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

DRUG INEFFECTIVE ( 645 FDA reports)
NAUSEA ( 620 FDA reports)
HEADACHE ( 562 FDA reports)
FATIGUE ( 513 FDA reports)
PAIN ( 512 FDA reports)
VOMITING ( 480 FDA reports)
DEPRESSION ( 461 FDA reports)
ANXIETY ( 454 FDA reports)
DIZZINESS ( 428 FDA reports)
DYSPNOEA ( 424 FDA reports)
CHEST PAIN ( 421 FDA reports)
MYOCARDIAL INFARCTION ( 410 FDA reports)
PYREXIA ( 352 FDA reports)
BACK PAIN ( 351 FDA reports)
HYPERTENSION ( 345 FDA reports)
DIARRHOEA ( 334 FDA reports)
ASTHENIA ( 333 FDA reports)
PAIN IN EXTREMITY ( 305 FDA reports)
ABDOMINAL PAIN UPPER ( 302 FDA reports)
ARTHRALGIA ( 300 FDA reports)
ABDOMINAL PAIN ( 279 FDA reports)
ANAEMIA ( 269 FDA reports)
CEREBROVASCULAR ACCIDENT ( 265 FDA reports)
OEDEMA PERIPHERAL ( 262 FDA reports)
RASH ( 259 FDA reports)
CORONARY ARTERY DISEASE ( 257 FDA reports)
FALL ( 251 FDA reports)
INSOMNIA ( 241 FDA reports)
CONDITION AGGRAVATED ( 235 FDA reports)
RENAL FAILURE ACUTE ( 235 FDA reports)
WEIGHT DECREASED ( 234 FDA reports)
PRURITUS ( 218 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 212 FDA reports)
HYPOAESTHESIA ( 209 FDA reports)
PULMONARY EMBOLISM ( 207 FDA reports)
INJURY ( 199 FDA reports)
PARAESTHESIA ( 199 FDA reports)
CONSTIPATION ( 193 FDA reports)
EMOTIONAL DISTRESS ( 193 FDA reports)
DEEP VEIN THROMBOSIS ( 188 FDA reports)
BLOOD PRESSURE INCREASED ( 185 FDA reports)
HYPERSENSITIVITY ( 184 FDA reports)
WEIGHT INCREASED ( 182 FDA reports)
OVERDOSE ( 179 FDA reports)
SOMNOLENCE ( 178 FDA reports)
COUGH ( 175 FDA reports)
FEELING ABNORMAL ( 174 FDA reports)
CHOLELITHIASIS ( 166 FDA reports)
MYALGIA ( 165 FDA reports)
URTICARIA ( 164 FDA reports)
HYPOTENSION ( 162 FDA reports)
MALAISE ( 159 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 158 FDA reports)
URINARY TRACT INFECTION ( 158 FDA reports)
RENAL FAILURE ( 156 FDA reports)
CONVULSION ( 153 FDA reports)
DEHYDRATION ( 151 FDA reports)
VISION BLURRED ( 151 FDA reports)
PNEUMONIA ( 150 FDA reports)
DYSPEPSIA ( 146 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 143 FDA reports)
HYPERHIDROSIS ( 143 FDA reports)
MIGRAINE ( 143 FDA reports)
PALPITATIONS ( 142 FDA reports)
CHEST DISCOMFORT ( 141 FDA reports)
MUSCLE SPASMS ( 139 FDA reports)
RECTAL HAEMORRHAGE ( 138 FDA reports)
PLEURAL EFFUSION ( 133 FDA reports)
SWELLING FACE ( 133 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 130 FDA reports)
ABDOMINAL DISTENSION ( 129 FDA reports)
GASTROINTESTINAL DISORDER ( 129 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 125 FDA reports)
ERYTHEMA ( 125 FDA reports)
COLITIS ULCERATIVE ( 124 FDA reports)
SYNCOPE ( 120 FDA reports)
DRUG HYPERSENSITIVITY ( 117 FDA reports)
OSTEOARTHRITIS ( 117 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 116 FDA reports)
HAEMOGLOBIN DECREASED ( 116 FDA reports)
GAIT DISTURBANCE ( 115 FDA reports)
HEART RATE INCREASED ( 115 FDA reports)
TREMOR ( 114 FDA reports)
CONFUSIONAL STATE ( 113 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 112 FDA reports)
BLOOD GLUCOSE INCREASED ( 111 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 111 FDA reports)
SINUSITIS ( 111 FDA reports)
DRUG EFFECT DECREASED ( 110 FDA reports)
ABDOMINAL DISCOMFORT ( 109 FDA reports)
MITRAL VALVE INCOMPETENCE ( 105 FDA reports)
CROHN'S DISEASE ( 104 FDA reports)
COLITIS ( 103 FDA reports)
GASTRITIS ( 103 FDA reports)
SUICIDAL IDEATION ( 103 FDA reports)
TACHYCARDIA ( 103 FDA reports)
DYSPHAGIA ( 102 FDA reports)
CHILLS ( 100 FDA reports)
LOSS OF CONSCIOUSNESS ( 97 FDA reports)
ATRIAL FIBRILLATION ( 94 FDA reports)
DECREASED APPETITE ( 94 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 94 FDA reports)
ANGINA PECTORIS ( 93 FDA reports)
FLUSHING ( 93 FDA reports)
MEMORY IMPAIRMENT ( 93 FDA reports)
INFLUENZA LIKE ILLNESS ( 92 FDA reports)
LYMPHADENOPATHY ( 92 FDA reports)
BALANCE DISORDER ( 91 FDA reports)
CARDIAC DISORDER ( 91 FDA reports)
CONTUSION ( 91 FDA reports)
DIABETES MELLITUS ( 91 FDA reports)
HYPOKALAEMIA ( 91 FDA reports)
HEPATIC ENZYME INCREASED ( 90 FDA reports)
HYPERLIPIDAEMIA ( 90 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 90 FDA reports)
NECK PAIN ( 89 FDA reports)
THROMBOSIS ( 88 FDA reports)
MUSCULAR WEAKNESS ( 87 FDA reports)
ARTHROPATHY ( 85 FDA reports)
NEPHROLITHIASIS ( 85 FDA reports)
BONE DISORDER ( 83 FDA reports)
BONE PAIN ( 83 FDA reports)
AMNESIA ( 82 FDA reports)
BRONCHITIS ( 82 FDA reports)
PANIC ATTACK ( 80 FDA reports)
CELLULITIS ( 79 FDA reports)
OSTEONECROSIS ( 79 FDA reports)
ANOREXIA ( 78 FDA reports)
JOINT SWELLING ( 78 FDA reports)
SWELLING ( 76 FDA reports)
CHOLECYSTITIS CHRONIC ( 75 FDA reports)
DRY SKIN ( 75 FDA reports)
HYPERCHOLESTEROLAEMIA ( 75 FDA reports)
LETHARGY ( 75 FDA reports)
SUICIDE ATTEMPT ( 75 FDA reports)
ALOPECIA ( 74 FDA reports)
INFECTION ( 74 FDA reports)
JAUNDICE ( 74 FDA reports)
EPISTAXIS ( 73 FDA reports)
INFLAMMATION ( 72 FDA reports)
IRRITABLE BOWEL SYNDROME ( 72 FDA reports)
ARTHRITIS ( 71 FDA reports)
BLOOD CREATININE INCREASED ( 71 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 71 FDA reports)
DYSPNOEA EXERTIONAL ( 71 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 71 FDA reports)
ANHEDONIA ( 70 FDA reports)
CARDIAC ARREST ( 70 FDA reports)
DYSURIA ( 70 FDA reports)
INCORRECT DOSE ADMINISTERED ( 70 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 70 FDA reports)
DISTURBANCE IN ATTENTION ( 69 FDA reports)
FLATULENCE ( 69 FDA reports)
HEPATITIS ( 69 FDA reports)
DYSGEUSIA ( 67 FDA reports)
BURNING SENSATION ( 66 FDA reports)
MUSCULOSKELETAL PAIN ( 66 FDA reports)
ASTHMA ( 65 FDA reports)
INTENTIONAL OVERDOSE ( 65 FDA reports)
NEUROPATHY PERIPHERAL ( 65 FDA reports)
STRESS ( 65 FDA reports)
VERTIGO ( 65 FDA reports)
BLOOD BILIRUBIN INCREASED ( 64 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 64 FDA reports)
LUNG DISORDER ( 64 FDA reports)
NERVOUSNESS ( 64 FDA reports)
AGITATION ( 63 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 63 FDA reports)
SLEEP APNOEA SYNDROME ( 63 FDA reports)
CORONARY ARTERY OCCLUSION ( 62 FDA reports)
DRY MOUTH ( 62 FDA reports)
MULTI-ORGAN DISORDER ( 62 FDA reports)
TOOTH EXTRACTION ( 62 FDA reports)
HIATUS HERNIA ( 61 FDA reports)
PANCREATITIS ( 61 FDA reports)
PANCYTOPENIA ( 61 FDA reports)
PLATELET COUNT DECREASED ( 61 FDA reports)
RESPIRATORY FAILURE ( 61 FDA reports)
DRUG INTERACTION ( 60 FDA reports)
INJECTION SITE PAIN ( 60 FDA reports)
IRRITABILITY ( 60 FDA reports)
TINNITUS ( 60 FDA reports)
HAEMATEMESIS ( 59 FDA reports)
HAEMATOCHEZIA ( 59 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 59 FDA reports)
VISUAL DISTURBANCE ( 59 FDA reports)
DIVERTICULITIS ( 58 FDA reports)
EYE SWELLING ( 58 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 58 FDA reports)
STEVENS-JOHNSON SYNDROME ( 58 FDA reports)
BLOOD PRESSURE DECREASED ( 57 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 57 FDA reports)
INFLUENZA ( 57 FDA reports)
INTESTINAL HAEMORRHAGE ( 57 FDA reports)
DRUG TOXICITY ( 56 FDA reports)
HERPES ZOSTER ( 56 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 56 FDA reports)
ROTATOR CUFF SYNDROME ( 56 FDA reports)
THROMBOCYTOPENIA ( 56 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 55 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 55 FDA reports)
SLEEP DISORDER ( 55 FDA reports)
ANAPHYLACTIC REACTION ( 54 FDA reports)
LEUKOPENIA ( 54 FDA reports)
MYOCARDIAL ISCHAEMIA ( 54 FDA reports)
OEDEMA ( 54 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 54 FDA reports)
ARRHYTHMIA ( 53 FDA reports)
ATELECTASIS ( 53 FDA reports)
FAECES DISCOLOURED ( 53 FDA reports)
HOT FLUSH ( 53 FDA reports)
RHINORRHOEA ( 53 FDA reports)
SWOLLEN TONGUE ( 53 FDA reports)
CATARACT ( 52 FDA reports)
INJECTION SITE ERYTHEMA ( 52 FDA reports)
BRADYCARDIA ( 51 FDA reports)
CARDIAC MURMUR ( 51 FDA reports)
CORONARY ARTERY STENOSIS ( 51 FDA reports)
CRYING ( 51 FDA reports)
HEPATIC STEATOSIS ( 51 FDA reports)
NASOPHARYNGITIS ( 51 FDA reports)
CARDIOMEGALY ( 50 FDA reports)
GALLBLADDER DISORDER ( 50 FDA reports)
MOUTH ULCERATION ( 50 FDA reports)
MULTIPLE SCLEROSIS ( 50 FDA reports)
NEUTROPENIA ( 50 FDA reports)
RESPIRATORY DISTRESS ( 50 FDA reports)
EMOTIONAL DISORDER ( 49 FDA reports)
GASTRIC ULCER ( 49 FDA reports)
HAEMORRHAGE ( 49 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 49 FDA reports)
STAPHYLOCOCCAL INFECTION ( 49 FDA reports)
AGGRESSION ( 48 FDA reports)
ANGER ( 48 FDA reports)
CYSTITIS ( 48 FDA reports)
EYE PAIN ( 48 FDA reports)
HEAD INJURY ( 48 FDA reports)
PAIN IN JAW ( 48 FDA reports)
SKIN EXFOLIATION ( 48 FDA reports)
SPEECH DISORDER ( 48 FDA reports)
ADVERSE EVENT ( 47 FDA reports)
HAEMATURIA ( 47 FDA reports)
HYPOTHYROIDISM ( 47 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 47 FDA reports)
PRODUCT QUALITY ISSUE ( 47 FDA reports)
PULMONARY OEDEMA ( 47 FDA reports)
CARPAL TUNNEL SYNDROME ( 46 FDA reports)
HAEMATOCRIT DECREASED ( 46 FDA reports)
OSTEOMYELITIS ( 46 FDA reports)
RENAL DISORDER ( 46 FDA reports)
AORTIC VALVE INCOMPETENCE ( 45 FDA reports)
DEATH ( 45 FDA reports)
HYPONATRAEMIA ( 45 FDA reports)
RHEUMATOID ARTHRITIS ( 45 FDA reports)
ROAD TRAFFIC ACCIDENT ( 45 FDA reports)
ABSCESS ( 44 FDA reports)
BACK INJURY ( 44 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 44 FDA reports)
RASH GENERALISED ( 44 FDA reports)
SCAR ( 44 FDA reports)
SINUS TACHYCARDIA ( 44 FDA reports)
SPINAL OSTEOARTHRITIS ( 44 FDA reports)
VENTRICULAR HYPERTROPHY ( 44 FDA reports)
BREAST CANCER ( 43 FDA reports)
DEPRESSED MOOD ( 43 FDA reports)
DISORIENTATION ( 43 FDA reports)
HAEMORRHOIDS ( 43 FDA reports)
LIP SWELLING ( 43 FDA reports)
THROAT IRRITATION ( 43 FDA reports)
BLOOD POTASSIUM DECREASED ( 42 FDA reports)
CYTOLYTIC HEPATITIS ( 42 FDA reports)
OSTEONECROSIS OF JAW ( 42 FDA reports)
PHARYNGEAL OEDEMA ( 42 FDA reports)
ASCITES ( 41 FDA reports)
EAR PAIN ( 41 FDA reports)
HYPOAESTHESIA ORAL ( 41 FDA reports)
METASTASES TO BONE ( 41 FDA reports)
RENAL CYST ( 41 FDA reports)
TENDONITIS ( 41 FDA reports)
URINARY RETENTION ( 41 FDA reports)
ABNORMAL BEHAVIOUR ( 40 FDA reports)
DIPLOPIA ( 40 FDA reports)
DISEASE PROGRESSION ( 40 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 40 FDA reports)
DYSARTHRIA ( 40 FDA reports)
LEUKOCYTOSIS ( 40 FDA reports)
RASH PRURITIC ( 40 FDA reports)
STOMATITIS ( 40 FDA reports)
TREATMENT NONCOMPLIANCE ( 40 FDA reports)
VIRAL INFECTION ( 40 FDA reports)
ANGINA UNSTABLE ( 39 FDA reports)
BASAL CELL CARCINOMA ( 39 FDA reports)
CARDIOMYOPATHY ( 39 FDA reports)
COLONIC POLYP ( 39 FDA reports)
DRUG DEPENDENCE ( 39 FDA reports)
FEAR ( 39 FDA reports)
FEELING HOT ( 39 FDA reports)
HERNIA ( 39 FDA reports)
MENTAL DISORDER ( 39 FDA reports)
MENTAL IMPAIRMENT ( 39 FDA reports)
OSTEOPOROSIS ( 39 FDA reports)
PLATELET COUNT INCREASED ( 39 FDA reports)
STOMACH DISCOMFORT ( 39 FDA reports)
CEREBRAL INFARCTION ( 38 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 38 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 38 FDA reports)
MELAENA ( 38 FDA reports)
MENISCUS LESION ( 38 FDA reports)
PHOTOPHOBIA ( 38 FDA reports)
RENAL FAILURE CHRONIC ( 38 FDA reports)
ABASIA ( 37 FDA reports)
CHOLECYSTITIS ( 37 FDA reports)
ILL-DEFINED DISORDER ( 37 FDA reports)
LIP DRY ( 37 FDA reports)
SEPSIS ( 37 FDA reports)
TOOTH DISORDER ( 37 FDA reports)
VISUAL IMPAIRMENT ( 37 FDA reports)
CARDIOVASCULAR DISORDER ( 36 FDA reports)
FACE OEDEMA ( 36 FDA reports)
HAEMODIALYSIS ( 36 FDA reports)
HEMIPARESIS ( 36 FDA reports)
HYPOXIA ( 36 FDA reports)
RIB FRACTURE ( 36 FDA reports)
TOXIC SKIN ERUPTION ( 36 FDA reports)
VISUAL ACUITY REDUCED ( 36 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 36 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 35 FDA reports)
DRUG ADMINISTRATION ERROR ( 35 FDA reports)
OESOPHAGITIS ( 35 FDA reports)
OVARIAN CYST ( 35 FDA reports)
SKIN DISCOLOURATION ( 35 FDA reports)
VAGINAL HAEMORRHAGE ( 35 FDA reports)
ABDOMINAL TENDERNESS ( 34 FDA reports)
APHASIA ( 34 FDA reports)
DIVERTICULUM ( 34 FDA reports)
FIBROMYALGIA ( 34 FDA reports)
GASTRIC DISORDER ( 34 FDA reports)
HEPATIC FAILURE ( 34 FDA reports)
HERPES SIMPLEX ( 34 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 34 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 34 FDA reports)
LIVER DISORDER ( 34 FDA reports)
LUNG INFILTRATION ( 34 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 34 FDA reports)
NIGHT SWEATS ( 34 FDA reports)
ORAL PAIN ( 34 FDA reports)
OXYGEN SATURATION DECREASED ( 34 FDA reports)
PSORIASIS ( 34 FDA reports)
PSYCHOTIC DISORDER ( 34 FDA reports)
RENAL PAIN ( 34 FDA reports)
SINUS BRADYCARDIA ( 34 FDA reports)
TENSION ( 34 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 33 FDA reports)
CHROMATURIA ( 33 FDA reports)
EYELID OEDEMA ( 33 FDA reports)
