CARDIAC TAMPONADE ( 2 FDA reports)
CATHETER RELATED INFECTION ( 2 FDA reports)
CELL DEATH ( 2 FDA reports)
CEREBRAL CALCIFICATION ( 2 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 2 FDA reports)
CERVICITIS ( 2 FDA reports)
CERVIX DISORDER ( 2 FDA reports)
CERVIX INFLAMMATION ( 2 FDA reports)
CHOLANGITIS ( 2 FDA reports)
CHOLELITHIASIS OBSTRUCTIVE ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
CHRONIC HEPATIC FAILURE ( 2 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 2 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 2 FDA reports)
CLOSTRIDIUM COLITIS ( 2 FDA reports)
CLUBBING ( 2 FDA reports)
COGWHEEL RIGIDITY ( 2 FDA reports)
COMA SCALE ABNORMAL ( 2 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 2 FDA reports)
CONGENITAL ABSENCE OF CRANIAL VAULT ( 2 FDA reports)
CONGENITAL NYSTAGMUS ( 2 FDA reports)
CONTINUOUS POSITIVE AIRWAY PRESSURE ( 2 FDA reports)
CORNEAL DYSTROPHY ( 2 FDA reports)
CORONARY ANGIOPLASTY ( 2 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 2 FDA reports)
CORONARY ARTERY BYPASS ( 2 FDA reports)
CRYOTHERAPY ( 2 FDA reports)
CYSTITIS INTERSTITIAL ( 2 FDA reports)
CYSTOSCOPY ( 2 FDA reports)
CYTOREDUCTIVE SURGERY ( 2 FDA reports)
DEAFNESS UNILATERAL ( 2 FDA reports)
DEATH OF RELATIVE ( 2 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 2 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 2 FDA reports)
DENTAL CARE ( 2 FDA reports)
DENTAL PULP DISORDER ( 2 FDA reports)
DERMATITIS EXFOLIATIVE ( 2 FDA reports)
DEVICE FAILURE ( 2 FDA reports)
DIABETES INSIPIDUS ( 2 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 2 FDA reports)
DIABETIC COMPLICATION ( 2 FDA reports)
DIABETIC EYE DISEASE ( 2 FDA reports)
DIABETIC FOOT ( 2 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 2 FDA reports)
DIABETIC RETINAL OEDEMA ( 2 FDA reports)
DISLOCATION OF VERTEBRA ( 2 FDA reports)
DIZZINESS POSTURAL ( 2 FDA reports)
DRUG DELIVERY DEVICE IMPLANTATION ( 2 FDA reports)
DRUG EFFECT INCREASED ( 2 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
DRUG LEVEL CHANGED ( 2 FDA reports)
DRUG TOLERANCE DECREASED ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 2 FDA reports)
DUODENAL POLYP ( 2 FDA reports)
EAR INFECTION ( 2 FDA reports)
EAR OPERATION ( 2 FDA reports)
EJECTION FRACTION ( 2 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 2 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 2 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 2 FDA reports)
ENAMEL ANOMALY ( 2 FDA reports)
ENCEPHALITIS VIRAL ( 2 FDA reports)
ENCEPHALOMALACIA ( 2 FDA reports)
ENDOMETRIOSIS ( 2 FDA reports)
ENERGY INCREASED ( 2 FDA reports)
ENTERITIS INFECTIOUS ( 2 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 2 FDA reports)
ENTEROCUTANEOUS FISTULA ( 2 FDA reports)
EOSINOPHIL COUNT INCREASED ( 2 FDA reports)
ERYTHEMA NODOSUM ( 2 FDA reports)
ESCHERICHIA INFECTION ( 2 FDA reports)
ESCHERICHIA TEST POSITIVE ( 2 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 2 FDA reports)
EXERCISE TOLERANCE DECREASED ( 2 FDA reports)
EXPIRED DRUG ADMINISTERED ( 2 FDA reports)
EXPLORATIVE LAPAROTOMY ( 2 FDA reports)
EXPOSED BONE IN JAW ( 2 FDA reports)
EXTERNAL EAR PAIN ( 2 FDA reports)
EXTREMITY NECROSIS ( 2 FDA reports)
EYE PRURITUS ( 2 FDA reports)
FAECAL VOMITING ( 2 FDA reports)
FEBRILE NONHAEMOLYTIC TRANSFUSION REACTION ( 2 FDA reports)
FISTULA DISCHARGE ( 2 FDA reports)
FLAT ANTERIOR CHAMBER OF EYE ( 2 FDA reports)
FLUID REPLACEMENT ( 2 FDA reports)
FOOT OPERATION ( 2 FDA reports)
FOREIGN BODY ( 2 FDA reports)
FRACTURE NONUNION ( 2 FDA reports)
FRACTURED SACRUM ( 2 FDA reports)
GAIT SPASTIC ( 2 FDA reports)
GASTRIC DILATATION ( 2 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 2 FDA reports)
GASTROINTESTINAL BACTERIAL INFECTION ( 2 FDA reports)
GASTROINTESTINAL PAIN ( 2 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 2 FDA reports)
GASTROSTOMY TUBE INSERTION ( 2 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 2 FDA reports)
GINGIVAL ATROPHY ( 2 FDA reports)
GINGIVAL ERYTHEMA ( 2 FDA reports)
GINGIVAL RECESSION ( 2 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 2 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 2 FDA reports)
GRIP STRENGTH DECREASED ( 2 FDA reports)
GUN SHOT WOUND ( 2 FDA reports)
HAEMATOCRIT INCREASED ( 2 FDA reports)
HAEMATOLOGICAL MALIGNANCY ( 2 FDA reports)
HAEMOPHILUS INFECTION ( 2 FDA reports)
HAEMORRHAGIC CYST ( 2 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 2 FDA reports)
HAIR COLOUR CHANGES ( 2 FDA reports)
HAND-FOOT-AND-MOUTH DISEASE ( 2 FDA reports)
HEMIANOPIA ( 2 FDA reports)
HEPATIC FIBROSIS ( 2 FDA reports)
HEPATIC NECROSIS ( 2 FDA reports)
HEPATITIS CHOLESTATIC ( 2 FDA reports)
HERPES ZOSTER DISSEMINATED ( 2 FDA reports)
HIP DEFORMITY ( 2 FDA reports)
HIP DYSPLASIA ( 2 FDA reports)
HUMERUS FRACTURE ( 2 FDA reports)
HYDROCEPHALUS ( 2 FDA reports)
HYPERACUSIS ( 2 FDA reports)
HYPERBILIRUBINAEMIA NEONATAL ( 2 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 2 FDA reports)
HYPERREFLEXIA ( 2 FDA reports)
HYPERTENSIVE CRISIS ( 2 FDA reports)
HYPERTHYROIDISM ( 2 FDA reports)
HYPERTONIA ( 2 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 2 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 2 FDA reports)
HYPOPERFUSION ( 2 FDA reports)
HYPOPROTEINAEMIA ( 2 FDA reports)
HYPOTHALAMO-PITUITARY DISORDER ( 2 FDA reports)
ILIUM FRACTURE ( 2 FDA reports)
IMMUNODEFICIENCY ( 2 FDA reports)
IMMUNOGLOBULINS DECREASED ( 2 FDA reports)
IMPLANT SITE PAIN ( 2 FDA reports)
INCISION SITE HAEMORRHAGE ( 2 FDA reports)
INCISION SITE INFECTION ( 2 FDA reports)
INDURATION ( 2 FDA reports)
INFECTED NEOPLASM ( 2 FDA reports)
INFECTED SKIN ULCER ( 2 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 2 FDA reports)
INJECTION SITE EXTRAVASATION ( 2 FDA reports)
INJECTION SITE NECROSIS ( 2 FDA reports)
