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

NAUSEA ( 846 FDA reports)
PAIN ( 747 FDA reports)
DIZZINESS ( 736 FDA reports)
NO ADVERSE EVENT ( 722 FDA reports)
HEADACHE ( 696 FDA reports)
DYSPNOEA ( 675 FDA reports)
ARTHRALGIA ( 626 FDA reports)
HYPERSENSITIVITY ( 624 FDA reports)
ABDOMINAL PAIN UPPER ( 560 FDA reports)
FATIGUE ( 510 FDA reports)
PRURITUS ( 507 FDA reports)
BACK PAIN ( 496 FDA reports)
VOMITING ( 496 FDA reports)
CHEST PAIN ( 476 FDA reports)
ANXIETY ( 437 FDA reports)
OEDEMA PERIPHERAL ( 429 FDA reports)
ASTHENIA ( 411 FDA reports)
DIARRHOEA ( 407 FDA reports)
BLOOD PRESSURE INCREASED ( 388 FDA reports)
URTICARIA ( 382 FDA reports)
DEPRESSION ( 374 FDA reports)
SWELLING FACE ( 363 FDA reports)
PAIN IN EXTREMITY ( 353 FDA reports)
INSOMNIA ( 338 FDA reports)
RASH ( 337 FDA reports)
MYOCARDIAL INFARCTION ( 336 FDA reports)
CONSTIPATION ( 334 FDA reports)
HYPERTENSION ( 320 FDA reports)
ABDOMINAL PAIN ( 308 FDA reports)
ERYTHEMA ( 298 FDA reports)
ANAEMIA ( 294 FDA reports)
CEREBROVASCULAR ACCIDENT ( 294 FDA reports)
SOMNOLENCE ( 291 FDA reports)
DYSPEPSIA ( 290 FDA reports)
DRUG INEFFECTIVE ( 269 FDA reports)
FALL ( 267 FDA reports)
HAEMATOCHEZIA ( 266 FDA reports)
HYPOAESTHESIA ( 257 FDA reports)
PYREXIA ( 234 FDA reports)
ABDOMINAL DISCOMFORT ( 233 FDA reports)
LOSS OF CONSCIOUSNESS ( 232 FDA reports)
PARAESTHESIA ( 229 FDA reports)
FEELING ABNORMAL ( 228 FDA reports)
MYALGIA ( 222 FDA reports)
WEIGHT DECREASED ( 218 FDA reports)
RECTAL HAEMORRHAGE ( 215 FDA reports)
INJURY ( 203 FDA reports)
STOMACH DISCOMFORT ( 202 FDA reports)
MUSCLE SPASMS ( 201 FDA reports)
ARTHRITIS ( 199 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 190 FDA reports)
CHEST DISCOMFORT ( 183 FDA reports)
CONTUSION ( 180 FDA reports)
GAIT DISTURBANCE ( 178 FDA reports)
EMOTIONAL DISTRESS ( 176 FDA reports)
FAECES DISCOLOURED ( 176 FDA reports)
BLOOD GLUCOSE INCREASED ( 168 FDA reports)
MALAISE ( 168 FDA reports)
PNEUMONIA ( 168 FDA reports)
SWELLING ( 164 FDA reports)
HYPOTENSION ( 162 FDA reports)
PALPITATIONS ( 161 FDA reports)
DYSPHAGIA ( 160 FDA reports)
HYPERHIDROSIS ( 160 FDA reports)
ABDOMINAL DISTENSION ( 155 FDA reports)
CONVULSION ( 154 FDA reports)
JOINT SWELLING ( 154 FDA reports)
COUGH ( 146 FDA reports)
LIP SWELLING ( 144 FDA reports)
SYNCOPE ( 144 FDA reports)
VISION BLURRED ( 143 FDA reports)
EYE SWELLING ( 142 FDA reports)
TREMOR ( 142 FDA reports)
DEHYDRATION ( 141 FDA reports)
MUSCULAR WEAKNESS ( 140 FDA reports)
WEIGHT INCREASED ( 140 FDA reports)
OSTEOARTHRITIS ( 139 FDA reports)
CHOLELITHIASIS ( 138 FDA reports)
HEART RATE INCREASED ( 137 FDA reports)
SWOLLEN TONGUE ( 135 FDA reports)
BURNING SENSATION ( 132 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 129 FDA reports)
CHILLS ( 128 FDA reports)
RENAL FAILURE ( 126 FDA reports)
SINUSITIS ( 122 FDA reports)
HAEMORRHAGE ( 120 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 119 FDA reports)
URINARY TRACT INFECTION ( 119 FDA reports)
MUSCULOSKELETAL PAIN ( 118 FDA reports)
PULMONARY EMBOLISM ( 117 FDA reports)
ANAPHYLACTIC REACTION ( 115 FDA reports)
GASTRIC ULCER ( 115 FDA reports)
THROAT IRRITATION ( 115 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 114 FDA reports)
PRURITUS GENERALISED ( 114 FDA reports)
DYSURIA ( 110 FDA reports)
FLUSHING ( 110 FDA reports)
NEUROPATHY PERIPHERAL ( 108 FDA reports)
MIGRAINE ( 107 FDA reports)
CONFUSIONAL STATE ( 106 FDA reports)
HAEMATEMESIS ( 106 FDA reports)
HAEMOGLOBIN DECREASED ( 106 FDA reports)
BLOOD PRESSURE DECREASED ( 105 FDA reports)
BRONCHITIS ( 105 FDA reports)
DECREASED APPETITE ( 105 FDA reports)
DRY MOUTH ( 105 FDA reports)
NECK PAIN ( 105 FDA reports)
OSTEONECROSIS OF JAW ( 105 FDA reports)
PAIN IN JAW ( 103 FDA reports)
ANHEDONIA ( 102 FDA reports)
DYSGEUSIA ( 102 FDA reports)
NERVOUSNESS ( 102 FDA reports)
OVERDOSE ( 102 FDA reports)
ANAPHYLACTIC SHOCK ( 101 FDA reports)
CONDITION AGGRAVATED ( 101 FDA reports)
RENAL FAILURE ACUTE ( 99 FDA reports)
THROAT TIGHTNESS ( 99 FDA reports)
EPISTAXIS ( 98 FDA reports)
FEELING HOT ( 98 FDA reports)
BONE DISORDER ( 96 FDA reports)
HAEMORRHOIDS ( 96 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 96 FDA reports)
DEEP VEIN THROMBOSIS ( 94 FDA reports)
BLOOD URINE PRESENT ( 93 FDA reports)
CARDIAC DISORDER ( 92 FDA reports)
PLEURAL EFFUSION ( 92 FDA reports)
CORONARY ARTERY DISEASE ( 91 FDA reports)
UNEVALUABLE EVENT ( 90 FDA reports)
BLISTER ( 89 FDA reports)
OSTEOMYELITIS ( 89 FDA reports)
RASH MACULAR ( 88 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 86 FDA reports)
THROMBOSIS ( 85 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 84 FDA reports)
AMNESIA ( 83 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 83 FDA reports)
GASTRIC HAEMORRHAGE ( 83 FDA reports)
DRUG HYPERSENSITIVITY ( 82 FDA reports)
OSTEONECROSIS ( 82 FDA reports)
INFECTION ( 81 FDA reports)
BONE PAIN ( 80 FDA reports)
HIATUS HERNIA ( 80 FDA reports)
SUICIDAL IDEATION ( 79 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 79 FDA reports)
DEATH ( 77 FDA reports)
INFLUENZA LIKE ILLNESS ( 77 FDA reports)
TOOTH EXTRACTION ( 77 FDA reports)
ANOREXIA ( 76 FDA reports)
STRESS ( 76 FDA reports)
FLATULENCE ( 73 FDA reports)
GASTRITIS ( 73 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 73 FDA reports)
WHEEZING ( 73 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 72 FDA reports)
ALOPECIA ( 71 FDA reports)
SPINAL OSTEOARTHRITIS ( 71 FDA reports)
METASTASES TO BONE ( 70 FDA reports)
SCAR ( 70 FDA reports)
ADVERSE EVENT ( 69 FDA reports)
CARDIAC MURMUR ( 69 FDA reports)
SEPSIS ( 69 FDA reports)
ANGINA PECTORIS ( 68 FDA reports)
ATRIAL FIBRILLATION ( 68 FDA reports)
RASH PRURITIC ( 68 FDA reports)
TINNITUS ( 68 FDA reports)
VAGINAL HAEMORRHAGE ( 68 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 67 FDA reports)
ASTHMA ( 67 FDA reports)
FLUID RETENTION ( 67 FDA reports)
GASTROINTESTINAL DISORDER ( 67 FDA reports)
HEPATIC ENZYME INCREASED ( 66 FDA reports)
RASH ERYTHEMATOUS ( 66 FDA reports)
RASH GENERALISED ( 66 FDA reports)
RENAL PAIN ( 66 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 65 FDA reports)
CHOLECYSTITIS CHRONIC ( 65 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 64 FDA reports)
HOT FLUSH ( 64 FDA reports)
MOBILITY DECREASED ( 64 FDA reports)
NEPHROLITHIASIS ( 64 FDA reports)
PULMONARY OEDEMA ( 64 FDA reports)
THROMBOCYTOPENIA ( 64 FDA reports)
BALANCE DISORDER ( 63 FDA reports)
DIABETES MELLITUS ( 63 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 63 FDA reports)
MEMORY IMPAIRMENT ( 63 FDA reports)
CELLULITIS ( 62 FDA reports)
COLITIS ULCERATIVE ( 62 FDA reports)
PHARYNGEAL OEDEMA ( 62 FDA reports)
GASTRIC DISORDER ( 61 FDA reports)
INJECTION SITE ERYTHEMA ( 61 FDA reports)
TOOTHACHE ( 61 FDA reports)
ATELECTASIS ( 60 FDA reports)
FOREIGN BODY TRAUMA ( 60 FDA reports)
TACHYCARDIA ( 60 FDA reports)
CARDIOMEGALY ( 59 FDA reports)
DIVERTICULUM ( 59 FDA reports)
OSTEOPENIA ( 59 FDA reports)
BLOOD CREATININE INCREASED ( 58 FDA reports)
DENTAL CARIES ( 58 FDA reports)
HYPOKALAEMIA ( 58 FDA reports)
LYMPHADENOPATHY ( 58 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 58 FDA reports)
OSTEOPOROSIS ( 58 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 57 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 57 FDA reports)
EAR PAIN ( 57 FDA reports)
HYPOAESTHESIA ORAL ( 56 FDA reports)
CROHN'S DISEASE ( 55 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 55 FDA reports)
CATARACT ( 54 FDA reports)
DYSMENORRHOEA ( 54 FDA reports)
IRRITABLE BOWEL SYNDROME ( 54 FDA reports)
POLLAKIURIA ( 54 FDA reports)
METASTASES TO LIVER ( 53 FDA reports)
MITRAL VALVE INCOMPETENCE ( 53 FDA reports)
DRY SKIN ( 52 FDA reports)
HAEMOPTYSIS ( 52 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 52 FDA reports)
RESPIRATORY FAILURE ( 52 FDA reports)
ULCER HAEMORRHAGE ( 52 FDA reports)
URINARY RETENTION ( 52 FDA reports)
HERPES ZOSTER ( 51 FDA reports)
RENAL FAILURE CHRONIC ( 51 FDA reports)
ARTHROPATHY ( 50 FDA reports)
CHROMATURIA ( 50 FDA reports)
DYSPHONIA ( 50 FDA reports)
GALLBLADDER DISORDER ( 50 FDA reports)
RENAL CYST ( 50 FDA reports)
SKIN DISCOLOURATION ( 50 FDA reports)
VERTIGO ( 50 FDA reports)
ACCIDENTAL EXPOSURE ( 49 FDA reports)
CORONARY ARTERY OCCLUSION ( 49 FDA reports)
DISTURBANCE IN ATTENTION ( 49 FDA reports)
GLOSSODYNIA ( 49 FDA reports)
HYPERLIPIDAEMIA ( 49 FDA reports)
SPEECH DISORDER ( 49 FDA reports)
TOOTH DISORDER ( 49 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 49 FDA reports)
EYE DISORDER ( 48 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 48 FDA reports)
ROAD TRAFFIC ACCIDENT ( 48 FDA reports)
TENDONITIS ( 48 FDA reports)
DEFORMITY ( 47 FDA reports)
DYSARTHRIA ( 47 FDA reports)
FEELING JITTERY ( 47 FDA reports)
NASOPHARYNGITIS ( 47 FDA reports)
RENAL DISORDER ( 47 FDA reports)
RENAL IMPAIRMENT ( 47 FDA reports)
SCOLIOSIS ( 47 FDA reports)
SLEEP DISORDER ( 47 FDA reports)
CARDIAC ARREST ( 46 FDA reports)
DIFFICULTY IN WALKING ( 46 FDA reports)
DYSPNOEA EXERTIONAL ( 46 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 46 FDA reports)
AGITATION ( 45 FDA reports)
HEART RATE DECREASED ( 45 FDA reports)
ORAL DISCOMFORT ( 45 FDA reports)
SINUS CONGESTION ( 45 FDA reports)
ATRIAL SEPTAL DEFECT ( 44 FDA reports)
COLITIS ( 44 FDA reports)
DISABILITY ( 44 FDA reports)
EXOSTOSIS ( 44 FDA reports)
HEART RATE IRREGULAR ( 44 FDA reports)
MELAENA ( 44 FDA reports)
NEUTROPENIA ( 44 FDA reports)
OROPHARYNGEAL PAIN ( 44 FDA reports)
SKIN DISORDER ( 44 FDA reports)
SUICIDE ATTEMPT ( 44 FDA reports)
ULCER ( 44 FDA reports)
URINARY INCONTINENCE ( 44 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 44 FDA reports)
GENERALISED ERYTHEMA ( 43 FDA reports)
INJECTION SITE PAIN ( 43 FDA reports)
MOUTH ULCERATION ( 43 FDA reports)
STAPHYLOCOCCAL INFECTION ( 43 FDA reports)
BLOOD GLUCOSE DECREASED ( 42 FDA reports)
CHRONIC SINUSITIS ( 42 FDA reports)
FEELING COLD ( 42 FDA reports)
OEDEMA ( 42 FDA reports)
RESPIRATORY DISORDER ( 42 FDA reports)
SCIATICA ( 42 FDA reports)
TOOTH ABSCESS ( 42 FDA reports)
DENTURE WEARER ( 41 FDA reports)
HEPATIC STEATOSIS ( 41 FDA reports)
LOCAL SWELLING ( 41 FDA reports)
METRORRHAGIA ( 41 FDA reports)
MULTIPLE SCLEROSIS ( 41 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 41 FDA reports)
NOCTURIA ( 41 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 41 FDA reports)
ABASIA ( 40 FDA reports)
ARRHYTHMIA ( 40 FDA reports)
HAEMATURIA ( 40 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 40 FDA reports)
RESPIRATORY ARREST ( 40 FDA reports)
HYPOTHYROIDISM ( 39 FDA reports)
NASAL CONGESTION ( 39 FDA reports)
RHINORRHOEA ( 39 FDA reports)
SINUS DISORDER ( 39 FDA reports)
DISORIENTATION ( 38 FDA reports)
HAEMATOCRIT DECREASED ( 38 FDA reports)
HERNIA ( 37 FDA reports)
INFLAMMATION ( 37 FDA reports)
LETHARGY ( 37 FDA reports)
MENTAL STATUS CHANGES ( 37 FDA reports)
PERIODONTAL DISEASE ( 37 FDA reports)
RHEUMATOID ARTHRITIS ( 37 FDA reports)
ANGER ( 36 FDA reports)
DERMATITIS CONTACT ( 36 FDA reports)
HALLUCINATION ( 36 FDA reports)
HYPERGLYCAEMIA ( 36 FDA reports)
LEUKOCYTOSIS ( 36 FDA reports)
MUSCLE TIGHTNESS ( 36 FDA reports)
ORAL CANDIDIASIS ( 36 FDA reports)
ABDOMINAL PAIN LOWER ( 35 FDA reports)
BLOOD CALCIUM DECREASED ( 35 FDA reports)
HYPOPHAGIA ( 35 FDA reports)
LACRIMATION INCREASED ( 35 FDA reports)
NEURALGIA ( 35 FDA reports)
NIGHT SWEATS ( 35 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 35 FDA reports)
RIB FRACTURE ( 35 FDA reports)
SKIN LESION ( 35 FDA reports)
SPINAL COMPRESSION FRACTURE ( 35 FDA reports)
DRUG EFFECT DECREASED ( 34 FDA reports)
DRUG SCREEN POSITIVE ( 34 FDA reports)
FUNGAL INFECTION ( 34 FDA reports)
HEMIPLEGIA ( 34 FDA reports)
HYPERCHOLESTEROLAEMIA ( 34 FDA reports)
IMPAIRED DRIVING ABILITY ( 34 FDA reports)
LUNG DISORDER ( 34 FDA reports)
ORAL PAIN ( 34 FDA reports)
PANCYTOPENIA ( 34 FDA reports)
PRIMARY SEQUESTRUM ( 34 FDA reports)
VISUAL DISTURBANCE ( 34 FDA reports)
DISCOMFORT ( 33 FDA reports)
FACIAL PAIN ( 33 FDA reports)
GASTRITIS EROSIVE ( 33 FDA reports)
GOUT ( 33 FDA reports)
HEMIPARESIS ( 33 FDA reports)
HYPOXIA ( 33 FDA reports)
MEDICATION ERROR ( 33 FDA reports)
MUSCLE TWITCHING ( 33 FDA reports)
PANCREATITIS ( 33 FDA reports)
RASH PAPULAR ( 33 FDA reports)
TOOTH LOSS ( 33 FDA reports)
VIRAL INFECTION ( 33 FDA reports)
VISUAL ACUITY REDUCED ( 33 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 32 FDA reports)
CYANOSIS ( 32 FDA reports)
DIPLOPIA ( 32 FDA reports)
FEAR ( 32 FDA reports)
FIBROSIS ( 32 FDA reports)
ILEUS ( 32 FDA reports)
LIP DRY ( 32 FDA reports)
MENTAL IMPAIRMENT ( 32 FDA reports)
OCULAR HYPERAEMIA ( 32 FDA reports)
ORTHOSTATIC HYPOTENSION ( 32 FDA reports)
PLATELET COUNT DECREASED ( 32 FDA reports)
SENSORY DISTURBANCE ( 32 FDA reports)
BRADYCARDIA ( 31 FDA reports)
CYSTITIS ( 31 FDA reports)
DERMATITIS ( 31 FDA reports)
FACIAL PALSY ( 31 FDA reports)
IMPAIRED HEALING ( 31 FDA reports)
IRRITABILITY ( 31 FDA reports)
JAUNDICE ( 31 FDA reports)
LUNG NEOPLASM MALIGNANT ( 31 FDA reports)
MASS ( 31 FDA reports)
MYOCARDIAL ISCHAEMIA ( 31 FDA reports)
OXYGEN SATURATION DECREASED ( 31 FDA reports)
PARAESTHESIA ORAL ( 31 FDA reports)
SHOCK ( 31 FDA reports)
SKIN EXFOLIATION ( 31 FDA reports)
VAGINAL INFECTION ( 31 FDA reports)
VENTRICULAR HYPERTROPHY ( 31 FDA reports)
ANGIOEDEMA ( 30 FDA reports)
CARDIOVASCULAR DISORDER ( 30 FDA reports)
CAROTID ARTERY STENOSIS ( 30 FDA reports)
CEREBRAL HAEMORRHAGE ( 30 FDA reports)
DEPRESSED MOOD ( 30 FDA reports)
DIVERTICULITIS ( 30 FDA reports)
FLANK PAIN ( 30 FDA reports)
INCORRECT DOSE ADMINISTERED ( 30 FDA reports)
KYPHOSIS ( 30 FDA reports)
MOOD SWINGS ( 30 FDA reports)
PROCEDURAL PAIN ( 30 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 30 FDA reports)
SENSATION OF FOREIGN BODY ( 30 FDA reports)
BACK DISORDER ( 29 FDA reports)
BACTERIAL INFECTION ( 29 FDA reports)
BLOOD UREA INCREASED ( 29 FDA reports)
DYSKINESIA ( 29 FDA reports)
GROIN PAIN ( 29 FDA reports)
INFLUENZA ( 29 FDA reports)
INTENTIONAL OVERDOSE ( 29 FDA reports)
INTESTINAL HAEMORRHAGE ( 29 FDA reports)
METASTASES TO LUNG ( 29 FDA reports)
MUCOSAL INFLAMMATION ( 29 FDA reports)
OEDEMA MOUTH ( 29 FDA reports)
PULMONARY VALVE STENOSIS ( 29 FDA reports)
SOMNAMBULISM ( 29 FDA reports)
SPINAL COLUMN STENOSIS ( 29 FDA reports)
BLOOD URINE ( 28 FDA reports)
BONE LESION ( 28 FDA reports)
BREAST CANCER ( 28 FDA reports)
CARPAL TUNNEL SYNDROME ( 28 FDA reports)
DRUG INTERACTION ( 28 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 28 FDA reports)
MENTAL DISORDER ( 28 FDA reports)
PALLOR ( 28 FDA reports)
RESTLESSNESS ( 28 FDA reports)
STOMATITIS ( 28 FDA reports)