HEPATOTOXICITY ( 33 FDA reports)
HYPERGLYCAEMIA ( 33 FDA reports)
MEDICATION ERROR ( 33 FDA reports)
MENORRHAGIA ( 33 FDA reports)
MENTAL STATUS CHANGES ( 33 FDA reports)
MOBILITY DECREASED ( 33 FDA reports)
NOCTURIA ( 33 FDA reports)
PNEUMONITIS ( 33 FDA reports)
RASH ERYTHEMATOUS ( 33 FDA reports)
VENTRICULAR TACHYCARDIA ( 33 FDA reports)
COAGULOPATHY ( 32 FDA reports)
IMPAIRED HEALING ( 32 FDA reports)
INJECTION SITE REACTION ( 32 FDA reports)
MUSCLE TWITCHING ( 32 FDA reports)
RENAL TUBULAR NECROSIS ( 32 FDA reports)
THYROID DISORDER ( 32 FDA reports)
AFFECT LABILITY ( 31 FDA reports)
CAROTID ARTERY STENOSIS ( 31 FDA reports)
ENCEPHALOPATHY ( 31 FDA reports)
LUMBAR RADICULOPATHY ( 31 FDA reports)
MULTI-ORGAN FAILURE ( 31 FDA reports)
PHARYNGITIS ( 31 FDA reports)
POLYP ( 31 FDA reports)
SCIATICA ( 31 FDA reports)
WHEEZING ( 31 FDA reports)
AGEUSIA ( 30 FDA reports)
APHTHOUS STOMATITIS ( 30 FDA reports)
HAEMOPTYSIS ( 30 FDA reports)
HEART RATE IRREGULAR ( 30 FDA reports)
MALNUTRITION ( 30 FDA reports)
NIGHTMARE ( 30 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 30 FDA reports)
POLLAKIURIA ( 30 FDA reports)
SINUS DISORDER ( 30 FDA reports)
TOOTH ABSCESS ( 30 FDA reports)
URINARY INCONTINENCE ( 30 FDA reports)
ACCIDENTAL OVERDOSE ( 29 FDA reports)
ATRIAL SEPTAL DEFECT ( 29 FDA reports)
BACK DISORDER ( 29 FDA reports)
BLOOD UREA INCREASED ( 29 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 29 FDA reports)
COMA ( 29 FDA reports)
DENTAL CARIES ( 29 FDA reports)
DERMATITIS ( 29 FDA reports)
EYE DISORDER ( 29 FDA reports)
GASTROENTERITIS ( 29 FDA reports)
HEPATOMEGALY ( 29 FDA reports)
JOINT INJURY ( 29 FDA reports)
MASS ( 29 FDA reports)
METABOLIC ACIDOSIS ( 29 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 29 FDA reports)
PLEURITIC PAIN ( 29 FDA reports)
PNEUMOTHORAX ( 29 FDA reports)
PRURITUS GENERALISED ( 29 FDA reports)
RASH MACULAR ( 29 FDA reports)
RESTLESSNESS ( 29 FDA reports)
TACHYPNOEA ( 29 FDA reports)
ARTERIOSCLEROSIS ( 28 FDA reports)
BLOOD GLUCOSE DECREASED ( 28 FDA reports)
BREAST CYST ( 28 FDA reports)
DECREASED INTEREST ( 28 FDA reports)
DIALYSIS ( 28 FDA reports)
ECCHYMOSIS ( 28 FDA reports)
ECZEMA ( 28 FDA reports)
FEBRILE NEUTROPENIA ( 28 FDA reports)
LACRIMATION INCREASED ( 28 FDA reports)
MENINGIOMA ( 28 FDA reports)
PARAESTHESIA ORAL ( 28 FDA reports)
PARALYSIS ( 28 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 28 FDA reports)
RESPIRATORY DISORDER ( 28 FDA reports)
SPINAL COMPRESSION FRACTURE ( 28 FDA reports)
ACUTE SINUSITIS ( 27 FDA reports)
BLOOD SODIUM DECREASED ( 27 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 27 FDA reports)
FEELING JITTERY ( 27 FDA reports)
FLUID RETENTION ( 27 FDA reports)
GLOSSODYNIA ( 27 FDA reports)
HYPERCOAGULATION ( 27 FDA reports)
LOBAR PNEUMONIA ( 27 FDA reports)
LUNG NEOPLASM ( 27 FDA reports)
NERVOUS SYSTEM DISORDER ( 27 FDA reports)
ORTHOSTATIC HYPOTENSION ( 27 FDA reports)
PANCREATITIS ACUTE ( 27 FDA reports)
POST PROCEDURAL COMPLICATION ( 27 FDA reports)
RENAL IMPAIRMENT ( 27 FDA reports)
SKIN DISORDER ( 27 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 27 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 27 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 26 FDA reports)
BACTERIAL INFECTION ( 26 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 26 FDA reports)
COGNITIVE DISORDER ( 26 FDA reports)
DRUG DOSE OMISSION ( 26 FDA reports)
FEELING COLD ( 26 FDA reports)
FUNGAL INFECTION ( 26 FDA reports)
HALLUCINATION ( 26 FDA reports)
IMPAIRED WORK ABILITY ( 26 FDA reports)
LACUNAR INFARCTION ( 26 FDA reports)
PROTHROMBIN TIME PROLONGED ( 26 FDA reports)
SURGERY ( 26 FDA reports)
TONGUE DISORDER ( 26 FDA reports)
ANAPHYLACTIC SHOCK ( 25 FDA reports)
DILATATION ATRIAL ( 25 FDA reports)
INJECTION SITE HAEMATOMA ( 25 FDA reports)
INJECTION SITE HAEMORRHAGE ( 25 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 25 FDA reports)
MASTICATION DISORDER ( 25 FDA reports)
MOOD SWINGS ( 25 FDA reports)
NON-CARDIAC CHEST PAIN ( 25 FDA reports)
ORAL DISCOMFORT ( 25 FDA reports)
PULMONARY HYPERTENSION ( 25 FDA reports)
RASH PAPULAR ( 25 FDA reports)
RESTLESS LEGS SYNDROME ( 25 FDA reports)
STENT OCCLUSION ( 25 FDA reports)
TENDERNESS ( 25 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 24 FDA reports)
ANAL FISTULA ( 24 FDA reports)
CARDIAC FAILURE ( 24 FDA reports)
DEFORMITY ( 24 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 24 FDA reports)
DIFFICULTY IN WALKING ( 24 FDA reports)
DISABILITY ( 24 FDA reports)
DYSKINESIA ( 24 FDA reports)
DYSPHONIA ( 24 FDA reports)
DYSSTASIA ( 24 FDA reports)
ERECTILE DYSFUNCTION ( 24 FDA reports)
ERYTHEMA MULTIFORME ( 24 FDA reports)
GLAUCOMA ( 24 FDA reports)
LOOSE TOOTH ( 24 FDA reports)
OROPHARYNGEAL PAIN ( 24 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 24 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 24 FDA reports)
RASH MACULO-PAPULAR ( 24 FDA reports)
THROAT TIGHTNESS ( 24 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 23 FDA reports)
CYANOSIS ( 23 FDA reports)
INTENTIONAL DRUG MISUSE ( 23 FDA reports)
INTESTINAL OBSTRUCTION ( 23 FDA reports)
METRORRHAGIA ( 23 FDA reports)
NASAL CONGESTION ( 23 FDA reports)
PALLOR ( 23 FDA reports)
PULMONARY INFARCTION ( 23 FDA reports)
RESPIRATORY ARREST ( 23 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 23 FDA reports)
SYNOVIAL CYST ( 23 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 23 FDA reports)
ACOUSTIC NEUROMA ( 22 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 22 FDA reports)
BLISTER ( 22 FDA reports)
CHANGE OF BOWEL HABIT ( 22 FDA reports)
COELIAC DISEASE ( 22 FDA reports)
ENDODONTIC PROCEDURE ( 22 FDA reports)
EYE HAEMORRHAGE ( 22 FDA reports)
FOOT FRACTURE ( 22 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 22 FDA reports)
GOUT ( 22 FDA reports)
HYPOPHAGIA ( 22 FDA reports)
HYPOVOLAEMIA ( 22 FDA reports)
MAJOR DEPRESSION ( 22 FDA reports)
METASTASES TO LIVER ( 22 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 22 FDA reports)
PLATELET DISORDER ( 22 FDA reports)
VASCULITIS ( 22 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 22 FDA reports)
ACCIDENTAL EXPOSURE ( 21 FDA reports)
ANXIETY DISORDER ( 21 FDA reports)
BLINDNESS ( 21 FDA reports)
BLOOD POTASSIUM INCREASED ( 21 FDA reports)
CALCULUS URETERIC ( 21 FDA reports)
CHOLESTASIS ( 21 FDA reports)
COMPLETED SUICIDE ( 21 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 21 FDA reports)
EJECTION FRACTION DECREASED ( 21 FDA reports)
ERUCTATION ( 21 FDA reports)
HALLUCINATION, VISUAL ( 21 FDA reports)
HYPERTHYROIDISM ( 21 FDA reports)
IMPAIRED DRIVING ABILITY ( 21 FDA reports)
INFUSION RELATED REACTION ( 21 FDA reports)
ISCHAEMIC STROKE ( 21 FDA reports)
LACERATION ( 21 FDA reports)
LIMB INJURY ( 21 FDA reports)
MOOD ALTERED ( 21 FDA reports)
MOUTH HAEMORRHAGE ( 21 FDA reports)
MUSCLE CRAMP ( 21 FDA reports)
ORAL INFECTION ( 21 FDA reports)
OTITIS MEDIA ( 21 FDA reports)
PAIN OF SKIN ( 21 FDA reports)
PRODUCTIVE COUGH ( 21 FDA reports)
PURPURA ( 21 FDA reports)
RHABDOMYOLYSIS ( 21 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 21 FDA reports)
UNEVALUABLE EVENT ( 21 FDA reports)
VIRAL PHARYNGITIS ( 21 FDA reports)
ABDOMINAL PAIN LOWER ( 20 FDA reports)
BILIARY DYSKINESIA ( 20 FDA reports)
BLINDNESS UNILATERAL ( 20 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 20 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 20 FDA reports)
CALCULUS URINARY ( 20 FDA reports)
CHRONIC SINUSITIS ( 20 FDA reports)
CONJUNCTIVITIS ( 20 FDA reports)
DEAFNESS ( 20 FDA reports)
DEBRIDEMENT ( 20 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 20 FDA reports)
DUODENAL ULCER ( 20 FDA reports)
ECONOMIC PROBLEM ( 20 FDA reports)
FELTY'S SYNDROME ( 20 FDA reports)
HAEMATOMA ( 20 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 20 FDA reports)
HYPERTONIC BLADDER ( 20 FDA reports)
LABORATORY TEST ABNORMAL ( 20 FDA reports)
LARYNGITIS ( 20 FDA reports)
LIBIDO DECREASED ( 20 FDA reports)
LIPOMA ( 20 FDA reports)
MIDDLE INSOMNIA ( 20 FDA reports)
MYOPIA ( 20 FDA reports)
OTITIS EXTERNA ( 20 FDA reports)
PELVIC PAIN ( 20 FDA reports)
PHOTOSENSITIVITY REACTION ( 20 FDA reports)
PNEUMONIA INFLUENZAL ( 20 FDA reports)
PROSTATITIS ( 20 FDA reports)
RESPIRATORY TRACT INFECTION ( 20 FDA reports)
SKIN LACERATION ( 20 FDA reports)
SKIN LESION ( 20 FDA reports)
SNEEZING ( 20 FDA reports)
TOOTH LOSS ( 20 FDA reports)
TOOTHACHE ( 20 FDA reports)
ULCER ( 20 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 20 FDA reports)
URTICARIA GENERALISED ( 20 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 20 FDA reports)
WOUND DEHISCENCE ( 20 FDA reports)
AORTIC ANEURYSM ( 19 FDA reports)
BLINDNESS TRANSIENT ( 19 FDA reports)
BLOOD ALBUMIN DECREASED ( 19 FDA reports)
BONE DEBRIDEMENT ( 19 FDA reports)
CEREBRAL HAEMORRHAGE ( 19 FDA reports)
CHEILITIS ( 19 FDA reports)
DELIRIUM ( 19 FDA reports)
DRY EYE ( 19 FDA reports)
GINGIVAL PAIN ( 19 FDA reports)
GRAND MAL CONVULSION ( 19 FDA reports)
HELICOBACTER INFECTION ( 19 FDA reports)
HEPATITIS CHOLESTATIC ( 19 FDA reports)
HYPERTHERMIA ( 19 FDA reports)
HYPOGLYCAEMIA ( 19 FDA reports)
KERATITIS HERPETIC ( 19 FDA reports)
MENSTRUATION IRREGULAR ( 19 FDA reports)
NECK INJURY ( 19 FDA reports)
NYSTAGMUS ( 19 FDA reports)
PETECHIAE ( 19 FDA reports)
PLEURISY ( 19 FDA reports)
RHINITIS ( 19 FDA reports)
SEPTIC SHOCK ( 19 FDA reports)
SNORING ( 19 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 19 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 19 FDA reports)
THINKING ABNORMAL ( 19 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 19 FDA reports)
ABNORMAL DREAMS ( 18 FDA reports)
AZOTAEMIA ( 18 FDA reports)
BLADDER DISORDER ( 18 FDA reports)
BLOOD URINE PRESENT ( 18 FDA reports)
CAESAREAN SECTION ( 18 FDA reports)
CEREBRAL ISCHAEMIA ( 18 FDA reports)
CYST ( 18 FDA reports)
DEVELOPMENTAL DELAY ( 18 FDA reports)
DISCOMFORT ( 18 FDA reports)
DRUG INTOLERANCE ( 18 FDA reports)
DYSPAREUNIA ( 18 FDA reports)
EPICONDYLITIS ( 18 FDA reports)
GASTRIC HAEMORRHAGE ( 18 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 18 FDA reports)
IRON DEFICIENCY ANAEMIA ( 18 FDA reports)
NERVE INJURY ( 18 FDA reports)
OESOPHAGEAL DISORDER ( 18 FDA reports)
PATHOLOGICAL GAMBLING ( 18 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 18 FDA reports)
POLYURIA ( 18 FDA reports)
PROCEDURAL PAIN ( 18 FDA reports)
RALES ( 18 FDA reports)
SINUS CONGESTION ( 18 FDA reports)
SPINAL COLUMN STENOSIS ( 18 FDA reports)
TOOTH FRACTURE ( 18 FDA reports)
TRIGGER FINGER ( 18 FDA reports)
VENTRICULAR FIBRILLATION ( 18 FDA reports)
ACUTE CORONARY SYNDROME ( 17 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 17 FDA reports)
BLOOD CALCIUM DECREASED ( 17 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 17 FDA reports)
CHOLECYSTECTOMY ( 17 FDA reports)
CHOLECYSTITIS ACUTE ( 17 FDA reports)
DILATATION VENTRICULAR ( 17 FDA reports)
DYSLIPIDAEMIA ( 17 FDA reports)
EAR INFECTION ( 17 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 17 FDA reports)
EPISCLERITIS ( 17 FDA reports)
EUPHORIC MOOD ( 17 FDA reports)
HEART DISEASE CONGENITAL ( 17 FDA reports)
HYPOMAGNESAEMIA ( 17 FDA reports)
IMMUNE SYSTEM DISORDER ( 17 FDA reports)
IMMUNOGLOBULINS DECREASED ( 17 FDA reports)
INGUINAL HERNIA ( 17 FDA reports)
JOINT SPRAIN ( 17 FDA reports)
KERATITIS ( 17 FDA reports)
LARYNGITIS VIRAL ( 17 FDA reports)
LUMBAR SPINAL STENOSIS ( 17 FDA reports)
LYMPHOMA ( 17 FDA reports)
MOUTH INJURY ( 17 FDA reports)
MUSCLE TIGHTNESS ( 17 FDA reports)
NEURALGIA ( 17 FDA reports)
PARONYCHIA ( 17 FDA reports)
POLYTRAUMATISM ( 17 FDA reports)
PROSTATE CANCER ( 17 FDA reports)
PULMONARY CONGESTION ( 17 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 17 FDA reports)
RESPIRATORY RATE INCREASED ( 17 FDA reports)
ANURIA ( 16 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 16 FDA reports)
BARRETT'S OESOPHAGUS ( 16 FDA reports)
BRAIN DAMAGE ( 16 FDA reports)
BREAST CANCER METASTATIC ( 16 FDA reports)
CARDIO-RESPIRATORY ARREST ( 16 FDA reports)
COLLAPSE OF LUNG ( 16 FDA reports)
DISEASE RECURRENCE ( 16 FDA reports)
EATING DISORDER ( 16 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 16 FDA reports)
GASTROENTERITIS VIRAL ( 16 FDA reports)
GRANULOMA ( 16 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 16 FDA reports)
HIP ARTHROPLASTY ( 16 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 16 FDA reports)
HYPOTHERMIA ( 16 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 16 FDA reports)
MOVEMENT DISORDER ( 16 FDA reports)
MULTIPLE DRUG OVERDOSE ( 16 FDA reports)
OBESITY ( 16 FDA reports)
OPTIC NEURITIS ( 16 FDA reports)
PROTEINURIA ( 16 FDA reports)
RETCHING ( 16 FDA reports)
RHINITIS ALLERGIC ( 16 FDA reports)