INJECTION SITE NODULE ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 2 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 2 FDA reports)
INTESTINAL DILATATION ( 2 FDA reports)
IRIS CYST ( 2 FDA reports)
JAUNDICE NEONATAL ( 2 FDA reports)
JOINT CONTRACTURE ( 2 FDA reports)
JOINT CREPITATION ( 2 FDA reports)
JOINT LOCK ( 2 FDA reports)
KLEBSIELLA TEST POSITIVE ( 2 FDA reports)
LAPAROTOMY ( 2 FDA reports)
LARGE FOR DATES BABY ( 2 FDA reports)
LEIOMYOMA ( 2 FDA reports)
LEUKAEMIA ( 2 FDA reports)
LEUKOPLAKIA ORAL ( 2 FDA reports)
LHERMITTE'S SIGN ( 2 FDA reports)
LICHEN PLANUS ( 2 FDA reports)
LICHENIFICATION ( 2 FDA reports)
LIGAMENT INJURY ( 2 FDA reports)
LIMB DEFORMITY ( 2 FDA reports)
LIP OEDEMA ( 2 FDA reports)
LIPIDS INCREASED ( 2 FDA reports)
LIVEDO RETICULARIS ( 2 FDA reports)
LORDOSIS ( 2 FDA reports)
LOSS OF EMPLOYMENT ( 2 FDA reports)
LOW DENSITY LIPOPROTEIN ABNORMAL ( 2 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
LUDWIG ANGINA ( 2 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 2 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE 0 ( 2 FDA reports)
LUNG CONSOLIDATION ( 2 FDA reports)
LUPUS-LIKE SYNDROME ( 2 FDA reports)
MACULAR OEDEMA ( 2 FDA reports)
MACULAR REFLEX ABNORMAL ( 2 FDA reports)
MALIGNANT TUMOUR EXCISION ( 2 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 2 FDA reports)
MEAN CELL VOLUME INCREASED ( 2 FDA reports)
MECHANICAL VENTILATION ( 2 FDA reports)
MECHANICAL VENTILATION COMPLICATION ( 2 FDA reports)
MEDIASTINAL DISORDER ( 2 FDA reports)
MEDICAL DEVICE REMOVAL ( 2 FDA reports)
MEDICAL INDUCTION OF COMA ( 2 FDA reports)
MENINGITIS ASEPTIC ( 2 FDA reports)
MENINGITIS CHEMICAL ( 2 FDA reports)
MENOPAUSAL SYMPTOMS ( 2 FDA reports)
MENSTRUATION IRREGULAR ( 2 FDA reports)
METAPLASIA ( 2 FDA reports)
MITOCHONDRIAL TOXICITY ( 2 FDA reports)
MOLE EXCISION ( 2 FDA reports)
MONOCYTE COUNT INCREASED ( 2 FDA reports)
MOTOR NEURONE DISEASE ( 2 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 2 FDA reports)
MUSCLE CRAMP ( 2 FDA reports)
MUSCLE DISORDER ( 2 FDA reports)
MUSCLE NECROSIS ( 2 FDA reports)
MUSCLE SPASTICITY ( 2 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 2 FDA reports)
MYELOMA RECURRENCE ( 2 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 2 FDA reports)
NEONATAL RESPIRATORY DEPRESSION ( 2 FDA reports)
NEOPLASM SKIN ( 2 FDA reports)
NEPHROCALCINOSIS ( 2 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 2 FDA reports)
NO THERAPEUTIC RESPONSE ( 2 FDA reports)
NODULE ON EXTREMITY ( 2 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 2 FDA reports)
OESOPHAGEAL DISCOMFORT ( 2 FDA reports)
OESOPHAGEAL DISORDER ( 2 FDA reports)
OESOPHAGEAL RUPTURE ( 2 FDA reports)
OESOPHAGEAL STENOSIS ( 2 FDA reports)
OLIGODENDROGLIOMA ( 2 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 2 FDA reports)
ORGANISING PNEUMONIA ( 2 FDA reports)
OTOTOXICITY ( 2 FDA reports)
OVARIAN INFECTION ( 2 FDA reports)
OVERWEIGHT ( 2 FDA reports)
PARACHUTE MITRAL VALVE ( 2 FDA reports)
PARTNER STRESS ( 2 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 2 FDA reports)
PEAU D'ORANGE ( 2 FDA reports)
PERCUTANEOUS CORONARY INTERVENTION ( 2 FDA reports)
PERICARDIAL DISEASE ( 2 FDA reports)
PERINEPHRIC COLLECTION ( 2 FDA reports)
PERIORBITAL OEDEMA ( 2 FDA reports)
PERIPHERAL EMBOLISM ( 2 FDA reports)
PERIPHERAL NERVE DECOMPRESSION ( 2 FDA reports)
PERITONITIS ( 2 FDA reports)
PERITONITIS BACTERIAL ( 2 FDA reports)
PERNICIOUS ANAEMIA ( 2 FDA reports)
PERSISTENT FOETAL CIRCULATION ( 2 FDA reports)
PETECHIAE ( 2 FDA reports)
PHARYNGEAL DISORDER ( 2 FDA reports)
PHLEBITIS SUPERFICIAL ( 2 FDA reports)
PHYSIOTHERAPY ( 2 FDA reports)
PIRIFORMIS SYNDROME ( 2 FDA reports)
PLANTAR FASCIITIS ( 2 FDA reports)
PLATELET COUNT ABNORMAL ( 2 FDA reports)
PLEOCYTOSIS ( 2 FDA reports)
PNEUMONIA MYCOPLASMAL ( 2 FDA reports)
PO2 DECREASED ( 2 FDA reports)
POLYARTHRITIS ( 2 FDA reports)
POLYP COLORECTAL ( 2 FDA reports)
POOR DENTAL CONDITION ( 2 FDA reports)
PORTAL VEIN THROMBOSIS ( 2 FDA reports)
POSTOPERATIVE FEVER ( 2 FDA reports)
POSTURING ( 2 FDA reports)
PRESBYOESOPHAGUS ( 2 FDA reports)
PRIAPISM ( 2 FDA reports)
PROCEDURAL NAUSEA ( 2 FDA reports)
PRODUCT COUNTERFEIT ( 2 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 2 FDA reports)
PROSTATITIS ( 2 FDA reports)
PROSTHESIS IMPLANTATION ( 2 FDA reports)
PROTEIN C INCREASED ( 2 FDA reports)
PROTEIN S DECREASED ( 2 FDA reports)
PROTEIN-LOSING GASTROENTEROPATHY ( 2 FDA reports)
PROTHROMBIN TIME SHORTENED ( 2 FDA reports)
PROTRUSION TONGUE ( 2 FDA reports)
PTERYGIUM ( 2 FDA reports)
PULMONARY HAEMORRHAGE ( 2 FDA reports)
PULMONARY MYCOSIS ( 2 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 2 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 2 FDA reports)
PYELOCALIECTASIS ( 2 FDA reports)
RADIATION OESOPHAGITIS ( 2 FDA reports)
RADICULAR PAIN ( 2 FDA reports)
RADICULITIS ( 2 FDA reports)
RADICULITIS LUMBOSACRAL ( 2 FDA reports)
RASH PAPULOSQUAMOUS ( 2 FDA reports)
RAYNAUD'S PHENOMENON ( 2 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 2 FDA reports)
REFLUX LARYNGITIS ( 2 FDA reports)
RELAPSING-REMITTING MULTIPLE SCLEROSIS ( 2 FDA reports)
RENAL APLASIA ( 2 FDA reports)
RENAL CELL CARCINOMA ( 2 FDA reports)
RENAL HYPOPLASIA ( 2 FDA reports)
RENAL ONCOCYTOMA ( 2 FDA reports)
RENAL TUBULAR DISORDER ( 2 FDA reports)
RESPIRATION ABNORMAL ( 2 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS BRONCHIOLITIS ( 2 FDA reports)
RESPIRATORY TRACT CONGESTION ( 2 FDA reports)
RETINAL DISORDER ( 2 FDA reports)
RETINAL DYSTROPHY ( 2 FDA reports)
RETINAL HAEMORRHAGE ( 2 FDA reports)
RETINAL VASCULAR DISORDER ( 2 FDA reports)
RETROPERITONEAL HAEMATOMA ( 2 FDA reports)
RHEUMATOID FACTOR INCREASED ( 2 FDA reports)
RIGHT ATRIAL DILATATION ( 2 FDA reports)
SALPINGITIS ( 2 FDA reports)
SCROTAL SWELLING ( 2 FDA reports)
SEBORRHOEIC KERATOSIS ( 2 FDA reports)
SENSITIVITY OF TEETH ( 2 FDA reports)
