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

COMPLETED SUICIDE ( 1562 FDA reports)
PAIN ( 600 FDA reports)
ANXIETY ( 588 FDA reports)
CARDIAC ARREST ( 534 FDA reports)
RESPIRATORY ARREST ( 482 FDA reports)
CARDIO-RESPIRATORY ARREST ( 454 FDA reports)
DEPRESSION ( 454 FDA reports)
NAUSEA ( 446 FDA reports)
DYSPNOEA ( 384 FDA reports)
BACK PAIN ( 380 FDA reports)
CHEST PAIN ( 366 FDA reports)
INTENTIONAL DRUG MISUSE ( 344 FDA reports)
ANAEMIA ( 340 FDA reports)
VOMITING ( 328 FDA reports)
DEATH ( 307 FDA reports)
HEADACHE ( 296 FDA reports)
FALL ( 285 FDA reports)
FATIGUE ( 281 FDA reports)
DRUG ABUSE ( 280 FDA reports)
HYPERTENSION ( 276 FDA reports)
DIZZINESS ( 275 FDA reports)
INJURY ( 267 FDA reports)
DIARRHOEA ( 265 FDA reports)
INSOMNIA ( 262 FDA reports)
OEDEMA PERIPHERAL ( 262 FDA reports)
ARTHRALGIA ( 261 FDA reports)
MULTIPLE DRUG OVERDOSE ( 252 FDA reports)
OSTEOARTHRITIS ( 248 FDA reports)
OSTEONECROSIS OF JAW ( 246 FDA reports)
ASTHENIA ( 240 FDA reports)
PAIN IN EXTREMITY ( 238 FDA reports)
BONE DISORDER ( 234 FDA reports)
MYOCARDIAL INFARCTION ( 233 FDA reports)
PNEUMONIA ( 233 FDA reports)
WEIGHT DECREASED ( 232 FDA reports)
CONSTIPATION ( 220 FDA reports)
EMOTIONAL DISTRESS ( 220 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 213 FDA reports)
ABDOMINAL PAIN ( 208 FDA reports)
DRUG INEFFECTIVE ( 208 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 196 FDA reports)
DEEP VEIN THROMBOSIS ( 194 FDA reports)
HYPOTENSION ( 191 FDA reports)
PULMONARY EMBOLISM ( 190 FDA reports)
PYREXIA ( 188 FDA reports)
PAIN IN JAW ( 182 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 172 FDA reports)
HYPOAESTHESIA ( 171 FDA reports)
CORONARY ARTERY DISEASE ( 169 FDA reports)
TOOTH EXTRACTION ( 167 FDA reports)
POISONING ( 164 FDA reports)
DEHYDRATION ( 160 FDA reports)
OSTEOMYELITIS ( 158 FDA reports)
SOMNOLENCE ( 153 FDA reports)
LOSS OF CONSCIOUSNESS ( 151 FDA reports)
OVERDOSE ( 151 FDA reports)
INFECTION ( 149 FDA reports)
ABDOMINAL PAIN UPPER ( 146 FDA reports)
CEREBROVASCULAR ACCIDENT ( 144 FDA reports)
IMPAIRED HEALING ( 144 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 138 FDA reports)
PLEURAL EFFUSION ( 138 FDA reports)
VISION BLURRED ( 137 FDA reports)
CONFUSIONAL STATE ( 134 FDA reports)
MALAISE ( 131 FDA reports)
SINUSITIS ( 130 FDA reports)
HYPERHIDROSIS ( 129 FDA reports)
COUGH ( 127 FDA reports)
DENTAL CARIES ( 127 FDA reports)
DECREASED APPETITE ( 125 FDA reports)
OSTEONECROSIS ( 123 FDA reports)
SPINAL OSTEOARTHRITIS ( 123 FDA reports)
SYNCOPE ( 123 FDA reports)
RASH ( 122 FDA reports)
ROAD TRAFFIC ACCIDENT ( 122 FDA reports)
SINUS TACHYCARDIA ( 122 FDA reports)
TOOTH DISORDER ( 122 FDA reports)
URINARY TRACT INFECTION ( 122 FDA reports)
CONVULSION ( 117 FDA reports)
DYSPEPSIA ( 117 FDA reports)
ATELECTASIS ( 115 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 112 FDA reports)
NECK PAIN ( 111 FDA reports)
GAIT DISTURBANCE ( 109 FDA reports)
RENAL FAILURE ACUTE ( 108 FDA reports)
BRONCHITIS ( 107 FDA reports)
ROTATOR CUFF SYNDROME ( 106 FDA reports)
DRUG TOXICITY ( 103 FDA reports)
ATRIAL FIBRILLATION ( 102 FDA reports)
OSTEOPENIA ( 102 FDA reports)
RENAL FAILURE ( 102 FDA reports)
OSTEOPOROSIS ( 101 FDA reports)
DRY MOUTH ( 100 FDA reports)
CHOLELITHIASIS ( 99 FDA reports)
DIABETES MELLITUS ( 98 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 98 FDA reports)
MUSCLE SPASMS ( 98 FDA reports)
AMNESIA ( 96 FDA reports)
ANHEDONIA ( 95 FDA reports)
HYPOXIA ( 95 FDA reports)
DYSPHAGIA ( 94 FDA reports)
TREMOR ( 94 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 94 FDA reports)
HAEMORRHOIDS ( 93 FDA reports)
NEUROPATHY PERIPHERAL ( 93 FDA reports)
WEIGHT INCREASED ( 93 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 92 FDA reports)
CELLULITIS ( 91 FDA reports)
HYPERLIPIDAEMIA ( 91 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 90 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 90 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 88 FDA reports)
MENTAL STATUS CHANGES ( 88 FDA reports)
BLOOD GLUCOSE INCREASED ( 87 FDA reports)
HYPOPHAGIA ( 87 FDA reports)
CATARACT ( 86 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 85 FDA reports)
CARDIOMEGALY ( 85 FDA reports)
COMA ( 85 FDA reports)
METASTASES TO BONE ( 85 FDA reports)
MITRAL VALVE INCOMPETENCE ( 85 FDA reports)
PULMONARY OEDEMA ( 85 FDA reports)
SEPSIS ( 85 FDA reports)
CONTUSION ( 84 FDA reports)
RIB FRACTURE ( 84 FDA reports)
SCAR ( 84 FDA reports)
MUSCULAR WEAKNESS ( 82 FDA reports)
PALPITATIONS ( 82 FDA reports)
SUICIDE ATTEMPT ( 80 FDA reports)
ARTHROPATHY ( 79 FDA reports)
DYSURIA ( 79 FDA reports)
EXOSTOSIS ( 79 FDA reports)
PURULENT DISCHARGE ( 79 FDA reports)
SWELLING ( 79 FDA reports)
CHEST DISCOMFORT ( 78 FDA reports)
HYPOKALAEMIA ( 78 FDA reports)
LETHARGY ( 78 FDA reports)
MYALGIA ( 78 FDA reports)
ARTHRITIS ( 77 FDA reports)
DEFORMITY ( 77 FDA reports)
OEDEMA ( 77 FDA reports)
MUSCULOSKELETAL PAIN ( 76 FDA reports)
PRURITUS ( 76 FDA reports)
TOOTHACHE ( 76 FDA reports)
AGITATION ( 75 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 75 FDA reports)
CHILLS ( 75 FDA reports)
EMPHYSEMA ( 75 FDA reports)
GASTRITIS ( 75 FDA reports)
HAEMOGLOBIN DECREASED ( 75 FDA reports)
PARAESTHESIA ( 75 FDA reports)
BONE DENSITY DECREASED ( 74 FDA reports)
FEELING ABNORMAL ( 73 FDA reports)
HAEMORRHAGE ( 73 FDA reports)
BLOOD PRESSURE INCREASED ( 72 FDA reports)
ERYTHEMA ( 72 FDA reports)
THROMBOCYTOPENIA ( 72 FDA reports)
BLOOD CREATININE INCREASED ( 71 FDA reports)
BONE PAIN ( 70 FDA reports)
CARDIAC DISORDER ( 70 FDA reports)
CHOLECYSTITIS CHRONIC ( 69 FDA reports)
INTENTIONAL OVERDOSE ( 69 FDA reports)
RESPIRATORY FAILURE ( 69 FDA reports)
NEOPLASM MALIGNANT ( 68 FDA reports)
SWELLING FACE ( 68 FDA reports)
LOOSE TOOTH ( 67 FDA reports)
PULMONARY HYPERTENSION ( 67 FDA reports)
SUICIDAL IDEATION ( 67 FDA reports)
ANGINA PECTORIS ( 66 FDA reports)
ABDOMINAL DISCOMFORT ( 65 FDA reports)
GALLBLADDER DISORDER ( 65 FDA reports)
INFLAMMATION ( 65 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 65 FDA reports)
IRRITABILITY ( 65 FDA reports)
TACHYCARDIA ( 65 FDA reports)
HIATUS HERNIA ( 64 FDA reports)
HYPONATRAEMIA ( 64 FDA reports)
ARTERIOSCLEROSIS ( 63 FDA reports)
CARDIAC MURMUR ( 63 FDA reports)
DEBRIDEMENT ( 63 FDA reports)
JAW OPERATION ( 63 FDA reports)
STAPHYLOCOCCAL INFECTION ( 63 FDA reports)
ORAL PAIN ( 62 FDA reports)
MEMORY IMPAIRMENT ( 61 FDA reports)
PRIMARY SEQUESTRUM ( 61 FDA reports)
SKIN ULCER ( 60 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 59 FDA reports)
DECREASED INTEREST ( 59 FDA reports)
DRUG INTERACTION ( 59 FDA reports)
HAEMATURIA ( 59 FDA reports)
PROTHROMBIN TIME PROLONGED ( 59 FDA reports)
RHEUMATOID ARTHRITIS ( 59 FDA reports)
DIVERTICULUM ( 58 FDA reports)
FIBROMYALGIA ( 58 FDA reports)
SURGERY ( 58 FDA reports)
TOOTH INFECTION ( 58 FDA reports)
TYPE 2 DIABETES MELLITUS ( 58 FDA reports)
DISCOMFORT ( 57 FDA reports)
ENDODONTIC PROCEDURE ( 57 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 56 FDA reports)
HEART RATE INCREASED ( 56 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 56 FDA reports)
MOUTH ULCERATION ( 56 FDA reports)
RESPIRATORY DISTRESS ( 56 FDA reports)
BURSITIS ( 55 FDA reports)
DYSGEUSIA ( 55 FDA reports)
HYPERSENSITIVITY ( 55 FDA reports)
LIFE EXPECTANCY SHORTENED ( 55 FDA reports)
MEDICATION ERROR ( 55 FDA reports)
ORAL DISORDER ( 55 FDA reports)
PANCREATITIS ( 55 FDA reports)
POLLAKIURIA ( 55 FDA reports)
HALLUCINATION ( 54 FDA reports)
OBESITY ( 54 FDA reports)
OXYGEN SATURATION DECREASED ( 54 FDA reports)
PERIODONTITIS ( 54 FDA reports)
URINARY INCONTINENCE ( 54 FDA reports)
DRUG DEPENDENCE ( 53 FDA reports)
ECONOMIC PROBLEM ( 53 FDA reports)
JAW DISORDER ( 53 FDA reports)
LEFT ATRIAL DILATATION ( 53 FDA reports)
PLATELET COUNT DECREASED ( 53 FDA reports)
RENAL CYST ( 53 FDA reports)
TOOTH FRACTURE ( 53 FDA reports)
TOOTH LOSS ( 53 FDA reports)
GINGIVAL PAIN ( 52 FDA reports)
HERPES ZOSTER ( 52 FDA reports)
VERTIGO ( 52 FDA reports)
DRUG HYPERSENSITIVITY ( 51 FDA reports)
ERECTILE DYSFUNCTION ( 51 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 51 FDA reports)
JOINT SWELLING ( 51 FDA reports)
MULTIPLE INJURIES ( 51 FDA reports)
RECTAL HAEMORRHAGE ( 51 FDA reports)
URTICARIA ( 51 FDA reports)
DRUG ABUSER ( 50 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 50 FDA reports)
RADIOTHERAPY ( 50 FDA reports)
TOOTH ABSCESS ( 50 FDA reports)
AGGRESSION ( 49 FDA reports)
EPISTAXIS ( 49 FDA reports)
ABSCESS ( 48 FDA reports)
FISTULA ( 48 FDA reports)
STRESS ( 48 FDA reports)
BONE DEBRIDEMENT ( 47 FDA reports)
EATING DISORDER ( 47 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 47 FDA reports)
SKIN DISCOLOURATION ( 47 FDA reports)
BLOOD PRESSURE DECREASED ( 46 FDA reports)
GINGIVAL BLEEDING ( 46 FDA reports)
MENTAL DISORDER ( 46 FDA reports)
ALOPECIA ( 45 FDA reports)
ARRHYTHMIA ( 45 FDA reports)
BLOOD UREA INCREASED ( 45 FDA reports)
DRUG EFFECT DECREASED ( 45 FDA reports)
METASTASES TO SPINE ( 45 FDA reports)
NERVOUSNESS ( 45 FDA reports)
PATHOLOGICAL FRACTURE ( 45 FDA reports)
SLEEP DISORDER ( 45 FDA reports)
SPINAL COLUMN STENOSIS ( 45 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 45 FDA reports)
WHEEZING ( 45 FDA reports)
GYNAECOMASTIA ( 44 FDA reports)
INCORRECT DOSE ADMINISTERED ( 44 FDA reports)
NEURALGIA ( 44 FDA reports)
PANIC ATTACK ( 44 FDA reports)
SLEEP APNOEA SYNDROME ( 44 FDA reports)
BASAL CELL CARCINOMA ( 43 FDA reports)
BRADYCARDIA ( 43 FDA reports)
COMPRESSION FRACTURE ( 43 FDA reports)
DRY EYE ( 43 FDA reports)
LIMB INJURY ( 43 FDA reports)
MIGRAINE ( 43 FDA reports)
ACTINOMYCOSIS ( 42 FDA reports)
BONE LESION ( 42 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 42 FDA reports)
LUNG INFILTRATION ( 42 FDA reports)
LYMPHADENOPATHY ( 42 FDA reports)
NEPHROLITHIASIS ( 42 FDA reports)
PHYSICAL DISABILITY ( 42 FDA reports)
CONDITION AGGRAVATED ( 41 FDA reports)
DEPRESSED MOOD ( 41 FDA reports)
FEAR ( 41 FDA reports)
HAEMATOCHEZIA ( 41 FDA reports)
INFLUENZA ( 41 FDA reports)
JAUNDICE ( 41 FDA reports)
SOMNAMBULISM ( 41 FDA reports)
SPINAL FRACTURE ( 41 FDA reports)
TOOTH DEPOSIT ( 41 FDA reports)
TRISMUS ( 41 FDA reports)
UNRESPONSIVE TO STIMULI ( 41 FDA reports)
BONE SWELLING ( 40 FDA reports)
BIPOLAR DISORDER ( 39 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 39 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 39 FDA reports)
FIBROSIS ( 39 FDA reports)
FRACTURE ( 39 FDA reports)
HOT FLUSH ( 39 FDA reports)
HYPERGLYCAEMIA ( 39 FDA reports)
HYPOAESTHESIA ORAL ( 39 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 39 FDA reports)
MOOD SWINGS ( 39 FDA reports)
BODY TEMPERATURE INCREASED ( 38 FDA reports)
DYSARTHRIA ( 38 FDA reports)
HEART RATE DECREASED ( 38 FDA reports)
HEPATIC STEATOSIS ( 38 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 38 FDA reports)
SINUS BRADYCARDIA ( 38 FDA reports)
THROMBOSIS ( 38 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 37 FDA reports)
CARPAL TUNNEL SYNDROME ( 37 FDA reports)
MICTURITION URGENCY ( 37 FDA reports)
NASOPHARYNGITIS ( 37 FDA reports)
PRODUCTIVE COUGH ( 37 FDA reports)
TREATMENT NONCOMPLIANCE ( 37 FDA reports)
ADVERSE DRUG REACTION ( 36 FDA reports)
BACK DISORDER ( 36 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 36 FDA reports)
DRUG SCREEN POSITIVE ( 36 FDA reports)
EJECTION FRACTION DECREASED ( 36 FDA reports)
MUCOSAL INFLAMMATION ( 36 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 36 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 36 FDA reports)
ULCER ( 36 FDA reports)
ABDOMINAL DISTENSION ( 35 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 35 FDA reports)
ADVERSE EVENT ( 35 FDA reports)
ANGER ( 35 FDA reports)
ASTHMA ( 35 FDA reports)
BACK INJURY ( 35 FDA reports)
BREAST CANCER ( 35 FDA reports)
FEBRILE NEUTROPENIA ( 35 FDA reports)
FOOT FRACTURE ( 35 FDA reports)
HAEMATOCRIT DECREASED ( 35 FDA reports)
HYPOGLYCAEMIA ( 35 FDA reports)
INTENTIONAL MISUSE ( 35 FDA reports)
LEUKOCYTOSIS ( 35 FDA reports)
MASS ( 35 FDA reports)
ONYCHOMYCOSIS ( 35 FDA reports)
RHINORRHOEA ( 35 FDA reports)
URINARY RETENTION ( 35 FDA reports)
BLOOD POTASSIUM DECREASED ( 34 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 34 FDA reports)
GINGIVAL DISORDER ( 34 FDA reports)
HEPATOMEGALY ( 34 FDA reports)
IMPAIRED DRIVING ABILITY ( 34 FDA reports)
JOINT DISLOCATION ( 34 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 34 FDA reports)
PRESYNCOPE ( 34 FDA reports)
SKIN LESION ( 34 FDA reports)
BALANCE DISORDER ( 33 FDA reports)
BLOOD PRESSURE ABNORMAL ( 33 FDA reports)
COLONIC POLYP ( 33 FDA reports)
CYANOSIS ( 33 FDA reports)
DERMATITIS CONTACT ( 33 FDA reports)
GASTROENTERITIS ( 33 FDA reports)
HEPATIC CYST ( 33 FDA reports)
RENAL FAILURE CHRONIC ( 33 FDA reports)
SINUS DISORDER ( 33 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 33 FDA reports)
ABDOMINAL PAIN LOWER ( 32 FDA reports)
AORTIC VALVE INCOMPETENCE ( 32 FDA reports)
DECUBITUS ULCER ( 32 FDA reports)
DENTAL OPERATION ( 32 FDA reports)
DIPLOPIA ( 32 FDA reports)
DISABILITY ( 32 FDA reports)
DISTURBANCE IN ATTENTION ( 32 FDA reports)
ECCHYMOSIS ( 32 FDA reports)
HYPERPLASIA ( 32 FDA reports)
PERICARDIAL EFFUSION ( 32 FDA reports)
SEDATION ( 32 FDA reports)
VENTRICULAR FIBRILLATION ( 32 FDA reports)
VENTRICULAR TACHYCARDIA ( 32 FDA reports)
ABSCESS JAW ( 31 FDA reports)
CARDIAC FAILURE ( 31 FDA reports)
CARDIOMYOPATHY ( 31 FDA reports)
CARDIOVASCULAR DISORDER ( 31 FDA reports)
CHOLECYSTITIS ( 31 FDA reports)
CONJUNCTIVITIS ( 31 FDA reports)
COORDINATION ABNORMAL ( 31 FDA reports)
DYSLIPIDAEMIA ( 31 FDA reports)
GINGIVAL RECESSION ( 31 FDA reports)
HEPATIC ENZYME INCREASED ( 31 FDA reports)
HEPATIC FAILURE ( 31 FDA reports)