SCOLIOSIS ( 16 FDA reports)
SEDATION ( 16 FDA reports)
SELF-MEDICATION ( 16 FDA reports)
SKIN BURNING SENSATION ( 16 FDA reports)
STREPTOCOCCAL INFECTION ( 16 FDA reports)
THIRST ( 16 FDA reports)
TONGUE ULCERATION ( 16 FDA reports)
ACNE ( 15 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 15 FDA reports)
BILIARY COLIC ( 15 FDA reports)
BONE SCAN ABNORMAL ( 15 FDA reports)
BREAST CANCER IN SITU ( 15 FDA reports)
CANDIDIASIS ( 15 FDA reports)
CEREBRAL ATROPHY ( 15 FDA reports)
CHEST X-RAY ABNORMAL ( 15 FDA reports)
CHOKING ( 15 FDA reports)
COORDINATION ABNORMAL ( 15 FDA reports)
DERMATITIS EXFOLIATIVE ( 15 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 15 FDA reports)
DRUG ABUSER ( 15 FDA reports)
EMPHYSEMA ( 15 FDA reports)
FACIAL PALSY ( 15 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 15 FDA reports)
FOREIGN BODY ( 15 FDA reports)
GASTRITIS ATROPHIC ( 15 FDA reports)
GASTROINTESTINAL INFECTION ( 15 FDA reports)
GENERALISED OEDEMA ( 15 FDA reports)
LARYNGEAL OEDEMA ( 15 FDA reports)
NEUROTOXICITY ( 15 FDA reports)
ORAL INTAKE REDUCED ( 15 FDA reports)
OSTEOLYSIS ( 15 FDA reports)
PEPTIC ULCER ( 15 FDA reports)
REFLUX OESOPHAGITIS ( 15 FDA reports)
SEBORRHOEIC KERATOSIS ( 15 FDA reports)
SENSATION OF FOREIGN BODY ( 15 FDA reports)
SENSORY DISTURBANCE ( 15 FDA reports)
SPINAL DISORDER ( 15 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 15 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 15 FDA reports)
UNRESPONSIVE TO STIMULI ( 15 FDA reports)
URINE OUTPUT DECREASED ( 15 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 14 FDA reports)
ACTINOMYCOSIS ( 14 FDA reports)
ANGIOPATHY ( 14 FDA reports)
APNOEA ( 14 FDA reports)
BLOOD CULTURE POSITIVE ( 14 FDA reports)
BODY HEIGHT DECREASED ( 14 FDA reports)
BRAIN OEDEMA ( 14 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 14 FDA reports)
DUODENITIS ( 14 FDA reports)
ENTERITIS ( 14 FDA reports)
EYELID PTOSIS ( 14 FDA reports)
FACTOR V LEIDEN MUTATION ( 14 FDA reports)
FAECAL INCONTINENCE ( 14 FDA reports)
FLANK PAIN ( 14 FDA reports)
GENERALISED ERYTHEMA ( 14 FDA reports)
GINGIVAL BLEEDING ( 14 FDA reports)
HEARING IMPAIRED ( 14 FDA reports)
HEART RATE DECREASED ( 14 FDA reports)
HYPERKERATOSIS ( 14 FDA reports)
HYPERTENSIVE CRISIS ( 14 FDA reports)
HYSTERECTOMY ( 14 FDA reports)
ILEUS ( 14 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 14 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 14 FDA reports)
ISCHAEMIA ( 14 FDA reports)
JAW OPERATION ( 14 FDA reports)
LEARNING DISORDER ( 14 FDA reports)
LIPASE INCREASED ( 14 FDA reports)
LUNG NEOPLASM MALIGNANT ( 14 FDA reports)
METASTASES TO SPINE ( 14 FDA reports)
MICTURITION URGENCY ( 14 FDA reports)
NEUROLOGICAL SYMPTOM ( 14 FDA reports)
NO ADVERSE EVENT ( 14 FDA reports)
PERICARDIAL EFFUSION ( 14 FDA reports)
PERSONALITY CHANGE ( 14 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 14 FDA reports)
TRANSAMINASES INCREASED ( 14 FDA reports)
VENTRICULAR HYPOKINESIA ( 14 FDA reports)
VESTIBULAR DISORDER ( 14 FDA reports)
ABSCESS LIMB ( 13 FDA reports)
ANKLE FRACTURE ( 13 FDA reports)
ARTERIOVENOUS FISTULA, ACQUIRED ( 13 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 13 FDA reports)
BLOOD CHLORIDE DECREASED ( 13 FDA reports)
BURSITIS ( 13 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 13 FDA reports)
COSTOCHONDRITIS ( 13 FDA reports)
DERMATITIS BULLOUS ( 13 FDA reports)
DRUG SCREEN POSITIVE ( 13 FDA reports)
DYSGRAPHIA ( 13 FDA reports)
EAR DISORDER ( 13 FDA reports)
ENTEROCOCCAL INFECTION ( 13 FDA reports)
EXOSTOSIS ( 13 FDA reports)
FACIAL BONES FRACTURE ( 13 FDA reports)
FLUID OVERLOAD ( 13 FDA reports)
GINGIVAL RECESSION ( 13 FDA reports)
HEPATIC NECROSIS ( 13 FDA reports)
HYPERKALAEMIA ( 13 FDA reports)
HYPOACUSIS ( 13 FDA reports)
INCONTINENCE ( 13 FDA reports)
INTENTIONAL MISUSE ( 13 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 13 FDA reports)
MUSCLE STRAIN ( 13 FDA reports)
NEUROPATHY ( 13 FDA reports)
ONYCHOMYCOSIS ( 13 FDA reports)
PAROTITIS ( 13 FDA reports)
PERICARDITIS ( 13 FDA reports)
PERITONITIS ( 13 FDA reports)
PERSISTENT FOETAL CIRCULATION ( 13 FDA reports)
PHONOPHOBIA ( 13 FDA reports)
PILONIDAL CYST ( 13 FDA reports)
POLYMYALGIA RHEUMATICA ( 13 FDA reports)
PULMONARY VASCULAR DISORDER ( 13 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 13 FDA reports)
SALIVARY HYPERSECRETION ( 13 FDA reports)
SHOCK ( 13 FDA reports)
SPLENOMEGALY ( 13 FDA reports)
TRISMUS ( 13 FDA reports)
UTERINE LEIOMYOMA ( 13 FDA reports)
VENTRICULAR DYSFUNCTION ( 13 FDA reports)
VITREOUS FLOATERS ( 13 FDA reports)
ADVERSE DRUG REACTION ( 12 FDA reports)
ALLERGY TO CHEMICALS ( 12 FDA reports)
ANOSMIA ( 12 FDA reports)
ARTHROPOD STING ( 12 FDA reports)
ATAXIA ( 12 FDA reports)
ATHEROSCLEROSIS ( 12 FDA reports)
ATRIAL FLUTTER ( 12 FDA reports)
BLOOD CALCIUM INCREASED ( 12 FDA reports)
BONE LESION ( 12 FDA reports)
BONE MARROW FAILURE ( 12 FDA reports)
BREAST MASS ( 12 FDA reports)
BREAST TENDERNESS ( 12 FDA reports)
BRONCHOSPASM ( 12 FDA reports)
CHORIORETINOPATHY ( 12 FDA reports)
CIRCULATORY COLLAPSE ( 12 FDA reports)
CLOSTRIDIAL INFECTION ( 12 FDA reports)
DECUBITUS ULCER ( 12 FDA reports)
DRUG TOLERANCE ( 12 FDA reports)
EYE PRURITUS ( 12 FDA reports)
FACIAL PAIN ( 12 FDA reports)
FEEDING DISORDER ( 12 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 12 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 12 FDA reports)
HAIR PLUCKING ( 12 FDA reports)
HALLUCINATION, AUDITORY ( 12 FDA reports)
HERPES VIRUS INFECTION ( 12 FDA reports)
HYPOAESTHESIA FACIAL ( 12 FDA reports)
IMPULSIVE BEHAVIOUR ( 12 FDA reports)
INJECTION SITE RASH ( 12 FDA reports)
INJECTION SITE SWELLING ( 12 FDA reports)
INNER EAR DISORDER ( 12 FDA reports)
LABYRINTHITIS ( 12 FDA reports)
LOCALISED INFECTION ( 12 FDA reports)
LYMPHADENITIS ( 12 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 12 FDA reports)
METASTASIS ( 12 FDA reports)
NEOPLASM MALIGNANT ( 12 FDA reports)
NEUTROPHIL COUNT DECREASED ( 12 FDA reports)
NEUTROPHIL COUNT INCREASED ( 12 FDA reports)
OCULAR HYPERAEMIA ( 12 FDA reports)
OEDEMA MOUTH ( 12 FDA reports)
OPEN WOUND ( 12 FDA reports)
OSTEOPENIA ( 12 FDA reports)
OSTEOSCLEROSIS ( 12 FDA reports)
PLATELET AGGREGATION INCREASED ( 12 FDA reports)
POLYARTHRITIS ( 12 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 12 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 12 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 12 FDA reports)
PURULENCE ( 12 FDA reports)
RETINAL VEIN OCCLUSION ( 12 FDA reports)
SINUS ARRHYTHMIA ( 12 FDA reports)
TESTICULAR PAIN ( 12 FDA reports)
THERAPY NON-RESPONDER ( 12 FDA reports)
TOOTH INFECTION ( 12 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 12 FDA reports)
VERTEBROPLASTY ( 12 FDA reports)
WEIGHT FLUCTUATION ( 12 FDA reports)
ABDOMINAL ADHESIONS ( 11 FDA reports)
ABORTION SPONTANEOUS ( 11 FDA reports)
ACIDOSIS ( 11 FDA reports)
ADJUSTMENT DISORDER WITH DEPRESSED MOOD ( 11 FDA reports)
ATRIOVENTRICULAR BLOCK ( 11 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 11 FDA reports)
AUTOIMMUNE HEPATITIS ( 11 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 11 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 11 FDA reports)
BONE DENSITY DECREASED ( 11 FDA reports)
BONE NEOPLASM MALIGNANT ( 11 FDA reports)
BREATH SOUNDS ABNORMAL ( 11 FDA reports)
CAROTID ARTERY DISEASE ( 11 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 11 FDA reports)
CHOLANGITIS SCLEROSING ( 11 FDA reports)
COLITIS ISCHAEMIC ( 11 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 11 FDA reports)
EPIGASTRIC DISCOMFORT ( 11 FDA reports)
EXCORIATION ( 11 FDA reports)
EXTRASYSTOLES ( 11 FDA reports)
EYE OPERATION ( 11 FDA reports)
GINGIVAL ULCERATION ( 11 FDA reports)
HYPERGAMMAGLOBULINAEMIA BENIGN MONOCLONAL ( 11 FDA reports)
HYPOVENTILATION ( 11 FDA reports)
IMMUNOSUPPRESSION ( 11 FDA reports)
INCREASED TENDENCY TO BRUISE ( 11 FDA reports)
INJECTION SITE BRUISING ( 11 FDA reports)
JAW DISORDER ( 11 FDA reports)
KIDNEY INFECTION ( 11 FDA reports)
KNEE ARTHROPLASTY ( 11 FDA reports)
LIGAMENT SPRAIN ( 11 FDA reports)
LIVER INJURY ( 11 FDA reports)
LOCAL SWELLING ( 11 FDA reports)
LYMPHOPENIA ( 11 FDA reports)
MITRAL VALVE CALCIFICATION ( 11 FDA reports)
MUCOSAL INFLAMMATION ( 11 FDA reports)
MULTIPLE MYELOMA ( 11 FDA reports)
MUSCULOSKELETAL DISORDER ( 11 FDA reports)
NEPHRITIS INTERSTITIAL ( 11 FDA reports)
NEPHROPATHY TOXIC ( 11 FDA reports)
OCULAR ICTERUS ( 11 FDA reports)
ORAL CANDIDIASIS ( 11 FDA reports)
ORAL HERPES ( 11 FDA reports)
OROPHARYNGEAL SWELLING ( 11 FDA reports)
PARANOIA ( 11 FDA reports)
PERIORBITAL OEDEMA ( 11 FDA reports)
PURULENT DISCHARGE ( 11 FDA reports)
PYELONEPHRITIS ( 11 FDA reports)
PYODERMA GANGRENOSUM ( 11 FDA reports)
RADICULOPATHY ( 11 FDA reports)
RADIUS FRACTURE ( 11 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 11 FDA reports)
RENAL ARTERY STENOSIS ( 11 FDA reports)
RENAL TUBULAR DISORDER ( 11 FDA reports)
ROSACEA ( 11 FDA reports)
SEXUAL DYSFUNCTION ( 11 FDA reports)
SINUS POLYP ( 11 FDA reports)
SKIN FISSURES ( 11 FDA reports)
SKIN WARM ( 11 FDA reports)
SPONDYLITIS ( 11 FDA reports)
TEARFULNESS ( 11 FDA reports)
VASCULAR PSEUDOANEURYSM ( 11 FDA reports)
VITAMIN D DEFICIENCY ( 11 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 10 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 10 FDA reports)
BILE DUCT STONE ( 10 FDA reports)
BIPOLAR DISORDER ( 10 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 10 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 10 FDA reports)
CALCULUS BLADDER ( 10 FDA reports)
CERUMEN IMPACTION ( 10 FDA reports)
CHOLANGITIS ( 10 FDA reports)
CHRONIC FATIGUE SYNDROME ( 10 FDA reports)
CONCUSSION ( 10 FDA reports)
CULTURE URINE POSITIVE ( 10 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 10 FDA reports)
DENTAL DISCOMFORT ( 10 FDA reports)
DEPENDENCE ( 10 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 10 FDA reports)
DRUG LEVEL INCREASED ( 10 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 10 FDA reports)
EMPYEMA ( 10 FDA reports)
EYE INFECTION ( 10 FDA reports)
GINGIVAL INFECTION ( 10 FDA reports)
HAEMODYNAMIC INSTABILITY ( 10 FDA reports)
HEPATOCELLULAR DAMAGE ( 10 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 10 FDA reports)
HYPERSOMNIA ( 10 FDA reports)
INADEQUATE ANALGESIA ( 10 FDA reports)
INCOHERENT ( 10 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 10 FDA reports)
INTRACARDIAC THROMBUS ( 10 FDA reports)
KNEE OPERATION ( 10 FDA reports)
LACTIC ACIDOSIS ( 10 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 10 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 10 FDA reports)
MYOCARDITIS ( 10 FDA reports)
MYOSITIS ( 10 FDA reports)
NEURODERMATITIS ( 10 FDA reports)
OPEN REDUCTION OF FRACTURE ( 10 FDA reports)
PATHOLOGICAL FRACTURE ( 10 FDA reports)
PERIPHERAL COLDNESS ( 10 FDA reports)
PHOTOPSIA ( 10 FDA reports)
PLANTAR FASCIITIS ( 10 FDA reports)
PREGNANCY ( 10 FDA reports)
PRESCRIBED OVERDOSE ( 10 FDA reports)
RASH VESICULAR ( 10 FDA reports)
RETINAL DETACHMENT ( 10 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 10 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 10 FDA reports)
SEQUESTRECTOMY ( 10 FDA reports)
STENT PLACEMENT ( 10 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 10 FDA reports)
SUDDEN DEATH ( 10 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 10 FDA reports)
VARICELLA ( 10 FDA reports)
VARICOSE VEIN ( 10 FDA reports)
VITAMIN B12 DEFICIENCY ( 10 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 10 FDA reports)
YAWNING ( 10 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 9 FDA reports)
ALCOHOL USE ( 9 FDA reports)
AMENORRHOEA ( 9 FDA reports)
ANAL ABSCESS ( 9 FDA reports)
ANAL FISSURE ( 9 FDA reports)
ANGIOEDEMA ( 9 FDA reports)
ANTIBODY TEST POSITIVE ( 9 FDA reports)
AORTIC VALVE SCLEROSIS ( 9 FDA reports)
APHAGIA ( 9 FDA reports)
APPETITE DISORDER ( 9 FDA reports)
ARTHRITIS BACTERIAL ( 9 FDA reports)
BASEDOW'S DISEASE ( 9 FDA reports)
BENIGN BREAST NEOPLASM ( 9 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 9 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 9 FDA reports)
BRONCHITIS ACUTE ( 9 FDA reports)
CARCINOMA IN SITU OF SKIN ( 9 FDA reports)
CARDIOGENIC SHOCK ( 9 FDA reports)
CARTILAGE INJURY ( 9 FDA reports)
COMPLEX PARTIAL SEIZURES ( 9 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 9 FDA reports)
DEAFNESS NEUROSENSORY ( 9 FDA reports)
DEFAECATION URGENCY ( 9 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 9 FDA reports)
DIASTOLIC DYSFUNCTION ( 9 FDA reports)
EARLY SATIETY ( 9 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 9 FDA reports)
ENTEROCELE ( 9 FDA reports)
EOSINOPHIL COUNT INCREASED ( 9 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 9 FDA reports)