SEROCONVERSION TEST POSITIVE ( 2 FDA reports)
SHOULDER OPERATION ( 2 FDA reports)
SINUS ARREST ( 2 FDA reports)
SKELETAL INJURY ( 2 FDA reports)
SKIN HYPERPIGMENTATION ( 2 FDA reports)
SKIN NODULE ( 2 FDA reports)
SKIN OEDEMA ( 2 FDA reports)
SKIN WARM ( 2 FDA reports)
SLUGGISHNESS ( 2 FDA reports)
SMEAR CERVIX ABNORMAL ( 2 FDA reports)
SOMATOFORM DISORDER ( 2 FDA reports)
SPINAL FUSION ACQUIRED ( 2 FDA reports)
SPINAL NERVE STIMULATOR IMPLANTATION ( 2 FDA reports)
SPINAL OPERATION ( 2 FDA reports)
SPINAL X-RAY ABNORMAL ( 2 FDA reports)
SPLEEN CONGESTION ( 2 FDA reports)
SPLENIC INFARCTION ( 2 FDA reports)
SPUTUM CULTURE POSITIVE ( 2 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 2 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 2 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 2 FDA reports)
STRABISMUS ( 2 FDA reports)
STREPTOCOCCAL INFECTION ( 2 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 2 FDA reports)
SUBDURAL HAEMORRHAGE ( 2 FDA reports)
SUBSTANCE ABUSE ( 2 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 2 FDA reports)
TANDEM GAIT TEST ABNORMAL ( 2 FDA reports)
TEMPORAL LOBE EPILEPSY ( 2 FDA reports)
TOE AMPUTATION ( 2 FDA reports)
TONGUE DRY ( 2 FDA reports)
TONGUE INJURY ( 2 FDA reports)
TONGUE SPASM ( 2 FDA reports)
TONSILLAR DISORDER ( 2 FDA reports)
TOOTH DEPOSIT ( 2 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 2 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 2 FDA reports)
TRAUMATIC BRAIN INJURY ( 2 FDA reports)
TRIGGER FINGER ( 2 FDA reports)
TUNNEL VISION ( 2 FDA reports)
UHTHOFF'S PHENOMENON ( 2 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 2 FDA reports)
URETHRAL DISORDER ( 2 FDA reports)
URETHRITIS ( 2 FDA reports)
UROSEPSIS ( 2 FDA reports)
UTERINE CANCER ( 2 FDA reports)
UTERINE HAEMORRHAGE ( 2 FDA reports)
UTERINE INFECTION ( 2 FDA reports)
UVEITIS ( 2 FDA reports)
VARICOSE VEIN ( 2 FDA reports)
VASCULITIC RASH ( 2 FDA reports)
VASOCONSTRICTION ( 2 FDA reports)
VENOUS THROMBOSIS ( 2 FDA reports)
VENTRICULAR DYSFUNCTION ( 2 FDA reports)
VERTEBROPLASTY ( 2 FDA reports)
VIRAL RASH ( 2 FDA reports)
VULVOVAGINAL PAIN ( 2 FDA reports)
WHIPLASH INJURY ( 2 FDA reports)
WOUND INFECTION ( 2 FDA reports)
WOUND INFECTION BACTERIAL ( 2 FDA reports)
WRIST DEFORMITY ( 2 FDA reports)
YELLOW SKIN ( 2 FDA reports)
ABDOMINAL ADHESIONS ( 1 FDA reports)
ABDOMINAL INFECTION ( 1 FDA reports)
ABDOMINAL WALL ABSCESS ( 1 FDA reports)
ABNORMAL CLOTTING FACTOR ( 1 FDA reports)
ABNORMAL WEIGHT GAIN ( 1 FDA reports)
ABORTION ( 1 FDA reports)
ABSCESS INTESTINAL ( 1 FDA reports)
ACCELERATED HYPERTENSION ( 1 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACCIDENTAL NEEDLE STICK ( 1 FDA reports)
ACNE CYSTIC ( 1 FDA reports)
ACQUIRED CARDIAC SEPTAL DEFECT ( 1 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 1 FDA reports)
ACUTE PHOSPHATE NEPHROPATHY ( 1 FDA reports)
ACUTE POLYNEUROPATHY ( 1 FDA reports)
ADENOCARCINOMA ( 1 FDA reports)
ADENOMA BENIGN ( 1 FDA reports)
ADMINISTRATION SITE PAIN ( 1 FDA reports)
ADNEXA UTERI MASS ( 1 FDA reports)
ADNEXA UTERI PAIN ( 1 FDA reports)
ADRENAL DISORDER ( 1 FDA reports)
ADRENAL MASS ( 1 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 1 FDA reports)
ADRENOMEGALY ( 1 FDA reports)
AGITATED DEPRESSION ( 1 FDA reports)
AGORAPHOBIA ( 1 FDA reports)
AKINESIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ( 1 FDA reports)
ALCOHOL ABUSE ( 1 FDA reports)
ALCOHOL INTERACTION ( 1 FDA reports)
ALCOHOL PROBLEM ( 1 FDA reports)
ALOPECIA AREATA ( 1 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 1 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 1 FDA reports)
ALVEOLAR OSTEITIS ( 1 FDA reports)
AMBLYOPIA ( 1 FDA reports)
AMPUTATION STUMP PAIN ( 1 FDA reports)
ANAESTHESIA ( 1 FDA reports)
ANDROGEN DEFICIENCY ( 1 FDA reports)
ANGIOLIPOMA ( 1 FDA reports)
ANGIOMYOLIPOMA ( 1 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 1 FDA reports)
ANIMAL SCRATCH ( 1 FDA reports)
ANION GAP INCREASED ( 1 FDA reports)
ANKYLOSING SPONDYLITIS ( 1 FDA reports)
ANORGASMIA ( 1 FDA reports)
ANOXIA ( 1 FDA reports)
ANTEPARTUM HAEMORRHAGE ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 1 FDA reports)
ANTINUCLEAR ANTIBODY ( 1 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 1 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 1 FDA reports)
ANTISOCIAL PERSONALITY DISORDER ( 1 FDA reports)
ANXIETY DISORDER ( 1 FDA reports)
AORTIC ATHEROSCLEROSIS ( 1 FDA reports)
AORTIC DILATATION ( 1 FDA reports)
AORTIC DISSECTION ( 1 FDA reports)
AORTIC OCCLUSION ( 1 FDA reports)
AORTIC VALVE DISEASE ( 1 FDA reports)
APLASIA PURE RED CELL ( 1 FDA reports)
APNOEIC ATTACK ( 1 FDA reports)
APPARENT DEATH ( 1 FDA reports)
APPARENT LIFE THREATENING EVENT ( 1 FDA reports)
APPENDICECTOMY ( 1 FDA reports)
APPLICATION SITE DERMATITIS ( 1 FDA reports)
APPLICATION SITE PRURITUS ( 1 FDA reports)
APPLICATION SITE URTICARIA ( 1 FDA reports)
ARACHNOIDITIS ( 1 FDA reports)
ARNOLD-CHIARI MALFORMATION ( 1 FDA reports)
ARTERIAL HAEMORRHAGE ( 1 FDA reports)
ARTERIOGRAM CORONARY ( 1 FDA reports)
ARTERIOVENOUS SHUNT OPERATION ( 1 FDA reports)
ARTERY DISSECTION ( 1 FDA reports)
ARTHRITIS BACTERIAL ( 1 FDA reports)
ASEPTIC NECROSIS BONE ( 1 FDA reports)
ASPHYXIA ( 1 FDA reports)
ASPIRATION BRONCHIAL ( 1 FDA reports)
ATRIAL CONDUCTION TIME PROLONGATION ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
ATRIOVENTRICULAR DISSOCIATION ( 1 FDA reports)
AXILLARY MASS ( 1 FDA reports)
AXONAL NEUROPATHY ( 1 FDA reports)
B-CELL LYMPHOMA ( 1 FDA reports)
B-CELL LYMPHOMA STAGE III ( 1 FDA reports)
BACILLUS INFECTION ( 1 FDA reports)
BACTERIURIA ( 1 FDA reports)
BASEDOW'S DISEASE ( 1 FDA reports)
BENIGN CARDIAC NEOPLASM ( 1 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 1 FDA reports)
BENIGN OVARIAN TUMOUR ( 1 FDA reports)
BENIGN SMALL INTESTINAL NEOPLASM ( 1 FDA reports)
BILIARY DILATATION ( 1 FDA reports)