HYPERKALAEMIA ( 31 FDA reports)
PULMONARY CONGESTION ( 31 FDA reports)
RASH PRURITIC ( 31 FDA reports)
TINNITUS ( 31 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 31 FDA reports)
VISUAL ACUITY REDUCED ( 31 FDA reports)
ABNORMAL BEHAVIOUR ( 30 FDA reports)
ANGINA UNSTABLE ( 30 FDA reports)
BLOOD BILIRUBIN INCREASED ( 30 FDA reports)
BLOOD SODIUM DECREASED ( 30 FDA reports)
COLITIS ISCHAEMIC ( 30 FDA reports)
CRYING ( 30 FDA reports)
DENTAL PROSTHESIS USER ( 30 FDA reports)
GINGIVAL SWELLING ( 30 FDA reports)
MULTI-ORGAN FAILURE ( 30 FDA reports)
MULTIPLE MYELOMA ( 30 FDA reports)
SCIATICA ( 30 FDA reports)
SENSITIVITY OF TEETH ( 30 FDA reports)
SOFT TISSUE DISORDER ( 30 FDA reports)
VISUAL IMPAIRMENT ( 30 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 30 FDA reports)
CACHEXIA ( 29 FDA reports)
CEREBRAL ATROPHY ( 29 FDA reports)
CYST ( 29 FDA reports)
HYPOAESTHESIA FACIAL ( 29 FDA reports)
KYPHOSIS ( 29 FDA reports)
LUMBAR SPINAL STENOSIS ( 29 FDA reports)
MASTECTOMY ( 29 FDA reports)
METASTASES TO LUNG ( 29 FDA reports)
METASTASES TO LYMPH NODES ( 29 FDA reports)
NEUTROPENIA ( 29 FDA reports)
ORAL CAVITY FISTULA ( 29 FDA reports)
PATHOLOGICAL GAMBLING ( 29 FDA reports)
RESPIRATORY DEPRESSION ( 29 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 29 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 28 FDA reports)
ATRIAL SEPTAL DEFECT ( 28 FDA reports)
BLOOD ALBUMIN DECREASED ( 28 FDA reports)
DERMATITIS ( 28 FDA reports)
DISORIENTATION ( 28 FDA reports)
DIVERTICULUM INTESTINAL ( 28 FDA reports)
DYSPNOEA EXERTIONAL ( 28 FDA reports)
FUNGAL INFECTION ( 28 FDA reports)
HYPERCHOLESTEROLAEMIA ( 28 FDA reports)
KNEE ARTHROPLASTY ( 28 FDA reports)
MALNUTRITION ( 28 FDA reports)
OESOPHAGITIS ( 28 FDA reports)
PNEUMONIA ASPIRATION ( 28 FDA reports)
PNEUMOTHORAX ( 28 FDA reports)
POLYNEUROPATHY ( 28 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 28 FDA reports)
SEQUESTRECTOMY ( 28 FDA reports)
ANKLE FRACTURE ( 27 FDA reports)
BILE DUCT STONE ( 27 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 27 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 27 FDA reports)
COAGULOPATHY ( 27 FDA reports)
FEMUR FRACTURE ( 27 FDA reports)
GASTRIC ULCER ( 27 FDA reports)
HYPERKERATOSIS ( 27 FDA reports)
LIVER DISORDER ( 27 FDA reports)
METABOLIC ACIDOSIS ( 27 FDA reports)
MULTIPLE SCLEROSIS ( 27 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 27 FDA reports)
NIGHTMARE ( 27 FDA reports)
OVARIAN CYST ( 27 FDA reports)
POLYP ( 27 FDA reports)
VASCULITIS ( 27 FDA reports)
ANIMAL BITE ( 26 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 26 FDA reports)
ASPIRATION ( 26 FDA reports)
BACTERIAL INFECTION ( 26 FDA reports)
DELIRIUM ( 26 FDA reports)
EAR CONGESTION ( 26 FDA reports)
HEART RATE IRREGULAR ( 26 FDA reports)
HYPOKINESIA ( 26 FDA reports)
INTERMITTENT CLAUDICATION ( 26 FDA reports)
MAJOR DEPRESSION ( 26 FDA reports)
MYOCARDIAL ISCHAEMIA ( 26 FDA reports)
NIGHT SWEATS ( 26 FDA reports)
PNEUMONITIS ( 26 FDA reports)
PROCEDURAL PAIN ( 26 FDA reports)
PROSTATE CANCER METASTATIC ( 26 FDA reports)
RESPIRATORY DISORDER ( 26 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 26 FDA reports)
ACIDOSIS ( 25 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 25 FDA reports)
DIABETIC NEUROPATHY ( 25 FDA reports)
EMOTIONAL DISORDER ( 25 FDA reports)
ENCEPHALOPATHY ( 25 FDA reports)
GASTRIC DISORDER ( 25 FDA reports)
HEAD INJURY ( 25 FDA reports)
HEPATITIS C ( 25 FDA reports)
MIOSIS ( 25 FDA reports)
OROPHARYNGEAL PAIN ( 25 FDA reports)
PAROTITIS ( 25 FDA reports)
TACHYPNOEA ( 25 FDA reports)
ABNORMAL DREAMS ( 24 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 24 FDA reports)
CHRONIC SINUSITIS ( 24 FDA reports)
CORONARY ARTERY OCCLUSION ( 24 FDA reports)
EAR PAIN ( 24 FDA reports)
EROSIVE OESOPHAGITIS ( 24 FDA reports)
EYE PAIN ( 24 FDA reports)
HAEMANGIOMA ( 24 FDA reports)
HEART VALVE INCOMPETENCE ( 24 FDA reports)
HERNIA ( 24 FDA reports)
INFLUENZA LIKE ILLNESS ( 24 FDA reports)
LUNG DISORDER ( 24 FDA reports)
LUNG NEOPLASM ( 24 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 24 FDA reports)
ORAL DISCOMFORT ( 24 FDA reports)
RESORPTION BONE INCREASED ( 24 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 24 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 24 FDA reports)
APNOEA ( 23 FDA reports)
BLOOD CALCIUM DECREASED ( 23 FDA reports)
BREAST CANCER FEMALE ( 23 FDA reports)
BURNING SENSATION ( 23 FDA reports)
CERVICOBRACHIAL SYNDROME ( 23 FDA reports)
COGNITIVE DISORDER ( 23 FDA reports)
DEAFNESS ( 23 FDA reports)
DIASTOLIC DYSFUNCTION ( 23 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 23 FDA reports)
HYPOTHYROIDISM ( 23 FDA reports)
IRRITABLE BOWEL SYNDROME ( 23 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 23 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 23 FDA reports)
PURULENCE ( 23 FDA reports)
UTERINE LEIOMYOMA ( 23 FDA reports)
VAGINAL HAEMORRHAGE ( 23 FDA reports)
VERTIGO POSITIONAL ( 23 FDA reports)
VITAMIN D DEFICIENCY ( 23 FDA reports)
ANGIOEDEMA ( 22 FDA reports)
ANOREXIA ( 22 FDA reports)
APHAGIA ( 22 FDA reports)
DIVERTICULITIS ( 22 FDA reports)
FAECES DISCOLOURED ( 22 FDA reports)
HEART DISEASE CONGENITAL ( 22 FDA reports)
MELANOSIS COLI ( 22 FDA reports)
METASTATIC NEOPLASM ( 22 FDA reports)
NECROSIS ( 22 FDA reports)
ORAL SURGERY ( 22 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 22 FDA reports)
PLEURAL FIBROSIS ( 22 FDA reports)
POISONING DELIBERATE ( 22 FDA reports)
PROSTATE CANCER ( 22 FDA reports)
PROSTATITIS ( 22 FDA reports)
RESPIRATORY RATE INCREASED ( 22 FDA reports)
SKIN PAPILLOMA ( 22 FDA reports)
STOMATITIS ( 22 FDA reports)
VENTRICULAR DYSFUNCTION ( 22 FDA reports)
WOUND DEHISCENCE ( 22 FDA reports)
BREAST RECONSTRUCTION ( 21 FDA reports)
FAILURE TO THRIVE ( 21 FDA reports)
GASTROINTESTINAL DISORDER ( 21 FDA reports)
GLOSSODYNIA ( 21 FDA reports)
HICCUPS ( 21 FDA reports)
HYPOCALCAEMIA ( 21 FDA reports)
IMPAIRED WORK ABILITY ( 21 FDA reports)
INADEQUATE ANALGESIA ( 21 FDA reports)
INJECTION SITE ERYTHEMA ( 21 FDA reports)
INTERSTITIAL LUNG DISEASE ( 21 FDA reports)
JOINT SPRAIN ( 21 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 21 FDA reports)
MELAENA ( 21 FDA reports)
MUSCLE TWITCHING ( 21 FDA reports)
PROCTALGIA ( 21 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 21 FDA reports)
RENAL IMPAIRMENT ( 21 FDA reports)
STEM CELL TRANSPLANT ( 21 FDA reports)
UNEVALUABLE EVENT ( 21 FDA reports)
VITREOUS FLOATERS ( 21 FDA reports)
ACNE ( 20 FDA reports)
APPENDICECTOMY ( 20 FDA reports)
ATHEROSCLEROSIS ( 20 FDA reports)
ATRIOVENTRICULAR BLOCK ( 20 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 20 FDA reports)
BLINDNESS ( 20 FDA reports)
BLOOD PH DECREASED ( 20 FDA reports)
BONE FRAGMENTATION ( 20 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 20 FDA reports)
CANDIDIASIS ( 20 FDA reports)
CERVICAL SPINAL STENOSIS ( 20 FDA reports)
COLITIS ( 20 FDA reports)
CORONARY ARTERY STENOSIS ( 20 FDA reports)
ECZEMA ( 20 FDA reports)
EDENTULOUS ( 20 FDA reports)
FACE OEDEMA ( 20 FDA reports)
FAMILY STRESS ( 20 FDA reports)
FLANK PAIN ( 20 FDA reports)
GASTRITIS EROSIVE ( 20 FDA reports)
INCOHERENT ( 20 FDA reports)
LIVEDO RETICULARIS ( 20 FDA reports)
LYMPHADENECTOMY ( 20 FDA reports)
MARROW HYPERPLASIA ( 20 FDA reports)
MENISCUS LESION ( 20 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 20 FDA reports)
NEOPLASM ( 20 FDA reports)
OSTEITIS ( 20 FDA reports)
PLASMACYTOMA ( 20 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 20 FDA reports)
RASH GENERALISED ( 20 FDA reports)
SPEECH DISORDER ( 20 FDA reports)
TOOTH EROSION ( 20 FDA reports)
VERTEBROPLASTY ( 20 FDA reports)
ABASIA ( 19 FDA reports)
ACCIDENTAL OVERDOSE ( 19 FDA reports)
AMMONIA INCREASED ( 19 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 19 FDA reports)
ASCITES ( 19 FDA reports)
BILIARY DYSKINESIA ( 19 FDA reports)
CAROTID ARTERY STENOSIS ( 19 FDA reports)
FLUID OVERLOAD ( 19 FDA reports)
JOINT CREPITATION ( 19 FDA reports)
LOBAR PNEUMONIA ( 19 FDA reports)
MASTICATION DISORDER ( 19 FDA reports)
MOBILITY DECREASED ( 19 FDA reports)
PARAESTHESIA ORAL ( 19 FDA reports)
POOR PERSONAL HYGIENE ( 19 FDA reports)
PSYCHOTIC DISORDER ( 19 FDA reports)
SHOULDER ARTHROPLASTY ( 19 FDA reports)
SPINAL DISORDER ( 19 FDA reports)
TENDERNESS ( 19 FDA reports)
TENDON RUPTURE ( 19 FDA reports)
VENTRICULAR HYPOKINESIA ( 19 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 19 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 18 FDA reports)
AZOTAEMIA ( 18 FDA reports)
BLOOD CHLORIDE DECREASED ( 18 FDA reports)
BLOOD POTASSIUM INCREASED ( 18 FDA reports)
BONE LOSS ( 18 FDA reports)
BONE MARROW RETICULIN FIBROSIS ( 18 FDA reports)
CATARACT OPERATION ( 18 FDA reports)
CYSTITIS ( 18 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 18 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 18 FDA reports)
DYSKINESIA ( 18 FDA reports)
EMPYEMA ( 18 FDA reports)
EPIDIDYMITIS ( 18 FDA reports)
GENERALISED ANXIETY DISORDER ( 18 FDA reports)
GLAUCOMA ( 18 FDA reports)
HAEMATEMESIS ( 18 FDA reports)
HEMIPARESIS ( 18 FDA reports)
LIMB DISCOMFORT ( 18 FDA reports)
LUMBAR RADICULOPATHY ( 18 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 18 FDA reports)
MUSCLE TIGHTNESS ( 18 FDA reports)
OESOPHAGEAL ULCER ( 18 FDA reports)
OPEN REDUCTION OF FRACTURE ( 18 FDA reports)
PERIODONTAL DISEASE ( 18 FDA reports)
POLYSUBSTANCE ABUSE ( 18 FDA reports)
POST PROCEDURAL COMPLICATION ( 18 FDA reports)
PYODERMA GANGRENOSUM ( 18 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 18 FDA reports)
RETCHING ( 18 FDA reports)
TACHYARRHYTHMIA ( 18 FDA reports)
UTERINE HAEMORRHAGE ( 18 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 18 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 18 FDA reports)
ACUTE RESPIRATORY FAILURE ( 17 FDA reports)
AORTIC CALCIFICATION ( 17 FDA reports)
BIOPSY BREAST ABNORMAL ( 17 FDA reports)
BONE EROSION ( 17 FDA reports)
CLAVICLE FRACTURE ( 17 FDA reports)
COLD SWEAT ( 17 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 17 FDA reports)
DILATATION VENTRICULAR ( 17 FDA reports)
DRUG DOSE OMISSION ( 17 FDA reports)
FOOT DEFORMITY ( 17 FDA reports)
HEPATIC CIRRHOSIS ( 17 FDA reports)
INJECTION SITE PAIN ( 17 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 17 FDA reports)
OPEN WOUND ( 17 FDA reports)
ORAL INFECTION ( 17 FDA reports)
PALLOR ( 17 FDA reports)
PELVIC PAIN ( 17 FDA reports)
RADICULOPATHY ( 17 FDA reports)
RENAL PAIN ( 17 FDA reports)
RHABDOMYOLYSIS ( 17 FDA reports)
SKIN FISSURES ( 17 FDA reports)
SPINAL COMPRESSION FRACTURE ( 17 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 17 FDA reports)
ULNAR NEURITIS ( 17 FDA reports)
ADHESION ( 16 FDA reports)
ALCOHOLISM ( 16 FDA reports)
ANOGENITAL WARTS ( 16 FDA reports)
BODY TEMPERATURE DECREASED ( 16 FDA reports)
BONE ABSCESS ( 16 FDA reports)
BONE NEOPLASM MALIGNANT ( 16 FDA reports)
BONE OPERATION ( 16 FDA reports)
BRAIN OEDEMA ( 16 FDA reports)
BREAST MASS ( 16 FDA reports)
BUNION ( 16 FDA reports)
CAPILLARY LEAK SYNDROME ( 16 FDA reports)
CHOLECYSTECTOMY ( 16 FDA reports)
CONJUNCTIVOCHALASIS ( 16 FDA reports)
CORNEAL DYSTROPHY ( 16 FDA reports)
EXCORIATION ( 16 FDA reports)
EYE DISORDER ( 16 FDA reports)
FEELING HOT ( 16 FDA reports)
FLUSHING ( 16 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 16 FDA reports)
GLARE ( 16 FDA reports)
HEPATIC LESION ( 16 FDA reports)
HIP FRACTURE ( 16 FDA reports)
HYPOGONADISM ( 16 FDA reports)
INDURATION ( 16 FDA reports)
INTERTRIGO ( 16 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 16 FDA reports)
IRON DEFICIENCY ANAEMIA ( 16 FDA reports)
LIBIDO DECREASED ( 16 FDA reports)
LIP DISORDER ( 16 FDA reports)
LIPASE INCREASED ( 16 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 16 FDA reports)
NON-CARDIAC CHEST PAIN ( 16 FDA reports)
OSTEITIS DEFORMANS ( 16 FDA reports)
OTITIS MEDIA ( 16 FDA reports)
PAPILLOMA ( 16 FDA reports)
PEPTIC ULCER ( 16 FDA reports)
PHLEBITIS ( 16 FDA reports)
RADIUS FRACTURE ( 16 FDA reports)
RENAL DISORDER ( 16 FDA reports)
SHOULDER PAIN ( 16 FDA reports)
TENDONITIS ( 16 FDA reports)
TOOTH INJURY ( 16 FDA reports)
ACROCHORDON ( 15 FDA reports)
ALVEOLOPLASTY ( 15 FDA reports)
ARTHROPOD BITE ( 15 FDA reports)
BLOOD GLUCOSE DECREASED ( 15 FDA reports)
CARDIAC VALVE ABSCESS ( 15 FDA reports)
DYSAESTHESIA ( 15 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 15 FDA reports)
FISTULA DISCHARGE ( 15 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 15 FDA reports)
HYDROCELE ( 15 FDA reports)
INCREASED TENDENCY TO BRUISE ( 15 FDA reports)
JOINT STIFFNESS ( 15 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 15 FDA reports)
LYMPHOPENIA ( 15 FDA reports)
MYELODYSPLASTIC SYNDROME ( 15 FDA reports)
NEOPLASM PROGRESSION ( 15 FDA reports)
NEUTROPHIL COUNT DECREASED ( 15 FDA reports)
OFF LABEL USE ( 15 FDA reports)
OSTEORADIONECROSIS ( 15 FDA reports)
PERIPHERAL EMBOLISM ( 15 FDA reports)
PRODUCT QUALITY ISSUE ( 15 FDA reports)
RENAL ISCHAEMIA ( 15 FDA reports)
SENSORY LOSS ( 15 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 15 FDA reports)
TESTICULAR SWELLING ( 15 FDA reports)
TONGUE DISCOLOURATION ( 15 FDA reports)
TONGUE INJURY ( 15 FDA reports)
URINE ANALYSIS ABNORMAL ( 15 FDA reports)
VENTRICULAR HYPERTROPHY ( 15 FDA reports)
VISUAL DISTURBANCE ( 15 FDA reports)
ACCIDENTAL EXPOSURE ( 14 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 14 FDA reports)
ADRENAL INSUFFICIENCY ( 14 FDA reports)
ALCOHOL USE ( 14 FDA reports)
BACTERAEMIA ( 14 FDA reports)
BLOOD BICARBONATE DECREASED ( 14 FDA reports)
CEREBRAL INFARCTION ( 14 FDA reports)
CERVICAL MYELOPATHY ( 14 FDA reports)
DIABETIC KETOACIDOSIS ( 14 FDA reports)
DRUG DIVERSION ( 14 FDA reports)