EYE IRRITATION ( 9 FDA reports)
FEMUR FRACTURE ( 9 FDA reports)
FISTULA ( 9 FDA reports)
FRACTURE ( 9 FDA reports)
GASTRITIS EROSIVE ( 9 FDA reports)
GASTROINTESTINAL INJURY ( 9 FDA reports)
GINGIVITIS ( 9 FDA reports)
GROIN PAIN ( 9 FDA reports)
HEMIPLEGIA ( 9 FDA reports)
INITIAL INSOMNIA ( 9 FDA reports)
INJECTION SITE MASS ( 9 FDA reports)
INTERSTITIAL LUNG DISEASE ( 9 FDA reports)
INTESTINAL PERFORATION ( 9 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 9 FDA reports)
JOINT STIFFNESS ( 9 FDA reports)
LIFE EXPECTANCY SHORTENED ( 9 FDA reports)
LIMB DISCOMFORT ( 9 FDA reports)
LOCALISED OSTEOARTHRITIS ( 9 FDA reports)
MACULAR DEGENERATION ( 9 FDA reports)
METASTATIC NEOPLASM ( 9 FDA reports)
MITRAL VALVE PROLAPSE ( 9 FDA reports)
MUCOUS MEMBRANE DISORDER ( 9 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 9 FDA reports)
MUSCLE ATROPHY ( 9 FDA reports)
NASAL CYST ( 9 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 9 FDA reports)
ORAL FUNGAL INFECTION ( 9 FDA reports)
ORAL SURGERY ( 9 FDA reports)
PANCREATITIS CHRONIC ( 9 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 9 FDA reports)
PNEUMONIA ASPIRATION ( 9 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 9 FDA reports)
POSTOPERATIVE ADHESION ( 9 FDA reports)
PRODUCT LABEL ISSUE ( 9 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 9 FDA reports)
PSEUDOMONAS INFECTION ( 9 FDA reports)
PULMONARY ARTERY STENOSIS ( 9 FDA reports)
PULSE ABSENT ( 9 FDA reports)
PYELOCALIECTASIS ( 9 FDA reports)
RASH SCARLATINIFORM ( 9 FDA reports)
SHOULDER OPERATION ( 9 FDA reports)
SHOULDER PAIN ( 9 FDA reports)
SKIN ATROPHY ( 9 FDA reports)
SKIN IRRITATION ( 9 FDA reports)
SKIN PLAQUE ( 9 FDA reports)
SKIN ULCER ( 9 FDA reports)
SOFT TISSUE DISORDER ( 9 FDA reports)
SPINAL CORD COMPRESSION ( 9 FDA reports)
SPINAL FUSION SURGERY ( 9 FDA reports)
SPUTUM PURULENT ( 9 FDA reports)
SUBCUTANEOUS ABSCESS ( 9 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 9 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 9 FDA reports)
TONSILLITIS ( 9 FDA reports)
TOOTH DEPOSIT ( 9 FDA reports)
ULNA FRACTURE ( 9 FDA reports)
UTERINE HAEMORRHAGE ( 9 FDA reports)
VEIN DISORDER ( 9 FDA reports)
WISDOM TEETH REMOVAL ( 9 FDA reports)
ACUTE RESPIRATORY FAILURE ( 8 FDA reports)
ADJUSTMENT DISORDER ( 8 FDA reports)
AFFECTIVE DISORDER ( 8 FDA reports)
AGRANULOCYTOSIS ( 8 FDA reports)
ANGIONEUROTIC OEDEMA ( 8 FDA reports)
APATHY ( 8 FDA reports)
APPENDICITIS ( 8 FDA reports)
ASPIRATION ( 8 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 8 FDA reports)
AUTOIMMUNE DISORDER ( 8 FDA reports)
BACTERIAL SEPSIS ( 8 FDA reports)
BEDRIDDEN ( 8 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 8 FDA reports)
BLADDER DYSFUNCTION ( 8 FDA reports)
BLOOD ALBUMIN INCREASED ( 8 FDA reports)
BLOOD PRESSURE ABNORMAL ( 8 FDA reports)
BONE FORMATION INCREASED ( 8 FDA reports)
BREAST CANCER FEMALE ( 8 FDA reports)
BREAST PAIN ( 8 FDA reports)
CALCINOSIS ( 8 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 8 FDA reports)
CEREBROVASCULAR DISORDER ( 8 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 8 FDA reports)
CLOSED HEAD INJURY ( 8 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 8 FDA reports)
COLD SWEAT ( 8 FDA reports)
COLON CANCER ( 8 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 8 FDA reports)
DENTURE WEARER ( 8 FDA reports)
DIABETIC KETOACIDOSIS ( 8 FDA reports)
DIVERTICULUM INTESTINAL ( 8 FDA reports)
DRUG ABUSE ( 8 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 8 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 8 FDA reports)
EOSINOPHILIA ( 8 FDA reports)
EPILEPSY ( 8 FDA reports)
ERYSIPELAS ( 8 FDA reports)
EXPIRED DRUG ADMINISTERED ( 8 FDA reports)
FACET JOINT SYNDROME ( 8 FDA reports)
FALLOT'S TETRALOGY ( 8 FDA reports)
FIBULA FRACTURE ( 8 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 8 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 8 FDA reports)
GINGIVAL SWELLING ( 8 FDA reports)
GLOSSITIS ( 8 FDA reports)
HAEMORRHAGIC ANAEMIA ( 8 FDA reports)
HAEMORRHAGIC STROKE ( 8 FDA reports)
HEPATIC CIRRHOSIS ( 8 FDA reports)
HEPATIC LESION ( 8 FDA reports)
HEPATOCELLULAR INJURY ( 8 FDA reports)
HOMICIDAL IDEATION ( 8 FDA reports)
HOSTILITY ( 8 FDA reports)
HYPERCALCAEMIA ( 8 FDA reports)
HYPERNATRAEMIA ( 8 FDA reports)
HYPERPLASIA ( 8 FDA reports)
INCREASED APPETITE ( 8 FDA reports)
INGROWING NAIL ( 8 FDA reports)
INJECTION SITE DISCOMFORT ( 8 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 8 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 8 FDA reports)
JAUNDICE NEONATAL ( 8 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 8 FDA reports)
LEG AMPUTATION ( 8 FDA reports)
LOCALISED OEDEMA ( 8 FDA reports)
LOOSE BODY IN JOINT ( 8 FDA reports)
LOOSE STOOLS ( 8 FDA reports)
MICROANGIOPATHY ( 8 FDA reports)
MIOSIS ( 8 FDA reports)
MURPHY'S SIGN POSITIVE ( 8 FDA reports)
NAIL DISORDER ( 8 FDA reports)
NERVE COMPRESSION ( 8 FDA reports)
NO THERAPEUTIC RESPONSE ( 8 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 8 FDA reports)
OCCULT BLOOD POSITIVE ( 8 FDA reports)
OESOPHAGEAL ULCER ( 8 FDA reports)
OPTIC NERVE INJURY ( 8 FDA reports)
ORAL DISORDER ( 8 FDA reports)
PERIARTHRITIS ( 8 FDA reports)
PERSONALITY DISORDER ( 8 FDA reports)
PNEUMOCOCCAL INFECTION ( 8 FDA reports)
POLYDIPSIA ( 8 FDA reports)
PREMATURE BABY ( 8 FDA reports)
PRIMARY SEQUESTRUM ( 8 FDA reports)
PRODUCT ODOUR ABNORMAL ( 8 FDA reports)
PULMONARY HAEMORRHAGE ( 8 FDA reports)
RESPIRATORY RATE DECREASED ( 8 FDA reports)
SACROILIITIS ( 8 FDA reports)
SCAB ( 8 FDA reports)
SEBORRHOEIC DERMATITIS ( 8 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 8 FDA reports)
SKIN NECROSIS ( 8 FDA reports)
SPINAL FRACTURE ( 8 FDA reports)
SPONDYLOLISTHESIS ( 8 FDA reports)
SUPERINFECTION ( 8 FDA reports)
SYNCOPE VASOVAGAL ( 8 FDA reports)
TOOTH EROSION ( 8 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 8 FDA reports)
VULVOVAGINAL DRYNESS ( 8 FDA reports)
WOUND DRAINAGE ( 8 FDA reports)
ABDOMINAL SYMPTOM ( 7 FDA reports)
ABNORMAL FAECES ( 7 FDA reports)
ABNORMAL SENSATION IN EYE ( 7 FDA reports)
ACCIDENT ( 7 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 7 FDA reports)
ALCOHOLISM ( 7 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 7 FDA reports)
ANKYLOSING SPONDYLITIS ( 7 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 7 FDA reports)
AORTIC VALVE CALCIFICATION ( 7 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 7 FDA reports)
BACTERAEMIA ( 7 FDA reports)
BEREAVEMENT REACTION ( 7 FDA reports)
BLADDER DILATATION ( 7 FDA reports)
BLADDER NEOPLASM ( 7 FDA reports)
BLOOD AMYLASE INCREASED ( 7 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 7 FDA reports)
BLOOD CREATININE DECREASED ( 7 FDA reports)
BONE FRAGMENTATION ( 7 FDA reports)
BONE LOSS ( 7 FDA reports)
BONE MARROW DEPRESSION ( 7 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 7 FDA reports)
BRUXISM ( 7 FDA reports)
CAROTID ARTERY OCCLUSION ( 7 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 7 FDA reports)
CONGENITAL ANOMALY ( 7 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 7 FDA reports)
CORONARY ARTERY RESTENOSIS ( 7 FDA reports)
DACRYOCYSTITIS INFECTIVE ( 7 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 7 FDA reports)
DEMYELINATION ( 7 FDA reports)
DIABETES INSIPIDUS ( 7 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 7 FDA reports)
DRUG ERUPTION ( 7 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 7 FDA reports)
DUODENAL ULCER PERFORATION ( 7 FDA reports)
DYSMENORRHOEA ( 7 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 7 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 7 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 7 FDA reports)
FACE INJURY ( 7 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 7 FDA reports)
FIBRIN D DIMER INCREASED ( 7 FDA reports)
GALLBLADDER OPERATION ( 7 FDA reports)
GASTRIC ULCER PERFORATION ( 7 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 7 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 7 FDA reports)
HEAD TITUBATION ( 7 FDA reports)
HEPATIC CYST ( 7 FDA reports)
HUNGER ( 7 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 7 FDA reports)
HYPERBILIRUBINAEMIA ( 7 FDA reports)
HYPERPHAGIA ( 7 FDA reports)
HYPOALBUMINAEMIA ( 7 FDA reports)
INCORRECT DRUG DOSAGE FORM ADMINISTERED ( 7 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 7 FDA reports)
INTESTINAL POLYP ( 7 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 7 FDA reports)
JAW FRACTURE ( 7 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 7 FDA reports)
MENSTRUAL DISORDER ( 7 FDA reports)
METASTASES TO LUNG ( 7 FDA reports)
METASTASES TO THE MEDIASTINUM ( 7 FDA reports)
MICROCYTIC ANAEMIA ( 7 FDA reports)
NASAL FLARING ( 7 FDA reports)
NONSPECIFIC REACTION ( 7 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 7 FDA reports)
OROPHARYNGEAL BLISTERING ( 7 FDA reports)
OTITIS MEDIA ACUTE ( 7 FDA reports)
PAINFUL RESPIRATION ( 7 FDA reports)
PANIC REACTION ( 7 FDA reports)
PERIODONTITIS ( 7 FDA reports)
PHYSICAL DISABILITY ( 7 FDA reports)
PRESYNCOPE ( 7 FDA reports)
PROCTALGIA ( 7 FDA reports)
PRODUCT TASTE ABNORMAL ( 7 FDA reports)
PROTEIN TOTAL DECREASED ( 7 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 7 FDA reports)
PULMONARY ARTERY DILATATION ( 7 FDA reports)
QRS AXIS ABNORMAL ( 7 FDA reports)
RADIOTHERAPY ( 7 FDA reports)
RENAL ARTERY ATHEROSCLEROSIS ( 7 FDA reports)
RENAL CANCER METASTATIC ( 7 FDA reports)
RESORPTION BONE INCREASED ( 7 FDA reports)
RETINAL ARTERY OCCLUSION ( 7 FDA reports)
SALIVARY GLAND CALCULUS ( 7 FDA reports)
SCREAMING ( 7 FDA reports)
SKELETAL INJURY ( 7 FDA reports)
SKIN CANCER ( 7 FDA reports)
SLUGGISHNESS ( 7 FDA reports)
SOFT TISSUE INFLAMMATION ( 7 FDA reports)
STRESS FRACTURE ( 7 FDA reports)
SYNOVITIS ( 7 FDA reports)
TEMPERATURE INTOLERANCE ( 7 FDA reports)
THYROID NEOPLASM ( 7 FDA reports)
TIBIA FRACTURE ( 7 FDA reports)
TOOTH IMPACTED ( 7 FDA reports)
VAGINAL DISCHARGE ( 7 FDA reports)
VENOUS THROMBOSIS ( 7 FDA reports)
VISUAL FIELD DEFECT ( 7 FDA reports)
VULVAL DISORDER ( 7 FDA reports)
VULVITIS ( 7 FDA reports)
WALKING AID USER ( 7 FDA reports)
WRONG DRUG ADMINISTERED ( 7 FDA reports)
ABSCESS NECK ( 6 FDA reports)
ACUTE PRERENAL FAILURE ( 6 FDA reports)
ADRENAL GLAND CANCER METASTATIC ( 6 FDA reports)
ANAEMIA POSTOPERATIVE ( 6 FDA reports)
ANOXIC ENCEPHALOPATHY ( 6 FDA reports)
ANTIMITOCHONDRIAL ANTIBODY ( 6 FDA reports)
AORTIC ANEURYSM RUPTURE ( 6 FDA reports)
APTYALISM ( 6 FDA reports)
AREFLEXIA ( 6 FDA reports)
ARTHRITIS INFECTIVE ( 6 FDA reports)
BACTERIA URINE IDENTIFIED ( 6 FDA reports)
BLEEDING TIME PROLONGED ( 6 FDA reports)
BLEPHARITIS ( 6 FDA reports)
BLOOD BICARBONATE DECREASED ( 6 FDA reports)
BLOOD CHLORIDE INCREASED ( 6 FDA reports)
BLOOD DISORDER ( 6 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 6 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 6 FDA reports)
BODY TEMPERATURE INCREASED ( 6 FDA reports)
BONE OPERATION ( 6 FDA reports)
BONE TRIMMING ( 6 FDA reports)
BRAIN NEOPLASM ( 6 FDA reports)
BREAST CANCER RECURRENT ( 6 FDA reports)
CACHEXIA ( 6 FDA reports)
CAPSULE ISSUE ( 6 FDA reports)
CARDIAC FLUTTER ( 6 FDA reports)
CARDIAC VALVE DISEASE ( 6 FDA reports)
CARDIOPULMONARY FAILURE ( 6 FDA reports)
CAROTID BRUIT ( 6 FDA reports)
CATHETER RELATED INFECTION ( 6 FDA reports)
CERVICAL CYST ( 6 FDA reports)
CERVIX HAEMORRHAGE UTERINE ( 6 FDA reports)
CHORIORETINAL DISORDER ( 6 FDA reports)
CLAUSTROPHOBIA ( 6 FDA reports)
CONJUNCTIVAL DISORDER ( 6 FDA reports)
CONJUNCTIVITIS VIRAL ( 6 FDA reports)
CONVERSION DISORDER ( 6 FDA reports)
CORONARY ANGIOPLASTY ( 6 FDA reports)
CYTOMEGALOVIRUS TEST ( 6 FDA reports)
DELUSION ( 6 FDA reports)
DERMATITIS CONTACT ( 6 FDA reports)
DEVICE RELATED INFECTION ( 6 FDA reports)
DRUG LEVEL DECREASED ( 6 FDA reports)
DYSTHYMIC DISORDER ( 6 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 6 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 6 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 6 FDA reports)
ELECTROLYTE IMBALANCE ( 6 FDA reports)
ENCEPHALITIS ( 6 FDA reports)
ESSENTIAL HYPERTENSION ( 6 FDA reports)
EYELID FUNCTION DISORDER ( 6 FDA reports)
EYELID RETRACTION ( 6 FDA reports)
FAECES HARD ( 6 FDA reports)
FEELING DRUNK ( 6 FDA reports)
FEELING GUILTY ( 6 FDA reports)
FOOD POISONING ( 6 FDA reports)
FURUNCLE ( 6 FDA reports)
GANGRENE ( 6 FDA reports)
GASTRIC PH DECREASED ( 6 FDA reports)
GASTRIC POLYPS ( 6 FDA reports)
GASTRITIS HAEMORRHAGIC ( 6 FDA reports)
GASTROINTESTINAL ULCER ( 6 FDA reports)
GINGIVAL OPERATION ( 6 FDA reports)
GLOMERULONEPHRITIS ( 6 FDA reports)
GLOMERULONEPHRITIS ACUTE ( 6 FDA reports)
HEART RATE ABNORMAL ( 6 FDA reports)