BIOPSY BREAST ( 1 FDA reports)
BIPOLAR I DISORDER ( 1 FDA reports)
BLADDER NEOPLASM ( 1 FDA reports)
BLAST CELL PROLIFERATION ( 1 FDA reports)
BLEPHARITIS ( 1 FDA reports)
BLIGHTED OVUM ( 1 FDA reports)
BLINDNESS CONGENITAL ( 1 FDA reports)
BLISTER INFECTED ( 1 FDA reports)
BLOOD ACID PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD ALBUMIN INCREASED ( 1 FDA reports)
BLOOD ALCOHOL INCREASED ( 1 FDA reports)
BLOOD ALDOSTERONE INCREASED ( 1 FDA reports)
BLOOD CALCIUM ABNORMAL ( 1 FDA reports)
BLOOD CHLORIDE INCREASED ( 1 FDA reports)
BLOOD CHOLINESTERASE INCREASED ( 1 FDA reports)
BLOOD CORTICOTROPHIN INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 1 FDA reports)
BLOOD FOLATE DECREASED ( 1 FDA reports)
BLOOD HOMOCYSTEINE DECREASED ( 1 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
BLOOD PARATHYROID HORMONE DECREASED ( 1 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD SODIUM ABNORMAL ( 1 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 1 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO DECREASED ( 1 FDA reports)
BLOOD URIC ACID DECREASED ( 1 FDA reports)
BLOOD URINE ( 1 FDA reports)
BONE MARROW DISORDER ( 1 FDA reports)
BONE METABOLISM DISORDER ( 1 FDA reports)
BONE NEOPLASM ( 1 FDA reports)
BONE OPERATION ( 1 FDA reports)
BONE SARCOMA ( 1 FDA reports)
BOWEL SOUNDS ABNORMAL ( 1 FDA reports)
BOWEN'S DISEASE ( 1 FDA reports)
BRADYKINESIA ( 1 FDA reports)
BRADYPHRENIA ( 1 FDA reports)
BRAIN DAMAGE ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
BRAIN MIDLINE SHIFT ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BREAST CANCER STAGE I ( 1 FDA reports)
BREAST COSMETIC SURGERY ( 1 FDA reports)
BREAST CYST ( 1 FDA reports)
BREAST HYPERPLASIA ( 1 FDA reports)
BREAST MASS ( 1 FDA reports)
BREAST PROSTHESIS IMPLANTATION ( 1 FDA reports)
BREAST RECONSTRUCTION ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
BRONCHIAL CARCINOMA ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ALLERGIC ( 1 FDA reports)
BURN OF INTERNAL ORGANS ( 1 FDA reports)
CAECITIS ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CANCER PAIN ( 1 FDA reports)
CANDIDA TEST POSITIVE ( 1 FDA reports)
CAPILLARY LEAK SYNDROME ( 1 FDA reports)
CAPSULE PHYSICAL ISSUE ( 1 FDA reports)
CARCINOMA IN SITU OF SKIN ( 1 FDA reports)
CARDIAC AMYLOIDOSIS ( 1 FDA reports)
CARDIAC DISCOMFORT ( 1 FDA reports)
CARDIAC HYPERTROPHY ( 1 FDA reports)
CARDIAC OPERATION ( 1 FDA reports)
CARDIAC SEPTAL DEFECT ( 1 FDA reports)
CARDIAC STRESS TEST ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 1 FDA reports)
CARDIOPULMONARY FAILURE ( 1 FDA reports)
CARDIOTOXICITY ( 1 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 1 FDA reports)
CAROTIDYNIA ( 1 FDA reports)
CATARACT OPERATION ( 1 FDA reports)
CATHETER SITE INFECTION ( 1 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 1 FDA reports)
CELLULITIS ORBITAL ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 1 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 1 FDA reports)
CEREBRAL ATHEROSCLEROSIS ( 1 FDA reports)
CEREBRAL CYST ( 1 FDA reports)
CEREBRAL HAEMATOMA ( 1 FDA reports)
CEREBRAL MICROANGIOPATHY ( 1 FDA reports)
CEREBRAL PALSY ( 1 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 1 FDA reports)
CERVICAL MYELOPATHY ( 1 FDA reports)
CHEMICAL POISONING ( 1 FDA reports)
CHEST WALL OPERATION ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHONDROPATHY ( 1 FDA reports)
CHROMOSOME ANALYSIS ABNORMAL ( 1 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 1 FDA reports)
CHRONIC RESPIRATORY DISEASE ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE SEPSIS ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST ( 1 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 1 FDA reports)
COAGULATION TIME PROLONGED ( 1 FDA reports)
COLON CANCER METASTATIC ( 1 FDA reports)
COLON INJURY ( 1 FDA reports)
COLONIC FISTULA ( 1 FDA reports)
COLONOSCOPY ABNORMAL ( 1 FDA reports)
COLORECTAL CANCER METASTATIC ( 1 FDA reports)
COLOSTOMY CLOSURE ( 1 FDA reports)
COLOUR VISION TESTS ABNORMAL ( 1 FDA reports)
COMPARTMENT SYNDROME ( 1 FDA reports)
COMPULSIVE SHOPPING ( 1 FDA reports)
CONJUNCTIVAL EROSION ( 1 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 1 FDA reports)
CONSTRICTED AFFECT ( 1 FDA reports)
COR PULMONALE CHRONIC ( 1 FDA reports)
CORNEAL IMPLANT ( 1 FDA reports)
CORNEAL OPACITY ( 1 FDA reports)
CRYPTOCOCCOSIS ( 1 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 1 FDA reports)
CSF PRESSURE INCREASED ( 1 FDA reports)
CSF PROTEIN INCREASED ( 1 FDA reports)
CSF TEST ABNORMAL ( 1 FDA reports)
CUTANEOUS VASCULITIS ( 1 FDA reports)
CYSTITIS HAEMORRHAGIC ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DAYDREAMING ( 1 FDA reports)
DEATH NEONATAL ( 1 FDA reports)
DELUSIONAL PERCEPTION ( 1 FDA reports)
DENERVATION ATROPHY ( 1 FDA reports)
DENTAL DISCOMFORT ( 1 FDA reports)
DEPENDENCE ON ENABLING MACHINE OR DEVICE ( 1 FDA reports)
DEPENDENT PERSONALITY DISORDER ( 1 FDA reports)
DEPRESSION SUICIDAL ( 1 FDA reports)
DERMATITIS ATOPIC ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DERMATITIS HERPETIFORMIS ( 1 FDA reports)
DETOXIFICATION ( 1 FDA reports)
DEVELOPMENTAL DELAY ( 1 FDA reports)
DEVICE BREAKAGE ( 1 FDA reports)
DEVICE COMPONENT ISSUE ( 1 FDA reports)
DEVICE LEAKAGE ( 1 FDA reports)
DIABETIC AMYOTROPHY ( 1 FDA reports)
DIABETIC CARDIOMYOPATHY ( 1 FDA reports)
DIABETIC GASTROPARESIS ( 1 FDA reports)
DIABETIC NEUROPATHIC ULCER ( 1 FDA reports)
DIABETIC ULCER ( 1 FDA reports)
DIAPHRAGMATIC HERNIA ( 1 FDA reports)
DIET REFUSAL ( 1 FDA reports)
DIEULAFOY'S VASCULAR MALFORMATION ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DISSEMINATED TUBERCULOSIS ( 1 FDA reports)
DISSOCIATIVE DISORDER ( 1 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DNA ANTIBODY POSITIVE ( 1 FDA reports)
DROP ATTACKS ( 1 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG DIVERSION ( 1 FDA reports)