DYSSTASIA ( 14 FDA reports)
EYE SWELLING ( 14 FDA reports)
EYELID OEDEMA ( 14 FDA reports)
FLATULENCE ( 14 FDA reports)
FLUID RETENTION ( 14 FDA reports)
FORAMEN MAGNUM STENOSIS ( 14 FDA reports)
GANGRENE ( 14 FDA reports)
GASTRIC HAEMORRHAGE ( 14 FDA reports)
GINGIVAL ERYTHEMA ( 14 FDA reports)
HAEMOPTYSIS ( 14 FDA reports)
HALLUCINATION, VISUAL ( 14 FDA reports)
HIP ARTHROPLASTY ( 14 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 14 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 14 FDA reports)
MENOPAUSE ( 14 FDA reports)
MICROANGIOPATHY ( 14 FDA reports)
MYOSITIS ( 14 FDA reports)
NASAL CONGESTION ( 14 FDA reports)
NOCTURIA ( 14 FDA reports)
ORTHOPNOEA ( 14 FDA reports)
OSTEOSCLEROSIS ( 14 FDA reports)
OSTEOSYNTHESIS ( 14 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 14 FDA reports)
PARANOIA ( 14 FDA reports)
PLEURITIC PAIN ( 14 FDA reports)
POST THROMBOTIC SYNDROME ( 14 FDA reports)
QUALITY OF LIFE DECREASED ( 14 FDA reports)
RADICULAR PAIN ( 14 FDA reports)
RASH ERYTHEMATOUS ( 14 FDA reports)
RESTLESSNESS ( 14 FDA reports)
RHINITIS ALLERGIC ( 14 FDA reports)
SKIN DISORDER ( 14 FDA reports)
SWOLLEN TONGUE ( 14 FDA reports)
VENOUS INSUFFICIENCY ( 14 FDA reports)
VENOUS THROMBOSIS LIMB ( 14 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 14 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 13 FDA reports)
CHEILITIS ( 13 FDA reports)
CHONDROMALACIA ( 13 FDA reports)
COLLAPSE OF LUNG ( 13 FDA reports)
DISEASE PROGRESSION ( 13 FDA reports)
DYSPHONIA ( 13 FDA reports)
EYE INFECTION ( 13 FDA reports)
GOUT ( 13 FDA reports)
HYPERAESTHESIA ( 13 FDA reports)
HYPERSOMNIA ( 13 FDA reports)
ILL-DEFINED DISORDER ( 13 FDA reports)
INTENTIONAL SELF-INJURY ( 13 FDA reports)
JOINT INJURY ( 13 FDA reports)
LACUNAR INFARCTION ( 13 FDA reports)
LOCALISED INFECTION ( 13 FDA reports)
MELANOCYTIC NAEVUS ( 13 FDA reports)
METASTASES TO BONE MARROW ( 13 FDA reports)
METASTASES TO LIVER ( 13 FDA reports)
METASTASES TO REPRODUCTIVE ORGAN ( 13 FDA reports)
MITRAL VALVE PROLAPSE ( 13 FDA reports)
MUCOSAL ULCERATION ( 13 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 13 FDA reports)
MUSCLE STRAIN ( 13 FDA reports)
NECK INJURY ( 13 FDA reports)
NEOPLASM RECURRENCE ( 13 FDA reports)
OROPHARYNGEAL PLAQUE ( 13 FDA reports)
PANCREATITIS ACUTE ( 13 FDA reports)
PAPULE ( 13 FDA reports)
PHARYNGEAL OEDEMA ( 13 FDA reports)
PHOTOPHOBIA ( 13 FDA reports)
POLYURIA ( 13 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 13 FDA reports)
RESPIRATORY RATE DECREASED ( 13 FDA reports)
SHOCK ( 13 FDA reports)
SKELETAL INJURY ( 13 FDA reports)
SKIN CANCER ( 13 FDA reports)
SPINAL CORD COMPRESSION ( 13 FDA reports)
SPONDYLITIS ( 13 FDA reports)
TARDIVE DYSKINESIA ( 13 FDA reports)
THROMBOCYTOSIS ( 13 FDA reports)
VENOUS OCCLUSION ( 13 FDA reports)
WOUND SECRETION ( 13 FDA reports)
ACTINIC KERATOSIS ( 12 FDA reports)
AMENORRHOEA ( 12 FDA reports)
APPENDICITIS ( 12 FDA reports)
BIOPSY LYMPH GLAND ( 12 FDA reports)
BLOOD MAGNESIUM DECREASED ( 12 FDA reports)
BREAST PROSTHESIS REMOVAL ( 12 FDA reports)
CHOLECYSTITIS ACUTE ( 12 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 12 FDA reports)
DRUG DISPENSING ERROR ( 12 FDA reports)
EJECTION FRACTION ABNORMAL ( 12 FDA reports)
ENTEROCUTANEOUS FISTULA ( 12 FDA reports)
FEELING COLD ( 12 FDA reports)
FRACTURE DELAYED UNION ( 12 FDA reports)
GINGIVAL INFECTION ( 12 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 12 FDA reports)
HYPERMETROPIA ( 12 FDA reports)
HYPOVOLAEMIA ( 12 FDA reports)
INCISIONAL DRAINAGE ( 12 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 12 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 12 FDA reports)
JAW LESION EXCISION ( 12 FDA reports)
LABYRINTHITIS ( 12 FDA reports)
LACERATION ( 12 FDA reports)
MALIGNANT TUMOUR EXCISION ( 12 FDA reports)
METASTASIS ( 12 FDA reports)
MOTOR DEVELOPMENTAL DELAY ( 12 FDA reports)
MYDRIASIS ( 12 FDA reports)
NO THERAPEUTIC RESPONSE ( 12 FDA reports)
ODYNOPHAGIA ( 12 FDA reports)
ORCHITIS ( 12 FDA reports)
PERSONALITY CHANGE ( 12 FDA reports)
RADIATION SKIN INJURY ( 12 FDA reports)
RADIOTHERAPY TO BRAIN ( 12 FDA reports)
RESTLESS LEGS SYNDROME ( 12 FDA reports)
SINUS HEADACHE ( 12 FDA reports)
SUBCUTANEOUS NODULE ( 12 FDA reports)
TESTICULAR PAIN ( 12 FDA reports)
TROPONIN INCREASED ( 12 FDA reports)
VULVOVAGINAL DRYNESS ( 12 FDA reports)
WITHDRAWAL SYNDROME ( 12 FDA reports)
WOUND ( 12 FDA reports)
ABSCESS DRAINAGE ( 11 FDA reports)
AFFECT LABILITY ( 11 FDA reports)
AFFECTIVE DISORDER ( 11 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 11 FDA reports)
ANXIETY DISORDER ( 11 FDA reports)
AORTIC DISORDER ( 11 FDA reports)
AORTIC STENOSIS ( 11 FDA reports)
AUTOIMMUNE DISORDER ( 11 FDA reports)
BENIGN TUMOUR EXCISION ( 11 FDA reports)
BILIARY COLIC ( 11 FDA reports)
BLADDER CATHETERISATION ( 11 FDA reports)
BLOOD URINE PRESENT ( 11 FDA reports)
BONE NEOPLASM ( 11 FDA reports)
BRAIN DEATH ( 11 FDA reports)
BREAST DISCHARGE ( 11 FDA reports)
BUNION OPERATION ( 11 FDA reports)
BUTTERFLY RASH ( 11 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 11 FDA reports)
CARDIOGENIC SHOCK ( 11 FDA reports)
CEREBRAL HAEMORRHAGE ( 11 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 11 FDA reports)
DEAFNESS NEUROSENSORY ( 11 FDA reports)
DEVICE RELATED INFECTION ( 11 FDA reports)
DILATATION ATRIAL ( 11 FDA reports)
DRY SKIN ( 11 FDA reports)
ERYTHEMA NODOSUM ( 11 FDA reports)
ERYTHEMA OF EYELID ( 11 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 11 FDA reports)
EYE DISCHARGE ( 11 FDA reports)
FACET JOINT SYNDROME ( 11 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 11 FDA reports)
GALLBLADDER INJURY ( 11 FDA reports)
GASTROSTOMY TUBE INSERTION ( 11 FDA reports)
GLOMERULAR FILTRATION RATE ABNORMAL ( 11 FDA reports)
HALLUCINATION, AUDITORY ( 11 FDA reports)
HOSPITALISATION ( 11 FDA reports)
INJECTION SITE SWELLING ( 11 FDA reports)
JAUNDICE CHOLESTATIC ( 11 FDA reports)
JOINT CONTRACTURE ( 11 FDA reports)
JOINT EFFUSION ( 11 FDA reports)
LACRIMATION INCREASED ( 11 FDA reports)
LIPOMA ( 11 FDA reports)
LOOSE BODY IN JOINT ( 11 FDA reports)
MICROCYTOSIS ( 11 FDA reports)
NASAL DISORDER ( 11 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 11 FDA reports)
ORAL HERPES ( 11 FDA reports)
PAROTIDECTOMY ( 11 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 11 FDA reports)
PHYSICAL ASSAULT ( 11 FDA reports)
PSORIASIS ( 11 FDA reports)
PULPITIS DENTAL ( 11 FDA reports)
PYELONEPHRITIS ( 11 FDA reports)
SEBORRHOEIC KERATOSIS ( 11 FDA reports)
SKIN HYPERPIGMENTATION ( 11 FDA reports)
SKIN HYPERTROPHY ( 11 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 11 FDA reports)
THINKING ABNORMAL ( 11 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 11 FDA reports)
TUMOUR LYSIS SYNDROME ( 11 FDA reports)
UTERINE DISORDER ( 11 FDA reports)
VARICOSE VEIN ( 11 FDA reports)
ABDOMINAL MASS ( 10 FDA reports)
ACCIDENT AT WORK ( 10 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 10 FDA reports)
ADMINISTRATION SITE INFECTION ( 10 FDA reports)
ADRENAL NEOPLASM ( 10 FDA reports)
ALLERGY TO ARTHROPOD STING ( 10 FDA reports)
ANAEMIA POSTOPERATIVE ( 10 FDA reports)
ATAXIA ( 10 FDA reports)
BRAIN INJURY ( 10 FDA reports)
BRONCHITIS ACUTE ( 10 FDA reports)
CARDIAC VALVE DISEASE ( 10 FDA reports)
CORNEAL ABRASION ( 10 FDA reports)
CYSTOCELE ( 10 FDA reports)
DRUG ADMINISTRATION ERROR ( 10 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 10 FDA reports)
EYELID PTOSIS ( 10 FDA reports)
GALLBLADDER POLYP ( 10 FDA reports)
GENERAL SYMPTOM ( 10 FDA reports)
GRANULOMA ( 10 FDA reports)
HAEMODIALYSIS ( 10 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 10 FDA reports)
IMPLANT SITE THROMBOSIS ( 10 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 10 FDA reports)
INGROWING NAIL ( 10 FDA reports)
IODINE ALLERGY ( 10 FDA reports)
LABORATORY TEST ABNORMAL ( 10 FDA reports)
LIP SWELLING ( 10 FDA reports)
LOWER LIMB FRACTURE ( 10 FDA reports)
LUNG NEOPLASM MALIGNANT ( 10 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 10 FDA reports)
NEUTROPHIL COUNT ( 10 FDA reports)
NODULE ( 10 FDA reports)
ORAL CANDIDIASIS ( 10 FDA reports)
ORTHOSTATIC HYPOTENSION ( 10 FDA reports)
OSTEOPOROTIC FRACTURE ( 10 FDA reports)
OVERWEIGHT ( 10 FDA reports)
PARALYSIS ( 10 FDA reports)
PRINZMETAL ANGINA ( 10 FDA reports)
PULMONARY INFARCTION ( 10 FDA reports)
RECTOCELE ( 10 FDA reports)
RENAL TUBULAR NECROSIS ( 10 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 10 FDA reports)
SJOGREN'S SYNDROME ( 10 FDA reports)
SKIN DEGENERATIVE DISORDER ( 10 FDA reports)
SKIN INDURATION ( 10 FDA reports)
SKIN NEOPLASM EXCISION ( 10 FDA reports)
SLEEP-RELATED EATING DISORDER ( 10 FDA reports)
SNORING ( 10 FDA reports)
SPONDYLOARTHROPATHY ( 10 FDA reports)
SPONDYLOLISTHESIS ( 10 FDA reports)
STEVENS-JOHNSON SYNDROME ( 10 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 10 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 10 FDA reports)
TALIPES ( 10 FDA reports)
TEARFULNESS ( 10 FDA reports)
THYROIDITIS ( 10 FDA reports)
TYPE 1 DIABETES MELLITUS ( 10 FDA reports)
URINE OUTPUT DECREASED ( 10 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 10 FDA reports)
WOUND INFECTION ( 10 FDA reports)
ABDOMINAL ADHESIONS ( 9 FDA reports)
ANISOCYTOSIS ( 9 FDA reports)
AORTIC ANEURYSM ( 9 FDA reports)
AORTIC VALVE DISEASE ( 9 FDA reports)
APLASTIC ANAEMIA ( 9 FDA reports)
ATRIAL TACHYCARDIA ( 9 FDA reports)
BACTERIAL DISEASE CARRIER ( 9 FDA reports)
BLINDNESS UNILATERAL ( 9 FDA reports)
BLISTER ( 9 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 9 FDA reports)
BLOOD CREATININE DECREASED ( 9 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 9 FDA reports)
BLOOD UREA DECREASED ( 9 FDA reports)
BREAST CYST ( 9 FDA reports)
BREAST TENDERNESS ( 9 FDA reports)
CEREBRAL ISCHAEMIA ( 9 FDA reports)
COMPUTERISED TOMOGRAM CORONARY ARTERY ABNORMAL ( 9 FDA reports)
COSTOCHONDRITIS ( 9 FDA reports)
DENTURE WEARER ( 9 FDA reports)
DEPENDENCE ( 9 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 9 FDA reports)
DIABETIC NEPHROPATHY ( 9 FDA reports)
DISSOCIATIVE FUGUE ( 9 FDA reports)
DUODENAL ULCER ( 9 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 9 FDA reports)
EARLY SATIETY ( 9 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 9 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 9 FDA reports)
FACE INJURY ( 9 FDA reports)
FISTULA REPAIR ( 9 FDA reports)
FOOD POISONING ( 9 FDA reports)
HAEMATOMA ( 9 FDA reports)
HAEMORRHAGIC DIATHESIS ( 9 FDA reports)
HAND FRACTURE ( 9 FDA reports)
HYPERSEXUALITY ( 9 FDA reports)
HYPERVENTILATION ( 9 FDA reports)
HYPOCHROMASIA ( 9 FDA reports)
HYPOVENTILATION ( 9 FDA reports)
ILEITIS ( 9 FDA reports)
ILEUS ( 9 FDA reports)
IMMUNODEFICIENCY ( 9 FDA reports)
INJECTION SITE HAEMATOMA ( 9 FDA reports)
ISCHAEMIA ( 9 FDA reports)
LACTIC ACIDOSIS ( 9 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 9 FDA reports)
LIGAMENT SPRAIN ( 9 FDA reports)
METABOLIC DISORDER ( 9 FDA reports)
MUSCULOSKELETAL DISORDER ( 9 FDA reports)
MYELITIS TRANSVERSE ( 9 FDA reports)
NEUROPATHY ( 9 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 9 FDA reports)
OCCULT BLOOD POSITIVE ( 9 FDA reports)
OESOPHAGOGASTRODUODENOSCOPY ( 9 FDA reports)
ORGAN FAILURE ( 9 FDA reports)
OSTEOSARCOMA METASTATIC ( 9 FDA reports)
PANCYTOPENIA ( 9 FDA reports)
PAROTID GLAND ENLARGEMENT ( 9 FDA reports)
PERIORBITAL HAEMATOMA ( 9 FDA reports)
PLASTIC SURGERY TO THE FACE ( 9 FDA reports)
POLYCHROMASIA ( 9 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 9 FDA reports)
PUPIL FIXED ( 9 FDA reports)
RENAL INJURY ( 9 FDA reports)
RETINOPATHY ( 9 FDA reports)
ROTATOR CUFF REPAIR ( 9 FDA reports)
ROULEAUX FORMATION ( 9 FDA reports)
SENSATION OF HEAVINESS ( 9 FDA reports)
SEROTONIN SYNDROME ( 9 FDA reports)
SKIN CANDIDA ( 9 FDA reports)
SKIN NECROSIS ( 9 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 9 FDA reports)
SOFT TISSUE INFLAMMATION ( 9 FDA reports)
TENSION ( 9 FDA reports)
TESTICULAR ATROPHY ( 9 FDA reports)
THORACOTOMY ( 9 FDA reports)
THROAT IRRITATION ( 9 FDA reports)
TRANSAMINASES INCREASED ( 9 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 9 FDA reports)
WALKING DISABILITY ( 9 FDA reports)
WOUND DRAINAGE ( 9 FDA reports)
ACUTE CORONARY SYNDROME ( 8 FDA reports)
ADRENAL MASS ( 8 FDA reports)
ANGIOPATHY ( 8 FDA reports)
ANKYLOSING SPONDYLITIS ( 8 FDA reports)
BLADDER DISORDER ( 8 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 8 FDA reports)
BREAST CALCIFICATIONS ( 8 FDA reports)
BREAST PROSTHESIS IMPLANTATION ( 8 FDA reports)
BREATH SOUNDS ABNORMAL ( 8 FDA reports)
BRUXISM ( 8 FDA reports)
CATHETERISATION CARDIAC ( 8 FDA reports)
CENTRAL NERVOUS SYSTEM NEOPLASM ( 8 FDA reports)
CEREBROVASCULAR DISORDER ( 8 FDA reports)
CERUMEN IMPACTION ( 8 FDA reports)
CHORIORETINAL DISORDER ( 8 FDA reports)
CHORIORETINOPATHY ( 8 FDA reports)
CHROMATURIA ( 8 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 8 FDA reports)
COLON CANCER ( 8 FDA reports)
CONGENITAL ARTERIAL MALFORMATION ( 8 FDA reports)
CROHN'S DISEASE ( 8 FDA reports)
DEMENTIA ( 8 FDA reports)
DEVICE MALFUNCTION ( 8 FDA reports)
DIFFICULTY IN WALKING ( 8 FDA reports)
DRUG SCREEN NEGATIVE ( 8 FDA reports)
DRUG WITHDRAWAL CONVULSIONS ( 8 FDA reports)
DUODENAL OBSTRUCTION ( 8 FDA reports)
DYSTHYMIC DISORDER ( 8 FDA reports)
DYSTONIA ( 8 FDA reports)
ENTEROBACTER INFECTION ( 8 FDA reports)
EYE IRRITATION ( 8 FDA reports)
FACIAL PAIN ( 8 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 8 FDA reports)
FIBULA FRACTURE ( 8 FDA reports)
FOOD INTOLERANCE ( 8 FDA reports)
GASTROSTOMY ( 8 FDA reports)
GENERALISED OEDEMA ( 8 FDA reports)
GINGIVAL ABSCESS ( 8 FDA reports)
GINGIVAL OEDEMA ( 8 FDA reports)
GINGIVITIS ( 8 FDA reports)
HEPATITIS ( 8 FDA reports)