TENDERNESS ( 28 FDA reports)
VISUAL IMPAIRMENT ( 28 FDA reports)
HEPATIC FAILURE ( 27 FDA reports)
HYPONATRAEMIA ( 27 FDA reports)
METASTASES TO SPINE ( 27 FDA reports)
NEOPLASM MALIGNANT ( 27 FDA reports)
OROPHARYNGEAL SWELLING ( 27 FDA reports)
PANIC ATTACK ( 27 FDA reports)
POOR QUALITY SLEEP ( 27 FDA reports)
PULMONARY HYPERTENSION ( 27 FDA reports)
RETCHING ( 27 FDA reports)
SINUS TACHYCARDIA ( 27 FDA reports)
BREAST MASS ( 26 FDA reports)
COLD SWEAT ( 26 FDA reports)
DEBRIDEMENT ( 26 FDA reports)
DRUG DOSE OMISSION ( 26 FDA reports)
DRY EYE ( 26 FDA reports)
ERUCTATION ( 26 FDA reports)
EXCORIATION ( 26 FDA reports)
GINGIVITIS ( 26 FDA reports)
INGUINAL HERNIA ( 26 FDA reports)
LEUKOPENIA ( 26 FDA reports)
MENINGIOMA ( 26 FDA reports)
MYOSITIS ( 26 FDA reports)
PROCTALGIA ( 26 FDA reports)
PRODUCTIVE COUGH ( 26 FDA reports)
RASH MACULO-PAPULAR ( 26 FDA reports)
BLOOD POTASSIUM DECREASED ( 25 FDA reports)
CERVICOBRACHIAL SYNDROME ( 25 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 25 FDA reports)
EYE HAEMORRHAGE ( 25 FDA reports)
GENERALISED OEDEMA ( 25 FDA reports)
MENSTRUATION IRREGULAR ( 25 FDA reports)
MOOD ALTERED ( 25 FDA reports)
MULTI-ORGAN DISORDER ( 25 FDA reports)
MULTIPLE MYELOMA ( 25 FDA reports)
RHABDOMYOLYSIS ( 25 FDA reports)
SLEEP APNOEA SYNDROME ( 25 FDA reports)
ACTINOMYCOSIS ( 24 FDA reports)
ANGIONEUROTIC OEDEMA ( 24 FDA reports)
BLOOD PRESSURE ABNORMAL ( 24 FDA reports)
BLOOD SODIUM DECREASED ( 24 FDA reports)
CARDIAC VALVE DISEASE ( 24 FDA reports)
COLONIC POLYP ( 24 FDA reports)
COMPRESSION FRACTURE ( 24 FDA reports)
EYE PRURITUS ( 24 FDA reports)
GASTROINTESTINAL PAIN ( 24 FDA reports)
HEPATOMEGALY ( 24 FDA reports)
HYPOGLYCAEMIA ( 24 FDA reports)
JOINT DISLOCATION ( 24 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 24 FDA reports)
LUMBAR RADICULOPATHY ( 24 FDA reports)
LUNG NEOPLASM ( 24 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 24 FDA reports)
ORAL INFECTION ( 24 FDA reports)
PERICARDIAL EFFUSION ( 24 FDA reports)
RESPIRATORY DISTRESS ( 24 FDA reports)
RESPIRATORY RATE INCREASED ( 24 FDA reports)
ROTATOR CUFF SYNDROME ( 24 FDA reports)
SCAB ( 24 FDA reports)
SKIN LACERATION ( 24 FDA reports)
TREATMENT NONCOMPLIANCE ( 24 FDA reports)
UTERINE LEIOMYOMA ( 24 FDA reports)
ACOUSTIC NEUROMA ( 23 FDA reports)
AGGRESSION ( 23 FDA reports)
CARDIO-RESPIRATORY ARREST ( 23 FDA reports)
EMOTIONAL DISORDER ( 23 FDA reports)
FOREIGN BODY ( 23 FDA reports)
HEART DISEASE CONGENITAL ( 23 FDA reports)
MUSCLE STRAIN ( 23 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 23 FDA reports)
ONYCHOMYCOSIS ( 23 FDA reports)
ORAL DISORDER ( 23 FDA reports)
PETECHIAE ( 23 FDA reports)
POLYNEUROPATHY ( 23 FDA reports)
RESTLESS LEGS SYNDROME ( 23 FDA reports)
SEQUESTRECTOMY ( 23 FDA reports)
THYROID NEOPLASM ( 23 FDA reports)
ABSCESS ( 22 FDA reports)
BLINDNESS ( 22 FDA reports)
BLINDNESS UNILATERAL ( 22 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 22 FDA reports)
BODY TEMPERATURE INCREASED ( 22 FDA reports)
BONE DEBRIDEMENT ( 22 FDA reports)
BREATH ODOUR ( 22 FDA reports)
CERVICAL DYSPLASIA ( 22 FDA reports)
CHOLECYSTITIS ACUTE ( 22 FDA reports)
COGNITIVE DISORDER ( 22 FDA reports)
DISEASE PROGRESSION ( 22 FDA reports)
INJECTION SITE PRURITUS ( 22 FDA reports)
JOINT SPRAIN ( 22 FDA reports)
LIMB INJURY ( 22 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 22 FDA reports)
MULTI-ORGAN FAILURE ( 22 FDA reports)
NON-CARDIAC CHEST PAIN ( 22 FDA reports)
PROSTATE CANCER ( 22 FDA reports)
WOUND INFECTION ( 22 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 22 FDA reports)
ABNORMAL BEHAVIOUR ( 21 FDA reports)
ABNORMAL DREAMS ( 21 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 21 FDA reports)
AORTIC VALVE INCOMPETENCE ( 21 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 21 FDA reports)
CHOLECYSTITIS ( 21 FDA reports)
DEAFNESS ( 21 FDA reports)
DEVELOPMENTAL DELAY ( 21 FDA reports)
DRUG INTOLERANCE ( 21 FDA reports)
EYE IRRITATION ( 21 FDA reports)
EYE PAIN ( 21 FDA reports)
FAECAL INCONTINENCE ( 21 FDA reports)
GINGIVAL BLEEDING ( 21 FDA reports)
ILL-DEFINED DISORDER ( 21 FDA reports)
JOINT INJURY ( 21 FDA reports)
MENORRHAGIA ( 21 FDA reports)
PERONEAL NERVE PALSY ( 21 FDA reports)
PURULENT DISCHARGE ( 21 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 21 FDA reports)
APHTHOUS STOMATITIS ( 20 FDA reports)
CARDIAC FAILURE ( 20 FDA reports)
CARDIAC FLUTTER ( 20 FDA reports)
COAGULOPATHY ( 20 FDA reports)
CONGENITAL ANOMALY ( 20 FDA reports)
CORONARY ARTERY STENOSIS ( 20 FDA reports)
DYSSTASIA ( 20 FDA reports)
GASTRIC PERFORATION ( 20 FDA reports)
GINGIVAL SWELLING ( 20 FDA reports)
HAEMATOMA ( 20 FDA reports)
HAEMORRHAGIC DIATHESIS ( 20 FDA reports)
HEPATIC CIRRHOSIS ( 20 FDA reports)
HEPATOCELLULAR DAMAGE ( 20 FDA reports)
JAW OPERATION ( 20 FDA reports)
JOINT STIFFNESS ( 20 FDA reports)
KIDNEY INFECTION ( 20 FDA reports)
NASAL DISCOMFORT ( 20 FDA reports)
OSTEORADIONECROSIS ( 20 FDA reports)
RENAL INJURY ( 20 FDA reports)
SQUAMOUS CELL CARCINOMA ( 20 FDA reports)
SURGERY ( 20 FDA reports)
VENTRICULAR FIBRILLATION ( 20 FDA reports)
WALKING AID USER ( 20 FDA reports)
ABSCESS ORAL ( 19 FDA reports)
APHASIA ( 19 FDA reports)
BACK INJURY ( 19 FDA reports)
CEREBRAL INFARCTION ( 19 FDA reports)
CHRONIC FATIGUE SYNDROME ( 19 FDA reports)
COORDINATION ABNORMAL ( 19 FDA reports)
DUODENAL ULCER ( 19 FDA reports)
EATING DISORDER ( 19 FDA reports)
ECCHYMOSIS ( 19 FDA reports)
EYELID OEDEMA ( 19 FDA reports)
HIP FRACTURE ( 19 FDA reports)
INJECTION SITE REACTION ( 19 FDA reports)
INTENTIONAL DRUG MISUSE ( 19 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 19 FDA reports)
MACULE ( 19 FDA reports)
NASAL MUCOSAL DISORDER ( 19 FDA reports)
OSTEOSCLEROSIS ( 19 FDA reports)
PARALYSIS ( 19 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 19 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 19 FDA reports)
SINUS BRADYCARDIA ( 19 FDA reports)
SKIN BURNING SENSATION ( 19 FDA reports)
SNEEZING ( 19 FDA reports)
SPINAL DISORDER ( 19 FDA reports)
SPINAL LAMINECTOMY ( 19 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 18 FDA reports)
ARTHROPOD BITE ( 18 FDA reports)
BLOOD BILIRUBIN INCREASED ( 18 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 18 FDA reports)
CHOKING ( 18 FDA reports)
CLOSTRIDIUM COLITIS ( 18 FDA reports)
DRUG TOXICITY ( 18 FDA reports)
ENDODONTIC PROCEDURE ( 18 FDA reports)
FEBRILE NEUTROPENIA ( 18 FDA reports)
FOOD INTOLERANCE ( 18 FDA reports)
INFUSION RELATED REACTION ( 18 FDA reports)
JAW FRACTURE ( 18 FDA reports)
LIMB DISCOMFORT ( 18 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 18 FDA reports)
MELANOCYTIC NAEVUS ( 18 FDA reports)
MENINGITIS ( 18 FDA reports)
NIGHTMARE ( 18 FDA reports)
OTITIS MEDIA ( 18 FDA reports)
PERIODONTITIS ( 18 FDA reports)
POST PROCEDURAL COMPLICATION ( 18 FDA reports)
PSEUDOMONAS INFECTION ( 18 FDA reports)
PULMONARY CONGESTION ( 18 FDA reports)
PULMONARY MASS ( 18 FDA reports)
THINKING ABNORMAL ( 18 FDA reports)
UNRESPONSIVE TO STIMULI ( 18 FDA reports)
URINARY TRACT DISORDER ( 18 FDA reports)
ANGINA UNSTABLE ( 17 FDA reports)
ARTERIOSCLEROSIS ( 17 FDA reports)
BREAST CANCER RECURRENT ( 17 FDA reports)
CHOLECYSTECTOMY ( 17 FDA reports)
COELIAC DISEASE ( 17 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 17 FDA reports)
FACET JOINT SYNDROME ( 17 FDA reports)
FOOT FRACTURE ( 17 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 17 FDA reports)
HAEMANGIOMA OF LIVER ( 17 FDA reports)
HEPATITIS ( 17 FDA reports)
HODGKIN'S DISEASE ( 17 FDA reports)
INCREASED TENDENCY TO BRUISE ( 17 FDA reports)
INTESTINAL OBSTRUCTION ( 17 FDA reports)
LIVER INJURY ( 17 FDA reports)
LUNG INFILTRATION ( 17 FDA reports)
MENISCUS LESION ( 17 FDA reports)
METABOLIC ACIDOSIS ( 17 FDA reports)
ORAL INTAKE REDUCED ( 17 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 17 FDA reports)
STENT PLACEMENT ( 17 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 17 FDA reports)
ABNORMAL SENSATION IN EYE ( 16 FDA reports)
ABORTION SPONTANEOUS ( 16 FDA reports)
ACNE ( 16 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 16 FDA reports)
ASCITES ( 16 FDA reports)
CATHETER PLACEMENT ( 16 FDA reports)
COMA ( 16 FDA reports)
COSTOCHONDRITIS ( 16 FDA reports)
DRUG USE FOR UNKNOWN INDICATION ( 16 FDA reports)
EAR DISORDER ( 16 FDA reports)
GASTROENTERITIS VIRAL ( 16 FDA reports)
HYPOAESTHESIA FACIAL ( 16 FDA reports)
HYPOMAGNESAEMIA ( 16 FDA reports)
IMPAIRED WORK ABILITY ( 16 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 16 FDA reports)
INCOHERENT ( 16 FDA reports)
INITIAL INSOMNIA ( 16 FDA reports)
INTERSTITIAL LUNG DISEASE ( 16 FDA reports)
IRON DEFICIENCY ANAEMIA ( 16 FDA reports)
LIPOMA ( 16 FDA reports)
METAPLASIA ( 16 FDA reports)
MYELOPATHY ( 16 FDA reports)
NERVE INJURY ( 16 FDA reports)
NEURODERMATITIS ( 16 FDA reports)
OCCULT BLOOD POSITIVE ( 16 FDA reports)
ODYNOPHAGIA ( 16 FDA reports)
OESOPHAGEAL PAIN ( 16 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 16 FDA reports)
PANCREATITIS ACUTE ( 16 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 16 FDA reports)
PELVIC PAIN ( 16 FDA reports)
PHYSICAL DISABILITY ( 16 FDA reports)
PRESYNCOPE ( 16 FDA reports)
RADIOTHERAPY ( 16 FDA reports)
RHINITIS ALLERGIC ( 16 FDA reports)
SINUS HEADACHE ( 16 FDA reports)
SKIN HYPERTROPHY ( 16 FDA reports)
SPLENOMEGALY ( 16 FDA reports)
STREPTOCOCCAL INFECTION ( 16 FDA reports)
SUICIDAL BEHAVIOUR ( 16 FDA reports)
TOOTH REPAIR ( 16 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 16 FDA reports)
AORTIC ANEURYSM ( 15 FDA reports)
APPENDICITIS PERFORATED ( 15 FDA reports)
BEDRIDDEN ( 15 FDA reports)
BILIARY DYSKINESIA ( 15 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 15 FDA reports)
BONE MARROW FAILURE ( 15 FDA reports)
BONE SCAN ABNORMAL ( 15 FDA reports)
CHOKING SENSATION ( 15 FDA reports)
DIASTOLIC DYSFUNCTION ( 15 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 15 FDA reports)
FISTULA ( 15 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 15 FDA reports)
HYSTERECTOMY ( 15 FDA reports)
INCISION SITE INFECTION ( 15 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 15 FDA reports)
INTESTINAL PERFORATION ( 15 FDA reports)
LACERATION ( 15 FDA reports)
LIP BLISTER ( 15 FDA reports)
LOBAR PNEUMONIA ( 15 FDA reports)
MOUTH HAEMORRHAGE ( 15 FDA reports)
MOVEMENT DISORDER ( 15 FDA reports)
NEUROGENIC BLADDER ( 15 FDA reports)
NODULE ( 15 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 15 FDA reports)
OESOPHAGEAL ULCER ( 15 FDA reports)
ORAL SURGERY ( 15 FDA reports)
ORTHOSIS USER ( 15 FDA reports)
OTITIS EXTERNA ( 15 FDA reports)
PALMAR ERYTHEMA ( 15 FDA reports)
PERSISTENT FOETAL CIRCULATION ( 15 FDA reports)
POLYP ( 15 FDA reports)
POLYURIA ( 15 FDA reports)
PROTHROMBIN TIME PROLONGED ( 15 FDA reports)
PULMONARY HYPOPLASIA ( 15 FDA reports)
RECTAL POLYP ( 15 FDA reports)
SCROTAL CYST ( 15 FDA reports)
SENSATION OF HEAVINESS ( 15 FDA reports)
SPINAL CORD COMPRESSION ( 15 FDA reports)
TOOTH INFECTION ( 15 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 15 FDA reports)
TUMOUR INVASION ( 15 FDA reports)
VENTRICULAR DYSFUNCTION ( 15 FDA reports)
VENTRICULAR TACHYCARDIA ( 15 FDA reports)
ADVERSE DRUG REACTION ( 14 FDA reports)
AGEUSIA ( 14 FDA reports)
ALCOHOL USE ( 14 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 14 FDA reports)
BARRETT'S OESOPHAGUS ( 14 FDA reports)
BLOOD ALBUMIN DECREASED ( 14 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 14 FDA reports)
BRAIN MASS ( 14 FDA reports)
CEREBRAL ISCHAEMIA ( 14 FDA reports)
CRYING ( 14 FDA reports)
DEVICE RELATED INFECTION ( 14 FDA reports)
DILATATION ATRIAL ( 14 FDA reports)
DIVERTICULUM INTESTINAL ( 14 FDA reports)
DRUG ADMINISTRATION ERROR ( 14 FDA reports)
DRUG DEPENDENCE ( 14 FDA reports)
EJECTION FRACTION DECREASED ( 14 FDA reports)
GASTRIC ULCER PERFORATION ( 14 FDA reports)
GINGIVAL PAIN ( 14 FDA reports)
HAEMANGIOMA ( 14 FDA reports)
HEAD INJURY ( 14 FDA reports)
HEPATIC LESION ( 14 FDA reports)
HYDRONEPHROSIS ( 14 FDA reports)
HYPERCALCAEMIA ( 14 FDA reports)
HYPOACUSIS ( 14 FDA reports)
HYPOVOLAEMIA ( 14 FDA reports)
JOINT EFFUSION ( 14 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 14 FDA reports)
LOCALISED INFECTION ( 14 FDA reports)
LUNG CONSOLIDATION ( 14 FDA reports)
MIDDLE INSOMNIA ( 14 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 14 FDA reports)
NERVE COMPRESSION ( 14 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 14 FDA reports)
OFF LABEL USE ( 14 FDA reports)
PATHOLOGICAL GAMBLING ( 14 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 14 FDA reports)
PSORIASIS ( 14 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 14 FDA reports)
SHOULDER PAIN ( 14 FDA reports)
SKIN ULCER ( 14 FDA reports)
STEVENS-JOHNSON SYNDROME ( 14 FDA reports)
TOOTH FRACTURE ( 14 FDA reports)
WHEELCHAIR USER ( 14 FDA reports)
ABDOMINAL HERNIA ( 13 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 13 FDA reports)
BLOOD POTASSIUM INCREASED ( 13 FDA reports)
BODY TEMPERATURE DECREASED ( 13 FDA reports)
BRAIN DEATH ( 13 FDA reports)
BRONCHOSPASM ( 13 FDA reports)
CYSTITIS HAEMORRHAGIC ( 13 FDA reports)
DECREASED INTEREST ( 13 FDA reports)
EAR INFECTION ( 13 FDA reports)
ENCEPHALOPATHY ( 13 FDA reports)
EPIGASTRIC DISCOMFORT ( 13 FDA reports)
ERECTILE DYSFUNCTION ( 13 FDA reports)
EXTERNAL EAR DISORDER ( 13 FDA reports)
FALLOT'S TETRALOGY ( 13 FDA reports)
FEELING DRUNK ( 13 FDA reports)
FIBROMYALGIA ( 13 FDA reports)
GASTROINTESTINAL ULCER ( 13 FDA reports)
HEPATIC CYST ( 13 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 13 FDA reports)
JAW DISORDER ( 13 FDA reports)
LYMPHOEDEMA ( 13 FDA reports)
MALNUTRITION ( 13 FDA reports)
NERVOUS SYSTEM DISORDER ( 13 FDA reports)
NEUROENDOCRINE CARCINOMA ( 13 FDA reports)
OCULAR ICTERUS ( 13 FDA reports)
OVARIAN MASS ( 13 FDA reports)
PNEUMONIA ASPIRATION ( 13 FDA reports)
POST PROCEDURAL HYPOTHYROIDISM ( 13 FDA reports)
PULMONARY FIBROSIS ( 13 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 13 FDA reports)
SELF-INJURIOUS IDEATION ( 13 FDA reports)
SPINAL DECOMPRESSION ( 13 FDA reports)
SPONDYLOLISTHESIS ( 13 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 13 FDA reports)
TENDON INJURY ( 13 FDA reports)
AORTIC DISORDER ( 12 FDA reports)
APNOEA ( 12 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 12 FDA reports)
BLOOD COUNT ABNORMAL ( 12 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 12 FDA reports)
BODY HEIGHT DECREASED ( 12 FDA reports)
BRAIN OEDEMA ( 12 FDA reports)
COLON ADENOMA ( 12 FDA reports)
CYST ( 12 FDA reports)
DYSLIPIDAEMIA ( 12 FDA reports)
ECONOMIC PROBLEM ( 12 FDA reports)
EXPOSED BONE IN JAW ( 12 FDA reports)