DRUG THERAPEUTIC INCOMPATIBILITY ( 1 FDA reports)
DRUG TOLERANCE ( 1 FDA reports)
DRUG TOLERANCE INCREASED ( 1 FDA reports)
DRY GANGRENE ( 1 FDA reports)
DUODENAL NEOPLASM ( 1 FDA reports)
DUODENAL STENOSIS ( 1 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 1 FDA reports)
DYSAESTHESIA ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DYSPLASTIC NAEVUS ( 1 FDA reports)
DYSPLASTIC NAEVUS SYNDROME ( 1 FDA reports)
DYSTHYMIC DISORDER ( 1 FDA reports)
EAR INFECTION VIRAL ( 1 FDA reports)
EARLY MORNING AWAKENING ( 1 FDA reports)
ECTOPIC PREGNANCY ( 1 FDA reports)
EJECTION FRACTION ABNORMAL ( 1 FDA reports)
ELECTRIC SHOCK ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 1 FDA reports)
EMBOLIC STROKE ( 1 FDA reports)
EMPYEMA ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
ENDOMETRIAL CANCER ( 1 FDA reports)
ENDOMETRIAL CANCER STAGE II ( 1 FDA reports)
ENTEROBACTER INFECTION ( 1 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 1 FDA reports)
ENTHESOPATHY ( 1 FDA reports)
ENURESIS ( 1 FDA reports)
EPICONDYLITIS ( 1 FDA reports)
EPIGASTRIC DISCOMFORT ( 1 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 1 FDA reports)
EROSIVE DUODENITIS ( 1 FDA reports)
ERYTHEMA INFECTIOSUM ( 1 FDA reports)
ESCHERICHIA BACTERAEMIA ( 1 FDA reports)
ESCHERICHIA SEPSIS ( 1 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 1 FDA reports)
EXECUTIVE DYSFUNCTION ( 1 FDA reports)
EXERCISE LACK OF ( 1 FDA reports)
EXOPHTHALMOS ( 1 FDA reports)
EXPOSURE TO TOXIC AGENT ( 1 FDA reports)
EXTERNAL EAR CELLULITIS ( 1 FDA reports)
EYE DISCHARGE ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
EYE INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
EYE OEDEMA ( 1 FDA reports)
EYELID PTOSIS ( 1 FDA reports)
EYES SUNKEN ( 1 FDA reports)
FACE INJURY ( 1 FDA reports)
FACIAL WASTING ( 1 FDA reports)
FAILURE TO THRIVE ( 1 FDA reports)
FALSE POSITIVE INVESTIGATION RESULT ( 1 FDA reports)
FAT TISSUE INCREASED ( 1 FDA reports)
FEBRILE INFECTION ( 1 FDA reports)
FEEDING DISORDER ( 1 FDA reports)
FEMALE SEXUAL DYSFUNCTION ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FLAT AFFECT ( 1 FDA reports)
FLIGHT OF IDEAS ( 1 FDA reports)
FOETAL DISTRESS SYNDROME ( 1 FDA reports)
FOLLICLE CENTRE LYMPHOMA, FOLLICULAR GRADE I, II, III STAGE IV ( 1 FDA reports)
FOOD ALLERGY ( 1 FDA reports)
FOOD INTERACTION ( 1 FDA reports)
FOOT AMPUTATION ( 1 FDA reports)
FOREARM FRACTURE ( 1 FDA reports)
FOREIGN BODY ASPIRATION ( 1 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 1 FDA reports)
FRACTURED COCCYX ( 1 FDA reports)
FUNGAL PERITONITIS ( 1 FDA reports)
FUNGAL SKIN INFECTION ( 1 FDA reports)
FUNGUS CULTURE POSITIVE ( 1 FDA reports)
GALLBLADDER OPERATION ( 1 FDA reports)
GALLBLADDER PAIN ( 1 FDA reports)
GALLBLADDER PERFORATION ( 1 FDA reports)
GAMMOPATHY ( 1 FDA reports)
GASTRECTOMY ( 1 FDA reports)
GASTRIC POLYPS ( 1 FDA reports)
GASTRIC VARICES ( 1 FDA reports)
GASTROENTERITIS RADIATION ( 1 FDA reports)
GASTROINTESTINAL CARCINOMA ( 1 FDA reports)
GASTROINTESTINAL HYPERMOTILITY ( 1 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 1 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 1 FDA reports)
GASTROINTESTINAL ULCER ( 1 FDA reports)
GENERALISED ANXIETY DISORDER ( 1 FDA reports)
GENITAL BURNING SENSATION ( 1 FDA reports)
GENITAL EROSION ( 1 FDA reports)
GINGIVAL HYPERPLASIA ( 1 FDA reports)
GLIOBLASTOMA ( 1 FDA reports)
GLOBULINS INCREASED ( 1 FDA reports)
GLOSSOPTOSIS ( 1 FDA reports)
GLUCOSE TOLERANCE DECREASED ( 1 FDA reports)
GLUCOSE URINE ( 1 FDA reports)
GLYCOPEPTIDE ANTIBIOTIC RESISTANT ENTEROCOCCAL INFECTION ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
GRANULOCYTOSIS ( 1 FDA reports)
GRIEF REACTION ( 1 FDA reports)
GROWTH HORMONE DEFICIENCY ( 1 FDA reports)
GROWTH RETARDATION ( 1 FDA reports)
HAEMARTHROSIS ( 1 FDA reports)
HAEMOCHROMATOSIS ( 1 FDA reports)
HAEMOGLOBIN S DECREASED ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HAEMORRHAGE URINARY TRACT ( 1 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 1 FDA reports)
HAIR DISORDER ( 1 FDA reports)
HAIR GROWTH ABNORMAL ( 1 FDA reports)
HAIR TEXTURE ABNORMAL ( 1 FDA reports)
HALLUCINATION, TACTILE ( 1 FDA reports)
HEART INJURY ( 1 FDA reports)
HELICOBACTER TEST POSITIVE ( 1 FDA reports)
HEMIANOPIA HOMONYMOUS ( 1 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 1 FDA reports)
HEPATIC CALCIFICATION ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HEPATIC INFARCTION ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 1 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS ALCOHOLIC ( 1 FDA reports)
HEPATITIS CHRONIC ACTIVE ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HEPATORENAL FAILURE ( 1 FDA reports)
HEPATORENAL SYNDROME ( 1 FDA reports)
HERNIA REPAIR ( 1 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
HISTONE ANTIBODY POSITIVE ( 1 FDA reports)
HISTOPLASMOSIS ( 1 FDA reports)
HISTOPLASMOSIS DISSEMINATED ( 1 FDA reports)
HIV INFECTION ( 1 FDA reports)
HODGKIN'S DISEASE STAGE IV ( 1 FDA reports)
HOMICIDE ( 1 FDA reports)
HOMOCYSTINAEMIA ( 1 FDA reports)
HORMONE LEVEL ABNORMAL ( 1 FDA reports)
HORNER'S SYNDROME ( 1 FDA reports)
HOSPICE CARE ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 1 FDA reports)
HYPERGAMMAGLOBULINAEMIA BENIGN MONOCLONAL ( 1 FDA reports)
HYPERMETROPIA ( 1 FDA reports)
HYPEROSMOLAR STATE ( 1 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 1 FDA reports)
HYPERPHOSPHATAEMIA ( 1 FDA reports)
HYPERPLASTIC CHOLECYSTOPATHY ( 1 FDA reports)
HYPERPROLACTINAEMIA ( 1 FDA reports)
HYPERTHERMIA MALIGNANT ( 1 FDA reports)
HYPERTROPHY BREAST ( 1 FDA reports)
HYPERVISCOSITY SYNDROME ( 1 FDA reports)
HYPOCHOLESTEROLAEMIA ( 1 FDA reports)
HYPOCHONDRIASIS ( 1 FDA reports)
HYPOGONADISM ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOMENORRHOEA ( 1 FDA reports)
HYPOPLASTIC LEFT HEART SYNDROME ( 1 FDA reports)