HEMIANOPIA HOMONYMOUS ( 6 FDA reports)
HEPATIC ENCEPHALOPATHY ( 6 FDA reports)
HEPATIC FIBROSIS ( 6 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 6 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 6 FDA reports)
HIP FRACTURE ( 6 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 6 FDA reports)
HODGKIN'S DISEASE ( 6 FDA reports)
HYDRONEPHROSIS ( 6 FDA reports)
HYPERAESTHESIA ( 6 FDA reports)
HYPERTENSIVE HEART DISEASE ( 6 FDA reports)
HYPOKINESIA ( 6 FDA reports)
HYPOSPADIAS ( 6 FDA reports)
ILEUS PARALYTIC ( 6 FDA reports)
IMMUNODEFICIENCY ( 6 FDA reports)
INCISIONAL DRAINAGE ( 6 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 6 FDA reports)
INJECTION SITE PRURITUS ( 6 FDA reports)
INSPIRATORY CAPACITY DECREASED ( 6 FDA reports)
INTENTIONAL SELF-INJURY ( 6 FDA reports)
INTESTINAL ULCER ( 6 FDA reports)
INTRACRANIAL ANEURYSM ( 6 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 6 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 6 FDA reports)
IRITIS ( 6 FDA reports)
ISCHAEMIC HEPATITIS ( 6 FDA reports)
JOINT DISLOCATION ( 6 FDA reports)
JOINT INSTABILITY ( 6 FDA reports)
KELOID SCAR ( 6 FDA reports)
LACRIMAL DISORDER ( 6 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 6 FDA reports)
LIP OEDEMA ( 6 FDA reports)
LISTLESS ( 6 FDA reports)
LOSS OF PROPRIOCEPTION ( 6 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 6 FDA reports)
LYMPH NODE CALCIFICATION ( 6 FDA reports)
MONOCYTE COUNT INCREASED ( 6 FDA reports)
MONOPLEGIA ( 6 FDA reports)
MULTIPLE ALLERGIES ( 6 FDA reports)
MUSCLE DISORDER ( 6 FDA reports)
MUSCLE INJURY ( 6 FDA reports)
MYDRIASIS ( 6 FDA reports)
NAIL RIDGING ( 6 FDA reports)
NASAL SEPTUM DEVIATION ( 6 FDA reports)
NEPHROTIC SYNDROME ( 6 FDA reports)
OESOPHAGEAL PAIN ( 6 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 6 FDA reports)
ORCHITIS ( 6 FDA reports)
OSTEOMALACIA ( 6 FDA reports)
OSTEOMYELITIS ACUTE ( 6 FDA reports)
OTORRHOEA ( 6 FDA reports)
PANCREATIC ATROPHY ( 6 FDA reports)
PANCREATOBILIARY SPHINCTEROTOMY ( 6 FDA reports)
PARALYSIS FLACCID ( 6 FDA reports)
PAROSMIA ( 6 FDA reports)
PAROTID GLAND ENLARGEMENT ( 6 FDA reports)
PERIPHERAL ARTERY DISSECTION ( 6 FDA reports)
PERITONEAL EFFUSION ( 6 FDA reports)
PEYRONIE'S DISEASE ( 6 FDA reports)
PITTING OEDEMA ( 6 FDA reports)
POST THROMBOTIC SYNDROME ( 6 FDA reports)
PRESBYOPIA ( 6 FDA reports)
PROCTITIS ( 6 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 6 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 6 FDA reports)
PSORIATIC ARTHROPATHY ( 6 FDA reports)
PULMONARY VALVE STENOSIS ( 6 FDA reports)
PUPILLARY DISORDER ( 6 FDA reports)
RADIATION SKIN INJURY ( 6 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 6 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 6 FDA reports)
RETINAL DISORDER ( 6 FDA reports)
RHONCHI ( 6 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 6 FDA reports)
SCOTOMA ( 6 FDA reports)
SECRETION DISCHARGE ( 6 FDA reports)
SELF ESTEEM DECREASED ( 6 FDA reports)
SENSATION OF HEAVINESS ( 6 FDA reports)
SENSORY LOSS ( 6 FDA reports)
SEROMA ( 6 FDA reports)
SERUM FERRITIN DECREASED ( 6 FDA reports)
SKIN TOXICITY ( 6 FDA reports)
SMOOTH MUSCLE ANTIBODY ( 6 FDA reports)
SPINAL DEFORMITY ( 6 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 6 FDA reports)
STRESS SYMPTOMS ( 6 FDA reports)
TABLET PHYSICAL ISSUE ( 6 FDA reports)
TENDON DISORDER ( 6 FDA reports)
THROMBOPHLEBITIS ( 6 FDA reports)
TONGUE DISCOLOURATION ( 6 FDA reports)
TYPE 2 DIABETES MELLITUS ( 6 FDA reports)
UMBILICAL HERNIA ( 6 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 6 FDA reports)
UROSEPSIS ( 6 FDA reports)
UTERINE CERVICAL SQUAMOUS METAPLASIA ( 6 FDA reports)
VAGINAL DISORDER ( 6 FDA reports)
VAGINAL INFECTION ( 6 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 6 FDA reports)
ACCIDENT AT WORK ( 5 FDA reports)
ACUTE HEPATIC FAILURE ( 5 FDA reports)
AKATHISIA ( 5 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 5 FDA reports)
ALLERGIC BRONCHITIS ( 5 FDA reports)
ALPHA 1 GLOBULIN INCREASED ( 5 FDA reports)
ALVEOLOPLASTY ( 5 FDA reports)
AMMONIA INCREASED ( 5 FDA reports)
ANORECTAL DISORDER ( 5 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 5 FDA reports)
APPLICATION SITE REACTION ( 5 FDA reports)
ARTERIAL DISORDER ( 5 FDA reports)
ARTHROPOD BITE ( 5 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 5 FDA reports)
BICUSPID AORTIC VALVE ( 5 FDA reports)
BILE DUCT OBSTRUCTION ( 5 FDA reports)
BLOOD BICARBONATE INCREASED ( 5 FDA reports)
BLOOD CREATINE INCREASED ( 5 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 5 FDA reports)
BLOOD PH DECREASED ( 5 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 5 FDA reports)
BLOOD URIC ACID INCREASED ( 5 FDA reports)
BODY TEMPERATURE DECREASED ( 5 FDA reports)
BRONCHITIS BACTERIAL ( 5 FDA reports)
BUNION ( 5 FDA reports)
CARDIAC OUTPUT DECREASED ( 5 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 5 FDA reports)
CHONDROPLASTY ( 5 FDA reports)
CLUSTER HEADACHE ( 5 FDA reports)
COARCTATION OF THE AORTA ( 5 FDA reports)
COLON ADENOMA ( 5 FDA reports)
COMPARTMENT SYNDROME ( 5 FDA reports)
COMPRESSION FRACTURE ( 5 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 5 FDA reports)
CONGENITAL AORTIC STENOSIS ( 5 FDA reports)
CONGENITAL CORONARY ARTERY MALFORMATION ( 5 FDA reports)
CONGENITAL MITRAL VALVE STENOSIS ( 5 FDA reports)
CONGENITAL PULMONARY ARTERY ANOMALY ( 5 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 5 FDA reports)
CUSHING'S SYNDROME ( 5 FDA reports)
CYSTIC FIBROSIS ( 5 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 5 FDA reports)
DENTAL OPERATION ( 5 FDA reports)
DERMAL CYST ( 5 FDA reports)
DEVICE FAILURE ( 5 FDA reports)
DEVICE MALFUNCTION ( 5 FDA reports)
DIET REFUSAL ( 5 FDA reports)
DRY THROAT ( 5 FDA reports)
ECZEMA INFECTED ( 5 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 5 FDA reports)
EMBOLISM ( 5 FDA reports)
EROSIVE OESOPHAGITIS ( 5 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 5 FDA reports)
EYE DISCHARGE ( 5 FDA reports)
FORMICATION ( 5 FDA reports)
GASTRIC CANCER ( 5 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 5 FDA reports)
GINGIVAL DISORDER ( 5 FDA reports)
GLOMERULONEPHRITIS FOCAL ( 5 FDA reports)
GOITRE ( 5 FDA reports)
GUN SHOT WOUND ( 5 FDA reports)
HAEMANGIOMA ( 5 FDA reports)
HAEMARTHROSIS ( 5 FDA reports)
HAEMOGLOBIN INCREASED ( 5 FDA reports)
HAEMOLYSIS ( 5 FDA reports)
HAEMOLYTIC ANAEMIA ( 5 FDA reports)
HAEMOPHILUS INFECTION ( 5 FDA reports)
HAEMORRHAGIC DISORDER ( 5 FDA reports)
HAND FRACTURE ( 5 FDA reports)
HEART INJURY ( 5 FDA reports)
HEART VALVE STENOSIS ( 5 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 5 FDA reports)
HEPATOSPLENOMEGALY ( 5 FDA reports)
HERNIA REPAIR ( 5 FDA reports)
HUMERUS FRACTURE ( 5 FDA reports)
HYPERCAPNIA ( 5 FDA reports)
HYPERVENTILATION ( 5 FDA reports)
HYPOTONIA ( 5 FDA reports)
ILEITIS ( 5 FDA reports)
IMPULSE-CONTROL DISORDER ( 5 FDA reports)
INJECTION SITE CELLULITIS ( 5 FDA reports)
INJECTION SITE INDURATION ( 5 FDA reports)
INJECTION SITE STINGING ( 5 FDA reports)
INTERCOSTAL NEURALGIA ( 5 FDA reports)
INTERCOSTAL RETRACTION ( 5 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 5 FDA reports)
JUGULAR VEIN DISTENSION ( 5 FDA reports)
KAWASAKI'S DISEASE ( 5 FDA reports)
KIDNEY ENLARGEMENT ( 5 FDA reports)
KYPHOSIS ( 5 FDA reports)
LARYNGOCELE ( 5 FDA reports)
LEFT VENTRICLE OUTFLOW TRACT OBSTRUCTION ( 5 FDA reports)
LIP DISORDER ( 5 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 5 FDA reports)
LYMPHOEDEMA ( 5 FDA reports)
MALLORY-WEISS SYNDROME ( 5 FDA reports)
MANIA ( 5 FDA reports)
MEAN CELL VOLUME DECREASED ( 5 FDA reports)
METABOLIC DISORDER ( 5 FDA reports)
MITRAL VALVE DISEASE ( 5 FDA reports)
MUCOSAL ULCERATION ( 5 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 5 FDA reports)
MULTIPLE INJURIES ( 5 FDA reports)
MUSCLE RIGIDITY ( 5 FDA reports)
MYASTHENIA GRAVIS ( 5 FDA reports)
MYCOPLASMA INFECTION ( 5 FDA reports)
MYOCARDIAL FIBROSIS ( 5 FDA reports)
MYOPATHY ( 5 FDA reports)
NAIL TINEA ( 5 FDA reports)
NASAL OEDEMA ( 5 FDA reports)
NECROTISING FASCIITIS ( 5 FDA reports)
NEPHROSCLEROSIS ( 5 FDA reports)
NEURILEMMOMA ( 5 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 5 FDA reports)
NEUTROPHILIA ( 5 FDA reports)
OBSTRUCTION ( 5 FDA reports)
OBSTRUCTIVE UROPATHY ( 5 FDA reports)
OCULAR DISCOMFORT ( 5 FDA reports)
OFF LABEL USE ( 5 FDA reports)
OPTIC NEUROPATHY ( 5 FDA reports)
ORGAN FAILURE ( 5 FDA reports)
ORTHOPNOEA ( 5 FDA reports)
OVERWEIGHT ( 5 FDA reports)
PANIC DISORDER ( 5 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 5 FDA reports)
PERIODONTAL DESTRUCTION ( 5 FDA reports)
PERIODONTAL DISEASE ( 5 FDA reports)
PERIPHERAL ISCHAEMIA ( 5 FDA reports)
PHARYNGEAL ABSCESS ( 5 FDA reports)
PHARYNGEAL HYPOAESTHESIA ( 5 FDA reports)
PHARYNGOTONSILLITIS ( 5 FDA reports)
PIGMENTATION DISORDER ( 5 FDA reports)
PLEURAL DISORDER ( 5 FDA reports)
PLEURAL FIBROSIS ( 5 FDA reports)
PNEUMOCOCCAL SEPSIS ( 5 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 5 FDA reports)
PNEUMONIA VIRAL ( 5 FDA reports)
POOR QUALITY SLEEP ( 5 FDA reports)
POST PROCEDURAL FISTULA ( 5 FDA reports)
POSTURE ABNORMAL ( 5 FDA reports)
PRODUCT SIZE ISSUE ( 5 FDA reports)
PROTHROMBIN TIME SHORTENED ( 5 FDA reports)
PSEUDOCYST ( 5 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 5 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 5 FDA reports)
PSYCHOTHERAPY ( 5 FDA reports)
PULMONARY HYPOPLASIA ( 5 FDA reports)
RADICAL MASTECTOMY ( 5 FDA reports)
RASH PUSTULAR ( 5 FDA reports)
RENAL EMBOLISM ( 5 FDA reports)
RENAL INJURY ( 5 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS BRONCHIOLITIS ( 5 FDA reports)
RIB DEFORMITY ( 5 FDA reports)
SEASONAL ALLERGY ( 5 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 5 FDA reports)
SELF-INJURIOUS IDEATION ( 5 FDA reports)
SERUM FERRITIN INCREASED ( 5 FDA reports)
SHIFT TO THE LEFT ( 5 FDA reports)
SINUS HEADACHE ( 5 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 5 FDA reports)
SPEECH REHABILITATION ( 5 FDA reports)
STRIDOR ( 5 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 5 FDA reports)
SYSTOLIC HYPERTENSION ( 5 FDA reports)
THERMAL BURN ( 5 FDA reports)
THOUGHT BLOCKING ( 5 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 5 FDA reports)
TOBACCO ABUSE ( 5 FDA reports)
TONGUE INJURY ( 5 FDA reports)
TONGUE OEDEMA ( 5 FDA reports)
TRACHEOMALACIA ( 5 FDA reports)
TRANSPOSITION OF THE GREAT VESSELS ( 5 FDA reports)
TROPONIN INCREASED ( 5 FDA reports)
TUNNEL VISION ( 5 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 5 FDA reports)
URINARY TRACT DISORDER ( 5 FDA reports)
VAGINAL CONTRACEPTIVE DEVICE EXPELLED ( 5 FDA reports)
VASCULAR ANOMALY ( 5 FDA reports)
VASCULAR INSUFFICIENCY ( 5 FDA reports)
VASCULAR PURPURA ( 5 FDA reports)
VITH NERVE PARALYSIS ( 5 FDA reports)
WEST NILE VIRAL INFECTION ( 5 FDA reports)
WITHDRAWAL SYNDROME ( 5 FDA reports)
WOUND ( 5 FDA reports)
WOUND DEBRIDEMENT ( 5 FDA reports)
WOUND SECRETION ( 5 FDA reports)
XANTHELASMA ( 5 FDA reports)
ABDOMINAL NEOPLASM ( 4 FDA reports)
ABSCESS ORAL ( 4 FDA reports)
ABSCESS RUPTURE ( 4 FDA reports)
ACUTE LUNG INJURY ( 4 FDA reports)
ADNEXA UTERI MASS ( 4 FDA reports)
ADRENAL DISORDER ( 4 FDA reports)
AKINESIA ( 4 FDA reports)
ALPHA 2 GLOBULIN INCREASED ( 4 FDA reports)
AMYOTROPHY ( 4 FDA reports)
ANEURYSM ( 4 FDA reports)
ANTI FACTOR VIII ANTIBODY POSITIVE ( 4 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 4 FDA reports)
APALLIC SYNDROME ( 4 FDA reports)
ARTERIAL RUPTURE ( 4 FDA reports)
ASPHYXIA ( 4 FDA reports)
AURICULAR SWELLING ( 4 FDA reports)
B-CELL LYMPHOMA STAGE IV ( 4 FDA reports)
BLADDER CANCER ( 4 FDA reports)
BLOOD BLISTER ( 4 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 4 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 4 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 4 FDA reports)
BLOOD TEST ABNORMAL ( 4 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 4 FDA reports)
BONE CYST ( 4 FDA reports)
BONE SWELLING ( 4 FDA reports)
BRAIN MASS ( 4 FDA reports)
BRAIN STEM SYNDROME ( 4 FDA reports)
BREAST DISCHARGE ( 4 FDA reports)
BREATH ODOUR ( 4 FDA reports)
BRONCHOPNEUMONIA ( 4 FDA reports)
CARDIAC VALVE ABSCESS ( 4 FDA reports)
CEREBELLAR INFARCTION ( 4 FDA reports)
CEREBROVASCULAR STENOSIS ( 4 FDA reports)
CERVICAL SPINAL STENOSIS ( 4 FDA reports)
CHAPPED LIPS ( 4 FDA reports)
CHOLANGITIS ACUTE ( 4 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 4 FDA reports)
CLAVICLE FRACTURE ( 4 FDA reports)
COAGULATION FACTOR X LEVEL DECREASED ( 4 FDA reports)
COLON POLYPECTOMY ( 4 FDA reports)
COLOUR BLINDNESS ( 4 FDA reports)
COMPULSIVE SHOPPING ( 4 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 4 FDA reports)
COW'S MILK INTOLERANCE ( 4 FDA reports)