FAILURE TO THRIVE ( 12 FDA reports)
FLUID OVERLOAD ( 12 FDA reports)
GINGIVAL DISORDER ( 12 FDA reports)
HEPATITIS ACUTE ( 12 FDA reports)
HEPATITIS C ( 12 FDA reports)
HYDROCEPHALUS ( 12 FDA reports)
HYPERKALAEMIA ( 12 FDA reports)
HYPOKINESIA ( 12 FDA reports)
INJECTION SITE HAEMATOMA ( 12 FDA reports)
INJECTION SITE HAEMORRHAGE ( 12 FDA reports)
LIFE EXPECTANCY SHORTENED ( 12 FDA reports)
MAJOR DEPRESSION ( 12 FDA reports)
METASTATIC NEOPLASM ( 12 FDA reports)
MICTURITION URGENCY ( 12 FDA reports)
MUSCLE CRAMP ( 12 FDA reports)
NASAL SEPTUM DEVIATION ( 12 FDA reports)
PATHOLOGICAL FRACTURE ( 12 FDA reports)
PEPTIC ULCER ( 12 FDA reports)
PLASMACYTOSIS ( 12 FDA reports)
PLEURITIC PAIN ( 12 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 12 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 12 FDA reports)
PULMONARY HAEMORRHAGE ( 12 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 12 FDA reports)
SYNOVIAL CYST ( 12 FDA reports)
TACHYPNOEA ( 12 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 12 FDA reports)
VARICOSE VEIN ( 12 FDA reports)
ABNORMAL FAECES ( 11 FDA reports)
ACUTE RESPIRATORY FAILURE ( 11 FDA reports)
ANISOCYTOSIS ( 11 FDA reports)
ANKLE FRACTURE ( 11 FDA reports)
APPENDICECTOMY ( 11 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 11 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 11 FDA reports)
BLEEDING TIME PROLONGED ( 11 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 11 FDA reports)
BLOOD DISORDER ( 11 FDA reports)
BONE GRAFT ( 11 FDA reports)
BREECH PRESENTATION ( 11 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 11 FDA reports)
CALCULUS URETERIC ( 11 FDA reports)
CANDIDIASIS ( 11 FDA reports)
CARDIOMYOPATHY ( 11 FDA reports)
CAROTID ARTERY OCCLUSION ( 11 FDA reports)
CERVICITIS HUMAN PAPILLOMA VIRUS ( 11 FDA reports)
DENTAL OPERATION ( 11 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 11 FDA reports)
EAR DISCOMFORT ( 11 FDA reports)
ENTEROVESICAL FISTULA ( 11 FDA reports)
EYE MOVEMENT DISORDER ( 11 FDA reports)
FACIAL OPERATION ( 11 FDA reports)
FOLLICULITIS ( 11 FDA reports)
FRACTURE ( 11 FDA reports)
GRAND MAL CONVULSION ( 11 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 11 FDA reports)
HYPOVENTILATION ( 11 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 11 FDA reports)
ISCHAEMIA ( 11 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 11 FDA reports)
LIVER DISORDER ( 11 FDA reports)
MAXILLOFACIAL OPERATION ( 11 FDA reports)
MITRAL VALVE PROLAPSE ( 11 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 11 FDA reports)
PERIODONTAL OPERATION ( 11 FDA reports)
POSTPARTUM HAEMORRHAGE ( 11 FDA reports)
PREMATURE BABY ( 11 FDA reports)
PROCEDURAL COMPLICATION ( 11 FDA reports)
PROCEDURAL HYPERTENSION ( 11 FDA reports)
PROSTATOMEGALY ( 11 FDA reports)
RASH PUSTULAR ( 11 FDA reports)
RESPIRATORY TRACT INFECTION ( 11 FDA reports)
SKIN IRRITATION ( 11 FDA reports)
SKIN TIGHTNESS ( 11 FDA reports)
SLEEP-RELATED EATING DISORDER ( 11 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 11 FDA reports)
SYNOVITIS ( 11 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 11 FDA reports)
THERMAL BURN ( 11 FDA reports)
THYROID DISORDER ( 11 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 11 FDA reports)
TONGUE DISCOLOURATION ( 11 FDA reports)
TORTICOLLIS ( 11 FDA reports)
UTERINE DISORDER ( 11 FDA reports)
ABDOMINAL ABSCESS ( 10 FDA reports)
ANAL HAEMORRHAGE ( 10 FDA reports)
ANGIOPATHY ( 10 FDA reports)
ANOSMIA ( 10 FDA reports)
ARTHRITIS INFECTIVE ( 10 FDA reports)
AURICULAR SWELLING ( 10 FDA reports)
AZOTAEMIA ( 10 FDA reports)
BASAL CELL CARCINOMA ( 10 FDA reports)
BIOPSY BONE MARROW ( 10 FDA reports)
BLADDER PAIN ( 10 FDA reports)
BLOOD IRON DECREASED ( 10 FDA reports)
BREAST CANCER METASTATIC ( 10 FDA reports)
BREATH SOUNDS ABNORMAL ( 10 FDA reports)
CAESAREAN SECTION ( 10 FDA reports)
CARDIOGENIC SHOCK ( 10 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 10 FDA reports)
CHOLESTASIS ( 10 FDA reports)
CIRCULATORY COLLAPSE ( 10 FDA reports)
DIZZINESS POSTURAL ( 10 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 10 FDA reports)
EMPYEMA ( 10 FDA reports)
EROSIVE OESOPHAGITIS ( 10 FDA reports)
EYE ROLLING ( 10 FDA reports)
GALLBLADDER INJURY ( 10 FDA reports)
GASTROENTERITIS ( 10 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 10 FDA reports)
GLAUCOMA ( 10 FDA reports)
HEARING IMPAIRED ( 10 FDA reports)
HYPERPLASIA ( 10 FDA reports)
HYPERSOMNIA ( 10 FDA reports)
INCREASED APPETITE ( 10 FDA reports)
ISCHAEMIC STROKE ( 10 FDA reports)
LUNG HYPERINFLATION ( 10 FDA reports)
LYMPHOMA ( 10 FDA reports)
METABOLIC DISORDER ( 10 FDA reports)
MUSCLE ATROPHY ( 10 FDA reports)
NECK MASS ( 10 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 10 FDA reports)
OESOPHAGEAL SPASM ( 10 FDA reports)
OESOPHAGITIS ( 10 FDA reports)
OESOPHAGITIS ULCERATIVE ( 10 FDA reports)
PERIPHERAL COLDNESS ( 10 FDA reports)
PHARYNGITIS ( 10 FDA reports)
PHOTOPHOBIA ( 10 FDA reports)
PILONIDAL CYST CONGENITAL ( 10 FDA reports)
POLYMYALGIA RHEUMATICA ( 10 FDA reports)
POOR DENTAL CONDITION ( 10 FDA reports)
PORTAL VEIN THROMBOSIS ( 10 FDA reports)
PULMONARY GRANULOMA ( 10 FDA reports)
PULMONARY VASCULAR DISORDER ( 10 FDA reports)
PYELONEPHRITIS ACUTE ( 10 FDA reports)
RENAL TUBULAR NECROSIS ( 10 FDA reports)
RHONCHI ( 10 FDA reports)
RIGHT VENTRICLE OUTFLOW TRACT OBSTRUCTION ( 10 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 10 FDA reports)
SKIN CANCER ( 10 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 10 FDA reports)
TENSION ( 10 FDA reports)
THERAPY NON-RESPONDER ( 10 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 10 FDA reports)
TONGUE DISORDER ( 10 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 10 FDA reports)
WEIGHT GAIN POOR ( 10 FDA reports)
WEST NILE VIRAL INFECTION ( 10 FDA reports)
ABSCESS DRAINAGE ( 9 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 9 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 9 FDA reports)
ALVEOLOPLASTY ( 9 FDA reports)
ANAL FISTULA ( 9 FDA reports)
ATRIAL FLUTTER ( 9 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 9 FDA reports)
BILE DUCT STONE ( 9 FDA reports)
BILIARY COLIC ( 9 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 9 FDA reports)
CERVICAL SPINAL STENOSIS ( 9 FDA reports)
COLLAPSE OF LUNG ( 9 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 9 FDA reports)
DIALYSIS ( 9 FDA reports)
DILATATION VENTRICULAR ( 9 FDA reports)
DISEASE RECURRENCE ( 9 FDA reports)
DISSOCIATIVE FUGUE ( 9 FDA reports)
DRUG ABUSE ( 9 FDA reports)
DRUG ABUSER ( 9 FDA reports)
EUPHORIC MOOD ( 9 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 9 FDA reports)
GASTROENTERITIS BACTERIAL ( 9 FDA reports)
GIANT CELL TUMOUR OF TENDON SHEATH ( 9 FDA reports)
GRANULOMA ( 9 FDA reports)
HAEMOPHILUS INFECTION ( 9 FDA reports)
HAIR FOLLICLE TUMOUR BENIGN ( 9 FDA reports)
HEAD TITUBATION ( 9 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 9 FDA reports)
HEPATOTOXICITY ( 9 FDA reports)
HOMICIDAL IDEATION ( 9 FDA reports)
HUMERUS FRACTURE ( 9 FDA reports)
HYPERAESTHESIA ( 9 FDA reports)
HYPERTROPHY ( 9 FDA reports)
IMMUNOGLOBULINS DECREASED ( 9 FDA reports)
INCONTINENCE ( 9 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 9 FDA reports)
JOINT CREPITATION ( 9 FDA reports)
LACUNAR INFARCTION ( 9 FDA reports)
LIGHT CHAIN ANALYSIS ( 9 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 9 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 9 FDA reports)
MASTICATION DISORDER ( 9 FDA reports)
MEDIASTINUM NEOPLASM ( 9 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 9 FDA reports)
MULTIPLE INJURIES ( 9 FDA reports)
MYOPIA ( 9 FDA reports)
OBSTRUCTION GASTRIC ( 9 FDA reports)
OESOPHAGEAL DISORDER ( 9 FDA reports)
OPTIC NERVE SHEATH HAEMORRHAGE ( 9 FDA reports)
ORAL PRURITUS ( 9 FDA reports)
OSTEITIS ( 9 FDA reports)
PAIN OF SKIN ( 9 FDA reports)
PARATHYROID TUMOUR BENIGN ( 9 FDA reports)
PLANTAR FASCIITIS ( 9 FDA reports)
PLASMACYTOMA ( 9 FDA reports)
PNEUMOTHORAX ( 9 FDA reports)
POOR PERSONAL HYGIENE ( 9 FDA reports)
PREGNANCY ( 9 FDA reports)
PROTEIN URINE ABSENT ( 9 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 9 FDA reports)
PULMONARY ARTERY STENOSIS ( 9 FDA reports)
PULMONARY THROMBOSIS ( 9 FDA reports)
PULSE ABSENT ( 9 FDA reports)
PYODERMA GANGRENOSUM ( 9 FDA reports)
RADIATION OESOPHAGITIS ( 9 FDA reports)
RED BLOOD CELL ABNORMALITY ( 9 FDA reports)
RESPIRATORY TRACT CONGESTION ( 9 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 9 FDA reports)
SKIN HYPERPIGMENTATION ( 9 FDA reports)
SKIN INFECTION ( 9 FDA reports)
SKIN WARM ( 9 FDA reports)
SKIN WRINKLING ( 9 FDA reports)
SNORING ( 9 FDA reports)
SPINAL FRACTURE ( 9 FDA reports)
SPINAL FUSION SURGERY ( 9 FDA reports)
TENDON DISORDER ( 9 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 9 FDA reports)
TRANSFUSION ( 9 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 9 FDA reports)
VASCULITIS ( 9 FDA reports)
VERTEBROPLASTY ( 9 FDA reports)
ABDOMINAL TENDERNESS ( 8 FDA reports)
ABDOMINAL WOUND DEHISCENCE ( 8 FDA reports)
ACANTHOMA ( 8 FDA reports)
ACCIDENT ( 8 FDA reports)
ACIDOSIS ( 8 FDA reports)
ACUTE SINUSITIS ( 8 FDA reports)
ANEURYSM ( 8 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 8 FDA reports)
AORTIC VALVE SCLEROSIS ( 8 FDA reports)
APHAGIA ( 8 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 8 FDA reports)
BLADDER DISORDER ( 8 FDA reports)
BLOOD BICARBONATE INCREASED ( 8 FDA reports)
BLOOD ZINC DECREASED ( 8 FDA reports)
BONE MARROW DISORDER ( 8 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 8 FDA reports)
CHEST WALL PAIN ( 8 FDA reports)
COCCYDYNIA ( 8 FDA reports)
CONGENITAL PULMONARY ARTERY ANOMALY ( 8 FDA reports)
CORONARY ARTERY BYPASS ( 8 FDA reports)
CRYOTHERAPY ( 8 FDA reports)
DEMYELINATION ( 8 FDA reports)
DERMAL CYST ( 8 FDA reports)
DIAPHRAGMATIC HERNIA ( 8 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 8 FDA reports)
DYSTHYMIC DISORDER ( 8 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 8 FDA reports)
EMPHYSEMA ( 8 FDA reports)
ENERGY INCREASED ( 8 FDA reports)
ESCHERICHIA SEPSIS ( 8 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 8 FDA reports)
FACE OEDEMA ( 8 FDA reports)
FEMUR FRACTURE ( 8 FDA reports)
FORMICATION ( 8 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 8 FDA reports)
GASTRECTOMY ( 8 FDA reports)
GASTRIC CANCER RECURRENT ( 8 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 8 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 8 FDA reports)
HEPATIC NECROSIS ( 8 FDA reports)
HYPERPHAGIA ( 8 FDA reports)
HYPOCALCAEMIA ( 8 FDA reports)
HYPOSPADIAS ( 8 FDA reports)
IMMUNODEFICIENCY ( 8 FDA reports)
INJECTION SITE DISCOLOURATION ( 8 FDA reports)
INJECTION SITE SWELLING ( 8 FDA reports)
INTERCOSTAL RETRACTION ( 8 FDA reports)
JOINT CONTRACTURE ( 8 FDA reports)
LABORATORY TEST ABNORMAL ( 8 FDA reports)
LOOSE TOOTH ( 8 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 8 FDA reports)
METASTASES TO LYMPH NODES ( 8 FDA reports)
MULTIPLE ALLERGIES ( 8 FDA reports)
MUSCLE DISORDER ( 8 FDA reports)
NAIL DISORDER ( 8 FDA reports)
NASAL FLARING ( 8 FDA reports)
NEPHRITIS INTERSTITIAL ( 8 FDA reports)
NEPHROPATHY TOXIC ( 8 FDA reports)
NEUROFIBROMA ( 8 FDA reports)
NEUTROPHILIA ( 8 FDA reports)
OPTIC NEURITIS ( 8 FDA reports)
OSTEOLYSIS ( 8 FDA reports)
PAINFUL RESPIRATION ( 8 FDA reports)
PERIPHERAL NERVE INJURY ( 8 FDA reports)
PHOTOSENSITIVITY REACTION ( 8 FDA reports)
PLEURODESIS ( 8 FDA reports)
PNEUMONIA HAEMOPHILUS ( 8 FDA reports)
PRESCRIBED OVERDOSE ( 8 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 8 FDA reports)
PROTEIN TOTAL DECREASED ( 8 FDA reports)
PSORIATIC ARTHROPATHY ( 8 FDA reports)
PULMONARY ARTERY DILATATION ( 8 FDA reports)
PULMONARY INFARCTION ( 8 FDA reports)
PYELOCALIECTASIS ( 8 FDA reports)
QUALITY OF LIFE DECREASED ( 8 FDA reports)
RADICULAR PAIN ( 8 FDA reports)
RIB DEFORMITY ( 8 FDA reports)
SKIN HAEMORRHAGE ( 8 FDA reports)
SKIN PAPILLOMA ( 8 FDA reports)
SLUGGISHNESS ( 8 FDA reports)
SPINAL DEFORMITY ( 8 FDA reports)
STEM CELL TRANSPLANT ( 8 FDA reports)
STRIDOR ( 8 FDA reports)
THORACOSTOMY ( 8 FDA reports)
TONGUE DRY ( 8 FDA reports)
TYPE 2 DIABETES MELLITUS ( 8 FDA reports)
URINARY HESITATION ( 8 FDA reports)
VERTIGO POSITIONAL ( 8 FDA reports)
VISUAL FIELD DEFECT ( 8 FDA reports)
ACCIDENTAL OVERDOSE ( 7 FDA reports)
ADNEXA UTERI MASS ( 7 FDA reports)
APPETITE DISORDER ( 7 FDA reports)
ARTERIOSPASM CORONARY ( 7 FDA reports)
ATAXIA ( 7 FDA reports)
AUTOIMMUNE DISORDER ( 7 FDA reports)
BLADDER CANCER ( 7 FDA reports)
BLINDNESS TRANSIENT ( 7 FDA reports)
BLOOD PH DECREASED ( 7 FDA reports)
BODY TINEA ( 7 FDA reports)
BONE EROSION ( 7 FDA reports)
BONE OPERATION ( 7 FDA reports)
BONE SWELLING ( 7 FDA reports)
BONE TRIMMING ( 7 FDA reports)
BREAST ABSCESS ( 7 FDA reports)
BURSITIS ( 7 FDA reports)
CAROTID ARTERY DISEASE ( 7 FDA reports)
CATHETER SITE HAEMATOMA ( 7 FDA reports)
CEREBELLAR INFARCTION ( 7 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 7 FDA reports)
CONGENITAL PULMONARY HYPERTENSION ( 7 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 7 FDA reports)
CORRECTIVE LENS USER ( 7 FDA reports)
DEVICE FAILURE ( 7 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 7 FDA reports)
ECZEMA ( 7 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 7 FDA reports)
EPILEPSY ( 7 FDA reports)
EXTRASYSTOLES ( 7 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 7 FDA reports)
GASTRIC POLYPS ( 7 FDA reports)
GLIOSIS ( 7 FDA reports)
GOITRE ( 7 FDA reports)
HEAD DISCOMFORT ( 7 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 7 FDA reports)
HEPATIC INFARCTION ( 7 FDA reports)
HIGH-PITCHED CRYING ( 7 FDA reports)
HYPERCAPNIA ( 7 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 7 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 7 FDA reports)
INJECTION SITE RASH ( 7 FDA reports)
KNEE OPERATION ( 7 FDA reports)
LIP ULCERATION ( 7 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED RECURRENT ( 7 FDA reports)
LYMPHATIC DISORDER ( 7 FDA reports)
MENSTRUAL DISORDER ( 7 FDA reports)
METABOLIC SYNDROME ( 7 FDA reports)
METASTATIC PAIN ( 7 FDA reports)
MULTIPLE DRUG OVERDOSE ( 7 FDA reports)
MUSCULOSKELETAL DISORDER ( 7 FDA reports)
NASAL DRYNESS ( 7 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 7 FDA reports)
OBESITY ( 7 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 7 FDA reports)
ORAL HERPES ( 7 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 7 FDA reports)
PARANOIA ( 7 FDA reports)
PERFORMANCE STATUS DECREASED ( 7 FDA reports)
PERINEAL LACERATION ( 7 FDA reports)
PLATELET COUNT INCREASED ( 7 FDA reports)