HEPATOTOXICITY ( 8 FDA reports)
HYPERTENSIVE HEART DISEASE ( 8 FDA reports)
HYPERTONIC BLADDER ( 8 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 8 FDA reports)
INGUINAL HERNIA ( 8 FDA reports)
INTRACRANIAL ANEURYSM ( 8 FDA reports)
ISCHAEMIC STROKE ( 8 FDA reports)
JAUNDICE NEONATAL ( 8 FDA reports)
KLEBSIELLA INFECTION ( 8 FDA reports)
LOW TURNOVER OSTEOPATHY ( 8 FDA reports)
LUNG INFECTION ( 8 FDA reports)
MENINGITIS ( 8 FDA reports)
MENORRHAGIA ( 8 FDA reports)
MUSCLE ATROPHY ( 8 FDA reports)
MUSCLE CRAMP ( 8 FDA reports)
MYOPATHY ( 8 FDA reports)
NERVE COMPRESSION ( 8 FDA reports)
NEURITIS ( 8 FDA reports)
NODAL RHYTHM ( 8 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 8 FDA reports)
ODONTOGENIC CYST ( 8 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 8 FDA reports)
ORAL TORUS ( 8 FDA reports)
PANIC DISORDER ( 8 FDA reports)
PANIC REACTION ( 8 FDA reports)
PARONYCHIA ( 8 FDA reports)
PERITONITIS ( 8 FDA reports)
PO2 DECREASED ( 8 FDA reports)
POOR DENTAL CONDITION ( 8 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 8 FDA reports)
POST LAMINECTOMY SYNDROME ( 8 FDA reports)
POST PROCEDURAL HAEMATOMA ( 8 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 8 FDA reports)
PROSTATECTOMY ( 8 FDA reports)
PROSTATIC DISORDER ( 8 FDA reports)
PRURITUS GENERALISED ( 8 FDA reports)
RETINAL DISORDER ( 8 FDA reports)
SACROILIITIS ( 8 FDA reports)
SEPSIS NEONATAL ( 8 FDA reports)
SEPTIC SHOCK ( 8 FDA reports)
SEPTOPLASTY ( 8 FDA reports)
SEROMA ( 8 FDA reports)
SKIN EXFOLIATION ( 8 FDA reports)
SKIN LACERATION ( 8 FDA reports)
SKIN SWELLING ( 8 FDA reports)
TENDON DISORDER ( 8 FDA reports)
TENDON INJURY ( 8 FDA reports)
TENDON PAIN ( 8 FDA reports)
TENSION HEADACHE ( 8 FDA reports)
THERMAL BURN ( 8 FDA reports)
THROMBOPHLEBITIS ( 8 FDA reports)
VAGINAL INFECTION ( 8 FDA reports)
VASCULAR OCCLUSION ( 8 FDA reports)
VIITH NERVE PARALYSIS ( 8 FDA reports)
ACCIDENT ( 7 FDA reports)
ADDISON'S DISEASE ( 7 FDA reports)
AGORAPHOBIA ( 7 FDA reports)
ANEURYSM ( 7 FDA reports)
APLASIA PURE RED CELL ( 7 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 7 FDA reports)
BACTERIAL SEPSIS ( 7 FDA reports)
BARRETT'S OESOPHAGUS ( 7 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 7 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 7 FDA reports)
BLOOD LACTIC ACID INCREASED ( 7 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 7 FDA reports)
BONE MARROW FAILURE ( 7 FDA reports)
BREAST CELLULITIS ( 7 FDA reports)
BRONCHOPNEUMONIA ( 7 FDA reports)
CARDIAC ANEURYSM ( 7 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 7 FDA reports)
CAROTID BRUIT ( 7 FDA reports)
CARTILAGE ATROPHY ( 7 FDA reports)
CHLOASMA ( 7 FDA reports)
CONVERSION DISORDER ( 7 FDA reports)
CONVULSION NEONATAL ( 7 FDA reports)
DERMAL CYST ( 7 FDA reports)
DIALYSIS ( 7 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 7 FDA reports)
DUODENAL STENOSIS ( 7 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 7 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 7 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 7 FDA reports)
FEELING DRUNK ( 7 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 7 FDA reports)
HAEMORRHAGIC STROKE ( 7 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 7 FDA reports)
HEART RATE ABNORMAL ( 7 FDA reports)
HEPATIC FIBROSIS ( 7 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 7 FDA reports)
HODGKIN'S DISEASE ( 7 FDA reports)
HOMICIDE ( 7 FDA reports)
HYDRONEPHROSIS ( 7 FDA reports)
HYPERCALCAEMIA ( 7 FDA reports)
IMPLANT SITE HAEMATOMA ( 7 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 7 FDA reports)
INTESTINAL HAEMORRHAGE ( 7 FDA reports)
INTESTINAL ISCHAEMIA ( 7 FDA reports)
INTRAMEDULLARY ROD INSERTION ( 7 FDA reports)
IRON DEFICIENCY ( 7 FDA reports)
LABILE HYPERTENSION ( 7 FDA reports)
MAMMOPLASTY ( 7 FDA reports)
MIDDLE INSOMNIA ( 7 FDA reports)
MITRAL VALVE DISEASE ( 7 FDA reports)
MONOCYTE COUNT INCREASED ( 7 FDA reports)
MULTIPLE FRACTURES ( 7 FDA reports)
MUSCLE INJURY ( 7 FDA reports)
NEPHROPATHY ( 7 FDA reports)
OCCIPITAL NEURALGIA ( 7 FDA reports)
OCULAR HYPERAEMIA ( 7 FDA reports)
OPERATIVE HAEMORRHAGE ( 7 FDA reports)
OSTEOTOMY ( 7 FDA reports)
PERIPHERAL COLDNESS ( 7 FDA reports)
PERONEAL NERVE PALSY ( 7 FDA reports)
PETECHIAE ( 7 FDA reports)
PHARYNGITIS ( 7 FDA reports)
POSTOPERATIVE ILEUS ( 7 FDA reports)
PREMATURE BABY ( 7 FDA reports)
PROTEIN TOTAL DECREASED ( 7 FDA reports)
PROTEIN URINE PRESENT ( 7 FDA reports)
PULMONARY ARTERY STENOSIS ( 7 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 7 FDA reports)
RESPIRATORY TRACT CONGESTION ( 7 FDA reports)
SECRETION DISCHARGE ( 7 FDA reports)
SEXUAL ABUSE ( 7 FDA reports)
SICK SINUS SYNDROME ( 7 FDA reports)
SINUS ARRHYTHMIA ( 7 FDA reports)
SINUS CONGESTION ( 7 FDA reports)
SKIN INFECTION ( 7 FDA reports)
SOCIAL PROBLEM ( 7 FDA reports)
STENT PLACEMENT ( 7 FDA reports)
STRESS INCONTINENCE ( 7 FDA reports)
THALASSAEMIA BETA ( 7 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 7 FDA reports)
THYROID DISORDER ( 7 FDA reports)
TONGUE GEOGRAPHIC ( 7 FDA reports)
UMBILICAL HERNIA ( 7 FDA reports)
UPPER LIMB FRACTURE ( 7 FDA reports)
URINE FLOW DECREASED ( 7 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 7 FDA reports)
ABDOMINAL BRUIT ( 6 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 6 FDA reports)
ACUTE PULMONARY OEDEMA ( 6 FDA reports)
ANAL FISSURE ( 6 FDA reports)
ANAPHYLACTIC REACTION ( 6 FDA reports)
ANION GAP INCREASED ( 6 FDA reports)
ARTERIOSPASM CORONARY ( 6 FDA reports)
ATRIAL FLUTTER ( 6 FDA reports)
ATROPHY ( 6 FDA reports)
BEREAVEMENT REACTION ( 6 FDA reports)
BIOPSY ENDOMETRIUM ( 6 FDA reports)
BLADDER OBSTRUCTION ( 6 FDA reports)
BONE DEVELOPMENT ABNORMAL ( 6 FDA reports)
BONE MARROW OEDEMA ( 6 FDA reports)
BREAST LUMP REMOVAL ( 6 FDA reports)
BREAST PAIN ( 6 FDA reports)
CARDIAC ENZYMES INCREASED ( 6 FDA reports)
CARDIORENAL SYNDROME ( 6 FDA reports)
CAROTID ARTERY DISEASE ( 6 FDA reports)
CHEST X-RAY ABNORMAL ( 6 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 6 FDA reports)
COARCTATION OF THE AORTA ( 6 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 6 FDA reports)
CONJUNCTIVAL DISCOLOURATION ( 6 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 6 FDA reports)
DENTAL FISTULA ( 6 FDA reports)
DERMATOPHYTOSIS ( 6 FDA reports)
DERMOID CYST ( 6 FDA reports)
DEVICE LEAKAGE ( 6 FDA reports)
DIAPHRAGMATIC HERNIA ( 6 FDA reports)
EMBOLISM ( 6 FDA reports)
EPHELIDES ( 6 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 6 FDA reports)
ESSENTIAL HYPERTENSION ( 6 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 6 FDA reports)
EYE PRURITUS ( 6 FDA reports)
FEELING GUILTY ( 6 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 6 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 6 FDA reports)
GLIOSIS ( 6 FDA reports)
GRAND MAL CONVULSION ( 6 FDA reports)
GROIN PAIN ( 6 FDA reports)
HAEMODYNAMIC INSTABILITY ( 6 FDA reports)
HAEMOTHORAX ( 6 FDA reports)
HEARING IMPAIRED ( 6 FDA reports)
HEPATIC CONGESTION ( 6 FDA reports)
HEPATOCELLULAR DAMAGE ( 6 FDA reports)
HOUSE DUST ALLERGY ( 6 FDA reports)
HYPOPARATHYROIDISM ( 6 FDA reports)
HYPOPLASTIC LEFT HEART SYNDROME ( 6 FDA reports)
ICHTHYOSIS ( 6 FDA reports)
IMPLANT SITE PAIN ( 6 FDA reports)
INAPPROPRIATE AFFECT ( 6 FDA reports)
INJECTION SITE PRURITUS ( 6 FDA reports)
INJECTION SITE REACTION ( 6 FDA reports)
INTESTINAL OBSTRUCTION ( 6 FDA reports)
INTRACARDIAC THROMBUS ( 6 FDA reports)
INTRAOCULAR LENS IMPLANT ( 6 FDA reports)
JOINT DISLOCATION REDUCTION ( 6 FDA reports)
LIPODYSTROPHY ACQUIRED ( 6 FDA reports)
MASS EXCISION ( 6 FDA reports)
MENTAL IMPAIRMENT ( 6 FDA reports)
MOVEMENT DISORDER ( 6 FDA reports)
MULTIPLE ALLERGIES ( 6 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 6 FDA reports)
NERVE INJURY ( 6 FDA reports)
NO ADVERSE EVENT ( 6 FDA reports)
OESOPHAGEAL STENOSIS ( 6 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 6 FDA reports)
PLEURISY ( 6 FDA reports)
PNEUMONIA BACTERIAL ( 6 FDA reports)
POST CONCUSSION SYNDROME ( 6 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 6 FDA reports)
PRESCRIBED OVERDOSE ( 6 FDA reports)
PUPILS UNEQUAL ( 6 FDA reports)
QRS AXIS ABNORMAL ( 6 FDA reports)
RALES ( 6 FDA reports)
RASH VESICULAR ( 6 FDA reports)
RHINITIS SEASONAL ( 6 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 6 FDA reports)
SCOLIOSIS ( 6 FDA reports)
SICCA SYNDROME ( 6 FDA reports)
SKIN GRAFT ( 6 FDA reports)
SKIN WARM ( 6 FDA reports)
STRESS SYMPTOMS ( 6 FDA reports)
STRESS URINARY INCONTINENCE ( 6 FDA reports)
SUBDURAL HAEMORRHAGE ( 6 FDA reports)
SUICIDAL BEHAVIOUR ( 6 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 6 FDA reports)
TORSADE DE POINTES ( 6 FDA reports)
TRAUMATIC BRAIN INJURY ( 6 FDA reports)
TROPONIN I INCREASED ( 6 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 6 FDA reports)
UTERINE POLYP ( 6 FDA reports)
VASCULAR INSUFFICIENCY ( 6 FDA reports)
VASOSPASM ( 6 FDA reports)
VENA CAVA FILTER INSERTION ( 6 FDA reports)
VERTEBRAL WEDGING ( 6 FDA reports)
VIRAL INFECTION ( 6 FDA reports)
VITAMIN D DECREASED ( 6 FDA reports)
WEST NILE VIRAL INFECTION ( 6 FDA reports)
WHEELCHAIR USER ( 6 FDA reports)
YAWNING ( 6 FDA reports)
ABDOMINAL HERNIA ( 5 FDA reports)
ACUTE SINUSITIS ( 5 FDA reports)
ACUTE STRESS DISORDER ( 5 FDA reports)
ADENOCARCINOMA ( 5 FDA reports)
ALCOHOL ABUSE ( 5 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 5 FDA reports)
ALVEOLAR OSTEITIS ( 5 FDA reports)
ANAEMIA MACROCYTIC ( 5 FDA reports)
ANOXIC ENCEPHALOPATHY ( 5 FDA reports)
APHASIA ( 5 FDA reports)
ASPIRATION BREAST ( 5 FDA reports)
ATROPHIC VULVOVAGINITIS ( 5 FDA reports)
BEDRIDDEN ( 5 FDA reports)
BILE DUCT OBSTRUCTION ( 5 FDA reports)
BILIARY NEOPLASM ( 5 FDA reports)
BIOPSY BREAST ( 5 FDA reports)
BIOPSY LYMPH GLAND ABNORMAL ( 5 FDA reports)
BLOOD AMYLASE INCREASED ( 5 FDA reports)
BLOOD PH INCREASED ( 5 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 5 FDA reports)
BODY HEIGHT DECREASED ( 5 FDA reports)
BONE FORMATION DECREASED ( 5 FDA reports)
BORDERLINE PERSONALITY DISORDER ( 5 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 5 FDA reports)
BREAST CANCER IN SITU ( 5 FDA reports)
BREAST DISORDER FEMALE ( 5 FDA reports)
BREAST FIBROSIS ( 5 FDA reports)
BREAST HAEMATOMA ( 5 FDA reports)
BREAST HYPERPLASIA ( 5 FDA reports)
BRONCHIAL OBSTRUCTION ( 5 FDA reports)
BRONCHIECTASIS ( 5 FDA reports)
CARDIAC PACEMAKER INSERTION ( 5 FDA reports)
CIRCULATORY COLLAPSE ( 5 FDA reports)
COELIAC ARTERY OCCLUSION ( 5 FDA reports)
CONDUCTION DISORDER ( 5 FDA reports)
DELUSION ( 5 FDA reports)
DEVELOPMENTAL DELAY ( 5 FDA reports)
DRUG PRESCRIBING ERROR ( 5 FDA reports)
DRUG TOLERANCE INCREASED ( 5 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 5 FDA reports)
DYSPAREUNIA ( 5 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 5 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 5 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 5 FDA reports)
EROSIVE DUODENITIS ( 5 FDA reports)
FACIAL PALSY ( 5 FDA reports)
FAECAL INCONTINENCE ( 5 FDA reports)
FALLOT'S TETRALOGY ( 5 FDA reports)
FEELING JITTERY ( 5 FDA reports)
FLATBACK SYNDROME ( 5 FDA reports)
FOREIGN BODY ( 5 FDA reports)
HEART VALVE STENOSIS ( 5 FDA reports)
HEPATITIS B ( 5 FDA reports)
HEPATOBILIARY SCAN ABNORMAL ( 5 FDA reports)
HERPES SIMPLEX ( 5 FDA reports)
HILAR LYMPHADENOPATHY ( 5 FDA reports)
HYPERTROPHY ( 5 FDA reports)
HYPOMAGNESAEMIA ( 5 FDA reports)
IMPAIRED FASTING GLUCOSE ( 5 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 5 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 5 FDA reports)
INFUSION RELATED REACTION ( 5 FDA reports)
INJECTION SITE RASH ( 5 FDA reports)
INJECTION SITE WARMTH ( 5 FDA reports)
LATEX ALLERGY ( 5 FDA reports)
LEFT VENTRICLE OUTFLOW TRACT OBSTRUCTION ( 5 FDA reports)
LOCAL SWELLING ( 5 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 5 FDA reports)
MACROCYTOSIS ( 5 FDA reports)
MUCOUS MEMBRANE DISORDER ( 5 FDA reports)
NARCOTIC INTOXICATION ( 5 FDA reports)
NEOPLASM SKIN ( 5 FDA reports)
NERVOUS SYSTEM DISORDER ( 5 FDA reports)
NEUROGENIC BLADDER ( 5 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 5 FDA reports)
NEUROPATHIC PAIN ( 5 FDA reports)
NICOTINE DEPENDENCE ( 5 FDA reports)
NON-SMALL CELL LUNG CANCER ( 5 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 5 FDA reports)
OCULAR ICTERUS ( 5 FDA reports)
OESTRADIOL DECREASED ( 5 FDA reports)
OLIGURIA ( 5 FDA reports)
ORAL DISCHARGE ( 5 FDA reports)
OVARIAN CANCER ( 5 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 5 FDA reports)
PELVIC HAEMATOMA ( 5 FDA reports)
PERSISTENT FOETAL CIRCULATION ( 5 FDA reports)
POLYMYALGIA RHEUMATICA ( 5 FDA reports)
PORTAL HYPERTENSION ( 5 FDA reports)
PRODUCT TASTE ABNORMAL ( 5 FDA reports)
PULMONARY MASS ( 5 FDA reports)
RASH MACULO-PAPULAR ( 5 FDA reports)
RECALL PHENOMENON ( 5 FDA reports)
REFLUX GASTRITIS ( 5 FDA reports)
RESPIRATION ABNORMAL ( 5 FDA reports)
RETROGRADE EJACULATION ( 5 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 5 FDA reports)
SCRATCH ( 5 FDA reports)
SCREAMING ( 5 FDA reports)
SCROTAL IRRITATION ( 5 FDA reports)
SELF-MEDICATION ( 5 FDA reports)
SKIN ATROPHY ( 5 FDA reports)
SKIN IRRITATION ( 5 FDA reports)
SKIN TIGHTNESS ( 5 FDA reports)
SKIN TURGOR DECREASED ( 5 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 5 FDA reports)
SPERMATOCELE ( 5 FDA reports)
SPINAL FUSION SURGERY ( 5 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 5 FDA reports)
STOMACH DISCOMFORT ( 5 FDA reports)
SUDDEN CARDIAC DEATH ( 5 FDA reports)
THERAPY NON-RESPONDER ( 5 FDA reports)
THYROID CANCER ( 5 FDA reports)
TINEA CRURIS ( 5 FDA reports)
TUMOUR MARKER INCREASED ( 5 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 5 FDA reports)