DECREASED ACTIVITY ( 4 FDA reports)
DENTAL FISTULA ( 4 FDA reports)
DERMATOMYOSITIS ( 4 FDA reports)
DISSEMINATED TUBERCULOSIS ( 4 FDA reports)
DIZZINESS POSTURAL ( 4 FDA reports)
DYSAESTHESIA ( 4 FDA reports)
EAR DISCOMFORT ( 4 FDA reports)
EFFUSION ( 4 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 4 FDA reports)
ENTEROBACTER INFECTION ( 4 FDA reports)
EPIDIDYMITIS ( 4 FDA reports)
ESCHERICHIA INFECTION ( 4 FDA reports)
ESCHERICHIA SEPSIS ( 4 FDA reports)
EYE MOVEMENT DISORDER ( 4 FDA reports)
EYE OEDEMA ( 4 FDA reports)
EYELID CYST ( 4 FDA reports)
FALLOPIAN TUBE CYST ( 4 FDA reports)
FEELING OF DESPAIR ( 4 FDA reports)
FIBROUS HISTIOCYTOMA ( 4 FDA reports)
FLUID INTAKE REDUCED ( 4 FDA reports)
FOAMING AT MOUTH ( 4 FDA reports)
GALLBLADDER INJURY ( 4 FDA reports)
GASTRIC MUCOSAL LESION ( 4 FDA reports)
GASTROENTERITIS RADIATION ( 4 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA ( 4 FDA reports)
GASTROINTESTINAL PAIN ( 4 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 4 FDA reports)
GAZE PALSY ( 4 FDA reports)
GENERALISED ANXIETY DISORDER ( 4 FDA reports)
GINGIVAL EROSION ( 4 FDA reports)
HEAD DISCOMFORT ( 4 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 4 FDA reports)
HEPATIC PAIN ( 4 FDA reports)
HEPATITIS ACUTE ( 4 FDA reports)
HEPATITIS B ( 4 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 4 FDA reports)
HIGH-PITCHED CRYING ( 4 FDA reports)
HORDEOLUM ( 4 FDA reports)
HORNER'S SYNDROME ( 4 FDA reports)
HYDROCEPHALUS ( 4 FDA reports)
HYPERSEXUALITY ( 4 FDA reports)
HYPOCALCAEMIA ( 4 FDA reports)
HYPOTRICHOSIS ( 4 FDA reports)
IMMOBILE ( 4 FDA reports)
INAPPROPRIATE AFFECT ( 4 FDA reports)
INCISION SITE COMPLICATION ( 4 FDA reports)
INDURATION ( 4 FDA reports)
INFARCTION ( 4 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 4 FDA reports)
INJECTION SITE IRRITATION ( 4 FDA reports)
JOINT EFFUSION ( 4 FDA reports)
KLEBSIELLA INFECTION ( 4 FDA reports)
LABORATORY TEST INTERFERENCE ( 4 FDA reports)
LAXATIVE ABUSE ( 4 FDA reports)
LID LAG ( 4 FDA reports)
LIFE SUPPORT ( 4 FDA reports)
LIP BLISTER ( 4 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 4 FDA reports)
MALABSORPTION ( 4 FDA reports)
MEDIASTINAL DISORDER ( 4 FDA reports)
MEDIASTINAL MASS ( 4 FDA reports)
MEDICAL DEVICE COMPLICATION ( 4 FDA reports)
MELANOSIS COLI ( 4 FDA reports)
MENINGITIS ( 4 FDA reports)
MENINGOCOCCAL SEPSIS ( 4 FDA reports)
MENOPAUSAL SYMPTOMS ( 4 FDA reports)
METABOLIC ALKALOSIS ( 4 FDA reports)
METASTASES TO SKIN ( 4 FDA reports)
MUSCLE FATIGUE ( 4 FDA reports)
MUTISM ( 4 FDA reports)
NAIL INFECTION ( 4 FDA reports)
NASAL DISCOMFORT ( 4 FDA reports)
NASAL DISORDER ( 4 FDA reports)
NASAL SEPTUM ULCERATION ( 4 FDA reports)
NASAL TURBINATE HYPERTROPHY ( 4 FDA reports)
NECROSIS ( 4 FDA reports)
NEOPLASM ( 4 FDA reports)
NEPHRECTOMY ( 4 FDA reports)
NEURITIS ( 4 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 4 FDA reports)
OESOPHAGEAL SPASM ( 4 FDA reports)
OLIGOHYDRAMNIOS ( 4 FDA reports)
OPPORTUNISTIC INFECTION ( 4 FDA reports)
OVARIAN NEOPLASM ( 4 FDA reports)
PANCREATIC INSUFFICIENCY ( 4 FDA reports)
PAPILLOMA ( 4 FDA reports)
PARAPSORIASIS ( 4 FDA reports)
PATELLA FRACTURE ( 4 FDA reports)
PELVI-URETERIC OBSTRUCTION ( 4 FDA reports)
PELVIC HAEMATOMA ( 4 FDA reports)
PELVIC VENOUS THROMBOSIS ( 4 FDA reports)
PERINEAL LACERATION ( 4 FDA reports)
PERINEPHRIC ABSCESS ( 4 FDA reports)
PERIORBITAL CELLULITIS ( 4 FDA reports)
PERNICIOUS ANAEMIA ( 4 FDA reports)
PERONEAL NERVE PALSY ( 4 FDA reports)
PHLEBITIS ( 4 FDA reports)
PNEUMONIA BACTERIAL ( 4 FDA reports)
PNEUMONIA NECROTISING ( 4 FDA reports)
POLYNEUROPATHY ( 4 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 4 FDA reports)
POSTOPERATIVE ILEUS ( 4 FDA reports)
POSTPARTUM HAEMORRHAGE ( 4 FDA reports)
PREGNANCY INDUCED HYPERTENSION ( 4 FDA reports)
PROCEDURAL COMPLICATION ( 4 FDA reports)
PROCEDURAL HYPOTENSION ( 4 FDA reports)
PRODUCT CLOSURE ISSUE ( 4 FDA reports)
PRODUCT CONTAINER ISSUE ( 4 FDA reports)
PROTEIN S DEFICIENCY ( 4 FDA reports)
PROTEIN TOTAL INCREASED ( 4 FDA reports)
PROTEIN URINE PRESENT ( 4 FDA reports)
PSYCHIATRIC SYMPTOM ( 4 FDA reports)
PULMONARY MASS ( 4 FDA reports)
RADIATION INJURY ( 4 FDA reports)
RAYNAUD'S PHENOMENON ( 4 FDA reports)
RECTAL CANCER ( 4 FDA reports)
RECTAL POLYP ( 4 FDA reports)
RECURRENT CANCER ( 4 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 4 FDA reports)
REFLUX LARYNGITIS ( 4 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 4 FDA reports)
RENAL INFARCT ( 4 FDA reports)
RESPIRATORY TRACT CONGESTION ( 4 FDA reports)
RIGHT ATRIAL DILATATION ( 4 FDA reports)
SARCOIDOSIS ( 4 FDA reports)
SELF MUTILATION ( 4 FDA reports)
SENSITIVITY OF TEETH ( 4 FDA reports)
SEROTONIN SYNDROME ( 4 FDA reports)
SKIN PAPILLOMA ( 4 FDA reports)
SKIN TURGOR DECREASED ( 4 FDA reports)
SMALL INTESTINAL PERFORATION ( 4 FDA reports)
SPUTUM DISCOLOURED ( 4 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 4 FDA reports)
STRABISMUS ( 4 FDA reports)
SUBACUTE ENDOCARDITIS ( 4 FDA reports)
SUFFOCATION FEELING ( 4 FDA reports)
SUNBURN ( 4 FDA reports)
TENOSYNOVITIS ( 4 FDA reports)
TENOSYNOVITIS STENOSANS ( 4 FDA reports)
TENSION HEADACHE ( 4 FDA reports)
THROMBOCYTHAEMIA ( 4 FDA reports)
TONGUE BLACK HAIRY ( 4 FDA reports)
TONGUE HAEMORRHAGE ( 4 FDA reports)
TRANSFUSION REACTION ( 4 FDA reports)
ULCER HAEMORRHAGE ( 4 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 4 FDA reports)
URINE ABNORMALITY ( 4 FDA reports)
URINE ODOUR ABNORMAL ( 4 FDA reports)
UTERINE DISORDER ( 4 FDA reports)
UTERINE POLYP ( 4 FDA reports)
VASCULAR GRAFT OCCLUSION ( 4 FDA reports)
VENOUS STENOSIS ( 4 FDA reports)
VERTIGO POSITIONAL ( 4 FDA reports)
VOLVULUS ( 4 FDA reports)
WRIST FRACTURE ( 4 FDA reports)
XANTHOGRANULOMA ( 4 FDA reports)
ABDOMINAL RIGIDITY ( 3 FDA reports)
ABSCESS JAW ( 3 FDA reports)
ACTINIC KERATOSIS ( 3 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 3 FDA reports)
ADENOMA BENIGN ( 3 FDA reports)
ADHESION ( 3 FDA reports)
ADRENAL MASS ( 3 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 3 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 3 FDA reports)
ANAPHYLACTOID REACTION ( 3 FDA reports)
ANORECTAL DISCOMFORT ( 3 FDA reports)
ANTI-THYROID ANTIBODY POSITIVE ( 3 FDA reports)
AORTIC ATHEROSCLEROSIS ( 3 FDA reports)
APHONIA ( 3 FDA reports)
APPENDICITIS PERFORATED ( 3 FDA reports)
APPLICATION SITE VESICLES ( 3 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 3 FDA reports)
ARTERIOSPASM CORONARY ( 3 FDA reports)
ARTERY DISSECTION ( 3 FDA reports)
ASTHENOPIA ( 3 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 3 FDA reports)
BILE DUCT STENOSIS ( 3 FDA reports)
BIOPSY BONE MARROW ( 3 FDA reports)
BIOPSY THYMUS GLAND ABNORMAL ( 3 FDA reports)
BLADDER SPASM ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 3 FDA reports)
BLOOD CHOLESTEROL ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 3 FDA reports)
BLOOD CREATININE ABNORMAL ( 3 FDA reports)
BLOOD FOLATE INCREASED ( 3 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 3 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 3 FDA reports)
BLOOD IRON DECREASED ( 3 FDA reports)
BLOOD LACTIC ACID INCREASED ( 3 FDA reports)
BLOOD MAGNESIUM DECREASED ( 3 FDA reports)
BLOOD SODIUM INCREASED ( 3 FDA reports)
BLOOD UREA DECREASED ( 3 FDA reports)
BODY TINEA ( 3 FDA reports)
BONE GRAFT ( 3 FDA reports)
BONE MARROW DISORDER ( 3 FDA reports)
BONE MARROW TOXICITY ( 3 FDA reports)
BRAIN HERNIATION ( 3 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 3 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 3 FDA reports)
BREAKTHROUGH PAIN ( 3 FDA reports)
BREATHING-RELATED SLEEP DISORDER ( 3 FDA reports)
BRONCHIAL OBSTRUCTION ( 3 FDA reports)
BRONCHITIS CHRONIC ( 3 FDA reports)
BUTTOCK PAIN ( 3 FDA reports)
CAPSULE PHYSICAL ISSUE ( 3 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 3 FDA reports)
CATARACT OPERATION ( 3 FDA reports)
CATHETERISATION CARDIAC ( 3 FDA reports)
CD4 LYMPHOCYTES INCREASED ( 3 FDA reports)
CELLULITIS STREPTOCOCCAL ( 3 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 3 FDA reports)
CERVICOBRACHIAL SYNDROME ( 3 FDA reports)
CHOKING SENSATION ( 3 FDA reports)
CHOLESTEROSIS ( 3 FDA reports)
CHRONIC HEPATITIS ( 3 FDA reports)
COAGULATION FACTOR VIII LEVEL DECREASED ( 3 FDA reports)
COAGULATION TIME PROLONGED ( 3 FDA reports)
COLON CANCER STAGE II ( 3 FDA reports)
COLONOSCOPY ( 3 FDA reports)
COMPLICATED MIGRAINE ( 3 FDA reports)
CONGENITAL MEGACOLON ( 3 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 3 FDA reports)
CORONARY OSTIAL STENOSIS ( 3 FDA reports)
CRANIAL NEUROPATHY ( 3 FDA reports)
CULTURE THROAT POSITIVE ( 3 FDA reports)
CUSHINGOID ( 3 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 3 FDA reports)
DACRYOCYSTITIS ( 3 FDA reports)
DEAFNESS BILATERAL ( 3 FDA reports)
DENTAL CARE ( 3 FDA reports)
DENTAL PLAQUE ( 3 FDA reports)
DERMATITIS ALLERGIC ( 3 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 3 FDA reports)
DIABETIC RETINOPATHY ( 3 FDA reports)
DIARRHOEA INFECTIOUS ( 3 FDA reports)
DIPLEGIA ( 3 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 3 FDA reports)
DRUG CLEARANCE INCREASED ( 3 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 3 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 3 FDA reports)
DRUG TOLERANCE INCREASED ( 3 FDA reports)
DYSPLASIA ( 3 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 3 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 3 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 3 FDA reports)
EMBOLISM ARTERIAL ( 3 FDA reports)
EMBOLISM VENOUS ( 3 FDA reports)
ENDOCARDITIS BACTERIAL ( 3 FDA reports)
ENDOMETRIAL CANCER STAGE II ( 3 FDA reports)
ENDOMETRIOSIS ( 3 FDA reports)
ENERGY INCREASED ( 3 FDA reports)
ENTEROVIRUS INFECTION ( 3 FDA reports)
ERECTION INCREASED ( 3 FDA reports)
ESCHAR ( 3 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 3 FDA reports)
EXANTHEM ( 3 FDA reports)
EXERCISE TOLERANCE DECREASED ( 3 FDA reports)
EXOPHTHALMOS ( 3 FDA reports)
EYE INFLAMMATION ( 3 FDA reports)
FIBROSIS ( 3 FDA reports)
FOOD CRAVING ( 3 FDA reports)
FOOT DEFORMITY ( 3 FDA reports)
FOREIGN BODY IN EYE ( 3 FDA reports)
FOREIGN BODY TRAUMA ( 3 FDA reports)
FRUSTRATION ( 3 FDA reports)
FULL BLOOD COUNT DECREASED ( 3 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 3 FDA reports)
GAMBLING ( 3 FDA reports)
GASTRIC BYPASS ( 3 FDA reports)
GASTROENTERITIS NORWALK VIRUS ( 3 FDA reports)
GASTROINTESTINAL NECROSIS ( 3 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 3 FDA reports)
GENITAL HERPES ( 3 FDA reports)
GENITAL LESION ( 3 FDA reports)
GENITAL TRACT INFLAMMATION ( 3 FDA reports)
GESTATIONAL HYPERTENSION ( 3 FDA reports)
GINGIVAL OEDEMA ( 3 FDA reports)
GLIOSIS ( 3 FDA reports)
GOUTY ARTHRITIS ( 3 FDA reports)
GRANULOCYTOPENIA ( 3 FDA reports)
HAEMANGIOMA OF LIVER ( 3 FDA reports)
HAEMORRHAGIC ASCITES ( 3 FDA reports)
HANGOVER ( 3 FDA reports)
HEPATITIS C ( 3 FDA reports)
HEPATITIS VIRAL ( 3 FDA reports)
HEPATORENAL SYNDROME ( 3 FDA reports)
HOARSENESS ( 3 FDA reports)
HYDROMETRA ( 3 FDA reports)
HYPOPHOSPHATAEMIA ( 3 FDA reports)
IIIRD NERVE PARALYSIS ( 3 FDA reports)
IMPATIENCE ( 3 FDA reports)
IMPETIGO ( 3 FDA reports)
INCISION SITE HAEMORRHAGE ( 3 FDA reports)
INJECTION SITE INFECTION ( 3 FDA reports)
INJECTION SITE NECROSIS ( 3 FDA reports)
INJECTION SITE NODULE ( 3 FDA reports)
INJECTION SITE PAPULE ( 3 FDA reports)
INSULIN RESISTANCE ( 3 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 3 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 3 FDA reports)
IRON DEFICIENCY ( 3 FDA reports)
JOINT CONTRACTURE ( 3 FDA reports)
JUVENILE ARTHRITIS ( 3 FDA reports)
KERATOACANTHOMA ( 3 FDA reports)
KNEE DEFORMITY ( 3 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 3 FDA reports)
LUNG CANCER METASTATIC ( 3 FDA reports)
LUNG CONSOLIDATION ( 3 FDA reports)
LUNG INFECTION ( 3 FDA reports)
LUPUS-LIKE SYNDROME ( 3 FDA reports)
MACULAR OEDEMA ( 3 FDA reports)
MACULOPATHY ( 3 FDA reports)
MALFORMATION VENOUS ( 3 FDA reports)
MASTECTOMY ( 3 FDA reports)
MEDIASTINAL BIOPSY ( 3 FDA reports)
MELANOCYTIC NAEVUS ( 3 FDA reports)
MENINGITIS ASEPTIC ( 3 FDA reports)
MENINGITIS BACTERIAL ( 3 FDA reports)
MENINGITIS PNEUMOCOCCAL ( 3 FDA reports)
MENINGITIS VIRAL ( 3 FDA reports)
METASTASES TO LYMPH NODES ( 3 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 3 FDA reports)
MONARTHRITIS ( 3 FDA reports)
MONONUCLEOSIS SYNDROME ( 3 FDA reports)
MORBID THOUGHTS ( 3 FDA reports)
MOTOR DYSFUNCTION ( 3 FDA reports)
MUCOSAL EROSION ( 3 FDA reports)
MUSCLE ABSCESS ( 3 FDA reports)
MUSCLE SPASTICITY ( 3 FDA reports)
MYELODYSPLASTIC SYNDROME ( 3 FDA reports)
MYODESOPSIA ( 3 FDA reports)
NAIL HYPERTROPHY ( 3 FDA reports)
NASAL ODOUR ( 3 FDA reports)