PNEUMONIA KLEBSIELLA ( 7 FDA reports)
PNEUMOTHORAX TRAUMATIC ( 7 FDA reports)
PRURITUS GENITAL ( 7 FDA reports)
PULMONARY MALFORMATION ( 7 FDA reports)
SELF-MEDICATION ( 7 FDA reports)
SEROSITIS ( 7 FDA reports)
SIALOADENITIS ( 7 FDA reports)
SKIN ATROPHY ( 7 FDA reports)
SKIN FISSURES ( 7 FDA reports)
SLEEP TALKING ( 7 FDA reports)
SPINAL CLAUDICATION ( 7 FDA reports)
SPONDYLOSIS ( 7 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 7 FDA reports)
TONGUE INJURY ( 7 FDA reports)
UPPER LIMB FRACTURE ( 7 FDA reports)
URINE ODOUR ABNORMAL ( 7 FDA reports)
VAGOTOMY ( 7 FDA reports)
VASCULAR RUPTURE ( 7 FDA reports)
VENOUS INSUFFICIENCY ( 7 FDA reports)
VIITH NERVE PARALYSIS ( 7 FDA reports)
VULVAL DISORDER ( 7 FDA reports)
WITHDRAWAL SYNDROME ( 7 FDA reports)
WOUND DEHISCENCE ( 7 FDA reports)
XANTHELASMA ( 7 FDA reports)
ABDOMINAL RIGIDITY ( 6 FDA reports)
ACUTE HEPATIC FAILURE ( 6 FDA reports)
ACUTE PRERENAL FAILURE ( 6 FDA reports)
ALCOHOLISM ( 6 FDA reports)
AMMONIA INCREASED ( 6 FDA reports)
AORTIC STENOSIS ( 6 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 6 FDA reports)
AUTOIMMUNE HEPATITIS ( 6 FDA reports)
BACTERIA TISSUE SPECIMEN IDENTIFIED ( 6 FDA reports)
BLADDER CATHETERISATION ( 6 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 6 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 6 FDA reports)
BLOOD SODIUM INCREASED ( 6 FDA reports)
BLOOD TEST ABNORMAL ( 6 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 6 FDA reports)
BONE MARROW TRANSPLANT ( 6 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 6 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 6 FDA reports)
CARDIAC DISCOMFORT ( 6 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 6 FDA reports)
CEREBRAL THROMBOSIS ( 6 FDA reports)
CHAPPED LIPS ( 6 FDA reports)
COARCTATION OF THE AORTA ( 6 FDA reports)
COLITIS ISCHAEMIC ( 6 FDA reports)
COMPLETED SUICIDE ( 6 FDA reports)
CYSTITIS INTERSTITIAL ( 6 FDA reports)
DECREASED ACTIVITY ( 6 FDA reports)
DELIRIUM ( 6 FDA reports)
DISSEMINATED TUBERCULOSIS ( 6 FDA reports)
DROOLING ( 6 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 6 FDA reports)
DRY THROAT ( 6 FDA reports)
DUODENAL ULCER PERFORATION ( 6 FDA reports)
DYSMORPHISM ( 6 FDA reports)
ELECTROLYTE IMBALANCE ( 6 FDA reports)
EOSINOPHIL COUNT INCREASED ( 6 FDA reports)
ERYTHEMA MULTIFORME ( 6 FDA reports)
ESCHERICHIA INFECTION ( 6 FDA reports)
FACE INJURY ( 6 FDA reports)
FAECALURIA ( 6 FDA reports)
FLUID INTAKE REDUCED ( 6 FDA reports)
GALLBLADDER PAIN ( 6 FDA reports)
GASTRIC INFECTION ( 6 FDA reports)
HAEMOLYTIC ANAEMIA ( 6 FDA reports)
HAEMOPHILUS BACTERAEMIA ( 6 FDA reports)
HAEMORRHAGIC STROKE ( 6 FDA reports)
HALLUCINATION, VISUAL ( 6 FDA reports)
HANGOVER ( 6 FDA reports)
HEART INJURY ( 6 FDA reports)
HYDROCELE ( 6 FDA reports)
HYPERBILIRUBINAEMIA ( 6 FDA reports)
HYPERVENTILATION ( 6 FDA reports)
INJECTION SITE NODULE ( 6 FDA reports)
INTENTIONAL SELF-INJURY ( 6 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 6 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 6 FDA reports)
JAUNDICE CHOLESTATIC ( 6 FDA reports)
KNEE ARTHROPLASTY ( 6 FDA reports)
LARYNGITIS ( 6 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 6 FDA reports)
LEIOMYOSARCOMA METASTATIC ( 6 FDA reports)
LIBIDO DECREASED ( 6 FDA reports)
LUNG ADENOCARCINOMA ( 6 FDA reports)
LUNG INJURY ( 6 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 6 FDA reports)
MACULAR DEGENERATION ( 6 FDA reports)
MANIA ( 6 FDA reports)
MEDICATION RESIDUE ( 6 FDA reports)
MICTURITION DISORDER ( 6 FDA reports)
MICTURITION FREQUENCY DECREASED ( 6 FDA reports)
MYELODYSPLASTIC SYNDROME ( 6 FDA reports)
NASAL OEDEMA ( 6 FDA reports)
NERVE BLOCK ( 6 FDA reports)
NEUROPATHY ( 6 FDA reports)
NO ADVERSE DRUG EFFECT ( 6 FDA reports)
NOONAN SYNDROME ( 6 FDA reports)
OPEN REDUCTION OF FRACTURE ( 6 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 6 FDA reports)
OROPHARYNGEAL BLISTERING ( 6 FDA reports)
OVERWEIGHT ( 6 FDA reports)
PANCREATIC CARCINOMA ( 6 FDA reports)
PENILE HAEMORRHAGE ( 6 FDA reports)
PERFORATED ULCER ( 6 FDA reports)
PERITONITIS ( 6 FDA reports)
PILONIDAL CYST ( 6 FDA reports)
PITTING OEDEMA ( 6 FDA reports)
POLYARTHRITIS ( 6 FDA reports)
PROCTITIS ( 6 FDA reports)
PRURITUS ANI ( 6 FDA reports)
PURULENCE ( 6 FDA reports)
PYOGENIC GRANULOMA ( 6 FDA reports)
RAYNAUD'S PHENOMENON ( 6 FDA reports)
REHABILITATION THERAPY ( 6 FDA reports)
RENAL ATROPHY ( 6 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS BRONCHIOLITIS ( 6 FDA reports)
RHINITIS SEASONAL ( 6 FDA reports)
SCLERODACTYLIA ( 6 FDA reports)
SEDATION ( 6 FDA reports)
SENSATION OF PRESSURE ( 6 FDA reports)
SKIN FIBROSIS ( 6 FDA reports)
SKIN INDURATION ( 6 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 6 FDA reports)
SPONDYLITIS ( 6 FDA reports)
SPONDYLOLISTHESIS ACQUIRED ( 6 FDA reports)
SPUTUM DISCOLOURED ( 6 FDA reports)
STENT OCCLUSION ( 6 FDA reports)
SYNCOPE VASOVAGAL ( 6 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 6 FDA reports)
TENDON PAIN ( 6 FDA reports)
TRACHEOBRONCHITIS ( 6 FDA reports)
TRACHEOMALACIA ( 6 FDA reports)
UMBILICAL CORD ABNORMALITY ( 6 FDA reports)
URTICARIA GENERALISED ( 6 FDA reports)
VASCULAR BYPASS GRAFT ( 6 FDA reports)
VITAMIN B12 DEFICIENCY ( 6 FDA reports)
VITAMIN D DEFICIENCY ( 6 FDA reports)
WRIST FRACTURE ( 6 FDA reports)
ABSCESS LIMB ( 5 FDA reports)
ADRENAL MASS ( 5 FDA reports)
ANAL ABSCESS ( 5 FDA reports)
ANAL DISCOMFORT ( 5 FDA reports)
ANAL FISSURE ( 5 FDA reports)
ANURIA ( 5 FDA reports)
AORTIC VALVE CALCIFICATION ( 5 FDA reports)
ASPIRATION ( 5 FDA reports)
ATHEROSCLEROSIS ( 5 FDA reports)
BACTERAEMIA ( 5 FDA reports)
BACTERIAL TEST POSITIVE ( 5 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 5 FDA reports)
BLOOD CALCIUM INCREASED ( 5 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 5 FDA reports)
BLOOD MAGNESIUM DECREASED ( 5 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 5 FDA reports)
BREAST PAIN ( 5 FDA reports)
BREAST TENDERNESS ( 5 FDA reports)
BRONCHOPNEUMONIA ( 5 FDA reports)
CARDIAC FAILURE ACUTE ( 5 FDA reports)
CATARACT OPERATION ( 5 FDA reports)
CEREBROVASCULAR DISORDER ( 5 FDA reports)
CLOSTRIDIAL INFECTION ( 5 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 5 FDA reports)
DELUSION ( 5 FDA reports)
DRUG DISPENSING ERROR ( 5 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 5 FDA reports)
ENTEROCOCCAL INFECTION ( 5 FDA reports)
EYELID PTOSIS ( 5 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 5 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 5 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 5 FDA reports)
GENERAL SYMPTOM ( 5 FDA reports)
GENITAL HAEMORRHAGE ( 5 FDA reports)
GESTATIONAL HYPERTENSION ( 5 FDA reports)
GROIN ABSCESS ( 5 FDA reports)
HEART VALVE INCOMPETENCE ( 5 FDA reports)
HEPATOSPLENOMEGALY ( 5 FDA reports)
HICCUPS ( 5 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 5 FDA reports)
HIP SURGERY ( 5 FDA reports)
HYPERCHLORHYDRIA ( 5 FDA reports)
HYPERTENSIVE HEART DISEASE ( 5 FDA reports)
IMMUNE SYSTEM DISORDER ( 5 FDA reports)
INGROWING NAIL ( 5 FDA reports)
INJECTION SITE IRRITATION ( 5 FDA reports)
INTRACRANIAL ANEURYSM ( 5 FDA reports)
LARGE INTESTINAL ULCER ( 5 FDA reports)
LIGAMENT INJURY ( 5 FDA reports)
LIP DISORDER ( 5 FDA reports)
LOWER LIMB FRACTURE ( 5 FDA reports)
LUNG ABSCESS ( 5 FDA reports)
MALIGNANT ASCITES ( 5 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 5 FDA reports)
MICROCYTOSIS ( 5 FDA reports)
MIOSIS ( 5 FDA reports)
MITRAL VALVE CALCIFICATION ( 5 FDA reports)
MOUNTAIN SICKNESS ACUTE ( 5 FDA reports)
MYDRIASIS ( 5 FDA reports)
MYOCLONUS ( 5 FDA reports)
NERVE ROOT COMPRESSION ( 5 FDA reports)
NEURILEMMOMA ( 5 FDA reports)
NEUTROPHIL COUNT DECREASED ( 5 FDA reports)
NO THERAPEUTIC RESPONSE ( 5 FDA reports)
NODULE ON EXTREMITY ( 5 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 5 FDA reports)
OESOPHAGEAL PERFORATION ( 5 FDA reports)
OLIGOMENORRHOEA ( 5 FDA reports)
OPERATIVE HAEMORRHAGE ( 5 FDA reports)
ORGAN FAILURE ( 5 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 5 FDA reports)
OS TRIGONUM SYNDROME ( 5 FDA reports)
OVARIAN CYST ( 5 FDA reports)
PANIC DISORDER ( 5 FDA reports)
PARTNER STRESS ( 5 FDA reports)
PENIS DISORDER ( 5 FDA reports)
PERIORBITAL HAEMATOMA ( 5 FDA reports)
PERSONALITY DISORDER ( 5 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 5 FDA reports)
PHLEBITIS ( 5 FDA reports)
PHOTOPSIA ( 5 FDA reports)
PNEUMONITIS ( 5 FDA reports)
PORTAL HYPERTENSION ( 5 FDA reports)
POSTNASAL DRIP ( 5 FDA reports)
PRODUCT QUALITY ISSUE ( 5 FDA reports)
PROTEIN URINE PRESENT ( 5 FDA reports)
PROTHROMBIN TIME SHORTENED ( 5 FDA reports)
PULMONARY AIR LEAKAGE ( 5 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 5 FDA reports)
PURPURA ( 5 FDA reports)
PYELONEPHRITIS ( 5 FDA reports)
RADICULITIS ( 5 FDA reports)
RADICULOPATHY ( 5 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 5 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 5 FDA reports)
RENAL ARTERY STENOSIS ( 5 FDA reports)
RESORPTION BONE INCREASED ( 5 FDA reports)
RESUSCITATION ( 5 FDA reports)
RETINAL HAEMORRHAGE ( 5 FDA reports)
RETINAL VEIN OCCLUSION ( 5 FDA reports)
RHINITIS ( 5 FDA reports)
RIGHT VENTRICULAR FAILURE ( 5 FDA reports)
SEBORRHOEIC DERMATITIS ( 5 FDA reports)
SENSITIVITY OF TEETH ( 5 FDA reports)
SEXUAL DYSFUNCTION ( 5 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 5 FDA reports)
SKIN LESION EXCISION ( 5 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 5 FDA reports)
STRESS FRACTURE ( 5 FDA reports)
SUDDEN CARDIAC DEATH ( 5 FDA reports)
SUDDEN DEATH ( 5 FDA reports)
TENOSYNOVITIS ( 5 FDA reports)
THIRST ( 5 FDA reports)
THROMBOCYTHAEMIA ( 5 FDA reports)
TINEA PEDIS ( 5 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 5 FDA reports)
TRISMUS ( 5 FDA reports)
TUBERCULOSIS ( 5 FDA reports)
UNINTENDED PREGNANCY ( 5 FDA reports)
UROSEPSIS ( 5 FDA reports)
UTERINE POLYP ( 5 FDA reports)
VAGINAL DISCHARGE ( 5 FDA reports)
VENTRICULAR HYPOKINESIA ( 5 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 5 FDA reports)
VITREOUS FLOATERS ( 5 FDA reports)
VOCAL CORD DISORDER ( 5 FDA reports)
VOLUME BLOOD DECREASED ( 5 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 5 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 4 FDA reports)
ACUTE CORONARY SYNDROME ( 4 FDA reports)
ACUTE LEUKAEMIA ( 4 FDA reports)
ACUTE PULMONARY OEDEMA ( 4 FDA reports)
ADENOCARCINOMA ( 4 FDA reports)
ADJUSTMENT DISORDER ( 4 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 4 FDA reports)
AMENORRHOEA ( 4 FDA reports)
ANALGESIA ( 4 FDA reports)
ANKYLOSING SPONDYLITIS ( 4 FDA reports)
ANORECTAL DISORDER ( 4 FDA reports)
ANOXIC ENCEPHALOPATHY ( 4 FDA reports)
ANXIETY DISORDER ( 4 FDA reports)
APPLICATION SITE REACTION ( 4 FDA reports)
ARTERIAL RUPTURE ( 4 FDA reports)
ATRIOVENTRICULAR BLOCK ( 4 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 4 FDA reports)
AUTISM ( 4 FDA reports)
AUTISM SPECTRUM DISORDER ( 4 FDA reports)
BALANITIS ( 4 FDA reports)
BILIARY TRACT DISORDER ( 4 FDA reports)
BLOOD BLISTER ( 4 FDA reports)
BLOOD CREATINE INCREASED ( 4 FDA reports)
BLOOD CULTURE POSITIVE ( 4 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 4 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 4 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 4 FDA reports)
BLOOD URIC ACID INCREASED ( 4 FDA reports)
BONE DENSITY DECREASED ( 4 FDA reports)
BONE FORMATION INCREASED ( 4 FDA reports)
BONE LOSS ( 4 FDA reports)
BOWEL SOUNDS ABNORMAL ( 4 FDA reports)
BRAIN DAMAGE ( 4 FDA reports)
BREAST ATROPHY ( 4 FDA reports)
BREAST CANCER FEMALE ( 4 FDA reports)
BREAST DISORDER ( 4 FDA reports)
CALCINOSIS ( 4 FDA reports)
CARDIAC PACEMAKER INSERTION ( 4 FDA reports)
CAROTID BRUIT ( 4 FDA reports)
CARTILAGE INJURY ( 4 FDA reports)
CEREBROVASCULAR STENOSIS ( 4 FDA reports)
CHEST X-RAY ABNORMAL ( 4 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 4 FDA reports)
COLON CANCER ( 4 FDA reports)
CONCUSSION ( 4 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 4 FDA reports)
CULTURE URINE POSITIVE ( 4 FDA reports)
DEAFNESS BILATERAL ( 4 FDA reports)
DEAFNESS NEUROSENSORY ( 4 FDA reports)
DEMENTIA ( 4 FDA reports)
DENTAL EXAMINATION ABNORMAL ( 4 FDA reports)
DERMATITIS ACNEIFORM ( 4 FDA reports)
DERMATITIS ATOPIC ( 4 FDA reports)
DERMATITIS EXFOLIATIVE ( 4 FDA reports)
DEVICE MALFUNCTION ( 4 FDA reports)
DIABETIC RETINOPATHY ( 4 FDA reports)
DRUG LEVEL INCREASED ( 4 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 4 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 4 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 4 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 4 FDA reports)
ENDOMETRIAL SARCOMA ( 4 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 4 FDA reports)
EXERCISE TOLERANCE DECREASED ( 4 FDA reports)
EXOPHTHALMOS ( 4 FDA reports)
EXPIRED DRUG ADMINISTERED ( 4 FDA reports)
EYE INJURY ( 4 FDA reports)
FAECES HARD ( 4 FDA reports)
FALLOPIAN TUBE OPERATION ( 4 FDA reports)
FEMORAL ARTERY OCCLUSION ( 4 FDA reports)
FIBROUS HISTIOCYTOMA ( 4 FDA reports)
FOAMING AT MOUTH ( 4 FDA reports)
FRUSTRATION ( 4 FDA reports)
FURUNCLE ( 4 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 4 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 4 FDA reports)
GENITAL LESION ( 4 FDA reports)
GENITAL PRURITUS FEMALE ( 4 FDA reports)
GINGIVAL RECESSION ( 4 FDA reports)
GLOBAL AMNESIA ( 4 FDA reports)
GLOMERULONEPHRITIS FOCAL ( 4 FDA reports)
HAEMANGIOMA OF SKIN ( 4 FDA reports)
HAEMATOMA INFECTION ( 4 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 4 FDA reports)
HAEMORRHAGE URINARY TRACT ( 4 FDA reports)
HAIR TEXTURE ABNORMAL ( 4 FDA reports)
HALLUCINATION, AUDITORY ( 4 FDA reports)
HEART ALTERNATION ( 4 FDA reports)
HEART RATE ABNORMAL ( 4 FDA reports)
HELICOBACTER GASTRITIS ( 4 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 4 FDA reports)
HELICOBACTER TEST POSITIVE ( 4 FDA reports)
HEPATIC FIBROSIS ( 4 FDA reports)
HERPES VIRUS INFECTION ( 4 FDA reports)
HUNGER ( 4 FDA reports)
HYPERKERATOSIS ( 4 FDA reports)
HYPERTENSIVE CRISIS ( 4 FDA reports)
HYPOVITAMINOSIS ( 4 FDA reports)
IATROGENIC INJURY ( 4 FDA reports)
IMPATIENCE ( 4 FDA reports)
INCISIONAL DRAINAGE ( 4 FDA reports)
INJECTION SITE BRUISING ( 4 FDA reports)
INJECTION SITE INDURATION ( 4 FDA reports)
INTENTIONAL MISUSE ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 4 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 4 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 4 FDA reports)
IRON DEFICIENCY ( 4 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 4 FDA reports)
KIDNEY SMALL ( 4 FDA reports)