HYPOSPADIAS ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
HYPOVOLAEMIC SHOCK ( 1 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
ILEITIS ( 1 FDA reports)
ILLUSION ( 1 FDA reports)
IMMINENT ABORTION ( 1 FDA reports)
IMMUNOLOGY TEST ( 1 FDA reports)
IMPATIENCE ( 1 FDA reports)
IMPETIGO ( 1 FDA reports)
INABILITY TO CRAWL ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 1 FDA reports)
INCORRECT STORAGE OF DRUG ( 1 FDA reports)
INCREASED BRONCHIAL SECRETION ( 1 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 1 FDA reports)
INFLAMMATORY MARKER INCREASED ( 1 FDA reports)
INFLUENZA VIRUS TEST POSITIVE ( 1 FDA reports)
INFUSION SITE HAEMORRHAGE ( 1 FDA reports)
INGUINAL HERNIA ( 1 FDA reports)
INJECTION SITE ABSCESS STERILE ( 1 FDA reports)
INJECTION SITE ATROPHY ( 1 FDA reports)
INJECTION SITE BURNING ( 1 FDA reports)
INJECTION SITE CELLULITIS ( 1 FDA reports)
INJECTION SITE DERMATITIS ( 1 FDA reports)
INJECTION SITE EXFOLIATION ( 1 FDA reports)
INJECTION SITE INDURATION ( 1 FDA reports)
INJECTION SITE INFLAMMATION ( 1 FDA reports)
INJECTION SITE MASS ( 1 FDA reports)
INJECTION SITE SCAR ( 1 FDA reports)
INJECTION SITE STINGING ( 1 FDA reports)
INJECTION SITE ULCER ( 1 FDA reports)
INJECTION SITE URTICARIA ( 1 FDA reports)
INSULIN RESISTANCE ( 1 FDA reports)
INSULIN-LIKE GROWTH FACTOR DECREASED ( 1 FDA reports)
INTERCEPTED MEDICATION ERROR ( 1 FDA reports)
INTERCOSTAL RETRACTION ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 1 FDA reports)
INTESTINAL INFARCTION ( 1 FDA reports)
INTESTINAL ISCHAEMIA ( 1 FDA reports)
INTESTINAL OPERATION ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
INTRACRANIAL ANEURYSM ( 1 FDA reports)
INTRACRANIAL HYPOTENSION ( 1 FDA reports)
INTRACRANIAL INJURY ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 1 FDA reports)
INTUBATION ( 1 FDA reports)
INVESTIGATION ( 1 FDA reports)
IRITIS ( 1 FDA reports)
IRON BINDING CAPACITY TOTAL INCREASED ( 1 FDA reports)
IRON OVERLOAD ( 1 FDA reports)
IVTH NERVE PARALYSIS ( 1 FDA reports)
JC VIRUS INFECTION ( 1 FDA reports)
JOINT ARTHROPLASTY ( 1 FDA reports)
JOINT STIFFNESS ( 1 FDA reports)
KIDNEY ENLARGEMENT ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
KIDNEY RUPTURE ( 1 FDA reports)
KLEBSIELLA SEPSIS ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
LARYNGOMALACIA ( 1 FDA reports)
LEUKAEMIA PLASMACYTIC ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LIBIDO INCREASED ( 1 FDA reports)
LICHENOID KERATOSIS ( 1 FDA reports)
LID LAG ( 1 FDA reports)
LIFE SUPPORT ( 1 FDA reports)
LIGAMENT OPERATION ( 1 FDA reports)
LIGAMENT RUPTURE ( 1 FDA reports)
LIMB CRUSHING INJURY ( 1 FDA reports)
LIMB OPERATION ( 1 FDA reports)
LIP BLISTER ( 1 FDA reports)
LIP EROSION ( 1 FDA reports)
LIPIDS DECREASED ( 1 FDA reports)
LIPOGRANULOMA ( 1 FDA reports)
LISTLESS ( 1 FDA reports)
LIVER TRANSPLANT ( 1 FDA reports)
LIVER TRANSPLANT REJECTION ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
LOOP ELECTROSURGICAL EXCISION PROCEDURE ( 1 FDA reports)
LOSS OF CONTROL OF LEGS ( 1 FDA reports)
LOSS OF PROPRIOCEPTION ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION VIRAL ( 1 FDA reports)
LUNG ABSCESS ( 1 FDA reports)
LUNG ADENOCARCINOMA ( 1 FDA reports)
LUNG CANCER METASTATIC ( 1 FDA reports)
LUNG CREPITATION ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
LUPUS PNEUMONITIS ( 1 FDA reports)
LYMPH GLAND INFECTION ( 1 FDA reports)
LYMPHADENITIS ( 1 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
LYMPHOPENIA ( 1 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
MALABSORPTION ( 1 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 1 FDA reports)
MAMMOGRAM ( 1 FDA reports)
MARITAL PROBLEM ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MAY-THURNER SYNDROME ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 1 FDA reports)
MEDICAL DEVICE IMPLANTATION ( 1 FDA reports)
MEDICATION DILUTION ( 1 FDA reports)
MEDICATION RESIDUE ( 1 FDA reports)
MENIERE'S DISEASE ( 1 FDA reports)
MENINGIOMA SURGERY ( 1 FDA reports)
MENOMETRORRHAGIA ( 1 FDA reports)
MENTAL RETARDATION ( 1 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 1 FDA reports)
METABOLIC ALKALOSIS ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
METASTASES TO MENINGES ( 1 FDA reports)
METASTASES TO MUSCLE ( 1 FDA reports)
METASTASES TO PLEURA ( 1 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 1 FDA reports)
METASTATIC SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
MICROCEPHALY ( 1 FDA reports)
MICROCYTIC ANAEMIA ( 1 FDA reports)
MICROGNATHIA ( 1 FDA reports)
MICROGRAPHIC SKIN SURGERY ( 1 FDA reports)
MICTURITION FREQUENCY DECREASED ( 1 FDA reports)
MINERAL DEFICIENCY ( 1 FDA reports)
MINERAL METABOLISM DISORDER ( 1 FDA reports)
MITRAL VALVE DISEASE ( 1 FDA reports)
MITRAL VALVE STENOSIS ( 1 FDA reports)
MONONEUROPATHY ( 1 FDA reports)
MONOPARESIS ( 1 FDA reports)
MORBID THOUGHTS ( 1 FDA reports)
MORTON'S NEUROMA ( 1 FDA reports)
MOUTH BREATHING ( 1 FDA reports)
MUCOSAL DRYNESS ( 1 FDA reports)
MUCOSAL EROSION ( 1 FDA reports)
MULTIPLE FRACTURES ( 1 FDA reports)
MUMPS ( 1 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 1 FDA reports)
MUSCLE HAEMORRHAGE ( 1 FDA reports)
MUSCLE HYPERTROPHY ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
MUTISM ( 1 FDA reports)
MYELITIS TRANSVERSE ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
MYELOFIBROSIS ( 1 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 1 FDA reports)
MYOCARDITIS ( 1 FDA reports)
MYOCLONIC EPILEPSY ( 1 FDA reports)
NAIL DISCOLOURATION ( 1 FDA reports)
NARROW ANTERIOR CHAMBER ANGLE ( 1 FDA reports)
NASAL DISORDER ( 1 FDA reports)
NASAL ULCER ( 1 FDA reports)
NEGATIVE THOUGHTS ( 1 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
NEOPLASM PROSTATE ( 1 FDA reports)
NEOPLASM RECURRENCE ( 1 FDA reports)
NEURODERMATITIS ( 1 FDA reports)
NEUROGENIC BLADDER ( 1 FDA reports)