NEOPLASM PROGRESSION ( 3 FDA reports)
NEPHROPATHY ( 3 FDA reports)
NEUROPATHIC PAIN ( 3 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 3 FDA reports)
NON-SMALL CELL LUNG CANCER ( 3 FDA reports)
NUCHAL RIGIDITY ( 3 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 3 FDA reports)
OPERATIVE HAEMORRHAGE ( 3 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 3 FDA reports)
OSMOTIC DEMYELINATION SYNDROME ( 3 FDA reports)
OSTEOCHONDROSIS ( 3 FDA reports)
OVARIAN CYST RUPTURED ( 3 FDA reports)
PAIN EXACERBATED ( 3 FDA reports)
PANCREATIC ENZYMES INCREASED ( 3 FDA reports)
PAPILLOEDEMA ( 3 FDA reports)
PARVOVIRUS B19 SEROLOGY POSITIVE ( 3 FDA reports)
PCO2 DECREASED ( 3 FDA reports)
PELVIC ABSCESS ( 3 FDA reports)
PERFORATED ULCER ( 3 FDA reports)
PERFORMANCE STATUS DECREASED ( 3 FDA reports)
PERINEURIAL CYST ( 3 FDA reports)
PERIPHERAL NERVE INJURY ( 3 FDA reports)
PERITONEAL HAEMORRHAGE ( 3 FDA reports)
PERITONSILLAR ABSCESS ( 3 FDA reports)
PHARYNGEAL ERYTHEMA ( 3 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 3 FDA reports)
POST LAMINECTOMY SYNDROME ( 3 FDA reports)
POST PROCEDURAL DIARRHOEA ( 3 FDA reports)
POSTOPERATIVE INFECTION ( 3 FDA reports)
POUCHITIS ( 3 FDA reports)
PRIMARY MEDIASTINAL LARGE B-CELL LYMPHOMA STAGE II ( 3 FDA reports)
PROCTITIS ULCERATIVE ( 3 FDA reports)
PRODUCT COATING ISSUE ( 3 FDA reports)
PRODUCT DEPOSIT ( 3 FDA reports)
PRODUCT EXPIRATION DATE ISSUE ( 3 FDA reports)
PRODUCT LOT NUMBER ISSUE ( 3 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 3 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 3 FDA reports)
PROSTATE CANCER METASTATIC ( 3 FDA reports)
PROSTATOMEGALY ( 3 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 3 FDA reports)
PSOAS ABSCESS ( 3 FDA reports)
PULMONARY FIBROSIS ( 3 FDA reports)
PULMONARY PNEUMATOCELE ( 3 FDA reports)
PULMONARY TUBERCULOSIS ( 3 FDA reports)
PYELONEPHRITIS ACUTE ( 3 FDA reports)
QUALITY OF LIFE DECREASED ( 3 FDA reports)
RASH MORBILLIFORM ( 3 FDA reports)
RECTAL ABSCESS ( 3 FDA reports)
RECTAL DISCHARGE ( 3 FDA reports)
RENAL PAPILLARY NECROSIS ( 3 FDA reports)
RESPIRATORY ACIDOSIS ( 3 FDA reports)
RESPIRATORY DEPRESSION ( 3 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 3 FDA reports)
RETINAL HAEMORRHAGE ( 3 FDA reports)
RETROPHARYNGEAL ABSCESS ( 3 FDA reports)
REVERSIBLE AIRWAYS OBSTRUCTION ( 3 FDA reports)
RHINITIS SEASONAL ( 3 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 3 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 3 FDA reports)
SCRATCH ( 3 FDA reports)
SEPTIC EMBOLUS ( 3 FDA reports)
SICK SINUS SYNDROME ( 3 FDA reports)
SINUSITIS BACTERIAL ( 3 FDA reports)
SKIN DESQUAMATION ( 3 FDA reports)
SPINAL OPERATION ( 3 FDA reports)
SPUTUM CULTURE POSITIVE ( 3 FDA reports)
SPUTUM INCREASED ( 3 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 3 FDA reports)
STATUS ASTHMATICUS ( 3 FDA reports)
STRESS ULCER ( 3 FDA reports)
SUDDEN CARDIAC DEATH ( 3 FDA reports)
SUICIDAL BEHAVIOUR ( 3 FDA reports)
SUPERINFECTION BACTERIAL ( 3 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 3 FDA reports)
TARDIVE DYSKINESIA ( 3 FDA reports)
TENDON PAIN ( 3 FDA reports)
THEFT ( 3 FDA reports)
THERAPY CESSATION ( 3 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 3 FDA reports)
THROMBOCYTOSIS ( 3 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 3 FDA reports)
THYROID MASS ( 3 FDA reports)
TINEA CRURIS ( 3 FDA reports)
TONGUE COATED ( 3 FDA reports)
TOXIC SHOCK SYNDROME STREPTOCOCCAL ( 3 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 3 FDA reports)
TUBERCULOSIS ( 3 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 3 FDA reports)
UMBILICAL CORD AROUND NECK ( 3 FDA reports)
UNDERWEIGHT ( 3 FDA reports)
UNEXPECTED THERAPEUTIC DRUG EFFECT ( 3 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 3 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 3 FDA reports)
URINE ANALYSIS ABNORMAL ( 3 FDA reports)
URINE FLOW DECREASED ( 3 FDA reports)
URINE KETONE BODY PRESENT ( 3 FDA reports)
VARICES OESOPHAGEAL ( 3 FDA reports)
VENA CAVA THROMBOSIS ( 3 FDA reports)
VENTRICULAR DYSKINESIA ( 3 FDA reports)
VICTIM OF CRIME ( 3 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 3 FDA reports)
VISUAL ACUITY REDUCED TRANSIENTLY ( 3 FDA reports)
VITAMIN B12 INCREASED ( 3 FDA reports)
VOCAL CORD INFLAMMATION ( 3 FDA reports)
VULVAL ULCERATION ( 3 FDA reports)
WHEELCHAIR USER ( 3 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 3 FDA reports)
ABDOMINAL HERNIA ( 2 FDA reports)
ABNORMAL WITHDRAWAL BLEEDING ( 2 FDA reports)
ABORTION COMPLETE ( 2 FDA reports)
ABORTION MISSED ( 2 FDA reports)
ABSCESS DRAINAGE ( 2 FDA reports)
ABSCESS INTESTINAL ( 2 FDA reports)
ACANTHOMA ( 2 FDA reports)
ACANTHOSIS ( 2 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 2 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 2 FDA reports)
ADENOCARCINOMA ( 2 FDA reports)
ADNEXA UTERI PAIN ( 2 FDA reports)
ADRENAL INSUFFICIENCY ( 2 FDA reports)
AGORAPHOBIA ( 2 FDA reports)
ALCOHOL POISONING ( 2 FDA reports)
ALLERGY TEST POSITIVE ( 2 FDA reports)
ALOPECIA SCARRING ( 2 FDA reports)
AMBLYOPIA ( 2 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 2 FDA reports)
ANAEMIA MACROCYTIC ( 2 FDA reports)
ANALGESIC ASTHMA SYNDROME ( 2 FDA reports)
ANDROGENETIC ALOPECIA ( 2 FDA reports)
AORTIC DISORDER ( 2 FDA reports)
AORTIC DISSECTION ( 2 FDA reports)
AORTIC VALVE DISEASE ( 2 FDA reports)
AORTIC VALVE STENOSIS ( 2 FDA reports)
APLASTIC ANAEMIA ( 2 FDA reports)
APPLICATION SITE ERYTHEMA ( 2 FDA reports)
APPLICATION SITE IRRITATION ( 2 FDA reports)
APPLICATION SITE PAIN ( 2 FDA reports)
ARNOLD-CHIARI MALFORMATION ( 2 FDA reports)
ARTERIAL THROMBOSIS ( 2 FDA reports)
ARTHROSCOPY ( 2 FDA reports)
ASPIRATION PLEURAL CAVITY ( 2 FDA reports)
ATOPY ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK THIRD DEGREE ( 2 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 2 FDA reports)
AUTOIMMUNE THYROIDITIS ( 2 FDA reports)
AXILLARY MASS ( 2 FDA reports)
BACTERIAL CULTURE POSITIVE ( 2 FDA reports)
BACTERIAL TEST NEGATIVE ( 2 FDA reports)
BALANITIS ( 2 FDA reports)
BASAL GANGLION DEGENERATION ( 2 FDA reports)
BELLIGERENCE ( 2 FDA reports)
BENIGN NEOPLASM OF BLADDER ( 2 FDA reports)
BILIARY CYST ( 2 FDA reports)
BIOPSY ( 2 FDA reports)
BIOPSY LIVER ( 2 FDA reports)
BIOPSY LIVER ABNORMAL ( 2 FDA reports)
BLADDER CATHETERISATION ( 2 FDA reports)
BLADDER OPERATION ( 2 FDA reports)
BLADDER PROLAPSE ( 2 FDA reports)
BLOOD ALCOHOL INCREASED ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE ( 2 FDA reports)
BLOOD CORTISOL INCREASED ( 2 FDA reports)
BLOOD COUNT ABNORMAL ( 2 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 2 FDA reports)
BLOOD MAGNESIUM INCREASED ( 2 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 2 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 2 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 2 FDA reports)
BLOOD URIC ACID DECREASED ( 2 FDA reports)
BODY TEMPERATURE ( 2 FDA reports)
BONE EROSION ( 2 FDA reports)
BOWEL SOUNDS ABNORMAL ( 2 FDA reports)
BRACHIAL PLEXOPATHY ( 2 FDA reports)
BRADYPHRENIA ( 2 FDA reports)
BREAST FIBROSIS ( 2 FDA reports)
BREAST NECROSIS ( 2 FDA reports)
BREAST OPERATION ( 2 FDA reports)
BRONCHIAL HYPERACTIVITY ( 2 FDA reports)
BRONCHIECTASIS ( 2 FDA reports)
BRONCHOPNEUMOPATHY ( 2 FDA reports)
BUCCAL MUCOSAL ROUGHENING ( 2 FDA reports)
CARDIAC DISCOMFORT ( 2 FDA reports)
CARDIAC MURMUR FUNCTIONAL ( 2 FDA reports)
CARDIAC PACEMAKER MALFUNCTION ( 2 FDA reports)
CARDIAC PERFORATION ( 2 FDA reports)
CAROTIDYNIA ( 2 FDA reports)
CATHETER SITE HAEMORRHAGE ( 2 FDA reports)
CATHETER SITE RELATED REACTION ( 2 FDA reports)
CEREBELLAR HAEMORRHAGE ( 2 FDA reports)
CEREBRAL ARTERY STENOSIS ( 2 FDA reports)
CEREBRAL DISORDER ( 2 FDA reports)
CERVICAL DYSPLASIA ( 2 FDA reports)
CERVIX DISORDER ( 2 FDA reports)
CHEST INJURY ( 2 FDA reports)
CHOLECYSTITIS INFECTIVE ( 2 FDA reports)
CHONDRITIS ( 2 FDA reports)
CHONDROPATHY ( 2 FDA reports)
CHOREOATHETOSIS ( 2 FDA reports)
CHROMOSOME ANALYSIS ABNORMAL ( 2 FDA reports)
CITROBACTER INFECTION ( 2 FDA reports)
CLOSTRIDIUM COLITIS ( 2 FDA reports)
CLUMSINESS ( 2 FDA reports)
COAGULATION FACTOR DECREASED ( 2 FDA reports)
COLITIS COLLAGENOUS ( 2 FDA reports)
COMMUNICATION DISORDER ( 2 FDA reports)
CONFABULATION ( 2 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 2 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 2 FDA reports)
CONVULSIVE THRESHOLD LOWERED ( 2 FDA reports)
CORNEAL ABRASION ( 2 FDA reports)
CORNEAL TRANSPLANT ( 2 FDA reports)
CORNEAL ULCER ( 2 FDA reports)
CORONARY ARTERY ANEURYSM ( 2 FDA reports)
CORRECTIVE LENS USER ( 2 FDA reports)
CSF PROTEIN INCREASED ( 2 FDA reports)
CUBITAL TUNNEL SYNDROME ( 2 FDA reports)
CULTURE POSITIVE ( 2 FDA reports)
CUTANEOUS VASCULITIS ( 2 FDA reports)
CYSTOCELE ( 2 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 2 FDA reports)
DEAFNESS UNILATERAL ( 2 FDA reports)
DECEREBRATION ( 2 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 2 FDA reports)
DELIRIUM TREMENS ( 2 FDA reports)
DEMENTIA ( 2 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 2 FDA reports)
DEPENDENT PERSONALITY DISORDER ( 2 FDA reports)
DEPERSONALISATION ( 2 FDA reports)
DERMATITIS ATOPIC ( 2 FDA reports)
DERMOGRAPHISM ( 2 FDA reports)
DEVICE BREAKAGE ( 2 FDA reports)
DEVICE MATERIAL ISSUE ( 2 FDA reports)
DEXAMETHASONE SUPPRESSION TEST POSITIVE ( 2 FDA reports)
DIABETIC MICROANGIOPATHY ( 2 FDA reports)
DIAPHRAGMATIC DISORDER ( 2 FDA reports)
DIAPHRAGMATIC INJURY ( 2 FDA reports)
DISINHIBITION ( 2 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 2 FDA reports)
DIVERTICULAR PERFORATION ( 2 FDA reports)
DRUG DISPENSING ERROR ( 2 FDA reports)
DRUG EFFECT DELAYED ( 2 FDA reports)
DRUG EFFECT INCREASED ( 2 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 2 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
DRUG TOLERANCE DECREASED ( 2 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 2 FDA reports)
DYSPHASIA ( 2 FDA reports)
DYSPHEMIA ( 2 FDA reports)
DYSPNOEA AT REST ( 2 FDA reports)
DYSPRAXIA ( 2 FDA reports)
EAR CONGESTION ( 2 FDA reports)
EAR PRURITUS ( 2 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 2 FDA reports)
EMBOLIC STROKE ( 2 FDA reports)
ENANTHEMA ( 2 FDA reports)
ENCEPHALITIS VIRAL ( 2 FDA reports)
ENCEPHALOMALACIA ( 2 FDA reports)
ENDOCARDITIS ( 2 FDA reports)
ENDOCARDITIS STAPHYLOCOCCAL ( 2 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 2 FDA reports)
ENTERITIS INFECTIOUS ( 2 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 2 FDA reports)
ENTHESOPATHY ( 2 FDA reports)
ENZYME ABNORMALITY ( 2 FDA reports)
EPIDERMOLYSIS BULLOSA ( 2 FDA reports)
EPSTEIN-BARR VIRUS ANTIGEN POSITIVE ( 2 FDA reports)
EROSIVE DUODENITIS ( 2 FDA reports)
ERYTHEMA NODOSUM ( 2 FDA reports)
ERYTHEMA OF EYELID ( 2 FDA reports)
EXERCISE LACK OF ( 2 FDA reports)
EYE INFECTION STAPHYLOCOCCAL ( 2 FDA reports)
EYE INJURY ( 2 FDA reports)
EYELID DISORDER ( 2 FDA reports)
EYELIDS PRURITUS ( 2 FDA reports)
FACIAL NERVE DISORDER ( 2 FDA reports)
FACIAL PARESIS ( 2 FDA reports)
FACTOR VIII INHIBITION ( 2 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 2 FDA reports)
FAECES PALE ( 2 FDA reports)
FAILURE TO THRIVE ( 2 FDA reports)
FALSE POSITIVE INVESTIGATION RESULT ( 2 FDA reports)
FASCIITIS ( 2 FDA reports)
FEAR OF DEATH ( 2 FDA reports)
FEELINGS OF WORTHLESSNESS ( 2 FDA reports)
FIBRIN D DIMER NORMAL ( 2 FDA reports)
FISTULA DISCHARGE ( 2 FDA reports)
FOETAL HEART RATE DECREASED ( 2 FDA reports)
FOOD INTERACTION ( 2 FDA reports)
FOOD INTOLERANCE ( 2 FDA reports)
FRACTURED COCCYX ( 2 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 2 FDA reports)
FUNGAL SKIN INFECTION ( 2 FDA reports)
GALLBLADDER PAIN ( 2 FDA reports)
GALLBLADDER PERFORATION ( 2 FDA reports)
GASTRIC NEOPLASM ( 2 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 2 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 2 FDA reports)
GINGIVAL ABSCESS ( 2 FDA reports)
GRANULOCYTES MATURATION ARREST ( 2 FDA reports)
GYNAECOMASTIA ( 2 FDA reports)
H1N1 INFLUENZA ( 2 FDA reports)
HAEMATOCRIT INCREASED ( 2 FDA reports)
HAEMATOPOIETIC NEOPLASM ( 2 FDA reports)
HAEMATOSPERMIA ( 2 FDA reports)
HAEMATOTOXICITY ( 2 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 2 FDA reports)
HAEMORRHAGIC CYST ( 2 FDA reports)
HAIR GROWTH ABNORMAL ( 2 FDA reports)
HAIR TEXTURE ABNORMAL ( 2 FDA reports)
HAPTOGLOBIN DECREASED ( 2 FDA reports)
HELICOBACTER GASTRITIS ( 2 FDA reports)
HEMICEPHALALGIA ( 2 FDA reports)
HEPATIC CALCIFICATION ( 2 FDA reports)
HEPATIC CANCER METASTATIC ( 2 FDA reports)
HEPATIC INFILTRATION EOSINOPHILIC ( 2 FDA reports)
HEPATITIS A ( 2 FDA reports)
HEPATITIS ALCOHOLIC ( 2 FDA reports)
HEPATITIS FULMINANT ( 2 FDA reports)