LABILE BLOOD PRESSURE ( 4 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 4 FDA reports)
LISTERIA SEPSIS ( 4 FDA reports)
LIVEDO RETICULARIS ( 4 FDA reports)
LUNG INFECTION ( 4 FDA reports)
LYMPHATIC SYSTEM NEOPLASM ( 4 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 4 FDA reports)
MACULOPATHY ( 4 FDA reports)
MARROW HYPERPLASIA ( 4 FDA reports)
MENINGITIS VIRAL ( 4 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 4 FDA reports)
MITOCHONDRIAL TOXICITY ( 4 FDA reports)
MONOCYTE COUNT INCREASED ( 4 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 4 FDA reports)
MULTIPLE FRACTURES ( 4 FDA reports)
MUSCLE RIGIDITY ( 4 FDA reports)
NARCOTIC INTOXICATION ( 4 FDA reports)
NASAL DISORDER ( 4 FDA reports)
NASAL ULCER ( 4 FDA reports)
NEPHROCALCINOSIS ( 4 FDA reports)
NEPHROSCLEROSIS ( 4 FDA reports)
NEPHROTIC SYNDROME ( 4 FDA reports)
NEUTROPHIL COUNT INCREASED ( 4 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 4 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 4 FDA reports)
OESOPHAGEAL DISCOMFORT ( 4 FDA reports)
OESOPHAGITIS HAEMORRHAGIC ( 4 FDA reports)
OPTIC NEUROPATHY ( 4 FDA reports)
ORCHITIS ( 4 FDA reports)
PAINFUL DEFAECATION ( 4 FDA reports)
PALATAL OEDEMA ( 4 FDA reports)
PANCREATIC CYST ( 4 FDA reports)
PARESIS ( 4 FDA reports)
PAROSMIA ( 4 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 4 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 4 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 4 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 4 FDA reports)
PERSONALITY CHANGE ( 4 FDA reports)
PLATELET DISORDER ( 4 FDA reports)
POLYTRAUMATISM ( 4 FDA reports)
POST HERPETIC NEURALGIA ( 4 FDA reports)
POST LAMINECTOMY SYNDROME ( 4 FDA reports)
POST PROCEDURAL HAEMATOMA ( 4 FDA reports)
POST-TRAUMATIC PAIN ( 4 FDA reports)
POSTOPERATIVE INFECTION ( 4 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 4 FDA reports)
PROTEIN URINE ( 4 FDA reports)
PSYCHIATRIC SYMPTOM ( 4 FDA reports)
PULMONARY VALVE STENOSIS CONGENITAL ( 4 FDA reports)
REFLUX OESOPHAGITIS ( 4 FDA reports)
RENAL ARTERY OCCLUSION ( 4 FDA reports)
RENAL MASS ( 4 FDA reports)
RESPIRATORY RATE DECREASED ( 4 FDA reports)
RETINAL ARTERY OCCLUSION ( 4 FDA reports)
RETINAL DETACHMENT ( 4 FDA reports)
RETINAL TEAR ( 4 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 4 FDA reports)
SALIVARY GLAND DISORDER ( 4 FDA reports)
SALIVARY HYPERSECRETION ( 4 FDA reports)
SEASONAL ALLERGY ( 4 FDA reports)
SEBORRHOEIC KERATOSIS ( 4 FDA reports)
SELF MUTILATION ( 4 FDA reports)
SHIFT TO THE LEFT ( 4 FDA reports)
SKIN NODULE ( 4 FDA reports)
SKIN REACTION ( 4 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 4 FDA reports)
STARING ( 4 FDA reports)
STRESS SYMPTOMS ( 4 FDA reports)
TACHYARRHYTHMIA ( 4 FDA reports)
TEMPERATURE INTOLERANCE ( 4 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 4 FDA reports)
THYROID CYST ( 4 FDA reports)
TOE AMPUTATION ( 4 FDA reports)
TONGUE OEDEMA ( 4 FDA reports)
TRANSFERRIN INCREASED ( 4 FDA reports)
TRICHORRHEXIS ( 4 FDA reports)
TROPONIN INCREASED ( 4 FDA reports)
TUMOUR MARKER INCREASED ( 4 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 4 FDA reports)
UTERINE CERVICAL EROSION ( 4 FDA reports)
VAGINAL BURNING SENSATION ( 4 FDA reports)
VAGINAL MYCOSIS ( 4 FDA reports)
VAGINAL SWELLING ( 4 FDA reports)
VASCULAR PSEUDOANEURYSM ( 4 FDA reports)
VITH NERVE PARALYSIS ( 4 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 3 FDA reports)
ACCIDENT AT WORK ( 3 FDA reports)
ACCIDENTAL DEATH ( 3 FDA reports)
ADENOCARCINOMA PANCREAS ( 3 FDA reports)
ADVERSE REACTION ( 3 FDA reports)
AFFECTIVE DISORDER ( 3 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 3 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 3 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 3 FDA reports)
ANAPHYLACTOID REACTION ( 3 FDA reports)
ANORECTAL DISCOMFORT ( 3 FDA reports)
ANTEPARTUM HAEMORRHAGE ( 3 FDA reports)
APATHY ( 3 FDA reports)
APPENDIX DISORDER ( 3 FDA reports)
APPLICATION SITE ERYTHEMA ( 3 FDA reports)
ARTERIAL DISORDER ( 3 FDA reports)
ARTERIOVENOUS FISTULA, ACQUIRED ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 3 FDA reports)
ATRIAL TACHYCARDIA ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 3 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 3 FDA reports)
AVULSION FRACTURE ( 3 FDA reports)
BACTERIA URINE ( 3 FDA reports)
BENIGN BONE NEOPLASM ( 3 FDA reports)
BIOPSY ( 3 FDA reports)
BIPOLAR DISORDER ( 3 FDA reports)
BLOOD AMYLASE INCREASED ( 3 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 3 FDA reports)
BLOOD CREATININE DECREASED ( 3 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 3 FDA reports)
BLOOD MAGNESIUM INCREASED ( 3 FDA reports)
BRAIN HERNIATION ( 3 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 3 FDA reports)
BRAIN NEOPLASM BENIGN ( 3 FDA reports)
BREAST CANCER IN SITU ( 3 FDA reports)
BREAST LUMP REMOVAL ( 3 FDA reports)
BRONCHIAL CARCINOMA ( 3 FDA reports)
BRONCHIECTASIS ( 3 FDA reports)
BRUXISM ( 3 FDA reports)
BUNDLE BRANCH BLOCK ( 3 FDA reports)
BUTTOCK PAIN ( 3 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 3 FDA reports)
CATHETER RELATED COMPLICATION ( 3 FDA reports)
CATHETER RELATED INFECTION ( 3 FDA reports)
CATHETERISATION CARDIAC ( 3 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 3 FDA reports)
CEREBRAL ATROPHY ( 3 FDA reports)
CEREBRAL HAEMATOMA ( 3 FDA reports)
CERUMEN IMPACTION ( 3 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 3 FDA reports)
CHONDROPATHY ( 3 FDA reports)
CHOROIDAL DETACHMENT ( 3 FDA reports)
CHRONIC HEPATITIS ( 3 FDA reports)
CLAVICLE FRACTURE ( 3 FDA reports)
COLECTOMY ( 3 FDA reports)
COLONOSCOPY ABNORMAL ( 3 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 3 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 3 FDA reports)
CONJUNCTIVITIS ( 3 FDA reports)
CORONARY ARTERY THROMBOSIS ( 3 FDA reports)
COW'S MILK INTOLERANCE ( 3 FDA reports)
CRYSTAL ARTHROPATHY ( 3 FDA reports)
CYSTIC LYMPHANGIOMA ( 3 FDA reports)
CYSTITIS RADIATION ( 3 FDA reports)
DEAFNESS UNILATERAL ( 3 FDA reports)
DEATH OF SPOUSE ( 3 FDA reports)
DEFAECATION URGENCY ( 3 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 3 FDA reports)
DENTAL FISTULA ( 3 FDA reports)
DENTAL PLAQUE ( 3 FDA reports)
DERMATITIS ALLERGIC ( 3 FDA reports)
DIABETIC COMPLICATION ( 3 FDA reports)
DIABETIC FOOT ( 3 FDA reports)
DIABETIC GASTROPARESIS ( 3 FDA reports)
DIABETIC KETOACIDOSIS ( 3 FDA reports)
DIABETIC NEUROPATHY ( 3 FDA reports)
DIVERTICULAR PERFORATION ( 3 FDA reports)
DRUG ERUPTION ( 3 FDA reports)
DRUG WITHDRAWAL HEADACHE ( 3 FDA reports)
DUODENAL POLYP ( 3 FDA reports)
DYSGRAPHIA ( 3 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 3 FDA reports)
EAR CONGESTION ( 3 FDA reports)
EAR HAEMORRHAGE ( 3 FDA reports)
EAR PRURITUS ( 3 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 3 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 3 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 3 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 3 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 3 FDA reports)
EMBOLISM ( 3 FDA reports)
ENCEPHALITIS ( 3 FDA reports)
EOSINOPHILIA ( 3 FDA reports)
EOSINOPHILIC PNEUMONIA ( 3 FDA reports)
ERYSIPELAS ( 3 FDA reports)
ERYTHEMA OF EYELID ( 3 FDA reports)
EXTRAOCULAR MUSCLE PARESIS ( 3 FDA reports)
EYE INFECTION BACTERIAL ( 3 FDA reports)
EYE REDNESS ( 3 FDA reports)
FAECES PALE ( 3 FDA reports)
FAMILY STRESS ( 3 FDA reports)
FAT NECROSIS ( 3 FDA reports)
FEAR OF DISEASE ( 3 FDA reports)
FEELING HOT AND COLD ( 3 FDA reports)
FEELING OF RELAXATION ( 3 FDA reports)
FEMORAL NECK FRACTURE ( 3 FDA reports)
FISTULA DISCHARGE ( 3 FDA reports)
FLAT AFFECT ( 3 FDA reports)
FLIGHT OF IDEAS ( 3 FDA reports)
FOOD POISONING ( 3 FDA reports)
FOOT AMPUTATION ( 3 FDA reports)
FOOT DEFORMITY ( 3 FDA reports)
FOOT OPERATION ( 3 FDA reports)
FRACTURE NONUNION ( 3 FDA reports)
GALLBLADDER POLYP ( 3 FDA reports)
GASTRIC ULCER SURGERY ( 3 FDA reports)
GASTROENTERITIS EOSINOPHILIC ( 3 FDA reports)
GASTROINTESTINAL INJURY ( 3 FDA reports)
GASTROINTESTINAL NECROSIS ( 3 FDA reports)
GINGIVAL INFECTION ( 3 FDA reports)
GINGIVAL ULCERATION ( 3 FDA reports)
GRIP STRENGTH DECREASED ( 3 FDA reports)
GUILLAIN-BARRE SYNDROME ( 3 FDA reports)
HAEMATOSPERMIA ( 3 FDA reports)
HAEMODIALYSIS ( 3 FDA reports)
HAEMODYNAMIC INSTABILITY ( 3 FDA reports)
HAEMOLYSIS ( 3 FDA reports)
HAEMORRHAGIC ANAEMIA ( 3 FDA reports)
HAIR GROWTH ABNORMAL ( 3 FDA reports)
HAND DEFORMITY ( 3 FDA reports)
HELICOBACTER INFECTION ( 3 FDA reports)
HEMICEPHALALGIA ( 3 FDA reports)
HEPATIC PAIN ( 3 FDA reports)
HEPATITIS A ( 3 FDA reports)
HEPATOBILIARY SCAN ABNORMAL ( 3 FDA reports)
HEPATOCELLULAR INJURY ( 3 FDA reports)
HEPATORENAL SYNDROME ( 3 FDA reports)
HIDRADENITIS ( 3 FDA reports)
HYPERACUSIS ( 3 FDA reports)
HYPERCHLORAEMIA ( 3 FDA reports)
HYPERCOAGULATION ( 3 FDA reports)
HYPERPHOSPHATAEMIA ( 3 FDA reports)
HYPERTHYROIDISM ( 3 FDA reports)
HYPERTONIC BLADDER ( 3 FDA reports)
HYPERTRANSAMINASAEMIA ( 3 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 3 FDA reports)
HYPOCHROMASIA ( 3 FDA reports)
HYPOCOAGULABLE STATE ( 3 FDA reports)
HYPOGEUSIA ( 3 FDA reports)
HYPOPNOEA ( 3 FDA reports)
HYPOPROTEINAEMIA ( 3 FDA reports)
HYPOREFLEXIA ( 3 FDA reports)
HYPOTRICHOSIS ( 3 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 3 FDA reports)
ILEUS PARALYTIC ( 3 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 3 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 3 FDA reports)
INJECTION SITE MASS ( 3 FDA reports)
INJURY ASPHYXIATION ( 3 FDA reports)
INTESTINAL POLYP ( 3 FDA reports)
IRITIS ( 3 FDA reports)
KELOID SCAR ( 3 FDA reports)
KOUNIS SYNDROME ( 3 FDA reports)
LEG AMPUTATION ( 3 FDA reports)
LEGAL PROBLEM ( 3 FDA reports)
LIGAMENT DISORDER ( 3 FDA reports)
LIVER TRANSPLANT REJECTION ( 3 FDA reports)
LOCALISED OEDEMA ( 3 FDA reports)
LOOSE STOOLS ( 3 FDA reports)
LYME DISEASE ( 3 FDA reports)
LYMPHADENECTOMY ( 3 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 3 FDA reports)
MACULAR OEDEMA ( 3 FDA reports)
MALLORY-WEISS SYNDROME ( 3 FDA reports)
MECHANICAL COMPLICATION OF IMPLANT ( 3 FDA reports)
MENIERE'S DISEASE ( 3 FDA reports)
MENOPAUSAL SYMPTOMS ( 3 FDA reports)
METASTASIS ( 3 FDA reports)
MUCOUS MEMBRANE DISORDER ( 3 FDA reports)
MUCOUS STOOLS ( 3 FDA reports)
MULTIPLE SYSTEM ATROPHY ( 3 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 3 FDA reports)
MUSCLE INJURY ( 3 FDA reports)
MYOCARDIAL FIBROSIS ( 3 FDA reports)
MYOPERICARDITIS ( 3 FDA reports)
NECK INJURY ( 3 FDA reports)
NECROSIS ( 3 FDA reports)
NEOPLASM ( 3 FDA reports)
NEPHROGENIC ANAEMIA ( 3 FDA reports)
NEUROMA ( 3 FDA reports)
NEUROTOXICITY ( 3 FDA reports)
NIPPLE PAIN ( 3 FDA reports)
NOCTURNAL DYSPNOEA ( 3 FDA reports)
NYSTAGMUS ( 3 FDA reports)
OESOPHAGEAL STENOSIS ( 3 FDA reports)
OLIGURIA ( 3 FDA reports)
ONYCHALGIA ( 3 FDA reports)
OPEN WOUND ( 3 FDA reports)
OROANTRAL FISTULA ( 3 FDA reports)
ORTHOPNOEA ( 3 FDA reports)
OSTEOMYELITIS CHRONIC ( 3 FDA reports)
OTITIS MEDIA ACUTE ( 3 FDA reports)
OVARIAN CANCER ( 3 FDA reports)
PARKINSON'S DISEASE ( 3 FDA reports)
PELVI-URETERIC OBSTRUCTION ( 3 FDA reports)
PELVIC DISCOMFORT ( 3 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 3 FDA reports)
PERIARTHRITIS ( 3 FDA reports)
PERICARDITIS ( 3 FDA reports)
PERIORBITAL OEDEMA ( 3 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 3 FDA reports)
PEYRONIE'S DISEASE ( 3 FDA reports)
PHARYNGOLARYNGEAL DISCOMFORT ( 3 FDA reports)
PLACENTAL DISORDER ( 3 FDA reports)
PLASMA VISCOSITY DECREASED ( 3 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 3 FDA reports)
POISONING ( 3 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 3 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 3 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 3 FDA reports)
POSTERIOR CAPSULOTOMY ( 3 FDA reports)
POSTURE ABNORMAL ( 3 FDA reports)
PREGNANCY WITH CONTRACEPTIVE DEVICE ( 3 FDA reports)
PREMATURE LABOUR ( 3 FDA reports)
PROTEINURIA ( 3 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 3 FDA reports)
PSEUDOPOLYP ( 3 FDA reports)
PSYCHOTIC DISORDER ( 3 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 3 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 3 FDA reports)
RAPID EYE MOVEMENTS SLEEP ABNORMAL ( 3 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 3 FDA reports)
RENAL COLIC ( 3 FDA reports)
RENAL PAPILLARY NECROSIS ( 3 FDA reports)
RESPIRATORY ALKALOSIS ( 3 FDA reports)
RETINAL DEGENERATION ( 3 FDA reports)
RETINAL VASCULAR THROMBOSIS ( 3 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 3 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 3 FDA reports)
SCLERITIS ( 3 FDA reports)
SCOTOMA ( 3 FDA reports)
SCRATCH ( 3 FDA reports)
SCREAMING ( 3 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 3 FDA reports)
SEMINAL VESICULITIS ( 3 FDA reports)
SEPTIC SHOCK ( 3 FDA reports)
SEROTONIN SYNDROME ( 3 FDA reports)
SERUM FERRITIN INCREASED ( 3 FDA reports)
SIMILAR REACTION ON PREVIOUS EXPOSURE TO DRUG ( 3 FDA reports)
SIMPLE PARTIAL SEIZURES ( 3 FDA reports)
SINGLE FUNCTIONAL KIDNEY ( 3 FDA reports)
SPLENIC LESION ( 3 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 3 FDA reports)
SUDDEN HEARING LOSS ( 3 FDA reports)
SUNBURN ( 3 FDA reports)
SWEAT GLAND INFECTION ( 3 FDA reports)
TEMPERATURE REGULATION DISORDER ( 3 FDA reports)
TENSION HEADACHE ( 3 FDA reports)
THROAT CANCER ( 3 FDA reports)
THROMBOPHLEBITIS ( 3 FDA reports)
TONSILLAR DISORDER ( 3 FDA reports)
TONSILLITIS ( 3 FDA reports)
TRANSAMINASES INCREASED ( 3 FDA reports)
TRANSPLANT ( 3 FDA reports)
TUMOUR LYSIS SYNDROME ( 3 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 3 FDA reports)
UTERINE DILATION AND CURETTAGE ( 3 FDA reports)
UVEITIS ( 3 FDA reports)
VARICES OESOPHAGEAL ( 3 FDA reports)
VESTIBULAR DISORDER ( 3 FDA reports)
VITAL FUNCTIONS ABNORMAL ( 3 FDA reports)
VITAMIN B12 DECREASED ( 3 FDA reports)
VULVOVAGINAL DISCOMFORT ( 3 FDA reports)
WOUND ( 3 FDA reports)
ABNORMAL WITHDRAWAL BLEEDING ( 2 FDA reports)
ABSCESS INTESTINAL ( 2 FDA reports)
ABSCESS JAW ( 2 FDA reports)
ACCELERATED HYPERTENSION ( 2 FDA reports)
ACTINIC KERATOSIS ( 2 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 2 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 2 FDA reports)
ACUTE PHOSPHATE NEPHROPATHY ( 2 FDA reports)
ADENOMYOSIS ( 2 FDA reports)
ADRENAL ADENOMA ( 2 FDA reports)
ADRENAL INSUFFICIENCY ( 2 FDA reports)
AFFECT LABILITY ( 2 FDA reports)
ALBUMIN URINE PRESENT ( 2 FDA reports)
ALVEOLITIS ALLERGIC ( 2 FDA reports)
AMPHETAMINES POSITIVE ( 2 FDA reports)
ANAEMIA MACROCYTIC ( 2 FDA reports)
ANAL PRURITUS ( 2 FDA reports)
ANASTOMOTIC ULCER HAEMORRHAGE ( 2 FDA reports)