URINARY TRACT DISORDER ( 5 FDA reports)
UTERINE CERVICAL SQUAMOUS METAPLASIA ( 5 FDA reports)
WRIST FRACTURE ( 5 FDA reports)
ABDOMINAL TENDERNESS ( 4 FDA reports)
ABNORMAL FAECES ( 4 FDA reports)
ABNORMAL SENSATION IN EYE ( 4 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 4 FDA reports)
ALCOHOL POISONING ( 4 FDA reports)
AORTIC VALVE SCLEROSIS ( 4 FDA reports)
APATHY ( 4 FDA reports)
AREFLEXIA ( 4 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 4 FDA reports)
BACTERIA STOOL IDENTIFIED ( 4 FDA reports)
BENIGN BONE NEOPLASM ( 4 FDA reports)
BIPOLAR I DISORDER ( 4 FDA reports)
BIPOLAR II DISORDER ( 4 FDA reports)
BLOOD CALCIUM INCREASED ( 4 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 4 FDA reports)
BLOOD IRON DECREASED ( 4 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 4 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 4 FDA reports)
BONE MARROW TRANSPLANT ( 4 FDA reports)
BRAIN HERNIATION ( 4 FDA reports)
CARDIAC OUTPUT DECREASED ( 4 FDA reports)
CARDIOTOXICITY ( 4 FDA reports)
CARTILAGE INJURY ( 4 FDA reports)
CAUDA EQUINA SYNDROME ( 4 FDA reports)
CEREBRAL THROMBOSIS ( 4 FDA reports)
CHOKING SENSATION ( 4 FDA reports)
CHOLESTEROSIS ( 4 FDA reports)
CLAUSTROPHOBIA ( 4 FDA reports)
COLON POLYPECTOMY ( 4 FDA reports)
CONGENITAL AORTIC VALVE INCOMPETENCE ( 4 FDA reports)
CORONARY ARTERY BYPASS ( 4 FDA reports)
CULTURE URINE POSITIVE ( 4 FDA reports)
DECREASED ACTIVITY ( 4 FDA reports)
DIABETIC GASTROPARESIS ( 4 FDA reports)
DIABETIC RETINOPATHY ( 4 FDA reports)
DIZZINESS POSTURAL ( 4 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 4 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 4 FDA reports)
EAR DISCOMFORT ( 4 FDA reports)
EAR DISORDER ( 4 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 4 FDA reports)
ENDOMETRIOSIS ( 4 FDA reports)
ENTEROBACTER PNEUMONIA ( 4 FDA reports)
EOSINOPHILIA ( 4 FDA reports)
EUPHORIC MOOD ( 4 FDA reports)
EYE HAEMORRHAGE ( 4 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 4 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 4 FDA reports)
FOREIGN BODY REACTION ( 4 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 4 FDA reports)
GINGIVAL HYPERTROPHY ( 4 FDA reports)
HAIR TEXTURE ABNORMAL ( 4 FDA reports)
HALLUCINATION, OLFACTORY ( 4 FDA reports)
HEART SOUNDS ABNORMAL ( 4 FDA reports)
HEPATORENAL SYNDROME ( 4 FDA reports)
HEPATOSPLENOMEGALY ( 4 FDA reports)
HYPERCOAGULATION ( 4 FDA reports)
HYPERPHAGIA ( 4 FDA reports)
HYPERSPLENISM ( 4 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 4 FDA reports)
HYPERVOLAEMIA ( 4 FDA reports)
HYPOACUSIS ( 4 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 4 FDA reports)
ILEUS PARALYTIC ( 4 FDA reports)
INCISIONAL HERNIA, OBSTRUCTIVE ( 4 FDA reports)
INCONTINENCE ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 4 FDA reports)
INTESTINAL RESECTION ( 4 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 4 FDA reports)
INTRACRANIAL TUMOUR HAEMORRHAGE ( 4 FDA reports)
ISCHAEMIC HEPATITIS ( 4 FDA reports)
JUDGEMENT IMPAIRED ( 4 FDA reports)
KIDNEY INFECTION ( 4 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 4 FDA reports)
LARGE INTESTINE PERFORATION ( 4 FDA reports)
LEUKOENCEPHALOPATHY ( 4 FDA reports)
LEUKOPENIA ( 4 FDA reports)
LIGAMENT DISORDER ( 4 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 4 FDA reports)
LIVER INJURY ( 4 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 4 FDA reports)
LYMPHOMA ( 4 FDA reports)
MACULAR DEGENERATION ( 4 FDA reports)
MEDICAL DEVICE COMPLICATION ( 4 FDA reports)
MEDICATION RESIDUE ( 4 FDA reports)
MEGACOLON ( 4 FDA reports)
MOOD ALTERED ( 4 FDA reports)
MORTON'S NEUROMA ( 4 FDA reports)
MOUTH HAEMORRHAGE ( 4 FDA reports)
MULTI-ORGAN DISORDER ( 4 FDA reports)
MYOCLONUS ( 4 FDA reports)
NAIL DISORDER ( 4 FDA reports)
NAIL DYSTROPHY ( 4 FDA reports)
NECK MASS ( 4 FDA reports)
OBSESSIVE-COMPULSIVE PERSONALITY DISORDER ( 4 FDA reports)
OESOPHAGEAL SPASM ( 4 FDA reports)
ORAL INTAKE REDUCED ( 4 FDA reports)
OROANTRAL FISTULA ( 4 FDA reports)
ORTHOSIS USER ( 4 FDA reports)
PANCREATIC CARCINOMA ( 4 FDA reports)
PARAPLEGIA ( 4 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 4 FDA reports)
PCO2 INCREASED ( 4 FDA reports)
PELVIC PROLAPSE ( 4 FDA reports)
PERICARDIAL DISEASE ( 4 FDA reports)
PERICARDITIS ( 4 FDA reports)
PHYSIOTHERAPY ( 4 FDA reports)
PLATYBASIA ( 4 FDA reports)
PNEUMONIA KLEBSIELLA ( 4 FDA reports)
POLYCYSTIC OVARIES ( 4 FDA reports)
POLYPECTOMY ( 4 FDA reports)
POLYTRAUMATISM ( 4 FDA reports)
POOR QUALITY SLEEP ( 4 FDA reports)
POST-TRAUMATIC NECK SYNDROME ( 4 FDA reports)
PRODUCT ODOUR ABNORMAL ( 4 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 4 FDA reports)
PSYCHIATRIC SYMPTOM ( 4 FDA reports)
PULMONARY HILUM MASS ( 4 FDA reports)
RADICULITIS LUMBOSACRAL ( 4 FDA reports)
RAYNAUD'S PHENOMENON ( 4 FDA reports)
REFLUX OESOPHAGITIS ( 4 FDA reports)
RENAL COLIC ( 4 FDA reports)
RHEUMATOID LUNG ( 4 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 4 FDA reports)
SEROSITIS ( 4 FDA reports)
SKIN BURNING SENSATION ( 4 FDA reports)
SKIN INJURY ( 4 FDA reports)
SLEEP WALKING ( 4 FDA reports)
SPINAL CORPECTOMY ( 4 FDA reports)
SPONDYLOLYSIS ( 4 FDA reports)
SPONDYLOSIS ( 4 FDA reports)
SPUTUM CULTURE POSITIVE ( 4 FDA reports)
SQUAMOUS CELL CARCINOMA ( 4 FDA reports)
STASIS DERMATITIS ( 4 FDA reports)
STREPTOCOCCAL INFECTION ( 4 FDA reports)
SUBACUTE ENDOCARDITIS ( 4 FDA reports)
SUDDEN DEATH ( 4 FDA reports)
SYSTEMIC CANDIDA ( 4 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 4 FDA reports)
THORACIC OPERATION ( 4 FDA reports)
THROAT TIGHTNESS ( 4 FDA reports)
THYROID NEOPLASM ( 4 FDA reports)
ULCER HAEMORRHAGE ( 4 FDA reports)
URETHRAL DISCHARGE ( 4 FDA reports)
URINARY HESITATION ( 4 FDA reports)
URINE ABNORMALITY ( 4 FDA reports)
UTERINE CANCER ( 4 FDA reports)
VAGINAL DISCHARGE ( 4 FDA reports)
VAGINITIS ATROPHIC ( 4 FDA reports)
VAGINITIS BACTERIAL ( 4 FDA reports)
VARICELLA ( 4 FDA reports)
VENOUS BRUIT ( 4 FDA reports)
VISUAL FIELD DEFECT ( 4 FDA reports)
VITAMIN B12 DEFICIENCY ( 4 FDA reports)
WRONG DRUG ADMINISTERED ( 4 FDA reports)
XANTHOMA ( 4 FDA reports)
ABDOMINAL ABSCESS ( 3 FDA reports)
ABDOMINAL SEPSIS ( 3 FDA reports)
ABORTION SPONTANEOUS ( 3 FDA reports)
ACCELERATED HYPERTENSION ( 3 FDA reports)
ACCIDENTAL DEATH ( 3 FDA reports)
ADENOMYOSIS ( 3 FDA reports)
ADJUSTMENT DISORDER ( 3 FDA reports)
ADNEXA UTERI MASS ( 3 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 3 FDA reports)
AMYLOIDOSIS ( 3 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 3 FDA reports)
ANAL CANDIDIASIS ( 3 FDA reports)
ANAPHYLACTIC SHOCK ( 3 FDA reports)
ANGIOFIBROMA ( 3 FDA reports)
ANTICHOLINERGIC SYNDROME ( 3 FDA reports)
AORTIC OCCLUSION ( 3 FDA reports)
APHTHOUS STOMATITIS ( 3 FDA reports)
APPLICATION SITE PRURITUS ( 3 FDA reports)
ARTERIAL STENOSIS ( 3 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 3 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 3 FDA reports)
ASBESTOSIS ( 3 FDA reports)
B-CELL LYMPHOMA ( 3 FDA reports)
BENIGN SALIVARY GLAND NEOPLASM ( 3 FDA reports)
BLINDNESS TRANSIENT ( 3 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 3 FDA reports)
BLOOD SODIUM INCREASED ( 3 FDA reports)
BONE GRAFT ( 3 FDA reports)
BONE SCAN ABNORMAL ( 3 FDA reports)
BOWEL SOUNDS ABNORMAL ( 3 FDA reports)
BRONCHOPLEURAL FISTULA ( 3 FDA reports)
CARCINOID TUMOUR PULMONARY ( 3 FDA reports)
CARDIOVERSION ( 3 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 3 FDA reports)
CEREBELLAR INFARCTION ( 3 FDA reports)
CEREBRAL CALCIFICATION ( 3 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 3 FDA reports)
CHOLESTASIS ( 3 FDA reports)
CHRONIC FATIGUE SYNDROME ( 3 FDA reports)
CNS VENTRICULITIS ( 3 FDA reports)
COLITIS ULCERATIVE ( 3 FDA reports)
COLON ADENOMA ( 3 FDA reports)
COLOSTOMY ( 3 FDA reports)
CONGENITAL ANOMALY ( 3 FDA reports)
CONGENITAL PNEUMONIA ( 3 FDA reports)
CORONARY ARTERY THROMBOSIS ( 3 FDA reports)
CREATININE RENAL CLEARANCE ABNORMAL ( 3 FDA reports)
CREPITATIONS ( 3 FDA reports)
CUBITAL TUNNEL SYNDROME ( 3 FDA reports)
CYTOREDUCTIVE SURGERY ( 3 FDA reports)
DENTAL PULP DISORDER ( 3 FDA reports)
DERMATITIS ALLERGIC ( 3 FDA reports)
DEVICE ELECTRICAL FINDING ( 3 FDA reports)
DEVICE FAILURE ( 3 FDA reports)
DIABETIC COMA ( 3 FDA reports)
DIABETIC COMPLICATION ( 3 FDA reports)
DRUG EFFECT INCREASED ( 3 FDA reports)
DRUG INTOLERANCE ( 3 FDA reports)
DRUG LEVEL INCREASED ( 3 FDA reports)
DRUG TOLERANCE ( 3 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 3 FDA reports)
EAR INFECTION ( 3 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX SHORTENED ( 3 FDA reports)
ELECTROLYTE IMBALANCE ( 3 FDA reports)
EMBOLIC STROKE ( 3 FDA reports)
ENTERITIS ( 3 FDA reports)
EOSINOPHIL COUNT INCREASED ( 3 FDA reports)
EPIGASTRIC DISCOMFORT ( 3 FDA reports)
EVANS SYNDROME ( 3 FDA reports)
EXTRASYSTOLES ( 3 FDA reports)
EYE INFECTION FUNGAL ( 3 FDA reports)
FACIAL BONES FRACTURE ( 3 FDA reports)
FEEDING TUBE COMPLICATION ( 3 FDA reports)
FIBROUS HISTIOCYTOMA ( 3 FDA reports)
FOETAL DISTRESS SYNDROME ( 3 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 3 FDA reports)
FUNGAEMIA ( 3 FDA reports)
FURUNCLE ( 3 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 3 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 3 FDA reports)
GLYCOSURIA ( 3 FDA reports)
GOITRE ( 3 FDA reports)
GRANULOCYTE COUNT INCREASED ( 3 FDA reports)
HAEMOLYTIC ANAEMIA ( 3 FDA reports)
HAEMORRHAGIC ANAEMIA ( 3 FDA reports)
HAIR DISORDER ( 3 FDA reports)
HALLUCINATIONS, MIXED ( 3 FDA reports)
HAND DEFORMITY ( 3 FDA reports)
HEPATIC ADENOMA ( 3 FDA reports)
HEPATIC INFARCTION ( 3 FDA reports)
HEPATIC NECROSIS ( 3 FDA reports)
HISTOPLASMOSIS ( 3 FDA reports)
HISTOPLASMOSIS DISSEMINATED ( 3 FDA reports)
HOMICIDAL IDEATION ( 3 FDA reports)
HYPERNATRAEMIA ( 3 FDA reports)
HYPEROSMOLAR STATE ( 3 FDA reports)
HYPERTENSIVE EMERGENCY ( 3 FDA reports)
HYPERTHERMIA ( 3 FDA reports)
HYPERTHYROIDISM ( 3 FDA reports)
HYPOALBUMINAEMIA ( 3 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 3 FDA reports)
ILIAC ARTERY STENOSIS ( 3 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 3 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 3 FDA reports)
INJECTION SITE HAEMORRHAGE ( 3 FDA reports)
INTERVERTEBRAL DISC INJURY ( 3 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 3 FDA reports)
INTESTINAL PERFORATION ( 3 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 3 FDA reports)
INTRAVENOUS CATHETER MANAGEMENT ( 3 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 3 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE NEONATAL ( 3 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 3 FDA reports)
KNEE OPERATION ( 3 FDA reports)
KYPHOSCOLIOSIS ( 3 FDA reports)
LEG AMPUTATION ( 3 FDA reports)
LENTIGO ( 3 FDA reports)
LICHENOID KERATOSIS ( 3 FDA reports)
LIP DRY ( 3 FDA reports)
LOCALISED OEDEMA ( 3 FDA reports)
LOSS OF EMPLOYMENT ( 3 FDA reports)
LUNG CONSOLIDATION ( 3 FDA reports)
LUNG TRANSPLANT ( 3 FDA reports)
LUNG VOLUME REDUCTION SURGERY ( 3 FDA reports)
MALIGNANT HYPERTENSION ( 3 FDA reports)
MANIA ( 3 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 3 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 3 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 3 FDA reports)
MECHANICAL VENTILATION ( 3 FDA reports)
MEDIASTINOSCOPY ( 3 FDA reports)
MERALGIA PARAESTHETICA ( 3 FDA reports)
METABOLIC ENCEPHALOPATHY ( 3 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 3 FDA reports)
MICROVASCULAR ANGINA ( 3 FDA reports)
MITRAL VALVE ATRESIA ( 3 FDA reports)
MONONEUROPATHY ( 3 FDA reports)
MORBID THOUGHTS ( 3 FDA reports)
MUSCLE DISORDER ( 3 FDA reports)
MUSCLE HAEMORRHAGE ( 3 FDA reports)
MUSCLE RIGIDITY ( 3 FDA reports)
NAIL INFECTION ( 3 FDA reports)
NAIL OPERATION ( 3 FDA reports)
NARCOLEPSY ( 3 FDA reports)
NECROTISING FASCIITIS ( 3 FDA reports)
NEUTROPENIC SEPSIS ( 3 FDA reports)
NODAL ARRHYTHMIA ( 3 FDA reports)
OPEN ANGLE GLAUCOMA ( 3 FDA reports)
OPTIC ATROPHY ( 3 FDA reports)
OPTIC NEURITIS ( 3 FDA reports)
OSTEOMALACIA ( 3 FDA reports)
PACEMAKER COMPLICATION ( 3 FDA reports)
PANCREATITIS CHRONIC ( 3 FDA reports)
PATELLA FRACTURE ( 3 FDA reports)
PCO2 DECREASED ( 3 FDA reports)
PELVIC MASS ( 3 FDA reports)
PERIARTHRITIS ( 3 FDA reports)
PERICARDIAL DRAINAGE ( 3 FDA reports)
PERIORBITAL OEDEMA ( 3 FDA reports)
PERIPHERAL NERVE LESION ( 3 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 3 FDA reports)
PERNICIOUS ANAEMIA ( 3 FDA reports)
PERSONALITY DISORDER ( 3 FDA reports)
PHARMACOPHOBIA ( 3 FDA reports)
PHOTOSENSITIVITY REACTION ( 3 FDA reports)
PITTING OEDEMA ( 3 FDA reports)
PLANTAR FASCIITIS ( 3 FDA reports)
PNEUMOCOCCAL SEPSIS ( 3 FDA reports)
PNEUMONIA VIRAL ( 3 FDA reports)
POSITIONAL PLAGIOCEPHALY ( 3 FDA reports)
POST PROCEDURAL MYOCARDIAL INFARCTION ( 3 FDA reports)
POST-TRAUMATIC HEADACHE ( 3 FDA reports)
POSTURING ( 3 FDA reports)
PREMATURE LABOUR ( 3 FDA reports)
PRESBYOPIA ( 3 FDA reports)
PROCEDURAL COMPLICATION ( 3 FDA reports)
PROCTITIS ( 3 FDA reports)
PROSTATISM ( 3 FDA reports)
PSEUDODEMENTIA ( 3 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 3 FDA reports)
PSYCHOLOGICAL TRAUMA ( 3 FDA reports)
PULMONARY ARTERY STENOSIS CONGENITAL ( 3 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 3 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 3 FDA reports)
PULMONARY VALVE STENOSIS CONGENITAL ( 3 FDA reports)
PULSE ABSENT ( 3 FDA reports)
REGURGITATION ( 3 FDA reports)
RENAL ATROPHY ( 3 FDA reports)
RHEUMATOID NODULE ( 3 FDA reports)
RHONCHI ( 3 FDA reports)
RIGHT VENTRICLE OUTFLOW TRACT OBSTRUCTION ( 3 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 3 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 3 FDA reports)
SCLERODERMA ( 3 FDA reports)
SCROTAL GANGRENE ( 3 FDA reports)