NEUROGENIC BOWEL ( 1 FDA reports)
NEUROPATHIC ARTHROPATHY ( 1 FDA reports)
NEUROSIS ( 1 FDA reports)
NEUTROPENIC COLITIS ( 1 FDA reports)
NEUTROPHILIA ( 1 FDA reports)
NIPPLE DISORDER ( 1 FDA reports)
NO ADVERSE EFFECT ( 1 FDA reports)
OBSESSIVE-COMPULSIVE PERSONALITY DISORDER ( 1 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 1 FDA reports)
OESOPHAGEAL CARCINOMA ( 1 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 1 FDA reports)
OESOPHAGEAL HYPOMOTILITY ( 1 FDA reports)
OESOPHAGEAL SPASM ( 1 FDA reports)
OESOPHAGOSCOPY ABNORMAL ( 1 FDA reports)
OLIGOHYDRAMNIOS ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
OPEN ANGLE GLAUCOMA ( 1 FDA reports)
OPERATIVE HAEMORRHAGE ( 1 FDA reports)
OPPORTUNISTIC INFECTION ( 1 FDA reports)
OPTIC DISC DISORDER ( 1 FDA reports)
OPTIC NERVE CUPPING ( 1 FDA reports)
OPTIC NERVE INJURY ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
ORAL MUCOSAL PETECHIAE ( 1 FDA reports)
ORAL SUBMUCOSAL FIBROSIS ( 1 FDA reports)
ORGANIC ERECTILE DYSFUNCTION ( 1 FDA reports)
ORGASM ABNORMAL ( 1 FDA reports)
ORTHOPEDIC PROCEDURE ( 1 FDA reports)
OSTEOMALACIA ( 1 FDA reports)
OSTEOPOROTIC FRACTURE ( 1 FDA reports)
OSTEOTOMY ( 1 FDA reports)
OTITIS MEDIA ACUTE ( 1 FDA reports)
OVARIAN MASS ( 1 FDA reports)
OVARIAN NEOPLASM ( 1 FDA reports)
PAINFUL DEFAECATION ( 1 FDA reports)
PANCREATIC OPERATION ( 1 FDA reports)
PANIC DISORDER WITH AGORAPHOBIA ( 1 FDA reports)
PARASITE DNA TEST POSITIVE ( 1 FDA reports)
PARKINSONIAN GAIT ( 1 FDA reports)
PAROSMIA ( 1 FDA reports)
PAROTITIS ( 1 FDA reports)
PARTIAL SEIZURES ( 1 FDA reports)
PASTEURELLA INFECTION ( 1 FDA reports)
PATIENT ISOLATION ( 1 FDA reports)
PELVIC CONGESTION ( 1 FDA reports)
PELVIC HAEMORRHAGE ( 1 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 1 FDA reports)
PELVIC PROLAPSE ( 1 FDA reports)
PEMPHIGUS ( 1 FDA reports)
PENILE PAIN ( 1 FDA reports)
PERFORMANCE STATUS DECREASED ( 1 FDA reports)
PERIANAL ABSCESS ( 1 FDA reports)
PERIODONTAL DESTRUCTION ( 1 FDA reports)
PERIORBITAL DISORDER ( 1 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 1 FDA reports)
PERIPHERAL NERVE INJURY ( 1 FDA reports)
PETIT MAL EPILEPSY ( 1 FDA reports)
PHAEOCHROMOCYTOMA ( 1 FDA reports)
PHOBIA OF DRIVING ( 1 FDA reports)
PHOTOCOAGULATION ( 1 FDA reports)
PITTING OEDEMA ( 1 FDA reports)
PITUITARY TUMOUR ( 1 FDA reports)
PITUITARY TUMOUR REMOVAL ( 1 FDA reports)
PLASMACYTOSIS ( 1 FDA reports)
PLASMAPHERESIS ( 1 FDA reports)
PLICA SYNDROME ( 1 FDA reports)
PNEUMONIA FUNGAL ( 1 FDA reports)
POLYCYSTIC OVARIES ( 1 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 1 FDA reports)
POLYTRAUMATISM ( 1 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 1 FDA reports)
POOR VENOUS ACCESS ( 1 FDA reports)
PORTAL HYPERTENSION ( 1 FDA reports)
PORTAL HYPERTENSIVE GASTROPATHY ( 1 FDA reports)
POST LUMBAR PUNCTURE SYNDROME ( 1 FDA reports)
POST PROCEDURAL BILE LEAK ( 1 FDA reports)
POST-TRAUMATIC HEADACHE ( 1 FDA reports)
POST-TRAUMATIC PAIN ( 1 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 1 FDA reports)
POSTOPERATIVE ADHESION ( 1 FDA reports)
PREGNANCY OF PARTNER ( 1 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 1 FDA reports)
PRESCRIBED OVERDOSE ( 1 FDA reports)
PRESSURE OF SPEECH ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PROCEDURAL VOMITING ( 1 FDA reports)
PRODUCT CONTAINER SEAL ISSUE ( 1 FDA reports)
PRODUCT DEPOSIT ( 1 FDA reports)
PRODUCT FORMULATION ISSUE ( 1 FDA reports)
PRODUCT OUTER PACKAGING ISSUE ( 1 FDA reports)
PRODUCT PACKAGING QUANTITY ISSUE ( 1 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 1 FDA reports)
PROSTATE INFECTION ( 1 FDA reports)
PROTEIN C DECREASED ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PROTEIN URINE ( 1 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 1 FDA reports)
PSEUDOMONAL SEPSIS ( 1 FDA reports)
PSEUDOPORPHYRIA ( 1 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 1 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 1 FDA reports)
PULMONARY ARTERY STENOSIS CONGENITAL ( 1 FDA reports)
PULMONARY CALCIFICATION ( 1 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 1 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 1 FDA reports)
PULMONARY HYPOPLASIA ( 1 FDA reports)
PULMONARY MALFORMATION ( 1 FDA reports)
PULSE ABNORMAL ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 1 FDA reports)
PUPILS UNEQUAL ( 1 FDA reports)
PYOMYOSITIS ( 1 FDA reports)
PYOPNEUMOTHORAX ( 1 FDA reports)
Q FEVER ( 1 FDA reports)
QUADRIPLEGIA ( 1 FDA reports)
RADIAL NERVE PALSY ( 1 FDA reports)
RADIATION PNEUMONITIS ( 1 FDA reports)
RADICAL HYSTERECTOMY ( 1 FDA reports)
RADIUS FRACTURE ( 1 FDA reports)
RECTAL POLYP ( 1 FDA reports)
RED BLOOD CELL ABNORMALITY ( 1 FDA reports)
RED BLOOD CELLS CSF POSITIVE ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 1 FDA reports)
RED MAN SYNDROME ( 1 FDA reports)
REFLUX GASTRITIS ( 1 FDA reports)
REGURGITATION ( 1 FDA reports)
RELATIONSHIP BREAKDOWN ( 1 FDA reports)
RENAL ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL CANCER METASTATIC ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
RENAL COLIC ( 1 FDA reports)
RENAL CYST HAEMORRHAGE ( 1 FDA reports)
RENAL FUNCTION TEST ( 1 FDA reports)
RENAL HAEMATOMA ( 1 FDA reports)
RENAL INFARCT ( 1 FDA reports)
RENOVASCULAR HYPERTENSION ( 1 FDA reports)
REPETITIVE SPEECH ( 1 FDA reports)
RESPIRATORY FUME INHALATION DISORDER ( 1 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 1 FDA reports)
RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
RETAINED PLACENTA OR MEMBRANES ( 1 FDA reports)
RETINAL ARTERY OCCLUSION ( 1 FDA reports)
RETINAL ARTERY STENOSIS ( 1 FDA reports)
RETINAL PIGMENT EPITHELIOPATHY ( 1 FDA reports)
RETINAL TEAR ( 1 FDA reports)
RETINITIS PIGMENTOSA ( 1 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 1 FDA reports)
RHABDOMYOMA ( 1 FDA reports)
RHINOLARYNGITIS ( 1 FDA reports)