ANGIOMYOLIPOMA ( 2 FDA reports)
ANGIOPLASTY ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
ANTIMITOCHONDRIAL ANTIBODY POSITIVE ( 2 FDA reports)
AORTIC VALVE DISEASE ( 2 FDA reports)
AORTIC VALVE STENOSIS ( 2 FDA reports)
APLASIA PURE RED CELL ( 2 FDA reports)
APPLICATION SITE PAIN ( 2 FDA reports)
APPLICATION SITE RASH ( 2 FDA reports)
ARNOLD-CHIARI MALFORMATION ( 2 FDA reports)
ARTERIAL HAEMORRHAGE ( 2 FDA reports)
ARTERIOVENOUS FISTULA ( 2 FDA reports)
ARTERIOVENOUS MALFORMATION ( 2 FDA reports)
ASEPTIC NECROSIS BONE ( 2 FDA reports)
ATRIAL THROMBOSIS ( 2 FDA reports)
ATROPHY ( 2 FDA reports)
AUTONOMIC NEUROPATHY ( 2 FDA reports)
BACTERIAL SEPSIS ( 2 FDA reports)
BASAL GANGLION DEGENERATION ( 2 FDA reports)
BENIGN GASTROINTESTINAL NEOPLASM ( 2 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 2 FDA reports)
BIFASCICULAR BLOCK ( 2 FDA reports)
BILIARY CIRRHOSIS ( 2 FDA reports)
BIOPSY BONE ABNORMAL ( 2 FDA reports)
BIOPSY BREAST ABNORMAL ( 2 FDA reports)
BIOPSY PERIPHERAL NERVE ( 2 FDA reports)
BIOPSY STOMACH ( 2 FDA reports)
BLEPHARITIS ( 2 FDA reports)
BLOOD ALCOHOL INCREASED ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE ( 2 FDA reports)
BLOOD ERYTHROPOIETIN INCREASED ( 2 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 2 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 2 FDA reports)
BLOOD IRON INCREASED ( 2 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 2 FDA reports)
BODY FAT DISORDER ( 2 FDA reports)
BONE CYST ( 2 FDA reports)
BONE NEOPLASM MALIGNANT ( 2 FDA reports)
BORDERLINE GLAUCOMA ( 2 FDA reports)
BRADYKINESIA ( 2 FDA reports)
BRAIN ABSCESS ( 2 FDA reports)
BRAIN INJURY ( 2 FDA reports)
BREAST CANCER STAGE III ( 2 FDA reports)
BREAST CYST ( 2 FDA reports)
BREAST NEOPLASM ( 2 FDA reports)
BREAST RECONSTRUCTION ( 2 FDA reports)
BREAST SWELLING ( 2 FDA reports)
BREATH SOUNDS DECREASED ( 2 FDA reports)
BRONCHITIS CHRONIC ( 2 FDA reports)
BRONCHITIS VIRAL ( 2 FDA reports)
BUNION OPERATION ( 2 FDA reports)
CARDIAC FIBRILLATION ( 2 FDA reports)
CARDIAC OPERATION ( 2 FDA reports)
CARDIOVERSION ( 2 FDA reports)
CAROTID ARTERIAL EMBOLUS ( 2 FDA reports)
CAROTID ARTERY THROMBOSIS ( 2 FDA reports)
CATHETER SITE RELATED REACTION ( 2 FDA reports)
CAUDA EQUINA SYNDROME ( 2 FDA reports)
CEREBELLAR ATAXIA ( 2 FDA reports)
CEREBELLAR HAEMORRHAGE ( 2 FDA reports)
CHEILITIS ( 2 FDA reports)
CHONDROCALCINOSIS ( 2 FDA reports)
CHOREA ( 2 FDA reports)
CHOROIDAL EFFUSION ( 2 FDA reports)
CHROMOSOME ANALYSIS ABNORMAL ( 2 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 2 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 2 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 2 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 2 FDA reports)
CLUMSINESS ( 2 FDA reports)
COAGULATION TIME PROLONGED ( 2 FDA reports)
COLON NEOPLASM ( 2 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 2 FDA reports)
COMPULSIVE SHOPPING ( 2 FDA reports)
CONGENITAL EYE DISORDER ( 2 FDA reports)
CONGENITAL HYDRONEPHROSIS ( 2 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 2 FDA reports)
COR PULMONALE ( 2 FDA reports)
CORNEAL DISORDER ( 2 FDA reports)
CORNEAL OEDEMA ( 2 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 2 FDA reports)
CORONARY ARTERY RESTENOSIS ( 2 FDA reports)
CORYNEBACTERIUM INFECTION ( 2 FDA reports)
CRANIAL NERVE PARALYSIS ( 2 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 2 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 2 FDA reports)
CYSTITIS KLEBSIELLA ( 2 FDA reports)
CYSTITIS NONINFECTIVE ( 2 FDA reports)
CYSTOCELE ( 2 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 2 FDA reports)
DAYDREAMING ( 2 FDA reports)
DEAFNESS TRANSITORY ( 2 FDA reports)
DECUBITUS ULCER ( 2 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 2 FDA reports)
DEPERSONALISATION ( 2 FDA reports)
DEPRESSION SUICIDAL ( 2 FDA reports)
DERMATITIS BULLOUS ( 2 FDA reports)
DERMATOMYOSITIS ( 2 FDA reports)
DIABETIC NEPHROPATHY ( 2 FDA reports)
DIARRHOEA INFECTIOUS ( 2 FDA reports)
DISEASE COMPLICATION ( 2 FDA reports)
DISSOCIATIVE AMNESIA ( 2 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 2 FDA reports)
DREAMY STATE ( 2 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 2 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
DRUG LEVEL FLUCTUATING ( 2 FDA reports)
DRUG PRESCRIBING ERROR ( 2 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 2 FDA reports)
DRUG TOLERANCE DECREASED ( 2 FDA reports)
DUODENAL ULCER REPAIR ( 2 FDA reports)
DYSLEXIA ( 2 FDA reports)
DYSPNOEA EXACERBATED ( 2 FDA reports)
EAR OPERATION ( 2 FDA reports)
EARLY MORNING AWAKENING ( 2 FDA reports)
ECTOPIC PREGNANCY ( 2 FDA reports)
ECZEMA INFECTED ( 2 FDA reports)
EDENTULOUS ( 2 FDA reports)
EFFUSION ( 2 FDA reports)
ELECTRIC SHOCK ( 2 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 2 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 2 FDA reports)
ELEVATED MOOD ( 2 FDA reports)
EMBOLISM VENOUS ( 2 FDA reports)
ENDOCRINE DISORDER ( 2 FDA reports)
ENDOMETRIOSIS ( 2 FDA reports)
ENDOSCOPY ( 2 FDA reports)
ENTERITIS ( 2 FDA reports)
ENTERITIS INFECTIOUS ( 2 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 2 FDA reports)
EPIDERMAL GROWTH FACTOR RECEPTOR INCREASED ( 2 FDA reports)
ESSENTIAL HYPERTENSION ( 2 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 2 FDA reports)
EYE INFLAMMATION ( 2 FDA reports)
EYE OEDEMA ( 2 FDA reports)
EYELID DISORDER ( 2 FDA reports)
FACE PRESENTATION ( 2 FDA reports)
FAECAL VOLUME DECREASED ( 2 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 2 FDA reports)
FEAR OF DEATH ( 2 FDA reports)
FEBRILE CONVULSION ( 2 FDA reports)
FEELING OF DESPAIR ( 2 FDA reports)
FIBULA FRACTURE ( 2 FDA reports)
FLOPPY IRIS SYNDROME ( 2 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 2 FDA reports)
FOETAL GROWTH RETARDATION ( 2 FDA reports)
FOLATE DEFICIENCY ( 2 FDA reports)
FOREIGN BODY IN EYE ( 2 FDA reports)
FRACTURE DELAYED UNION ( 2 FDA reports)
FRACTURE DISPLACEMENT ( 2 FDA reports)
FULL BLOOD COUNT DECREASED ( 2 FDA reports)
FUMBLING ( 2 FDA reports)
FUNGAL SKIN INFECTION ( 2 FDA reports)
GALLBLADDER ENLARGEMENT ( 2 FDA reports)
GASTRIC CANCER ( 2 FDA reports)
GASTRIC OPERATION ( 2 FDA reports)
GASTRITIS HAEMORRHAGIC ( 2 FDA reports)
GASTROINTESTINAL MUCOSAL NECROSIS ( 2 FDA reports)
GASTROOESOPHAGEAL SPHINCTER INSUFFICIENCY ( 2 FDA reports)
GENERAL ANAESTHESIA ( 2 FDA reports)
GENERALISED ANXIETY DISORDER ( 2 FDA reports)
GENITAL BURNING SENSATION ( 2 FDA reports)
GINGIVAL BLISTER ( 2 FDA reports)
GINGIVAL EROSION ( 2 FDA reports)
GLARE ( 2 FDA reports)
GLOMERULONEPHRITIS PROLIFERATIVE ( 2 FDA reports)
GLOSSITIS ( 2 FDA reports)
GRAFT THROMBOSIS ( 2 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 2 FDA reports)
HEPATIC ENCEPHALOPATHY ( 2 FDA reports)
HEPATIC ENZYME ABNORMAL ( 2 FDA reports)
HEPATIC INFECTION ( 2 FDA reports)
HEPATIC NEOPLASM ( 2 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 2 FDA reports)
HEPATITIS B ( 2 FDA reports)
HEPATITIS FULMINANT ( 2 FDA reports)
HERNIA HIATUS REPAIR ( 2 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
HILAR LYMPHADENOPATHY ( 2 FDA reports)
HIP ARTHROPLASTY ( 2 FDA reports)
HOARSENESS ( 2 FDA reports)
HOMICIDE ( 2 FDA reports)
HOSPITALISATION ( 2 FDA reports)
HOSTILITY ( 2 FDA reports)
HYPERNATRAEMIA ( 2 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 2 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 2 FDA reports)
HYPERURICAEMIA ( 2 FDA reports)
HYPERVIGILANCE ( 2 FDA reports)
HYPOALBUMINAEMIA ( 2 FDA reports)
HYPOCHLORAEMIA ( 2 FDA reports)
HYPOCHONDRIASIS ( 2 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 2 FDA reports)
HYPOMANIA ( 2 FDA reports)
HYPOTONIA ( 2 FDA reports)
IIIRD NERVE PARALYSIS ( 2 FDA reports)
IMMOBILE ( 2 FDA reports)
IMMUNOSUPPRESSION ( 2 FDA reports)
INCISION SITE HAEMORRHAGE ( 2 FDA reports)
INCORRECT STORAGE OF DRUG ( 2 FDA reports)
INFARCTION ( 2 FDA reports)
INFECTED VARICOSE VEIN ( 2 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 2 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 2 FDA reports)
INGUINAL MASS ( 2 FDA reports)
INNER EAR DISORDER ( 2 FDA reports)
INTERTRIGO CANDIDA ( 2 FDA reports)
INTESTINAL ISCHAEMIA ( 2 FDA reports)
INTESTINAL ULCER ( 2 FDA reports)
INTRAOCULAR LENS IMPLANT ( 2 FDA reports)
INTUBATION ( 2 FDA reports)
INTUBATION COMPLICATION ( 2 FDA reports)
IRIDOCYCLITIS ( 2 FDA reports)
IUCD COMPLICATION ( 2 FDA reports)
JEJUNITIS ( 2 FDA reports)
JOINT SURGERY ( 2 FDA reports)
LABORATORY TEST INTERFERENCE ( 2 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 2 FDA reports)
LARGE INTESTINE PERFORATION ( 2 FDA reports)
LEGIONELLA INFECTION ( 2 FDA reports)
LEUKOCYTE VACUOLISATION ( 2 FDA reports)
LHERMITTE'S SIGN ( 2 FDA reports)
LIGAMENT SPRAIN ( 2 FDA reports)
LIGHT CHAIN DISEASE ( 2 FDA reports)
LIP EXFOLIATION ( 2 FDA reports)
LIPIDS INCREASED ( 2 FDA reports)
LOCALISED OSTEOARTHRITIS ( 2 FDA reports)
LOSS OF CONTROL OF LEGS ( 2 FDA reports)
LOW TURNOVER OSTEOPATHY ( 2 FDA reports)
LUNG LOBECTOMY ( 2 FDA reports)
LYMPHADENITIS ( 2 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 2 FDA reports)
LYMPHOCYTOSIS ( 2 FDA reports)
MALABSORPTION ( 2 FDA reports)
MALIGNANT FIBROUS HISTIOCYTOMA METASTATIC ( 2 FDA reports)
MALIGNANT HYPERTENSION ( 2 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 2 FDA reports)
MASTECTOMY ( 2 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 2 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 2 FDA reports)
MENINGITIS ASEPTIC ( 2 FDA reports)
MENOPAUSE ( 2 FDA reports)
MENSTRUATION DELAYED ( 2 FDA reports)
METABOLIC ENCEPHALOPATHY ( 2 FDA reports)
METASTASES TO SPLEEN ( 2 FDA reports)
METASTATIC CARCINOMA OF THE BLADDER ( 2 FDA reports)
MICROALBUMINURIA ( 2 FDA reports)
MIGRAINE WITH AURA ( 2 FDA reports)
MONARTHRITIS ( 2 FDA reports)
MONOPLEGIA ( 2 FDA reports)
MUSCLE CONTRACTURE ( 2 FDA reports)
MUSCLE SWELLING ( 2 FDA reports)
MYODESOPSIA ( 2 FDA reports)
NAIL DYSTROPHY ( 2 FDA reports)
NEOPLASM PROGRESSION ( 2 FDA reports)
NEPHRECTOMY ( 2 FDA reports)
NEPHROPATHY ( 2 FDA reports)
NEUTROPHIL TOXIC GRANULATION PRESENT ( 2 FDA reports)
NIGHT BLINDNESS ( 2 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 2 FDA reports)
NODAL OSTEOARTHRITIS ( 2 FDA reports)
NONSPECIFIC REACTION ( 2 FDA reports)
OBSTRUCTION ( 2 FDA reports)
OCULAR DISCOMFORT ( 2 FDA reports)
OEDEMA MUCOSAL ( 2 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 2 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 2 FDA reports)
OOPHORECTOMY ( 2 FDA reports)
OPEN ANGLE GLAUCOMA ( 2 FDA reports)
OPEN FRACTURE ( 2 FDA reports)
OPHTHALMOPLEGIA ( 2 FDA reports)
OPIATES POSITIVE ( 2 FDA reports)
OPTIC NERVE DISORDER ( 2 FDA reports)
ORAL MUCOSAL DISORDER ( 2 FDA reports)
OVARIAN ENLARGEMENT ( 2 FDA reports)
OVARIAN GRANULOSA-THECA CELL TUMOUR ( 2 FDA reports)
PAIN PROPHYLAXIS ( 2 FDA reports)
PANCREATIC ENZYMES INCREASED ( 2 FDA reports)
PANCREATIC MASS ( 2 FDA reports)
PANCREATITIS CHRONIC ( 2 FDA reports)
PAPILLOEDEMA ( 2 FDA reports)
PAPILLOMA ( 2 FDA reports)
PARADOXICAL DRUG REACTION ( 2 FDA reports)
PARAESTHESIA OF GENITAL MALE ( 2 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 2 FDA reports)
PARKINSONISM ( 2 FDA reports)
PARTIAL SEIZURES ( 2 FDA reports)
PATHOGEN RESISTANCE ( 2 FDA reports)
PCO2 INCREASED ( 2 FDA reports)
PELVIC FLOOR MUSCLE WEAKNESS ( 2 FDA reports)
PELVIC VENOUS THROMBOSIS ( 2 FDA reports)
PENILE PAIN ( 2 FDA reports)
PETIT MAL EPILEPSY ( 2 FDA reports)
PHARYNGEAL ERYTHEMA ( 2 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 2 FDA reports)
PHARYNGEAL HYPOAESTHESIA ( 2 FDA reports)
PHYSICAL ASSAULT ( 2 FDA reports)
PICA ( 2 FDA reports)
PITUITARY TUMOUR ( 2 FDA reports)
PLEURAL FIBROSIS ( 2 FDA reports)
POLYCHONDRITIS ( 2 FDA reports)
POLYDIPSIA ( 2 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 2 FDA reports)
POSTOPERATIVE ADHESION ( 2 FDA reports)
POSTURING ( 2 FDA reports)
POUCHITIS ( 2 FDA reports)
PREGNANCY INDUCED HYPERTENSION ( 2 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 2 FDA reports)
PROCEDURAL SITE REACTION ( 2 FDA reports)
PRODUCT COMMINGLING ( 2 FDA reports)
PULMONARY ARTERIAL WEDGE PRESSURE DECREASED ( 2 FDA reports)
PULSE ABNORMAL ( 2 FDA reports)
PUPIL FIXED ( 2 FDA reports)
QUADRUPLE VESSEL BYPASS GRAFT ( 2 FDA reports)
RALES ( 2 FDA reports)
RASH VESICULAR ( 2 FDA reports)
RATHKE'S CLEFT CYST ( 2 FDA reports)
RECTAL PERFORATION ( 2 FDA reports)
RECTAL PROLAPSE ( 2 FDA reports)
RECTAL TENESMUS ( 2 FDA reports)
RECTOCELE ( 2 FDA reports)
RED BLOOD CELLS SEMEN POSITIVE ( 2 FDA reports)
REGURGITATION ( 2 FDA reports)
RENAL ARTERIOSCLEROSIS ( 2 FDA reports)
RENAL CANCER ( 2 FDA reports)
RENAL CANCER METASTATIC ( 2 FDA reports)
RENAL CELL CARCINOMA ( 2 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 2 FDA reports)
RENAL INTERSTITIAL FIBROSIS ( 2 FDA reports)
RENAL TRANSPLANT ( 2 FDA reports)
RESPIRATION ABNORMAL ( 2 FDA reports)
RETINAL ISCHAEMIA ( 2 FDA reports)
RHEUMATIC FEVER ( 2 FDA reports)
ROTATOR CUFF REPAIR ( 2 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 2 FDA reports)
SARCOIDOSIS ( 2 FDA reports)
SCLEROMALACIA ( 2 FDA reports)
SCROTAL DISORDER ( 2 FDA reports)
SECRETION DISCHARGE ( 2 FDA reports)
SENSORY LOSS ( 2 FDA reports)
SERUM SICKNESS ( 2 FDA reports)
SKELETAL INJURY ( 2 FDA reports)
SKIN FRAGILITY ( 2 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 2 FDA reports)
SOFT TISSUE INFECTION ( 2 FDA reports)
SOLILOQUY ( 2 FDA reports)
SPLEEN DISORDER ( 2 FDA reports)
SPORTS INJURY ( 2 FDA reports)
STEATORRHOEA ( 2 FDA reports)
STRESS URINARY INCONTINENCE ( 2 FDA reports)
SUBCUTANEOUS NODULE ( 2 FDA reports)
SUTURE RELATED COMPLICATION ( 2 FDA reports)
TEARFULNESS ( 2 FDA reports)
TESTICULAR DISORDER ( 2 FDA reports)
TESTICULAR MASS ( 2 FDA reports)
TESTICULAR SWELLING ( 2 FDA reports)
THERAPEUTIC PRODUCT CONTAMINATION ( 2 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 2 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
THYROID CANCER METASTATIC ( 2 FDA reports)
THYROID MASS ( 2 FDA reports)
THYROIDECTOMY ( 2 FDA reports)
TOBACCO USER ( 2 FDA reports)
TONGUE NEOPLASM ( 2 FDA reports)
TONGUE ULCERATION ( 2 FDA reports)
TOOTH DEPOSIT ( 2 FDA reports)
TOOTH EROSION ( 2 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 2 FDA reports)
TRANSFUSION REACTION ( 2 FDA reports)
TRICHOMONIASIS ( 2 FDA reports)
TRIGEMINAL NEURALGIA ( 2 FDA reports)
TUNNEL VISION ( 2 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 2 FDA reports)
UMBILICAL HERNIA ( 2 FDA reports)
UNDERDOSE ( 2 FDA reports)
URETHRAL OBSTRUCTION ( 2 FDA reports)
URETHRITIS ( 2 FDA reports)
URGE INCONTINENCE ( 2 FDA reports)