SELF-INJURIOUS IDEATION ( 3 FDA reports)
SENSORY DISTURBANCE ( 3 FDA reports)
SIGMOIDECTOMY ( 3 FDA reports)
SLEEP TALKING ( 3 FDA reports)
SLUGGISHNESS ( 3 FDA reports)
SNEEZING ( 3 FDA reports)
SPINAL X-RAY ABNORMAL ( 3 FDA reports)
SPLENOMEGALY ( 3 FDA reports)
SPUTUM INCREASED ( 3 FDA reports)
STATUS MIGRAINOSUS ( 3 FDA reports)
STRESS CARDIOMYOPATHY ( 3 FDA reports)
SUBCUTANEOUS ABSCESS ( 3 FDA reports)
SYNOVIAL CYST ( 3 FDA reports)
TARSAL TUNNEL SYNDROME ( 3 FDA reports)
TETANY ( 3 FDA reports)
THORACIC HAEMORRHAGE ( 3 FDA reports)
TONGUE DISORDER ( 3 FDA reports)
TOOTH IMPACTED ( 3 FDA reports)
TORTICOLLIS ( 3 FDA reports)
TRANSIENT GLOBAL AMNESIA ( 3 FDA reports)
TRANSIENT TACHYPNOEA OF THE NEWBORN ( 3 FDA reports)
TRIGGER FINGER ( 3 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 3 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
URETERITIS ( 3 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 3 FDA reports)
URINE OUTPUT INCREASED ( 3 FDA reports)
VASCULAR GRAFT OCCLUSION ( 3 FDA reports)
VENA CAVA THROMBOSIS ( 3 FDA reports)
VISCERAL CONGESTION ( 3 FDA reports)
VOCAL CORD DISORDER ( 3 FDA reports)
VULVOVAGINAL PRURITUS ( 3 FDA reports)
XEROSIS ( 3 FDA reports)
ABDOMINAL AORTIC BRUIT ( 2 FDA reports)
ABSCESS ORAL ( 2 FDA reports)
ABSCESS RUPTURE ( 2 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 2 FDA reports)
ADJUSTMENT DISORDER WITH DEPRESSED MOOD ( 2 FDA reports)
ADVERSE REACTION ( 2 FDA reports)
AGONAL RHYTHM ( 2 FDA reports)
AKATHISIA ( 2 FDA reports)
AKINESIA ( 2 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 2 FDA reports)
ANAEMIA MEGALOBLASTIC ( 2 FDA reports)
ANALGESIC EFFECT ( 2 FDA reports)
ANAPHYLACTOID REACTION ( 2 FDA reports)
ANKLE OPERATION ( 2 FDA reports)
ANORGASMIA ( 2 FDA reports)
ANTI-CYCLIC CITRULLINATED PEPTIDE ANTIBODY POSITIVE ( 2 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 2 FDA reports)
ANTI-HBC IGG ANTIBODY POSITIVE ( 2 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 2 FDA reports)
ANURIA ( 2 FDA reports)
AORTIC DILATATION ( 2 FDA reports)
APPLICATION SITE ERYTHEMA ( 2 FDA reports)
APPLICATION SITE RASH ( 2 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 2 FDA reports)
ARTERIAL INJURY ( 2 FDA reports)
ARTERIAL INSUFFICIENCY ( 2 FDA reports)
ARTERIOVENOUS FISTULA ANEURYSM ( 2 FDA reports)
ARTHRITIS INFECTIVE ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 2 FDA reports)
ASPIRATION PLEURAL CAVITY ( 2 FDA reports)
AUTOIMMUNE HEPATITIS ( 2 FDA reports)
AZYGOS LOBE ( 2 FDA reports)
BASEDOW'S DISEASE ( 2 FDA reports)
BASOPHIL COUNT INCREASED ( 2 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 2 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 2 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 2 FDA reports)
BILIARY DILATATION ( 2 FDA reports)
BINGE EATING ( 2 FDA reports)
BLADDER PAIN ( 2 FDA reports)
BLEPHARITIS ( 2 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 2 FDA reports)
BLOOD COUNT ABNORMAL ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 2 FDA reports)
BLOOD CREATININE ABNORMAL ( 2 FDA reports)
BLOOD ETHANOL INCREASED ( 2 FDA reports)
BLOOD GASES ABNORMAL ( 2 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 2 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 2 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 2 FDA reports)
BONE MARROW DISORDER ( 2 FDA reports)
BRADYPHRENIA ( 2 FDA reports)
BRONCHOSPASM ( 2 FDA reports)
CALCULUS BLADDER ( 2 FDA reports)
CALCULUS URETERIC ( 2 FDA reports)
CALCULUS URETHRAL ( 2 FDA reports)
CARDIAC FAILURE CHRONIC ( 2 FDA reports)
CARDIAC FLUTTER ( 2 FDA reports)
CARDIAC TAMPONADE ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 2 FDA reports)
CATHETER RELATED INFECTION ( 2 FDA reports)
CELLULITIS GANGRENOUS ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 2 FDA reports)
CEREBRAL DISORDER ( 2 FDA reports)
CHEMICAL INJURY ( 2 FDA reports)
CHEMOTHERAPY ( 2 FDA reports)
CHOLELITHIASIS OBSTRUCTIVE ( 2 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 2 FDA reports)
CLOSTRIDIUM COLITIS ( 2 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 2 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 2 FDA reports)
CROUP INFECTIOUS ( 2 FDA reports)
CULTURE WOUND POSITIVE ( 2 FDA reports)
DEPRESSION SUICIDAL ( 2 FDA reports)
DEVICE DAMAGE ( 2 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 2 FDA reports)
DIZZINESS EXERTIONAL ( 2 FDA reports)
DRUG ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE ( 2 FDA reports)
DRUG ERUPTION ( 2 FDA reports)
DUODENITIS ( 2 FDA reports)
DYSMENORRHOEA ( 2 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 2 FDA reports)
ENDOCARDITIS ( 2 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 2 FDA reports)
ENDOTRACHEAL INTUBATION ( 2 FDA reports)
ENTEROCOCCAL INFECTION ( 2 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 2 FDA reports)
EPICONDYLITIS ( 2 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 2 FDA reports)
ERUCTATION ( 2 FDA reports)
EXERCISE TOLERANCE DECREASED ( 2 FDA reports)
EXPOSED BONE IN JAW ( 2 FDA reports)
EXTRADURAL HAEMATOMA ( 2 FDA reports)
EYE INJURY ( 2 FDA reports)
FACTOR V LEIDEN MUTATION ( 2 FDA reports)
FAECALOMA ( 2 FDA reports)
FAECES HARD ( 2 FDA reports)
FAT INTOLERANCE ( 2 FDA reports)
FAT NECROSIS ( 2 FDA reports)
FIBRIN D DIMER INCREASED ( 2 FDA reports)
FLAT AFFECT ( 2 FDA reports)
FOETAL CARDIAC DISORDER ( 2 FDA reports)
FORCED EXPIRATORY VOLUME DECREASED ( 2 FDA reports)
FOREIGN BODY ASPIRATION ( 2 FDA reports)
FOREIGN BODY TRAUMA ( 2 FDA reports)
FORMICATION ( 2 FDA reports)
FRACTURE NONUNION ( 2 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 2 FDA reports)
FUNGAL RHINITIS ( 2 FDA reports)
GALLOP RHYTHM PRESENT ( 2 FDA reports)
GANGLION ( 2 FDA reports)
GASTRIC OPERATION ( 2 FDA reports)
GASTRIC PH DECREASED ( 2 FDA reports)
GASTROENTERITIS VIRAL ( 2 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 2 FDA reports)
GINGIVAL ATROPHY ( 2 FDA reports)
GINGIVAL HYPERPLASIA ( 2 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 2 FDA reports)
GRAFT THROMBOSIS ( 2 FDA reports)
GUN SHOT WOUND ( 2 FDA reports)
HAEMATOCRIT INCREASED ( 2 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 2 FDA reports)
HEAD DISCOMFORT ( 2 FDA reports)
HEART VALVE INSUFFICIENCY ( 2 FDA reports)
HELICOBACTER GASTRITIS ( 2 FDA reports)
HELICOBACTER TEST POSITIVE ( 2 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 2 FDA reports)
HEPATITIS TOXIC ( 2 FDA reports)
HEPATORENAL FAILURE ( 2 FDA reports)
HERNIA REPAIR ( 2 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 2 FDA reports)
HORMONE LEVEL ABNORMAL ( 2 FDA reports)
HOSTILITY ( 2 FDA reports)
HUMERUS FRACTURE ( 2 FDA reports)
HYDROCEPHALUS ( 2 FDA reports)
HYDROPNEUMOTHORAX ( 2 FDA reports)
HYPERBILIRUBINAEMIA ( 2 FDA reports)
HYPERTENSIVE CRISIS ( 2 FDA reports)
HYPERTHERMIA MALIGNANT ( 2 FDA reports)
HYPERTONIA ( 2 FDA reports)
HYPOPERFUSION ( 2 FDA reports)
HYPOTHERMIA ( 2 FDA reports)
HYSTERECTOMY ( 2 FDA reports)
IATROGENIC INJURY ( 2 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 2 FDA reports)
IMPRISONMENT ( 2 FDA reports)
INCISIONAL HERNIA ( 2 FDA reports)
INCREASED APPETITE ( 2 FDA reports)
INCREASED BRONCHIAL SECRETION ( 2 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 2 FDA reports)
INJECTION SITE INFECTION ( 2 FDA reports)
INJECTION SITE URTICARIA ( 2 FDA reports)
INJECTION SITE VESICLES ( 2 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 2 FDA reports)
JOINT ANKYLOSIS ( 2 FDA reports)
JOINT WARMTH ( 2 FDA reports)
JUGULAR VEIN THROMBOSIS ( 2 FDA reports)
KIDNEY FIBROSIS ( 2 FDA reports)
LARYNGEAL OEDEMA ( 2 FDA reports)
LARYNGITIS ( 2 FDA reports)
LEFT VENTRICULAR FAILURE ( 2 FDA reports)
LEUKAEMIA ( 2 FDA reports)
LIBIDO INCREASED ( 2 FDA reports)
LISTLESS ( 2 FDA reports)
LONG QT SYNDROME ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFLAMMATION ( 2 FDA reports)
LUNG ABSCESS ( 2 FDA reports)
LUNG HYPERINFLATION ( 2 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 2 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 2 FDA reports)
LYMPHOEDEMA ( 2 FDA reports)
MALIGNANT MELANOMA ( 2 FDA reports)
MASTOIDITIS ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 2 FDA reports)
MEAN CELL VOLUME INCREASED ( 2 FDA reports)
MENINGIOMA ( 2 FDA reports)
MENSTRUATION IRREGULAR ( 2 FDA reports)
METABOLIC SYNDROME ( 2 FDA reports)
METASTASES TO PLEURA ( 2 FDA reports)
METASTASES TO SKIN ( 2 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 2 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST POSITIVE ( 2 FDA reports)
METRORRHAGIA ( 2 FDA reports)
MICROCYTIC ANAEMIA ( 2 FDA reports)
MIDDLE EAR EFFUSION ( 2 FDA reports)
MONOPLEGIA ( 2 FDA reports)
MUSCLE RUPTURE ( 2 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 2 FDA reports)
NAIL TINEA ( 2 FDA reports)
NASAL SEPTUM PERFORATION ( 2 FDA reports)
NASAL SINUS DRAINAGE ( 2 FDA reports)
NEGATIVE THOUGHTS ( 2 FDA reports)
NEPHROSCLEROSIS ( 2 FDA reports)
NEURALGIC AMYOTROPHY ( 2 FDA reports)
NIPPLE DISORDER ( 2 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 2 FDA reports)
OBSESSIVE THOUGHTS ( 2 FDA reports)
OBSTRUCTION ( 2 FDA reports)
OEDEMA MOUTH ( 2 FDA reports)
OESOPHAGEAL PAIN ( 2 FDA reports)
OESOPHAGOGASTRIC FUNDOPLASTY ( 2 FDA reports)
OPEN FRACTURE ( 2 FDA reports)
OPIATES POSITIVE ( 2 FDA reports)
OPTIC DISC DISORDER ( 2 FDA reports)
OPTIC NERVE CUP/DISC RATIO DECREASED ( 2 FDA reports)
ORAL MUCOSA ATROPHY ( 2 FDA reports)
OSTEOLYSIS ( 2 FDA reports)
OSTEOMYELITIS CHRONIC ( 2 FDA reports)
OTOTOXICITY ( 2 FDA reports)
PAIN EXACERBATED ( 2 FDA reports)
PANCREATITIS RELAPSING ( 2 FDA reports)
PARADOXICAL DRUG REACTION ( 2 FDA reports)
PARATHYROID DISORDER ( 2 FDA reports)
PARATHYROIDECTOMY ( 2 FDA reports)
PARTNER STRESS ( 2 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 2 FDA reports)
PELVIC DISCOMFORT ( 2 FDA reports)
PELVIC VENOUS THROMBOSIS ( 2 FDA reports)
PENIS DISORDER ( 2 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 2 FDA reports)
PERIPHERAL NERVE DECOMPRESSION ( 2 FDA reports)
PERITONEAL HAEMORRHAGE ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COUNTERFEIT ( 2 FDA reports)
PHARYNGEAL DISORDER ( 2 FDA reports)
PIGMENTED NAEVUS ( 2 FDA reports)
PIRIFORMIS SYNDROME ( 2 FDA reports)
PLATELET DISORDER ( 2 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 2 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 2 FDA reports)
PO2 INCREASED ( 2 FDA reports)
POLYARTHRITIS ( 2 FDA reports)
POLYCYTHAEMIA ( 2 FDA reports)
POLYMYOSITIS ( 2 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 2 FDA reports)
POOR VENOUS ACCESS ( 2 FDA reports)
POST PROCEDURAL INFECTION ( 2 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 2 FDA reports)
POSTURE ABNORMAL ( 2 FDA reports)
PROCEDURAL HYPOTENSION ( 2 FDA reports)
PROSTATE CANCER RECURRENT ( 2 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 2 FDA reports)
PROTEUS INFECTION ( 2 FDA reports)
PROTHROMBIN TIME SHORTENED ( 2 FDA reports)
PSYCHOMOTOR RETARDATION ( 2 FDA reports)
PULMONARY GRANULOMA ( 2 FDA reports)
PULMONARY HAEMORRHAGE ( 2 FDA reports)
PULMONARY VALVE STENOSIS ( 2 FDA reports)
PULMONARY VASCULAR DISORDER ( 2 FDA reports)
PUPILLARY DISORDER ( 2 FDA reports)
RADIAL TUNNEL SYNDROME ( 2 FDA reports)
RADICULAR SYNDROME ( 2 FDA reports)
RASH MACULAR ( 2 FDA reports)
RASH PAPULAR ( 2 FDA reports)
RECTAL ULCER ( 2 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 2 FDA reports)
RENAL ANEURYSM ( 2 FDA reports)
RENAL ARTERIOSCLEROSIS ( 2 FDA reports)
RENAL INFARCT ( 2 FDA reports)
RENAL VESSEL DISORDER ( 2 FDA reports)
REPETITIVE SPEECH ( 2 FDA reports)
RESPIRATORY TRACT INFECTION ( 2 FDA reports)
RESUSCITATION ( 2 FDA reports)
RETINAL TEAR ( 2 FDA reports)
RETROPERITONEAL HAEMATOMA ( 2 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 2 FDA reports)
RHINALGIA ( 2 FDA reports)
RIGHT VENTRICULAR FAILURE ( 2 FDA reports)
SARCOIDOSIS ( 2 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 2 FDA reports)
SCLERODACTYLIA ( 2 FDA reports)
SCOTOMA ( 2 FDA reports)
SEXUAL DYSFUNCTION ( 2 FDA reports)
SHOCK HAEMORRHAGIC ( 2 FDA reports)
SHORT-BOWEL SYNDROME ( 2 FDA reports)
SIALOADENITIS ( 2 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 2 FDA reports)
SKIN NODULE ( 2 FDA reports)
SKIN PLAQUE ( 2 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 2 FDA reports)
SOFT TISSUE INFECTION ( 2 FDA reports)
SPINAL CORD INJURY ( 2 FDA reports)
SPLEEN CONGESTION ( 2 FDA reports)
SPLENIC INFARCTION ( 2 FDA reports)
SPUTUM DISCOLOURED ( 2 FDA reports)
STATUS EPILEPTICUS ( 2 FDA reports)
STENOTROPHOMONAS INFECTION ( 2 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 2 FDA reports)
STUPOR ( 2 FDA reports)
SUBDURAL HAEMATOMA ( 2 FDA reports)
SUBMANDIBULAR MASS ( 2 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 2 FDA reports)
SYNCOPE VASOVAGAL ( 2 FDA reports)
SYNOVITIS ( 2 FDA reports)
TEETH BRITTLE ( 2 FDA reports)
TELANGIECTASIA ( 2 FDA reports)
TEMPERATURE INTOLERANCE ( 2 FDA reports)
TESTICULAR DISORDER ( 2 FDA reports)
THERAPY CESSATION ( 2 FDA reports)
THERMAL BURNS OF EYE ( 2 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 2 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
THYROIDECTOMY ( 2 FDA reports)
TOTAL LUNG CAPACITY INCREASED ( 2 FDA reports)
TOXOPLASMA SEROLOGY POSITIVE ( 2 FDA reports)
TRANSPLANT FAILURE ( 2 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 2 FDA reports)
TREATMENT FAILURE ( 2 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 2 FDA reports)
URETERIC OBSTRUCTION ( 2 FDA reports)
URINARY TRACT OBSTRUCTION ( 2 FDA reports)
URINE COLOUR ABNORMAL ( 2 FDA reports)
URINE KETONE BODY PRESENT ( 2 FDA reports)
VARICOSE ULCERATION ( 2 FDA reports)