RHYTHM IDIOVENTRICULAR ( 1 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
ROSACEA ( 1 FDA reports)
ROTATOR CUFF REPAIR ( 1 FDA reports)
SACRALISATION ( 1 FDA reports)
SCAB ( 1 FDA reports)
SCAN ABDOMEN ABNORMAL ( 1 FDA reports)
SCAN MYOCARDIAL PERFUSION ( 1 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 1 FDA reports)
SCLERODERMA ( 1 FDA reports)
SCOTOMA ( 1 FDA reports)
SCRATCH ( 1 FDA reports)
SCROTAL OEDEMA ( 1 FDA reports)
SCROTAL PAIN ( 1 FDA reports)
SECONDARY PROGRESSIVE MULTIPLE SCLEROSIS ( 1 FDA reports)
SENSITISATION ( 1 FDA reports)
SENSORIMOTOR DISORDER ( 1 FDA reports)
SERRATIA SEPSIS ( 1 FDA reports)
SERUM FERRITIN DECREASED ( 1 FDA reports)
SEXUALLY INAPPROPRIATE BEHAVIOUR ( 1 FDA reports)
SHIFT TO THE LEFT ( 1 FDA reports)
SIALOADENITIS ( 1 FDA reports)
SICCA SYNDROME ( 1 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 1 FDA reports)
SINUS CONGESTION ( 1 FDA reports)
SJOGREN'S SYNDROME ( 1 FDA reports)
SKIN DESQUAMATION ( 1 FDA reports)
SKIN EROSION ( 1 FDA reports)
SKIN FISSURES ( 1 FDA reports)
SKIN HAEMORRHAGE ( 1 FDA reports)
SKIN INJURY ( 1 FDA reports)
SKIN MACERATION ( 1 FDA reports)
SKIN PAPILLOMA ( 1 FDA reports)
SKIN PLAQUE ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SKIN STRIAE ( 1 FDA reports)
SKIN ULCER HAEMORRHAGE ( 1 FDA reports)
SLEEP TERROR ( 1 FDA reports)
SLEEP WALKING ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SOFT TISSUE DISORDER ( 1 FDA reports)
SOMATISATION DISORDER ( 1 FDA reports)
SPEECH REHABILITATION ( 1 FDA reports)
SPERMATOZOA ABNORMAL ( 1 FDA reports)
SPINAL CORD COMPRESSION ( 1 FDA reports)
SPINAL CORD INJURY ( 1 FDA reports)
SPLENIC LESION ( 1 FDA reports)
SPUTUM PURULENT ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STATUS MIGRAINOSUS ( 1 FDA reports)
STREPTOCOCCAL SEPSIS ( 1 FDA reports)
STUPOR ( 1 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 1 FDA reports)
SUBSTANCE ABUSER ( 1 FDA reports)
SUDDEN HEARING LOSS ( 1 FDA reports)
SYNOVIAL RUPTURE ( 1 FDA reports)
SYSTEMIC CANDIDA ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
TAKAYASU'S ARTERITIS ( 1 FDA reports)
TARSAL TUNNEL SYNDROME ( 1 FDA reports)
TENDON RUPTURE ( 1 FDA reports)
TENOSYNOVITIS STENOSANS ( 1 FDA reports)
TENSION ( 1 FDA reports)
TENSION HEADACHE ( 1 FDA reports)
TESTICULAR DISORDER ( 1 FDA reports)
TESTICULAR MASS ( 1 FDA reports)
TETANY ( 1 FDA reports)
THERAPEUTIC EMBOLISATION ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 1 FDA reports)
THERAPY CESSATION ( 1 FDA reports)
THERAPY REGIMEN CHANGED ( 1 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 1 FDA reports)
THROMBOPHLEBITIS ( 1 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 1 FDA reports)
THYMOL TURBIDITY TEST INCREASED ( 1 FDA reports)
THYROXINE INCREASED ( 1 FDA reports)
TINEA CRURIS ( 1 FDA reports)
TINEL'S SIGN ( 1 FDA reports)
TOBACCO USER ( 1 FDA reports)
TOE OPERATION ( 1 FDA reports)
TONGUE BITING ( 1 FDA reports)
TONGUE HAEMORRHAGE ( 1 FDA reports)
TONGUE OEDEMA ( 1 FDA reports)
TONSILLAR HYPERTROPHY ( 1 FDA reports)
TOOTH DISCOLOURATION ( 1 FDA reports)
TOOTH EROSION ( 1 FDA reports)
TRACHEOBRONCHITIS ( 1 FDA reports)
TRACHEOSTOMY ( 1 FDA reports)
TRANSIENT GLOBAL AMNESIA ( 1 FDA reports)
TRANSPLANT FAILURE ( 1 FDA reports)
TRANSPLANT REJECTION ( 1 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 1 FDA reports)
TRICUSPID VALVE DISEASE ( 1 FDA reports)
TUBERCULIN TEST POSITIVE ( 1 FDA reports)
TUBERCULOSIS TEST POSITIVE ( 1 FDA reports)
TUBEROUS SCLEROSIS ( 1 FDA reports)
TUBO-OVARIAN ABSCESS ( 1 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 1 FDA reports)
ULCERATIVE KERATITIS ( 1 FDA reports)
ULNA FRACTURE ( 1 FDA reports)
UNEMPLOYMENT ( 1 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 1 FDA reports)
URETERIC CANCER ( 1 FDA reports)
URINARY CASTS PRESENT ( 1 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 1 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 1 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 1 FDA reports)
URINARY TRACT OBSTRUCTION ( 1 FDA reports)
URINE ANALYSIS ABNORMAL ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
USE OF ACCESSORY RESPIRATORY MUSCLES ( 1 FDA reports)
UTERINE CYST ( 1 FDA reports)
UTERINE DISORDER ( 1 FDA reports)
VAGINAL INFLAMMATION ( 1 FDA reports)
VAGINAL ULCERATION ( 1 FDA reports)
VARICES OESOPHAGEAL ( 1 FDA reports)
VASCULAR ACCESS COMPLICATION ( 1 FDA reports)
VASCULAR GRAFT ( 1 FDA reports)
VASCULAR INJURY ( 1 FDA reports)
VASCULAR INSUFFICIENCY ( 1 FDA reports)
VASCULAR OPERATION ( 1 FDA reports)
VASCULAR RUPTURE ( 1 FDA reports)
VENA CAVA INJURY ( 1 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 1 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 1 FDA reports)
VENOUS STENOSIS ( 1 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 1 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 1 FDA reports)
VIRAL MYOCARDITIS ( 1 FDA reports)
VIRAL MYOSITIS ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VITAMIN B12 DECREASED ( 1 FDA reports)
VITAMIN D DEFICIENCY ( 1 FDA reports)
VITREOUS DETACHMENT ( 1 FDA reports)
VITREOUS FLOATERS ( 1 FDA reports)
VOCAL CORD INFLAMMATION ( 1 FDA reports)
VOLVULUS ( 1 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 1 FDA reports)
VULVOVAGINAL PRURITUS ( 1 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 1 FDA reports)
WALDENSTROM'S MACROGLOBULINAEMIA ( 1 FDA reports)
WATER INTOXICATION ( 1 FDA reports)
WEGENER'S GRANULOMATOSIS ( 1 FDA reports)
WEIGHT ( 1 FDA reports)
WEIGHT LOSS POOR ( 1 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
WOUND ABSCESS ( 1 FDA reports)
WOUND DEBRIDEMENT ( 1 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 1 FDA reports)
WOUND TREATMENT ( 1 FDA reports)
YAWNING ( 1 FDA reports)
YERSINIA INFECTION ( 1 FDA reports)
YOUNG'S SYNDROME ( 1 FDA reports)

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