URINE ANALYSIS ABNORMAL ( 2 FDA reports)
URINE COLOUR ABNORMAL ( 2 FDA reports)
URINE FLOW DECREASED ( 2 FDA reports)
UTERINE ENLARGEMENT ( 2 FDA reports)
VAGINAL ODOUR ( 2 FDA reports)
VASCULAR CALCIFICATION ( 2 FDA reports)
VASCULAR INJURY ( 2 FDA reports)
VASCULAR OCCLUSION ( 2 FDA reports)
VASODILATATION ( 2 FDA reports)
VEIN DISORDER ( 2 FDA reports)
VISUAL BRIGHTNESS ( 2 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 2 FDA reports)
WATER POLLUTION ( 2 FDA reports)
WEGENER'S GRANULOMATOSIS ( 2 FDA reports)
WOLFF-PARKINSON-WHITE SYNDROME ( 2 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 2 FDA reports)
XEROPHTHALMIA ( 2 FDA reports)
YAWNING ( 2 FDA reports)
ABDOMINAL MASS ( 1 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 1 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 1 FDA reports)
ACANTHOSIS ( 1 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 1 FDA reports)
ACNE PUSTULAR ( 1 FDA reports)
ADENOCARCINOMA OF THE CERVIX ( 1 FDA reports)
ADENOID CYSTIC CARCINOMA ( 1 FDA reports)
ADENOIDAL DISORDER ( 1 FDA reports)
ADENOLIPOMA ( 1 FDA reports)
ADNEXA UTERI PAIN ( 1 FDA reports)
ADRENAL DISORDER ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 1 FDA reports)
ALBUMIN GLOBULIN RATIO INCREASED ( 1 FDA reports)
ALCOHOLIC PANCREATITIS ( 1 FDA reports)
ALLERGY TO ANIMAL ( 1 FDA reports)
ALLERGY TO ARTHROPOD STING ( 1 FDA reports)
ALLERGY TO CHEMICALS ( 1 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 1 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 1 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 1 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 1 FDA reports)
ANAEMIA POSTOPERATIVE ( 1 FDA reports)
ANALGESIC DRUG LEVEL INCREASED ( 1 FDA reports)
ANASTOMOTIC ULCER PERFORATION ( 1 FDA reports)
ANDROGENETIC ALOPECIA ( 1 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 1 FDA reports)
ANIMAL SCRATCH ( 1 FDA reports)
ANOGENITAL WARTS ( 1 FDA reports)
ANORECTAL CELLULITIS ( 1 FDA reports)
ANORECTAL OPERATION ( 1 FDA reports)
ANORGASMIA ( 1 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 1 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST ( 1 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
ANTIBODY TEST POSITIVE ( 1 FDA reports)
ANTICOAGULANT THERAPY ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 1 FDA reports)
AORTIC DILATATION ( 1 FDA reports)
APHONIA ( 1 FDA reports)
APLASTIC ANAEMIA ( 1 FDA reports)
APPARENT DEATH ( 1 FDA reports)
APPLICATION SITE CELLULITIS ( 1 FDA reports)
APPLICATION SITE DERMATITIS ( 1 FDA reports)
APPLICATION SITE DISCOLOURATION ( 1 FDA reports)
APPLICATION SITE EROSION ( 1 FDA reports)
APPLICATION SITE EXFOLIATION ( 1 FDA reports)
APPLICATION SITE IRRITATION ( 1 FDA reports)
APPLICATION SITE PRURITUS ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ARTERIAL THROMBOSIS ( 1 FDA reports)
ARTERIOGRAM ABNORMAL ( 1 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 1 FDA reports)
ARTHROFIBROSIS ( 1 FDA reports)
ARTHROSCOPIC SURGERY ( 1 FDA reports)
ASPERGILLOSIS ( 1 FDA reports)
ASPERGILLUS TEST POSITIVE ( 1 FDA reports)
ASPIRATION BONE MARROW ABNORMAL ( 1 FDA reports)
ASTERIXIS ( 1 FDA reports)
ASTHENOPIA ( 1 FDA reports)
ASTHMATIC CRISIS ( 1 FDA reports)
ATONIC URINARY BLADDER ( 1 FDA reports)
ATROPHIC VULVOVAGINITIS ( 1 FDA reports)
AURA ( 1 FDA reports)
B-CELL LYMPHOMA ( 1 FDA reports)
BACTERIA STOOL IDENTIFIED ( 1 FDA reports)
BACTERIA URINE IDENTIFIED ( 1 FDA reports)
BALINT'S SYNDROME ( 1 FDA reports)
BAND NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
BASOSQUAMOUS CARCINOMA ( 1 FDA reports)
BEHCET'S SYNDROME ( 1 FDA reports)
BENIGN COLONIC NEOPLASM ( 1 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 1 FDA reports)
BENIGN LARYNGEAL NEOPLASM ( 1 FDA reports)
BENIGN NEOPLASM OF BLADDER ( 1 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 1 FDA reports)
BENIGN PANCREATIC NEOPLASM ( 1 FDA reports)
BEREAVEMENT REACTION ( 1 FDA reports)
BICUSPID AORTIC VALVE ( 1 FDA reports)
BILIARY CANCER METASTATIC ( 1 FDA reports)
BILIARY DILATATION ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BINGE EATING ( 1 FDA reports)
BINOCULAR EYE MOVEMENT DISORDER ( 1 FDA reports)
BIPOLAR I DISORDER ( 1 FDA reports)
BLADDER CANCER RECURRENT ( 1 FDA reports)
BLADDER CANCER STAGE III ( 1 FDA reports)
BLADDER DISCOMFORT ( 1 FDA reports)
BLADDER HYPERTROPHY ( 1 FDA reports)
BLADDER NEOPLASM ( 1 FDA reports)
BLADDER REPAIR ( 1 FDA reports)
BLADDER SPASM ( 1 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA STAGE II ( 1 FDA reports)
BLAST CRISIS IN MYELOGENOUS LEUKAEMIA ( 1 FDA reports)
BLEEDING VARICOSE VEIN ( 1 FDA reports)
BLEPHAROPLASTY ( 1 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 1 FDA reports)
BLOOD CANNABINOIDS ( 1 FDA reports)
BLOOD CARBON MONOXIDE INCREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CHLORIDE INCREASED ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD ERYTHROPOIETIN DECREASED ( 1 FDA reports)
BLOOD GLUCOSE ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 1 FDA reports)
BLOOD OESTROGEN INCREASED ( 1 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 1 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 1 FDA reports)
BLOOD PRESSURE ( 1 FDA reports)
BLOOD PRESSURE AMBULATORY DECREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 1 FDA reports)
BLOOD PRESSURE MANAGEMENT ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC ABNORMAL ( 1 FDA reports)
BLOOD VISCOSITY INCREASED ( 1 FDA reports)
BONE CALLUS EXCESSIVE ( 1 FDA reports)
BONE SARCOMA ( 1 FDA reports)
BRADYPHRENIA ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
BRAIN SCAN ABNORMAL ( 1 FDA reports)
BRAIN STEM STROKE ( 1 FDA reports)
BRAIN STEM SYNDROME ( 1 FDA reports)
BREAKTHROUGH PAIN ( 1 FDA reports)
BREAST DISCOLOURATION ( 1 FDA reports)
BREAST DYSPLASIA ( 1 FDA reports)
BREAST NECROSIS ( 1 FDA reports)
BREATHING-RELATED SLEEP DISORDER ( 1 FDA reports)
BRONCHIAL OBSTRUCTION ( 1 FDA reports)
BRONCHIAL SECRETION RETENTION ( 1 FDA reports)
BRONCHITIS BACTERIAL ( 1 FDA reports)
BUDD-CHIARI SYNDROME ( 1 FDA reports)
BURN OESOPHAGEAL ( 1 FDA reports)
BURNING SENSATION MUCOSAL ( 1 FDA reports)
BURNS FIRST DEGREE ( 1 FDA reports)
BURNS SECOND DEGREE ( 1 FDA reports)
BURNS THIRD DEGREE ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CALCIPHYLAXIS ( 1 FDA reports)
CALCIUM IONISED DECREASED ( 1 FDA reports)
CALCULUS URINARY ( 1 FDA reports)
CANCER PAIN ( 1 FDA reports)
CANDIDURIA ( 1 FDA reports)
CARCINOMA ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
CARDIAC IMAGING PROCEDURE ABNORMAL ( 1 FDA reports)
CARDIAC PERFORATION ( 1 FDA reports)
CARDIAC SEPTAL DEFECT ( 1 FDA reports)
CARDIAC VALVE VEGETATION ( 1 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 1 FDA reports)
CARNITINE PALMITOYLTRANSFERASE DEFICIENCY ( 1 FDA reports)
CAROTID ARTERY ATHEROMA ( 1 FDA reports)
CAROTID PULSE ABNORMAL ( 1 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 1 FDA reports)
CATAPLEXY ( 1 FDA reports)
CATARACT CORTICAL ( 1 FDA reports)
CATARACT OPERATION COMPLICATION ( 1 FDA reports)
CATHETER SITE ERYTHEMA ( 1 FDA reports)
CATHETER SITE HAEMORRHAGE ( 1 FDA reports)
CATHETER SITE INFECTION ( 1 FDA reports)
CATHETER SITE INFLAMMATION ( 1 FDA reports)
CATHETER SITE PAIN ( 1 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 1 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 1 FDA reports)
CEREBRAL ARTERY STENOSIS ( 1 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 1 FDA reports)
CERVICAL INCOMPETENCE ( 1 FDA reports)
CERVIX CARCINOMA ( 1 FDA reports)
CERVIX INFLAMMATION ( 1 FDA reports)
CHALAZION ( 1 FDA reports)
CHANGE OF BOWEL HABIT ( 1 FDA reports)
CHEMOTHERAPY ( 1 FDA reports)
CHEST INJURY ( 1 FDA reports)
CHEST TUBE INSERTION ( 1 FDA reports)
CHOLECYSTITIS INFECTIVE ( 1 FDA reports)
CHOLESTEROSIS ( 1 FDA reports)
CHONDRITIS ( 1 FDA reports)
CHORIOCARCINOMA ( 1 FDA reports)
CHROMATOPSIA ( 1 FDA reports)
CHRONIC GASTROINTESTINAL BLEEDING ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA STAGE 0 ( 1 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 1 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
CILIARY BODY DISORDER ( 1 FDA reports)
CIRCUMORAL OEDEMA ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 1 FDA reports)
CLUSTER HEADACHE ( 1 FDA reports)
COAGULATION TIME SHORTENED ( 1 FDA reports)
COITAL BLEEDING ( 1 FDA reports)
COLITIS COLLAGENOUS ( 1 FDA reports)
COLLAGEN DISORDER ( 1 FDA reports)
COLLAGEN-VASCULAR DISEASE ( 1 FDA reports)
COLON CANCER STAGE II ( 1 FDA reports)
COLOSTOMY ( 1 FDA reports)
COMPARTMENT SYNDROME ( 1 FDA reports)
COMPLEMENT FACTOR C4 DECREASED ( 1 FDA reports)
COMPLEX PARTIAL SEIZURES ( 1 FDA reports)
COMPLICATION OF DELIVERY ( 1 FDA reports)
COMPULSIONS ( 1 FDA reports)
COMPULSIVE LIP BITING ( 1 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 1 FDA reports)
CONGENITAL AORTIC STENOSIS ( 1 FDA reports)
CONJUNCTIVAL OEDEMA ( 1 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 1 FDA reports)
CONNECTIVE TISSUE DISORDER ( 1 FDA reports)
CORNEAL ABRASION ( 1 FDA reports)
CORONARY ARTERY SURGERY ( 1 FDA reports)
CRACKLES LUNG ( 1 FDA reports)
CRANIAL NEUROPATHY ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
CRUSH INJURY ( 1 FDA reports)
CULTURE STOOL POSITIVE ( 1 FDA reports)
CUTIS LAXA ( 1 FDA reports)
CYST REMOVAL ( 1 FDA reports)
CYST RUPTURE ( 1 FDA reports)
CYSTITIS ESCHERICHIA ( 1 FDA reports)
CYSTOSCOPY ABNORMAL ( 1 FDA reports)
DANDRUFF ( 1 FDA reports)
DEATH OF RELATIVE ( 1 FDA reports)
DEPENDENCE ( 1 FDA reports)
DEPRESSIVE SYMPTOM ( 1 FDA reports)
DERMABRASION ( 1 FDA reports)
DERMATITIS PSORIASIFORM ( 1 FDA reports)
DEVICE DISLOCATION ( 1 FDA reports)
DEVICE MIGRATION ( 1 FDA reports)
DIABETIC CARDIOMYOPATHY ( 1 FDA reports)
DIABETIC RETINAL OEDEMA ( 1 FDA reports)
DISLOCATION OF VERTEBRA ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DISTRACTIBILITY ( 1 FDA reports)
DIVERTICULAR HERNIA ( 1 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 1 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 1 FDA reports)
DRUG CLEARANCE DECREASED ( 1 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 1 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 1 FDA reports)
DUODENITIS ( 1 FDA reports)
DUPUYTREN'S CONTRACTURE ( 1 FDA reports)
DURAL TEAR ( 1 FDA reports)
DYSPHASIA ( 1 FDA reports)
DYSPHEMIA ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
DYSTROPHIC CALCIFICATION ( 1 FDA reports)
EARLY SATIETY ( 1 FDA reports)
EJECTION FRACTION ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 1 FDA reports)
EMBOLIC STROKE ( 1 FDA reports)
EMPYEMA DRAINAGE ( 1 FDA reports)
ENCEPHALITIS HERPES ( 1 FDA reports)
ENDOCARDIAL FIBROSIS ( 1 FDA reports)
ENDOMETRIAL DISORDER ( 1 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 1 FDA reports)
ENDOMETRIAL METAPLASIA ( 1 FDA reports)
ENDOTRACHEAL INTUBATION ( 1 FDA reports)
ENTEROBACTER BACTERAEMIA ( 1 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 1 FDA reports)
ENZYME ABNORMALITY ( 1 FDA reports)
EOSINOPHIL PERCENTAGE DECREASED ( 1 FDA reports)
EOSINOPHILIC FASCIITIS ( 1 FDA reports)
EPICONDYLITIS ( 1 FDA reports)
EPIGLOTTITIS ( 1 FDA reports)
ERECTION INCREASED ( 1 FDA reports)
ERYTHEMA NODOSUM ( 1 FDA reports)
ESSENTIAL TREMOR ( 1 FDA reports)
ETHMOID SINUS SURGERY ( 1 FDA reports)
EXCITABILITY ( 1 FDA reports)
EXERCISE ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
EXPOSURE TO ALLERGEN ( 1 FDA reports)
EXPOSURE TO TOXIC AGENT ( 1 FDA reports)
EXTRAVASATION ( 1 FDA reports)
EXTREMITY CONTRACTURE ( 1 FDA reports)
EXTRUSION OF DEVICE ( 1 FDA reports)
EYE ALLERGY ( 1 FDA reports)
EYE BURNS ( 1 FDA reports)
EYE DISCHARGE ( 1 FDA reports)
EYE INFECTION ( 1 FDA reports)
EYE INFECTION FUNGAL ( 1 FDA reports)
EYE INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
EYELID BLEEDING ( 1 FDA reports)
EYELID MARGIN CRUSTING ( 1 FDA reports)
FACIAL LESION EXCISION ( 1 FDA reports)
FACIAL PARESIS ( 1 FDA reports)
FACIAL WASTING ( 1 FDA reports)
FACTOR II DEFICIENCY ( 1 FDA reports)
FACTOR V DEFICIENCY ( 1 FDA reports)
FAECAL OCCULT BLOOD ( 1 FDA reports)
FAECALOMA ( 1 FDA reports)
FAILURE OF IMPLANT ( 1 FDA reports)
FANCONI SYNDROME ACQUIRED ( 1 FDA reports)
FAT INTOLERANCE ( 1 FDA reports)
FAT TISSUE INCREASED ( 1 FDA reports)
FATTY ACID DEFICIENCY ( 1 FDA reports)
FEELINGS OF WORTHLESSNESS ( 1 FDA reports)
FEMALE STERILISATION ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FIBROADENOMA OF BREAST ( 1 FDA reports)
FINGER DEFORMITY ( 1 FDA reports)
FOETAL CYSTIC HYGROMA ( 1 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
FOOD ALLERGY ( 1 FDA reports)
FOOD CRAVING ( 1 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 1 FDA reports)
FOREIGN TRAVEL ( 1 FDA reports)
FRACTURE MALUNION ( 1 FDA reports)
FRACTURED SACRUM ( 1 FDA reports)
FREE THYROXINE INDEX DECREASED ( 1 FDA reports)
FUNGAEMIA ( 1 FDA reports)
FUNGUS SPUTUM TEST POSITIVE ( 1 FDA reports)
GAIT DEVIATION ( 1 FDA reports)
GALLBLADDER OBSTRUCTION ( 1 FDA reports)
GALLBLADDER OPERATION ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ( 1 FDA reports)
GANGLION ( 1 FDA reports)
GASTRIC BYPASS ( 1 FDA reports)
GASTRIC DILATATION ( 1 FDA reports)
GASTRIC MUCOSAL LESION ( 1 FDA reports)
GASTRIC NEOPLASM ( 1 FDA reports)
GASTRIC OUTLET OBSTRUCTION ( 1 FDA reports)
GASTRO-INTESTINAL FISTULA ( 1 FDA reports)
GASTROENTERITIS NORWALK VIRUS ( 1 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
GASTROINTESTINAL INFECTION ( 1 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 1 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 1 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 1 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 1 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GENITAL ERYTHEMA ( 1 FDA reports)
GENITAL PAIN ( 1 FDA reports)
GENITAL RASH ( 1 FDA reports)
GINGIVAL ABSCESS ( 1 FDA reports)
GINGIVAL ERYTHEMA ( 1 FDA reports)
GLIOBLASTOMA MULTIFORME ( 1 FDA reports)
GLIOMA ( 1 FDA reports)
GLOBULINS DECREASED ( 1 FDA reports)
GLOMERULAR FILTRATION RATE INCREASED ( 1 FDA reports)
GLOMERULONEPHRITIS ( 1 FDA reports)
GLOMERULOSCLEROSIS ( 1 FDA reports)
GRAFT COMPLICATION ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
GRANULOMA ANNULARE ( 1 FDA reports)
GRAVITATIONAL OEDEMA ( 1 FDA reports)
GRIMACING ( 1 FDA reports)
GRUNTING ( 1 FDA reports)
GUN SHOT WOUND ( 1 FDA reports)
HAEMARTHROSIS ( 1 FDA reports)
HAEMOCONCENTRATION ( 1 FDA reports)
HAEMOGLOBIN ABNORMAL ( 1 FDA reports)
HAEMORRHAGIC ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
HAEMORRHAGIC DISORDER ( 1 FDA reports)
HAIR DISORDER ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