VASCULAR PUNCTURE SITE SEALING ( 2 FDA reports)
VENTRICULAR ARRHYTHMIA ( 2 FDA reports)
VESTIBULAR DISORDER ( 2 FDA reports)
VULVAL DISORDER ( 2 FDA reports)
VULVOVAGINAL DISCOMFORT ( 2 FDA reports)
WEIGHT BEARING DIFFICULTY ( 2 FDA reports)
WHITE BLOOD CELL DISORDER ( 2 FDA reports)
ABDOMINAL HERNIA REPAIR ( 1 FDA reports)
ABDOMINAL INFECTION ( 1 FDA reports)
ABDOMINAL INJURY ( 1 FDA reports)
ABSCESS NECK ( 1 FDA reports)
ACQUIRED MACROGLOSSIA ( 1 FDA reports)
ACUTE HEPATIC FAILURE ( 1 FDA reports)
ACUTE LUNG INJURY ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
ADRENAL ADENOMA ( 1 FDA reports)
ADRENAL DISORDER ( 1 FDA reports)
AEROPHAGIA ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
AIR EMBOLISM ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
ALLERGY TO CHEMICALS ( 1 FDA reports)
ALLODYNIA ( 1 FDA reports)
AMAUROSIS FUGAX ( 1 FDA reports)
AMMONIA DECREASED ( 1 FDA reports)
AMNESTIC DISORDER ( 1 FDA reports)
AMPHETAMINES POSITIVE ( 1 FDA reports)
ANAL HAEMORRHAGE ( 1 FDA reports)
ANALGESIC DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANALGESIC DRUG LEVEL INCREASED ( 1 FDA reports)
ANGIOGRAM ( 1 FDA reports)
ANGIOMYOLIPOMA ( 1 FDA reports)
ANGIOPLASTY ( 1 FDA reports)
ANOGENITAL DYSPLASIA ( 1 FDA reports)
ANOSMIA ( 1 FDA reports)
ANOXIA ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTIDIURETIC HORMONE ABNORMALITY ( 1 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 1 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 1 FDA reports)
ANTISOCIAL BEHAVIOUR ( 1 FDA reports)
AORTIC ANEURYSM RUPTURE ( 1 FDA reports)
AORTIC ATHEROSCLEROSIS ( 1 FDA reports)
AORTIC DISSECTION ( 1 FDA reports)
AORTIC THROMBOSIS ( 1 FDA reports)
AORTIC VALVE CALCIFICATION ( 1 FDA reports)
AORTIC VALVE REPLACEMENT ( 1 FDA reports)
APHONIA ( 1 FDA reports)
APNOEIC ATTACK ( 1 FDA reports)
APPETITE DISORDER ( 1 FDA reports)
APPLICATION SITE BURNING ( 1 FDA reports)
APPLICATION SITE INFECTION ( 1 FDA reports)
APPLICATION SITE URTICARIA ( 1 FDA reports)
ARNOLD-CHIARI MALFORMATION ( 1 FDA reports)
ARTERIAL HAEMORRHAGE ( 1 FDA reports)
ARTHROSCOPY ( 1 FDA reports)
ASPIRATION BIOPSY ( 1 FDA reports)
ATRIAL HYPERTROPHY ( 1 FDA reports)
ATRIAL THROMBOSIS ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
ATRIOVENTRICULAR SEPTAL DEFECT ( 1 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 1 FDA reports)
BACTERIAL TEST POSITIVE ( 1 FDA reports)
BAROTRAUMA ( 1 FDA reports)
BASAL GANGLIA INFARCTION ( 1 FDA reports)
BASE EXCESS DECREASED ( 1 FDA reports)
BELLIGERENCE ( 1 FDA reports)
BENIGN OVARIAN TUMOUR ( 1 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 1 FDA reports)
BICUSPID AORTIC VALVE ( 1 FDA reports)
BILE DUCT STENOSIS ( 1 FDA reports)
BILIARY CIRRHOSIS ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
BIOPSY LIVER ( 1 FDA reports)
BITE ( 1 FDA reports)
BLADDER DILATATION ( 1 FDA reports)
BLADDER INJURY ( 1 FDA reports)
BLADDER OPERATION ( 1 FDA reports)
BLAST CELLS PRESENT ( 1 FDA reports)
BLOOD ALCOHOL INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 1 FDA reports)
BLOOD BICARBONATE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN ( 1 FDA reports)
BLOOD BLISTER ( 1 FDA reports)
BLOOD CANNABINOIDS ( 1 FDA reports)
BLOOD CARBON MONOXIDE ABNORMAL ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD ERYTHROPOIETIN DECREASED ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 1 FDA reports)
BLOOD METHAEMOGLOBIN PRESENT ( 1 FDA reports)
BLOOD OSMOLARITY INCREASED ( 1 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 1 FDA reports)
BLOOD PH ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC DECREASED ( 1 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 1 FDA reports)
BLOOD UREA ABNORMAL ( 1 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 1 FDA reports)
BLOOD URINE ( 1 FDA reports)
BLOODY DISCHARGE ( 1 FDA reports)
BODY FAT DISORDER ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 1 FDA reports)
BRACHIAL PLEXUS INJURY ( 1 FDA reports)
BRAIN CONTUSION ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
BRAIN STEM SYNDROME ( 1 FDA reports)
BREAKTHROUGH PAIN ( 1 FDA reports)
BREAST CANCER METASTATIC ( 1 FDA reports)
BRONCHIAL HAEMORRHAGE ( 1 FDA reports)
BRONCHIOLITIS ( 1 FDA reports)
BRONCHITIS CHRONIC ( 1 FDA reports)
BRONCHOMALACIA ( 1 FDA reports)
BRONCHOSTENOSIS ( 1 FDA reports)
BUNDLE BRANCH BLOCK ( 1 FDA reports)
BURN OESOPHAGEAL ( 1 FDA reports)
BURNOUT SYNDROME ( 1 FDA reports)
BURNS SECOND DEGREE ( 1 FDA reports)
BURNS THIRD DEGREE ( 1 FDA reports)
BURSITIS INFECTIVE STAPHYLOCOCCAL ( 1 FDA reports)
BUTTOCK PAIN ( 1 FDA reports)
C-REACTIVE PROTEIN ABNORMAL ( 1 FDA reports)
CALCIUM IONISED DECREASED ( 1 FDA reports)
CALCULUS URINARY ( 1 FDA reports)
CAPILLARY NAIL REFILL TEST ABNORMAL ( 1 FDA reports)
CARBUNCLE ( 1 FDA reports)
CARCINOID TUMOUR OF THE SMALL BOWEL ( 1 FDA reports)
CARCINOMA ( 1 FDA reports)
CARCINOMA IN SITU ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
CARDIAC HYPERTROPHY ( 1 FDA reports)
CARDIAC OPERATION ( 1 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 1 FDA reports)
CARDIOSPASM ( 1 FDA reports)
CAROTID ARTERY OCCLUSION ( 1 FDA reports)
CAROTID ENDARTERECTOMY ( 1 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 1 FDA reports)
CATHETER SITE ERYTHEMA ( 1 FDA reports)
CATHETER SITE HAEMATOMA ( 1 FDA reports)
CATHETER SITE INFECTION ( 1 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 1 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 1 FDA reports)
CELLULITIS ORBITAL ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM STIMULATION ( 1 FDA reports)
CEREBELLAR HAEMORRHAGE ( 1 FDA reports)
CEREBELLAR ISCHAEMIA ( 1 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 1 FDA reports)
CEREBRAL HYPOPERFUSION ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT PROPHYLAXIS ( 1 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 1 FDA reports)
CERVIX CARCINOMA ( 1 FDA reports)
CHANGE OF BOWEL HABIT ( 1 FDA reports)
CHAPPED LIPS ( 1 FDA reports)
CHEST INJURY ( 1 FDA reports)
CHEST WALL PAIN ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHOLECYSTITIS INFECTIVE ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA TRANSFORMATION ( 1 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 1 FDA reports)
CLUMSINESS ( 1 FDA reports)
CLUSTER HEADACHE ( 1 FDA reports)
COAGULATION TIME PROLONGED ( 1 FDA reports)
COELIAC DISEASE ( 1 FDA reports)
COLITIS EROSIVE ( 1 FDA reports)
COLLAGEN DISORDER ( 1 FDA reports)
COLON CANCER METASTATIC ( 1 FDA reports)
COLONIC OBSTRUCTION ( 1 FDA reports)
COLONOSCOPY ( 1 FDA reports)
COLORECTAL CANCER ( 1 FDA reports)
COLORECTAL CANCER METASTATIC ( 1 FDA reports)
COLORECTAL CANCER RECURRENT ( 1 FDA reports)
COMA HEPATIC ( 1 FDA reports)
COMPARTMENT SYNDROME ( 1 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED LUNG ( 1 FDA reports)
COMPULSIVE SHOPPING ( 1 FDA reports)
CONCUSSION ( 1 FDA reports)
CONGENITAL AORTIC STENOSIS ( 1 FDA reports)
CONGENITAL CARDIOVASCULAR ANOMALY ( 1 FDA reports)
CONGENITAL MITRAL VALVE STENOSIS ( 1 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
COR PULMONALE ( 1 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 1 FDA reports)
CORONARY OSTIAL STENOSIS ( 1 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
CREATININE URINE INCREASED ( 1 FDA reports)
CRYSTAL URINE PRESENT ( 1 FDA reports)
CULTURE THROAT POSITIVE ( 1 FDA reports)
CULTURE TISSUE SPECIMEN POSITIVE ( 1 FDA reports)
CUSHINGOID ( 1 FDA reports)
CYCLIC VOMITING SYNDROME ( 1 FDA reports)
CYSTOURETHROCELE ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DEAFNESS UNILATERAL ( 1 FDA reports)
DEATH OF RELATIVE ( 1 FDA reports)
DELIRIUM TREMENS ( 1 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 1 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 1 FDA reports)
DEMYELINATION ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DIABETIC FOOT ( 1 FDA reports)
DISSOCIATION ( 1 FDA reports)
DISSOCIATIVE DISORDER ( 1 FDA reports)
DISTURBANCE IN SEXUAL AROUSAL ( 1 FDA reports)
DIVORCED ( 1 FDA reports)
DROWNING ( 1 FDA reports)
DRUG ADDICT ( 1 FDA reports)
DRUG EFFECT DELAYED ( 1 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 1 FDA reports)
DRUG LEVEL CHANGED ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DRY THROAT ( 1 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DYSHIDROSIS ( 1 FDA reports)
DYSKINESIA OESOPHAGEAL ( 1 FDA reports)
DYSMORPHISM ( 1 FDA reports)
DYSPHEMIA ( 1 FDA reports)
DYSPHORIA ( 1 FDA reports)
DYSPLASTIC NAEVUS ( 1 FDA reports)
EAR OPERATION ( 1 FDA reports)
EASTERN COOPERATIVE ONCOLOGY GROUP PERFORMANCE STATUS WORSENED ( 1 FDA reports)
ECZEMA NUMMULAR ( 1 FDA reports)
EJACULATION FAILURE ( 1 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM P PULMONALE ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
ENAMEL ANOMALY ( 1 FDA reports)
ENDOMETRIAL CANCER ( 1 FDA reports)
ENERGY INCREASED ( 1 FDA reports)
ENTEROBACTER SEPSIS ( 1 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 1 FDA reports)
ENTEROCOCCAL SEPSIS ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
ESCHERICHIA BACTERAEMIA ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
ESCHERICHIA SEPSIS ( 1 FDA reports)
EX-TOBACCO USER ( 1 FDA reports)
EXFOLIATIVE RASH ( 1 FDA reports)
EXPIRED DRUG ADMINISTERED ( 1 FDA reports)
EXPOSURE DURING BREAST FEEDING ( 1 FDA reports)
EXPOSURE TO TOXIC AGENT ( 1 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 1 FDA reports)
EXTRADURAL ABSCESS ( 1 FDA reports)
EYE ALLERGY ( 1 FDA reports)
EYE OEDEMA ( 1 FDA reports)
EYE ROLLING ( 1 FDA reports)
EYELID CYST ( 1 FDA reports)
EYELID DISORDER ( 1 FDA reports)
FACIAL PARESIS ( 1 FDA reports)
FACTITIOUS DISORDER ( 1 FDA reports)
FAILURE OF IMPLANT ( 1 FDA reports)
FEAR OF DEATH ( 1 FDA reports)
FEELING OF DESPAIR ( 1 FDA reports)
FEELINGS OF WORTHLESSNESS ( 1 FDA reports)
FEMALE STERILISATION ( 1 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 1 FDA reports)
FEMORAL ARTERY OCCLUSION ( 1 FDA reports)
FEMORAL BRUIT ( 1 FDA reports)
FIBROADENOMA OF BREAST ( 1 FDA reports)
FIBROSARCOMA ( 1 FDA reports)
FLASHBACK ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
FOCAL NODULAR HYPERPLASIA ( 1 FDA reports)
FOETAL HEART RATE INCREASED ( 1 FDA reports)
FOOT OPERATION ( 1 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 1 FDA reports)
FREEZING PHENOMENON ( 1 FDA reports)
FULL BLOOD COUNT INCREASED ( 1 FDA reports)
FUNGAL OESOPHAGITIS ( 1 FDA reports)
FUNGAL RASH ( 1 FDA reports)
GALLBLADDER ENLARGEMENT ( 1 FDA reports)
GASTRIC DILATATION ( 1 FDA reports)
GASTRIC POLYPS ( 1 FDA reports)
GASTROINTESTINAL DISORDER POSTOPERATIVE ( 1 FDA reports)
GASTROINTESTINAL EROSION ( 1 FDA reports)
GASTROINTESTINAL GANGRENE ( 1 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 1 FDA reports)
GASTROINTESTINAL MUCOSAL EXFOLIATION ( 1 FDA reports)
GASTROINTESTINAL NECROSIS ( 1 FDA reports)
GASTROINTESTINAL OEDEMA ( 1 FDA reports)
GASTROINTESTINAL PERFORATION ( 1 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 1 FDA reports)
GASTROINTESTINAL ULCER ( 1 FDA reports)
GASTROSCHISIS ( 1 FDA reports)
GENITAL HYPOAESTHESIA ( 1 FDA reports)
GENITAL LABIAL ADHESIONS ( 1 FDA reports)
GESTATIONAL DIABETES ( 1 FDA reports)
GINGIVAL INJURY ( 1 FDA reports)
GLIOBLASTOMA MULTIFORME ( 1 FDA reports)
GLOBULINS INCREASED ( 1 FDA reports)
GLUCOSE URINE PRESENT ( 1 FDA reports)
GLYCOPEPTIDE ANTIBIOTIC RESISTANT ENTEROCOCCAL INFECTION ( 1 FDA reports)
GRAFT COMPLICATION ( 1 FDA reports)
GRAVITATIONAL OEDEMA ( 1 FDA reports)
GRIP STRENGTH DECREASED ( 1 FDA reports)
GROWING PAINS ( 1 FDA reports)
GUTTATE PSORIASIS ( 1 FDA reports)
HAEMARTHROSIS ( 1 FDA reports)
HAEMATOCRIT ABNORMAL ( 1 FDA reports)
HAEMATOPOIETIC NEOPLASM ( 1 FDA reports)
HAEMATOTOXICITY ( 1 FDA reports)
HAEMODILUTION ( 1 FDA reports)
HAEMOGLOBIN ABNORMAL ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HAEMORRHAGIC CYST ( 1 FDA reports)
HAIR COLOUR CHANGES ( 1 FDA reports)
HAIR GROWTH ABNORMAL ( 1 FDA reports)
HALLUCINATION, TACTILE ( 1 FDA reports)
HEART INJURY ( 1 FDA reports)
HEART TRANSPLANT REJECTION ( 1 FDA reports)
HELICOBACTER INFECTION ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA TEST POSITIVE ( 1 FDA reports)
HEPATECTOMY ( 1 FDA reports)
HEPATIC CANCER METASTATIC ( 1 FDA reports)
HEPATIC MASS ( 1 FDA reports)
HEPATIC NEOPLASM ( 1 FDA reports)
HEPATIC PAIN ( 1 FDA reports)
HEPATIC TRAUMA ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HERPES ZOSTER OTICUS ( 1 FDA reports)
HIV INFECTION ( 1 FDA reports)
HOARSENESS ( 1 FDA reports)
HOSPICE CARE ( 1 FDA reports)
HYPERAMMONAEMIA ( 1 FDA reports)
HYPERCAPNIA ( 1 FDA reports)
HYPERHOMOCYSTEINAEMIA ( 1 FDA reports)
HYPERPROLACTINAEMIA ( 1 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 1 FDA reports)
HYPERURICAEMIA ( 1 FDA reports)
HYPOCHROMIC ANAEMIA ( 1 FDA reports)
HYPOCOAGULABLE STATE ( 1 FDA reports)
HYPOHIDROSIS ( 1 FDA reports)
HYPOMANIA ( 1 FDA reports)
HYPOPROTHROMBINAEMIA ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
HYPOVOLAEMIC SHOCK ( 1 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 1 FDA reports)
IDEAS OF REFERENCE ( 1 FDA reports)
ILEAL ULCER ( 1 FDA reports)
ILIAC VEIN OCCLUSION ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
IMPETIGO ( 1 FDA reports)
IMPULSE-CONTROL DISORDER ( 1 FDA reports)
IMPULSIVE BEHAVIOUR ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INBORN ERROR OF METABOLISM ( 1 FDA reports)
INCISION SITE PAIN ( 1 FDA reports)
INFECTED CYST ( 1 FDA reports)
INFERTILITY ( 1 FDA reports)
INHIBITORY DRUG INTERACTION ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
INJECTION SITE BURNING ( 1 FDA reports)
INJECTION SITE DISCOLOURATION ( 1 FDA reports)
INJECTION SITE DISCOMFORT ( 1 FDA reports)