HALO VISION ( 1 FDA reports)
HAND FRACTURE ( 1 FDA reports)
HEART SOUNDS ABNORMAL ( 1 FDA reports)
HEAT EXHAUSTION ( 1 FDA reports)
HEAT EXPOSURE INJURY ( 1 FDA reports)
HEMIANOPIA ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 1 FDA reports)
HEPATIC ATROPHY ( 1 FDA reports)
HEPATIC HAEMORRHAGE ( 1 FDA reports)
HEPATIC TRAUMA ( 1 FDA reports)
HEPATIC VEIN THROMBOSIS ( 1 FDA reports)
HEPATITIS C VIRUS ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HEPATITIS CHRONIC ACTIVE ( 1 FDA reports)
HEPATITIS GRANULOMATOUS ( 1 FDA reports)
HEPATITIS TOXIC ( 1 FDA reports)
HEPATORENAL FAILURE ( 1 FDA reports)
HERNIA PAIN ( 1 FDA reports)
HERNIA REPAIR ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HERPES SIMPLEX OPHTHALMIC ( 1 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 1 FDA reports)
HERPES ZOSTER DISSEMINATED ( 1 FDA reports)
HISTIOCYTOSIS ( 1 FDA reports)
HIV INFECTION ( 1 FDA reports)
HUMAN PAPILLOMA VIRUS TEST POSITIVE ( 1 FDA reports)
HUNTINGTON'S CHOREA ( 1 FDA reports)
HUNTINGTON'S DISEASE ( 1 FDA reports)
HYDROCHOLECYSTIS ( 1 FDA reports)
HYDROPNEUMOTHORAX ( 1 FDA reports)
HYDROURETER ( 1 FDA reports)
HYPERCALCIURIA ( 1 FDA reports)
HYPERMETABOLISM ( 1 FDA reports)
HYPERPARATHYROIDISM ( 1 FDA reports)
HYPERSEXUALITY ( 1 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 1 FDA reports)
HYPERTONIA ( 1 FDA reports)
HYPERTRICHOSIS ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
HYPERVITAMINOSIS ( 1 FDA reports)
HYPERVOLAEMIA ( 1 FDA reports)
HYPOCHROMIC ANAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 1 FDA reports)
HYPOPHARYNGEAL NEOPLASM ( 1 FDA reports)
HYPOSMIA ( 1 FDA reports)
HYPOTHALAMO-PITUITARY DISORDERS ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 1 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 1 FDA reports)
IDIOPATHIC URTICARIA ( 1 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 1 FDA reports)
IIIRD NERVE DISORDER ( 1 FDA reports)
ILIAC ARTERY STENOSIS ( 1 FDA reports)
ILLUSION ( 1 FDA reports)
IMPLANT EXPULSION ( 1 FDA reports)
IMPLANT SITE HAEMORRHAGE ( 1 FDA reports)
IMPRISONMENT ( 1 FDA reports)
IMPULSIVE BEHAVIOUR ( 1 FDA reports)
INABILITY TO CRAWL ( 1 FDA reports)
INCISION SITE HAEMATOMA ( 1 FDA reports)
INCISIONAL HERNIA ( 1 FDA reports)
INCISIONAL HERNIA REPAIR ( 1 FDA reports)
INDURATION ( 1 FDA reports)
INFECTED CYST ( 1 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 1 FDA reports)
INFUSION SITE ERYTHEMA ( 1 FDA reports)
INFUSION SITE RASH ( 1 FDA reports)
INFUSION SITE SWELLING ( 1 FDA reports)
INGROWN HAIR ( 1 FDA reports)
INGUINAL HERNIA REPAIR ( 1 FDA reports)
INJECTION SITE DISCHARGE ( 1 FDA reports)
INJECTION SITE DISCOMFORT ( 1 FDA reports)
INJECTION SITE EXTRAVASATION ( 1 FDA reports)
INJECTION SITE INFECTION ( 1 FDA reports)
INJECTION SITE PAPULE ( 1 FDA reports)
INJECTION SITE SCAR ( 1 FDA reports)
INJECTION SITE STINGING ( 1 FDA reports)
INJECTION SITE URTICARIA ( 1 FDA reports)
INJECTION SITE WARMTH ( 1 FDA reports)
INSOMNIA RELATED TO ANOTHER MENTAL CONDITION ( 1 FDA reports)
INTERMITTENT CLAUDICATION ( 1 FDA reports)
INTERVERTEBRAL DISCITIS ( 1 FDA reports)
INTESTINAL DILATATION ( 1 FDA reports)
INTESTINAL INFARCTION ( 1 FDA reports)
INTESTINAL OPERATION ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
INTRACRANIAL HAEMATOMA ( 1 FDA reports)
INTRACRANIAL TUMOUR HAEMORRHAGE ( 1 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 1 FDA reports)
INVESTIGATION ( 1 FDA reports)
IRON BINDING CAPACITY TOTAL INCREASED ( 1 FDA reports)
ISCHAEMIC ULCER ( 1 FDA reports)
IUD MIGRATION ( 1 FDA reports)
JAW CYST ( 1 FDA reports)
JC VIRUS INFECTION ( 1 FDA reports)
JC VIRUS TEST POSITIVE ( 1 FDA reports)
JOINT ANKYLOSIS ( 1 FDA reports)
JOINT INSTABILITY ( 1 FDA reports)
JOINT LOCK ( 1 FDA reports)
JUGULAR VEIN THROMBOSIS ( 1 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 1 FDA reports)
KERATOPATHY ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
KLEBSIELLA TEST POSITIVE ( 1 FDA reports)
LABILE HYPERTENSION ( 1 FDA reports)
LACTOSE INTOLERANCE ( 1 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
LARYNGEAL DISORDER ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
LATEX ALLERGY ( 1 FDA reports)
LAZINESS ( 1 FDA reports)
LEFT ATRIAL DILATATION ( 1 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 1 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
LENTICULAR OPACITIES ( 1 FDA reports)
LEUKAEMIA ( 1 FDA reports)
LEUKOARAIOSIS ( 1 FDA reports)
LICHEN PLANUS ( 1 FDA reports)
LICHEN SCLEROSUS ( 1 FDA reports)
LIFE SUPPORT ( 1 FDA reports)
LIMB ASYMMETRY ( 1 FDA reports)
LIMB DEFORMITY ( 1 FDA reports)
LIP DISCOLOURATION ( 1 FDA reports)
LIP INJURY ( 1 FDA reports)
LIP OEDEMA ( 1 FDA reports)
LIP PAIN ( 1 FDA reports)
LIVER TENDERNESS ( 1 FDA reports)
LOGORRHOEA ( 1 FDA reports)
LOSS OF LIBIDO ( 1 FDA reports)
LOW BIRTH WEIGHT BABY ( 1 FDA reports)
LOWER EXTREMITY MASS ( 1 FDA reports)
LUMBAR SPINAL STENOSIS ( 1 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
LUPUS NEPHRITIS ( 1 FDA reports)
LYMPHANGIECTASIA ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
LYMPHOPENIA ( 1 FDA reports)
MACROCYTOSIS ( 1 FDA reports)
MADAROSIS ( 1 FDA reports)
MAGNESIUM METABOLISM DISORDER ( 1 FDA reports)
MALIGNANT MELANOMA ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MAXILLOFACIAL SINUS NEOPLASM ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 1 FDA reports)
MEASLES ( 1 FDA reports)
MEDICAL DEVICE CHANGE ( 1 FDA reports)
MEDICAL DEVICE DISCOMFORT ( 1 FDA reports)
MEDICAL DIET ( 1 FDA reports)
MENINGEAL DISORDER ( 1 FDA reports)
MENINGITIS BACTERIAL ( 1 FDA reports)
MENSTRUAL DISCOMFORT ( 1 FDA reports)
METASTASES TO MENINGES ( 1 FDA reports)
METASTASES TO PELVIS ( 1 FDA reports)
METASTASES TO PERITONEUM ( 1 FDA reports)
METASTASES TO PLEURA ( 1 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST POSITIVE ( 1 FDA reports)
MICROANGIOPATHY ( 1 FDA reports)
MIDDLE EAR EFFUSION ( 1 FDA reports)
MITRAL VALVE REPAIR ( 1 FDA reports)
MITRAL VALVE SCLEROSIS ( 1 FDA reports)
MOANING ( 1 FDA reports)
MODIFIED RADICAL MASTECTOMY ( 1 FDA reports)
MONONUCLEOSIS SYNDROME ( 1 FDA reports)
MORBID THOUGHTS ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MOUTH INJURY ( 1 FDA reports)
MUCOSAL EXFOLIATION ( 1 FDA reports)
MULTIPLE PREGNANCY ( 1 FDA reports)
MUMPS ( 1 FDA reports)
MURPHY'S SIGN POSITIVE ( 1 FDA reports)
MUSCLE RUPTURE ( 1 FDA reports)
MUSCLE SPASTICITY ( 1 FDA reports)
MUSCULOSKELETAL DEFORMITY ( 1 FDA reports)
MYASTHENIA GRAVIS ( 1 FDA reports)
MYCOBACTERIA TEST ( 1 FDA reports)
MYCOBACTERIAL INFECTION ( 1 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 1 FDA reports)
MYCOPLASMA INFECTION ( 1 FDA reports)
MYOCARDIAL OEDEMA ( 1 FDA reports)
MYOCARDITIS ( 1 FDA reports)
MYRINGOPLASTY ( 1 FDA reports)
MYRINGOTOMY ( 1 FDA reports)
N-TELOPEPTIDE URINE DECREASED ( 1 FDA reports)
NAIL INFECTION ( 1 FDA reports)
NASAL ABSCESS ( 1 FDA reports)
NASAL POLYPS ( 1 FDA reports)
NECROLYTIC MIGRATORY ERYTHEMA ( 1 FDA reports)
NEONATAL DISORDER ( 1 FDA reports)
NEONATAL PNEUMONIA ( 1 FDA reports)
NEOPLASM RECURRENCE ( 1 FDA reports)
NEPHRITIS ( 1 FDA reports)
NEUTROPHIL COUNT ( 1 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 1 FDA reports)
NICOTINE DEPENDENCE ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA REFRACTORY ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER ( 1 FDA reports)
NOSOCOMIAL INFECTION ( 1 FDA reports)
OCCUPATIONAL PROBLEM ENVIRONMENTAL ( 1 FDA reports)
OCULAR HYPERTENSION ( 1 FDA reports)
OCULAR VASCULAR DISORDER ( 1 FDA reports)
OEDEMA GENITAL ( 1 FDA reports)
OESOPHAGEAL HYPOMOTILITY ( 1 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 1 FDA reports)
OLIGOHYDRAMNIOS ( 1 FDA reports)
OPTIC ATROPHY ( 1 FDA reports)
OPTIC NERVE CUP/DISC RATIO INCREASED ( 1 FDA reports)
OPTIC NERVE INJURY ( 1 FDA reports)
ORAL CAVITY FISTULA ( 1 FDA reports)
ORAL MUCOSAL BLISTERING ( 1 FDA reports)
ORAL MUCOSAL ERUPTION ( 1 FDA reports)
ORAL NEOPLASM ( 1 FDA reports)
ORAL SOFT TISSUE DISORDER ( 1 FDA reports)
ORBITAL OEDEMA ( 1 FDA reports)
OSTEOCHONDROSIS ( 1 FDA reports)
OSTEOGENESIS IMPERFECTA ( 1 FDA reports)
OVARIAN CYST RUPTURED ( 1 FDA reports)
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OXYGEN CONSUMPTION DECREASED ( 1 FDA reports)
OXYGEN SATURATION ABNORMAL ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PANCREATIC ENZYME ABNORMALITY ( 1 FDA reports)
PANCREATITIS RELAPSING ( 1 FDA reports)
PAPULE ( 1 FDA reports)
PARAKERATOSIS ( 1 FDA reports)
PARANASAL SINUS DISCOMFORT ( 1 FDA reports)
PARANEOPLASTIC SYNDROME ( 1 FDA reports)
PARASOMNIA ( 1 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 1 FDA reports)
PARENT-CHILD PROBLEM ( 1 FDA reports)
PAROTID GLAND ENLARGEMENT ( 1 FDA reports)
PATELLA FRACTURE ( 1 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 1 FDA reports)
PECTUS EXCAVATUM ( 1 FDA reports)
PELVIC FRACTURE ( 1 FDA reports)
PENILE ABSCESS ( 1 FDA reports)
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PENIS DEVIATION ( 1 FDA reports)
PERFUME SENSITIVITY ( 1 FDA reports)
PERICARDITIS RHEUMATIC ( 1 FDA reports)
PERIORBITAL CELLULITIS ( 1 FDA reports)
PERIRECTAL ABSCESS ( 1 FDA reports)
PERITONEAL EFFUSION ( 1 FDA reports)
PERITONEAL LESION ( 1 FDA reports)
PERITONSILLAR ABSCESS ( 1 FDA reports)
PHARYNGEAL ULCERATION ( 1 FDA reports)
PHOTODERMATOSIS ( 1 FDA reports)
PILOERECTION ( 1 FDA reports)
PITUITARY CYST ( 1 FDA reports)
PLASTIC SURGERY TO THE FACE ( 1 FDA reports)
PLATELET COUNT ABNORMAL ( 1 FDA reports)
PLATELET MORPHOLOGY ABNORMAL ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
PNEUMOMEDIASTINUM ( 1 FDA reports)
PNEUMONIA FUNGAL ( 1 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 1 FDA reports)
POIKILOCYTOSIS ( 1 FDA reports)
POLYCYTHAEMIA ( 1 FDA reports)
POLYDACTYLY ( 1 FDA reports)
POLYHYDRAMNIOS ( 1 FDA reports)
POLYMYALGIA ( 1 FDA reports)
POLYMYOSITIS ( 1 FDA reports)
POOR PERIPHERAL CIRCULATION ( 1 FDA reports)
POOR VENOUS ACCESS ( 1 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 1 FDA reports)
POST CHOLECYSTECTOMY SYNDROME ( 1 FDA reports)
POST COITAL BLEEDING ( 1 FDA reports)
POST CONCUSSION SYNDROME ( 1 FDA reports)
POST PROCEDURAL INFECTION ( 1 FDA reports)
POST PROCEDURAL NAUSEA ( 1 FDA reports)
POST PROCEDURAL PULMONARY EMBOLISM ( 1 FDA reports)
POST PROCEDURAL VOMITING ( 1 FDA reports)
POSTMENOPAUSE ( 1 FDA reports)
POSTOPERATIVE RENAL FAILURE ( 1 FDA reports)
PRE-EXISTING CONDITION IMPROVED ( 1 FDA reports)
PREGNANCY ON CONTRACEPTIVE ( 1 FDA reports)
PREMATURE DELIVERY ( 1 FDA reports)
PREPYLORIC STENOSIS ( 1 FDA reports)
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PROCTITIS ULCERATIVE ( 1 FDA reports)
PROCTOCOLITIS ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 1 FDA reports)
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PSYCHOLOGICAL TRAUMA ( 1 FDA reports)
PSYCHOMOTOR RETARDATION ( 1 FDA reports)
PULMONARY COCCIDIOIDES ( 1 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 1 FDA reports)
PULMONARY MICROEMBOLI ( 1 FDA reports)
PULMONARY TOXICITY ( 1 FDA reports)
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PULSE PRESSURE DECREASED ( 1 FDA reports)
PUNCTURE SITE DISCHARGE ( 1 FDA reports)
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PYELECTASIA ( 1 FDA reports)
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PYURIA ( 1 FDA reports)
RADIATION INJURY ( 1 FDA reports)
RADIATION PNEUMONITIS ( 1 FDA reports)
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RASH MORBILLIFORM ( 1 FDA reports)
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REACTION TO PRESERVATIVES ( 1 FDA reports)
READING DISORDER ( 1 FDA reports)
RECTAL ABSCESS ( 1 FDA reports)
RECTAL DISCHARGE ( 1 FDA reports)
RECTAL FISSURE ( 1 FDA reports)
RECTAL ULCER ( 1 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 1 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH DECREASED ( 1 FDA reports)
REFLEXES ABNORMAL ( 1 FDA reports)
REFUSAL OF EXAMINATION ( 1 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 1 FDA reports)
RELATIONSHIP BREAKDOWN ( 1 FDA reports)
REMOVAL OF INERT MATTER FROM SKIN OR SUBCUTANEOUS TISSUE ( 1 FDA reports)
RENAL ARTERY STENT PLACEMENT ( 1 FDA reports)
RENAL NEOPLASM ( 1 FDA reports)
RENAL TUBULAR ATROPHY ( 1 FDA reports)
RESPIRATORY ACIDOSIS ( 1 FDA reports)
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RESTRICTIVE PULMONARY DISEASE ( 1 FDA reports)
RETINAL DISORDER ( 1 FDA reports)
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RETROGRADE EJACULATION ( 1 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 1 FDA reports)
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RHEUMATOID LUNG ( 1 FDA reports)
RHEUMATOID NODULE ( 1 FDA reports)
RIFT VALLEY FEVER ( 1 FDA reports)
ROSACEA ( 1 FDA reports)
SALIVA ALTERED ( 1 FDA reports)
SALIVARY GLAND NEOPLASM ( 1 FDA reports)
SCAPULA FRACTURE ( 1 FDA reports)
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SCLERAL HYPERAEMIA ( 1 FDA reports)
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SCROTAL HAEMATOMA ( 1 FDA reports)
SCROTAL MASS ( 1 FDA reports)
SCROTAL OEDEMA ( 1 FDA reports)
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SECONDARY HYPERTENSION ( 1 FDA reports)
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SEPSIS PASTEURELLA ( 1 FDA reports)
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SICKLE CELL ANAEMIA WITH CRISIS ( 1 FDA reports)
SILICOSIS ( 1 FDA reports)
SINUS ANTROSTOMY ( 1 FDA reports)
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SMALL INTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
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SPHINCTER OF ODDI DYSFUNCTION ( 1 FDA reports)
SPINAL CORD DISORDER ( 1 FDA reports)
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STATUS ASTHMATICUS ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
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SYMBOLIC DYSFUNCTION ( 1 FDA reports)
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TARDIVE DYSKINESIA ( 1 FDA reports)
TEMPORAL ARTERITIS ( 1 FDA reports)
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TONIC CLONIC MOVEMENTS ( 1 FDA reports)
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TYPE 1 DIABETES MELLITUS ( 1 FDA reports)
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URETHRAL FISTULA ( 1 FDA reports)
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URINARY TRACT INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
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VERBAL ABUSE ( 1 FDA reports)
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