INJECTION SITE INDURATION ( 1 FDA reports)
INJECTION SITE IRRITATION ( 1 FDA reports)
INJURY ASPHYXIATION ( 1 FDA reports)
INTERNAL INJURY ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 1 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 1 FDA reports)
INTRA-UTERINE DEATH ( 1 FDA reports)
INTRAOCULAR MELANOMA ( 1 FDA reports)
INTUSSUSCEPTION ( 1 FDA reports)
INVESTIGATION ABNORMAL ( 1 FDA reports)
IRITIS ( 1 FDA reports)
ISCHAEMIC NEPHROPATHY ( 1 FDA reports)
JUGULAR VEIN DISTENSION ( 1 FDA reports)
KERATITIS ( 1 FDA reports)
KERATOACANTHOMA ( 1 FDA reports)
KETOACIDOSIS ( 1 FDA reports)
KETONURIA ( 1 FDA reports)
KNEE DEFORMITY ( 1 FDA reports)
KNEE MENISCECTOMY ( 1 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 1 FDA reports)
LARYNGEAL DISORDER ( 1 FDA reports)
LEUKOPLAKIA ORAL ( 1 FDA reports)
LIBIDO DISORDER ( 1 FDA reports)
LICHEN PLANUS ( 1 FDA reports)
LIGAMENT RUPTURE ( 1 FDA reports)
LIMB DEFORMITY ( 1 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 1 FDA reports)
LIP NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 1 FDA reports)
LIP OEDEMA ( 1 FDA reports)
LIP PAIN ( 1 FDA reports)
LIPASE URINE INCREASED ( 1 FDA reports)
LIPIDS INCREASED ( 1 FDA reports)
LOCALISED OSTEOARTHRITIS ( 1 FDA reports)
LOGORRHOEA ( 1 FDA reports)
LOOSE STOOLS ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
LUNG ADENOCARCINOMA ( 1 FDA reports)
LUNG ADENOCARCINOMA STAGE IV ( 1 FDA reports)
LUPUS-LIKE SYNDROME ( 1 FDA reports)
LYME DISEASE ( 1 FDA reports)
LYMPHADENITIS ( 1 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
MACULAR OEDEMA ( 1 FDA reports)
MACULE ( 1 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 1 FDA reports)
MAMMOGRAM ( 1 FDA reports)
MARITAL PROBLEM ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 1 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 1 FDA reports)
MEAN CELL VOLUME DECREASED ( 1 FDA reports)
MEAN PLATELET VOLUME INCREASED ( 1 FDA reports)
MEDIASTINAL MASS ( 1 FDA reports)
MEDIASTINITIS ( 1 FDA reports)
MENIERE'S DISEASE ( 1 FDA reports)
METABOLIC ALKALOSIS ( 1 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 1 FDA reports)
METASTASES TO ADRENALS ( 1 FDA reports)
METASTASES TO PELVIS ( 1 FDA reports)
METASTASES TO SOFT TISSUE ( 1 FDA reports)
METHAEMOGLOBINAEMIA ( 1 FDA reports)
MICROALBUMINURIA ( 1 FDA reports)
MICTURITION FREQUENCY DECREASED ( 1 FDA reports)
MILIA ( 1 FDA reports)
MINERAL DEFICIENCY ( 1 FDA reports)
MITRAL VALVE CALCIFICATION ( 1 FDA reports)
MITRAL VALVE DISEASE MIXED ( 1 FDA reports)
MITRAL VALVE STENOSIS ( 1 FDA reports)
MIXED HYPERLIPIDAEMIA ( 1 FDA reports)
MOANING ( 1 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
MORGANELLA INFECTION ( 1 FDA reports)
MORPHOEA ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 1 FDA reports)
MURPHY'S SIGN POSITIVE ( 1 FDA reports)
MUSCLE CONTRACTURE ( 1 FDA reports)
MUSCLE SPASTICITY ( 1 FDA reports)
MYCOBACTERIA SPUTUM TEST POSITIVE ( 1 FDA reports)
MYELOPATHY ( 1 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 1 FDA reports)
MYOCARDITIS ( 1 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 1 FDA reports)
MYOPIA ( 1 FDA reports)
MYOSCLEROSIS ( 1 FDA reports)
NAIL DISCOMFORT ( 1 FDA reports)
NASAL CYST ( 1 FDA reports)
NASAL DISCOMFORT ( 1 FDA reports)
NASAL DRYNESS ( 1 FDA reports)
NASAL MUCOSAL DISCOLOURATION ( 1 FDA reports)
NASAL MUCOSAL DISORDER ( 1 FDA reports)
NASAL SEPTUM DEVIATION ( 1 FDA reports)
NASAL SEPTUM DISORDER ( 1 FDA reports)
NASAL ULCER ( 1 FDA reports)
NEGATIVISM ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NEPHROGENIC ANAEMIA ( 1 FDA reports)
NERVE ROOT INJURY ( 1 FDA reports)
NEURODERMATITIS ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NEUTROPHIL FUNCTION DISORDER ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
NIGHT BLINDNESS ( 1 FDA reports)
NONSPECIFIC REACTION ( 1 FDA reports)
NYSTAGMUS ( 1 FDA reports)
OESOPHAGEAL CARCINOMA ( 1 FDA reports)
OESOPHAGEAL FISTULA ( 1 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 1 FDA reports)
OESOPHAGEAL PERFORATION ( 1 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 1 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 1 FDA reports)
OESOPHAGITIS ULCERATIVE ( 1 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 1 FDA reports)
OMPHALITIS ( 1 FDA reports)
ONYCHOMADESIS ( 1 FDA reports)
OPIATES ( 1 FDA reports)
OPTIC NERVE DISORDER ( 1 FDA reports)
OPTIC NERVE INFARCTION ( 1 FDA reports)
ORAL BACTERIAL INFECTION ( 1 FDA reports)
ORAL FUNGAL INFECTION ( 1 FDA reports)
ORGANIC ERECTILE DYSFUNCTION ( 1 FDA reports)
OROPHARYNGEAL BLISTERING ( 1 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 1 FDA reports)
ORTHOSTATIC INTOLERANCE ( 1 FDA reports)
OSTEOMYELITIS ACUTE ( 1 FDA reports)
OTITIS EXTERNA ( 1 FDA reports)
OTITIS MEDIA ACUTE ( 1 FDA reports)
OVARIAN CANCER STAGE III ( 1 FDA reports)
OXYGEN SATURATION INCREASED ( 1 FDA reports)
PAIN OF SKIN ( 1 FDA reports)
PAINFUL RESPIRATION ( 1 FDA reports)
PANCREATIC CYST ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PANCREATIC NECROSIS ( 1 FDA reports)
PANCREATIC PSEUDOCYST ( 1 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 1 FDA reports)
PANIC DISORDER WITH AGORAPHOBIA ( 1 FDA reports)
PARANOID PERSONALITY DISORDER ( 1 FDA reports)
PARASOMNIA ( 1 FDA reports)
PARATHYROID GLAND ENLARGEMENT ( 1 FDA reports)
PARESIS ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PATENT DUCTUS ARTERIOSUS REPAIR ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PCO2 ABNORMAL ( 1 FDA reports)
PELVIC ABSCESS ( 1 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 1 FDA reports)
PELVIC PERITONEAL ADHESIONS ( 1 FDA reports)
PENILE WART ( 1 FDA reports)
PEPTOSTREPTOCOCCUS INFECTION ( 1 FDA reports)
PERFORMANCE STATUS DECREASED ( 1 FDA reports)
PERIANAL ABSCESS ( 1 FDA reports)
PERICARDIAL HAEMORRHAGE ( 1 FDA reports)
PERIPHERAL ISCHAEMIA ( 1 FDA reports)
PERIPHERAL OCCLUSIVE DISEASE ( 1 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 1 FDA reports)
PERIPORTAL SINUS DILATATION ( 1 FDA reports)
PERIRECTAL ABSCESS ( 1 FDA reports)
PERITONEAL DISORDER ( 1 FDA reports)
PERITONEAL EFFLUENT ABNORMAL ( 1 FDA reports)
PERITONEAL FLUID ANALYSIS ABNORMAL ( 1 FDA reports)
PERITONITIS BACTERIAL ( 1 FDA reports)
PHAGOPHOBIA ( 1 FDA reports)
PHARYNGEAL INFLAMMATION ( 1 FDA reports)
PHARYNGEAL LEUKOPLAKIA ( 1 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PLATELET FUNCTION TEST ABNORMAL ( 1 FDA reports)
PNEUMOCEPHALUS ( 1 FDA reports)
PNEUMOCOCCAL INFECTION ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 1 FDA reports)
PO2 ABNORMAL ( 1 FDA reports)
POLYDIPSIA ( 1 FDA reports)
POST CHOLECYSTECTOMY SYNDROME ( 1 FDA reports)
POST INFLAMMATORY PIGMENTATION CHANGE ( 1 FDA reports)
POST LUMBAR PUNCTURE SYNDROME ( 1 FDA reports)
POST PROCEDURAL DISCOMFORT ( 1 FDA reports)
POST PROCEDURAL DRAINAGE ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
POST PROCEDURAL NAUSEA ( 1 FDA reports)
POST-TRAUMATIC PAIN ( 1 FDA reports)
POSTOPERATIVE ADHESION ( 1 FDA reports)
POSTOPERATIVE FEVER ( 1 FDA reports)
PREALBUMIN DECREASED ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PRESSURE OF SPEECH ( 1 FDA reports)
PROCEDURAL HYPERTENSION ( 1 FDA reports)
PROCEDURAL NAUSEA ( 1 FDA reports)
PROCEDURAL SITE REACTION ( 1 FDA reports)
PROCEDURAL VOMITING ( 1 FDA reports)
PRODUCT CONTAMINATION PHYSICAL ( 1 FDA reports)
PRODUCT SIZE ISSUE ( 1 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 1 FDA reports)
PROSTATOMEGALY ( 1 FDA reports)
PRURITUS ALLERGIC ( 1 FDA reports)
PSEUDOMONAL SEPSIS ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PSORIATIC ARTHROPATHY ( 1 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 1 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY MALFORMATION ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
PULMONARY TOXICITY ( 1 FDA reports)
PULSE ABNORMAL ( 1 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 1 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 1 FDA reports)
PYOTHORAX ( 1 FDA reports)
RADICAL HYSTERECTOMY ( 1 FDA reports)
RADICULITIS ( 1 FDA reports)
RASH MORBILLIFORM ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 1 FDA reports)
RECTAL CANCER ( 1 FDA reports)
RECTAL POLYP ( 1 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 1 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 1 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL ARTERY FIBROMUSCULAR DYSPLASIA ( 1 FDA reports)
RENAL ARTERY STENOSIS ( 1 FDA reports)
RENAL CANCER ( 1 FDA reports)
RENAL CANCER METASTATIC ( 1 FDA reports)
RENAL CELL CARCINOMA ( 1 FDA reports)
RENAL CYST HAEMORRHAGE ( 1 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 1 FDA reports)
RENAL MASS ( 1 FDA reports)
RENAL TRANSPLANT ( 1 FDA reports)
REPERFUSION ARRHYTHMIA ( 1 FDA reports)
RESPIRATORY ACIDOSIS ( 1 FDA reports)
RESPIRATORY ALKALOSIS ( 1 FDA reports)
RETICULOCYTE COUNT ABNORMAL ( 1 FDA reports)
RETINAL DETACHMENT ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
RETINAL PIGMENTATION ( 1 FDA reports)
RETINAL VASCULAR OCCLUSION ( 1 FDA reports)
RETROPERITONEAL FIBROSIS ( 1 FDA reports)
RETROPERITONEAL NEOPLASM ( 1 FDA reports)
RHINITIS ( 1 FDA reports)
SALPINGO-OOPHORECTOMY ( 1 FDA reports)
SALPINGO-OOPHORECTOMY UNILATERAL ( 1 FDA reports)
SCAB ( 1 FDA reports)
SCAN ABDOMEN ABNORMAL ( 1 FDA reports)
SCHIZOPHRENIA ( 1 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 1 FDA reports)
SCIATIC NERVE NEUROPATHY ( 1 FDA reports)
SCINTILLATING SCOTOMA ( 1 FDA reports)
SCROTAL OEDEMA ( 1 FDA reports)
SCROTAL SWELLING ( 1 FDA reports)
SEASONAL ALLERGY ( 1 FDA reports)
SELF ESTEEM DECREASED ( 1 FDA reports)
SENILE DEMENTIA ( 1 FDA reports)
SKIN HAEMORRHAGE ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SKIN STRIAE ( 1 FDA reports)
SKULL FRACTURED BASE ( 1 FDA reports)
SLEEP PARALYSIS ( 1 FDA reports)
SLEEP TERROR ( 1 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 1 FDA reports)
SOCIAL FEAR ( 1 FDA reports)
SOFT TISSUE HAEMORRHAGE ( 1 FDA reports)
SOMATOFORM DISORDER ( 1 FDA reports)
SPINA BIFIDA ( 1 FDA reports)
SPINAL CORD DISORDER ( 1 FDA reports)
SPINAL DECOMPRESSION ( 1 FDA reports)
SPINAL DEFORMITY ( 1 FDA reports)
SPINAL ROD INSERTION ( 1 FDA reports)
SPLENIC GRANULOMA ( 1 FDA reports)
SPLENITIS ( 1 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 1 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
STARING ( 1 FDA reports)
STATUS ASTHMATICUS ( 1 FDA reports)
STENT MALFUNCTION ( 1 FDA reports)
STERNAL FRACTURE ( 1 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 1 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 1 FDA reports)
SUBSTANCE ABUSE ( 1 FDA reports)
SUDDEN ONSET OF SLEEP ( 1 FDA reports)
SUNBURN ( 1 FDA reports)
SUPERIOR MESENTERIC ARTERY SYNDROME ( 1 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 1 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 1 FDA reports)
SUSPICIOUSNESS ( 1 FDA reports)
SWEAT GLAND INFECTION ( 1 FDA reports)
SYPHILIS ( 1 FDA reports)
SYRINGE ISSUE ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 1 FDA reports)
SYSTOLIC HYPERTENSION ( 1 FDA reports)
TANGENTIALITY ( 1 FDA reports)
TENODESIS ( 1 FDA reports)
TENOSYNOVITIS ( 1 FDA reports)
TERMINAL INSOMNIA ( 1 FDA reports)
THEFT ( 1 FDA reports)
THERAPEUTIC PRODUCT CONTAMINATION ( 1 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 1 FDA reports)
THIRST ( 1 FDA reports)
THORACIC CAVITY DRAINAGE TEST ABNORMAL ( 1 FDA reports)
THYROID CYST ( 1 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 1 FDA reports)
TINEA PEDIS ( 1 FDA reports)
TOE AMPUTATION ( 1 FDA reports)
TOE DEFORMITY ( 1 FDA reports)
TONGUE ATROPHY ( 1 FDA reports)
TONGUE BITING ( 1 FDA reports)
TONGUE BLISTERING ( 1 FDA reports)
TONIC CLONIC MOVEMENTS ( 1 FDA reports)
TONSILLITIS ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 1 FDA reports)
TRACHEAL HAEMORRHAGE ( 1 FDA reports)
TRANSFUSION ( 1 FDA reports)
TRANSPOSITION OF THE GREAT VESSELS ( 1 FDA reports)
TRAUMATIC HAEMATOMA ( 1 FDA reports)
TRIGEMINAL NEURALGIA ( 1 FDA reports)
TUBERCULIN TEST POSITIVE ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
TUMOUR COMPRESSION ( 1 FDA reports)
TUMOUR EMBOLISM ( 1 FDA reports)
ULCERATIVE KERATITIS ( 1 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 1 FDA reports)
UMBILICAL HERNIA, OBSTRUCTIVE ( 1 FDA reports)
UNDERWEIGHT ( 1 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
URETHRAL ABSCESS ( 1 FDA reports)
URETHRAL OBSTRUCTION ( 1 FDA reports)
URETHRAL STENOSIS ( 1 FDA reports)
URGE INCONTINENCE ( 1 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 1 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 1 FDA reports)
URINARY TRACT NEOPLASM ( 1 FDA reports)
URINE CALCIUM INCREASED ( 1 FDA reports)
URINE LEUKOCYTE ESTERASE ( 1 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 1 FDA reports)
URINE ODOUR ABNORMAL ( 1 FDA reports)
URINE SODIUM DECREASED ( 1 FDA reports)
UROSEPSIS ( 1 FDA reports)
UTERINE ENLARGEMENT ( 1 FDA reports)
UTERINE SPASM ( 1 FDA reports)
VASCULAR DEMENTIA ( 1 FDA reports)
VASCULAR INJURY ( 1 FDA reports)
VASCULAR PSEUDOANEURYSM ( 1 FDA reports)
VASCULAR SHUNT ( 1 FDA reports)
VASODILATATION ( 1 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 1 FDA reports)
VISCERAL OEDEMA ( 1 FDA reports)
VISUAL BRIGHTNESS ( 1 FDA reports)
VITREOUS HAEMORRHAGE ( 1 FDA reports)
VULVAL CELLULITIS ( 1 FDA reports)
VULVITIS ( 1 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 1 FDA reports)
VULVOVAGINAL ERYTHEMA ( 1 FDA reports)
WALDENSTROM'S MACROGLOBULINAEMIA ( 1 FDA reports)
WALKING AID USER ( 1 FDA reports)
WITHDRAWAL OF LIFE SUPPORT ( 1 FDA reports)
WOUND NECROSIS ( 1 FDA reports)
X-RAY ABNORMAL ( 1 FDA reports)
XANTHOPSIA ( 1 FDA reports)

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