HEPATITIS TOXIC ( 2 FDA reports)
HERPES OPHTHALMIC ( 2 FDA reports)
HIDRADENITIS ( 2 FDA reports)
HILAR LYMPHADENOPATHY ( 2 FDA reports)
HISTONE ANTIBODY POSITIVE ( 2 FDA reports)
HISTOPLASMOSIS ( 2 FDA reports)
HOMANS' SIGN ( 2 FDA reports)
HOMICIDE ( 2 FDA reports)
HORMONE LEVEL ABNORMAL ( 2 FDA reports)
HOSPICE CARE ( 2 FDA reports)
HUMAN EHRLICHIOSIS ( 2 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 2 FDA reports)
HYPERAEMIA ( 2 FDA reports)
HYPERCHLORHYDRIA ( 2 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 2 FDA reports)
HYPERPLASTIC CHOLECYSTOPATHY ( 2 FDA reports)
HYPERPROTEINAEMIA ( 2 FDA reports)
HYPERREFLEXIA ( 2 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 2 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 2 FDA reports)
HYPERTHERMIA MALIGNANT ( 2 FDA reports)
HYPERURICAEMIA ( 2 FDA reports)
HYPOAESTHESIA EYE ( 2 FDA reports)
HYPOCAPNIA ( 2 FDA reports)
HYPOVOLAEMIC SHOCK ( 2 FDA reports)
ILIAC ARTERY STENOSIS ( 2 FDA reports)
ILIAC VEIN OCCLUSION ( 2 FDA reports)
ILLUSION ( 2 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 2 FDA reports)
INABILITY TO CRAWL ( 2 FDA reports)
INCISIONAL HERNIA ( 2 FDA reports)
INFECTED SKIN ULCER ( 2 FDA reports)
INFECTIVE ANEURYSM ( 2 FDA reports)
INFUSION SITE REACTION ( 2 FDA reports)
INGUINAL HERNIA REPAIR ( 2 FDA reports)
INJECTION SITE ABSCESS ( 2 FDA reports)
INJECTION SITE DISCOLOURATION ( 2 FDA reports)
INTERMITTENT CLAUDICATION ( 2 FDA reports)
INTESTINAL ISCHAEMIA ( 2 FDA reports)
INTRA-UTERINE DEATH ( 2 FDA reports)
INTUSSUSCEPTION ( 2 FDA reports)
IRON OVERLOAD ( 2 FDA reports)
IUD MIGRATION ( 2 FDA reports)
JAUNDICE CHOLESTATIC ( 2 FDA reports)
JOINT ANKYLOSIS ( 2 FDA reports)
JOINT CREPITATION ( 2 FDA reports)
JOINT HYPEREXTENSION ( 2 FDA reports)
JOINT LOCK ( 2 FDA reports)
KIDNEY FIBROSIS ( 2 FDA reports)
LABELLED DRUG-FOOD INTERACTION MEDICATION ERROR ( 2 FDA reports)
LABILE BLOOD PRESSURE ( 2 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 2 FDA reports)
LACTOSE INTOLERANCE ( 2 FDA reports)
LARGE CELL CARCINOMA OF THE RESPIRATORY TRACT STAGE UNSPECIFIED ( 2 FDA reports)
LARGE INTESTINE PERFORATION ( 2 FDA reports)
LARYNGEAL DISORDER ( 2 FDA reports)
LARYNGOSPASM ( 2 FDA reports)
LATENT TUBERCULOSIS ( 2 FDA reports)
LEFT VENTRICULAR FAILURE ( 2 FDA reports)
LIBIDO INCREASED ( 2 FDA reports)
LIGAMENT RUPTURE ( 2 FDA reports)
LIPOATROPHY ( 2 FDA reports)
LIPOSARCOMA ( 2 FDA reports)
LIPOSUCTION ( 2 FDA reports)
LIVER ABSCESS ( 2 FDA reports)
LOCALISED EXFOLIATION ( 2 FDA reports)
LOSS OF CONTROL OF LEGS ( 2 FDA reports)
LOSS OF EMPLOYMENT ( 2 FDA reports)
LOW TURNOVER OSTEOPATHY ( 2 FDA reports)
LOWER LIMB FRACTURE ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 2 FDA reports)
LYMPHOCYTIC INFILTRATION ( 2 FDA reports)
MALIGNANT MELANOMA ( 2 FDA reports)
MAMMOGRAM ABNORMAL ( 2 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 2 FDA reports)
MARROW HYPERPLASIA ( 2 FDA reports)
MASTITIS ( 2 FDA reports)
MASTOIDITIS ( 2 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 2 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 2 FDA reports)
MAY-THURNER SYNDROME ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 2 FDA reports)
MENIERE'S DISEASE ( 2 FDA reports)
MENINGISM ( 2 FDA reports)
MENINGITIS LISTERIA ( 2 FDA reports)
MENOPAUSE ( 2 FDA reports)
METABOLIC SYNDROME ( 2 FDA reports)
METASTASES TO ADRENALS ( 2 FDA reports)
METASTASES TO PERITONEUM ( 2 FDA reports)
METATARSALGIA ( 2 FDA reports)
MICROCYTOSIS ( 2 FDA reports)
MIGRAINE WITH AURA ( 2 FDA reports)
MITRAL VALVE SCLEROSIS ( 2 FDA reports)
MITRAL VALVE STENOSIS ( 2 FDA reports)
MUIR-TORRE SYNDROME ( 2 FDA reports)
MULTIPLE CHEMICAL SENSITIVITY ( 2 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 2 FDA reports)
MUSCLE CONTRACTURE ( 2 FDA reports)
MUSCLE MASS ( 2 FDA reports)
MYOCLONIC EPILEPSY ( 2 FDA reports)
MYOCLONUS ( 2 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 2 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 2 FDA reports)
NAIL DISCOLOURATION ( 2 FDA reports)
NASAL DRYNESS ( 2 FDA reports)
NASAL MUCOSAL DISORDER ( 2 FDA reports)
NASAL OBSTRUCTION ( 2 FDA reports)
NEGATIVE THOUGHTS ( 2 FDA reports)
NEONATAL DISORDER ( 2 FDA reports)
NEPHRITIS ( 2 FDA reports)
NERVE BLOCK ( 2 FDA reports)
NEUROMA ( 2 FDA reports)
NEUTROPENIC SEPSIS ( 2 FDA reports)
NIKOLSKY'S SIGN ( 2 FDA reports)
NITRITE URINE PRESENT ( 2 FDA reports)
NODULE ( 2 FDA reports)
NODULE ON EXTREMITY ( 2 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 2 FDA reports)
OCCULT BLOOD ( 2 FDA reports)
ODYNOPHAGIA ( 2 FDA reports)
OEDEMATOUS PANCREATITIS ( 2 FDA reports)
OESOPHAGEAL ADENOCARCINOMA ( 2 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 2 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 2 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 2 FDA reports)
OESOPHAGITIS ULCERATIVE ( 2 FDA reports)
OLIGURIA ( 2 FDA reports)
ON AND OFF PHENOMENON ( 2 FDA reports)
ONYCHOCLASIS ( 2 FDA reports)
ONYCHOMADESIS ( 2 FDA reports)
OPTIC NEURITIS RETROBULBAR ( 2 FDA reports)
ORAL SOFT TISSUE DISORDER ( 2 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 2 FDA reports)
OSTEITIS ( 2 FDA reports)
OVARIAN ENLARGEMENT ( 2 FDA reports)
PAINFUL ERECTION ( 2 FDA reports)
PANCOAST'S TUMOUR ( 2 FDA reports)
PANCREATIC NECROSIS ( 2 FDA reports)
PANCREATIC PSEUDOCYST ( 2 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 2 FDA reports)
PANCREATITIS NECROTISING ( 2 FDA reports)
PAPILLARY THYROID CANCER ( 2 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 2 FDA reports)
PARTNER STRESS ( 2 FDA reports)
PATHOGEN RESISTANCE ( 2 FDA reports)
PCO2 INCREASED ( 2 FDA reports)
PERIORBITAL HAEMATOMA ( 2 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 2 FDA reports)
PERIPHERAL NERVE DECOMPRESSION ( 2 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 2 FDA reports)
PERIRECTAL ABSCESS ( 2 FDA reports)
PERITONEAL DIALYSIS ( 2 FDA reports)
PERITONITIS BACTERIAL ( 2 FDA reports)
PHARYNGEAL INFLAMMATION ( 2 FDA reports)
PHARYNX DISCOMFORT ( 2 FDA reports)
PHIMOSIS ( 2 FDA reports)
PHLEBITIS SUPERFICIAL ( 2 FDA reports)
PHLEBOLITH ( 2 FDA reports)
PHYSICAL ASSAULT ( 2 FDA reports)
PHYSIOTHERAPY ( 2 FDA reports)
PLATELET FUNCTION TEST ABNORMAL ( 2 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 2 FDA reports)
PNEUMOPERITONEUM ( 2 FDA reports)
PO2 DECREASED ( 2 FDA reports)
POLYHYDRAMNIOS ( 2 FDA reports)
POLYMENORRHOEA ( 2 FDA reports)
POLYPECTOMY ( 2 FDA reports)
POLYSUBSTANCE ABUSE ( 2 FDA reports)
PORTAL HYPERTENSION ( 2 FDA reports)
PORTAL VEIN OCCLUSION ( 2 FDA reports)
POST GASTRIC SURGERY SYNDROME ( 2 FDA reports)
POST HERPETIC NEURALGIA ( 2 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 2 FDA reports)
POSTOPERATIVE ABSCESS ( 2 FDA reports)
POSTPARTUM DEPRESSION ( 2 FDA reports)
POSTPERICARDIOTOMY SYNDROME ( 2 FDA reports)
POSTURAL ORTHOSTATIC TACHYCARDIA SYNDROME ( 2 FDA reports)
PRINZMETAL ANGINA ( 2 FDA reports)
PROCTOCOLITIS ( 2 FDA reports)
PRODUCT COMMINGLING ( 2 FDA reports)
PRODUCT CONTAINER SEAL ISSUE ( 2 FDA reports)
PRODUCT SHAPE ISSUE ( 2 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 2 FDA reports)
PROSTATIC DISORDER ( 2 FDA reports)
PROSTATISM ( 2 FDA reports)
PROTEIN S DECREASED ( 2 FDA reports)
PRURITUS GENITAL ( 2 FDA reports)
PSEUDOMONAL SEPSIS ( 2 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 2 FDA reports)
PULMONARY GRANULOMA ( 2 FDA reports)
PULMONARY NECROSIS ( 2 FDA reports)
PULSE PRESSURE DECREASED ( 2 FDA reports)
PURPURA FULMINANS ( 2 FDA reports)
RADICULAR SYNDROME ( 2 FDA reports)
RASH SCALY ( 2 FDA reports)
REACTION TO COLOURING ( 2 FDA reports)
RECTAL TENESMUS ( 2 FDA reports)
RECTOCELE ( 2 FDA reports)
RED BLOOD CELLS URINE ( 2 FDA reports)
REFLUX GASTRITIS ( 2 FDA reports)
REFRACTORY ANAEMIA ( 2 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 2 FDA reports)
RELAPSING-REMITTING MULTIPLE SCLEROSIS ( 2 FDA reports)
RENAL CELL CARCINOMA ( 2 FDA reports)
RENAL COLIC ( 2 FDA reports)
RENAL INTERSTITIAL FIBROSIS ( 2 FDA reports)
RENAL SURGERY ( 2 FDA reports)
RENAL TUBULAR ACIDOSIS ( 2 FDA reports)
RENAL VESSEL DISORDER ( 2 FDA reports)
RESPIRATORY ALKALOSIS ( 2 FDA reports)
RESPIRATORY TRACT INFLAMMATION ( 2 FDA reports)
RETINAL ISCHAEMIA ( 2 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 2 FDA reports)
ROTATOR CUFF REPAIR ( 2 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 2 FDA reports)
SEBACEOUS ADENOMA ( 2 FDA reports)
SENSATION OF BLOCK IN EAR ( 2 FDA reports)
SENSATION OF PRESSURE ( 2 FDA reports)
SENSE OF OPPRESSION ( 2 FDA reports)
SEPTAL PANNICULITIS ( 2 FDA reports)
SEPTIC ARTHRITIS STAPHYLOCOCCAL ( 2 FDA reports)
SEROSITIS ( 2 FDA reports)
SHOCK HAEMORRHAGIC ( 2 FDA reports)
SKIN HYPERPIGMENTATION ( 2 FDA reports)
SKIN NEOPLASM EXCISION ( 2 FDA reports)
SKIN TEST NEGATIVE ( 2 FDA reports)
SKIN TEST POSITIVE ( 2 FDA reports)
SKIN TIGHTNESS ( 2 FDA reports)
SKIN WRINKLING ( 2 FDA reports)
SLEEP PARALYSIS ( 2 FDA reports)
SMALL INTESTINE ULCER ( 2 FDA reports)
SMEAR CERVIX ABNORMAL ( 2 FDA reports)
SOCIAL PROBLEM ( 2 FDA reports)
SPINAL CORD INJURY ( 2 FDA reports)
SPINAL MYELOGRAM ABNORMAL ( 2 FDA reports)
SPLENIC INFARCTION ( 2 FDA reports)
SPLENIC LESION ( 2 FDA reports)
SQUAMOUS CELL CARCINOMA ( 2 FDA reports)
STAPHYLOCOCCAL OSTEOMYELITIS ( 2 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 2 FDA reports)
STARING ( 2 FDA reports)
STATUS EPILEPTICUS ( 2 FDA reports)
STEATORRHOEA ( 2 FDA reports)
STENOTROPHOMONAS INFECTION ( 2 FDA reports)
STREPTOCOCCAL SEPSIS ( 2 FDA reports)
STUPOR ( 2 FDA reports)
SUBCUTANEOUS NODULE ( 2 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 2 FDA reports)
T-LYMPHOCYTE COUNT INCREASED ( 2 FDA reports)
TANGENTIALITY ( 2 FDA reports)
TELANGIECTASIA ( 2 FDA reports)
TEMPORAL ARTERITIS ( 2 FDA reports)
TEMPORAL LOBE EPILEPSY ( 2 FDA reports)
TENDON INJURY ( 2 FDA reports)
TENDON OPERATION ( 2 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 2 FDA reports)
THORACIC OUTLET SYNDROME ( 2 FDA reports)
THYROTOXIC CRISIS ( 2 FDA reports)
THYROXINE DECREASED ( 2 FDA reports)
TINEA PEDIS ( 2 FDA reports)
TOE DEFORMITY ( 2 FDA reports)
TONGUE BITING ( 2 FDA reports)
TONGUE BLISTERING ( 2 FDA reports)
TONGUE PARALYSIS ( 2 FDA reports)
TONSILLITIS BACTERIAL ( 2 FDA reports)
TORTICOLLIS ( 2 FDA reports)
TOXIC SHOCK SYNDROME ( 2 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 2 FDA reports)
TRANSPLANT ( 2 FDA reports)
TRAUMATIC HAEMORRHAGE ( 2 FDA reports)
TRICUSPID VALVE STENOSIS ( 2 FDA reports)
UHTHOFF'S PHENOMENON ( 2 FDA reports)
ULCERATIVE KERATITIS ( 2 FDA reports)
UMBILICAL HERNIA, OBSTRUCTIVE ( 2 FDA reports)
URETERIC OBSTRUCTION ( 2 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 2 FDA reports)
URINE ANALYSIS ( 2 FDA reports)
UTERINE CONTRACTIONS ABNORMAL ( 2 FDA reports)
UTERINE CONTRACTIONS DURING PREGNANCY ( 2 FDA reports)
UTERINE ENLARGEMENT ( 2 FDA reports)
UTERINE INFLAMMATION ( 2 FDA reports)
UTERINE MASS ( 2 FDA reports)
UTERINE PERFORATION ( 2 FDA reports)
VAGINAL MYCOSIS ( 2 FDA reports)
VAGINAL OEDEMA ( 2 FDA reports)
VASCULAR DEMENTIA ( 2 FDA reports)
VASCULAR HEADACHE ( 2 FDA reports)
VASCULAR INJURY ( 2 FDA reports)
VENA CAVA INJURY ( 2 FDA reports)
VENOUS INSUFFICIENCY ( 2 FDA reports)
VENOUS STASIS ( 2 FDA reports)
VENTRICULAR ARRHYTHMIA ( 2 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 2 FDA reports)
VESICAL FISTULA ( 2 FDA reports)
VIRAL LABYRINTHITIS ( 2 FDA reports)
VIRAL RHINITIS ( 2 FDA reports)
VIRUS SEROLOGY TEST POSITIVE ( 2 FDA reports)
VITAMIN D DECREASED ( 2 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 2 FDA reports)
WEIGHT LOSS POOR ( 2 FDA reports)
WHITE BLOOD CELL COUNT ( 2 FDA reports)
ABNORMAL CHEST SOUND ( 1 FDA reports)
ABNORMAL LABOUR ( 1 FDA reports)
ABORTION INDUCED ( 1 FDA reports)
ABSCESS BACTERIAL ( 1 FDA reports)
ABSCESS OF SALIVARY GLAND ( 1 FDA reports)
ACCIDENTAL NEEDLE STICK ( 1 FDA reports)
ACIDOSIS HYPERCHLORAEMIC ( 1 FDA reports)
ACINETOBACTER INFECTION ( 1 FDA reports)
ACQUIRED PYLORIC STENOSIS ( 1 FDA reports)
ACTIVATED PROTEIN C RESISTANCE ( 1 FDA reports)
ACUTE CHEST SYNDROME ( 1 FDA reports)
ACUTE LEUKAEMIA ( 1 FDA reports)
ADENOCARCINOMA OF THE CERVIX ( 1 FDA reports)
ADHESIOLYSIS ( 1 FDA reports)
ADJUSTMENT DISORDER WITH MIXED DISTURBANCE OF EMOTION AND CONDUCT ( 1 FDA reports)
ADRENAL NEOPLASM ( 1 FDA reports)
AGE INDETERMINATE MYOCARDIAL INFARCTION ( 1 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ALBUMIN GLOBULIN RATIO INCREASED ( 1 FDA reports)
ALCOHOL INTERACTION ( 1 FDA reports)
ALCOHOL INTOLERANCE ( 1 FDA reports)
ALCOHOLIC PANCREATITIS ( 1 FDA reports)
ALDOLASE INCREASED ( 1 FDA reports)
ALLERGY TO ANIMAL ( 1 FDA reports)
ALLOGENIC BONE MARROW TRANSPLANTATION THERAPY ( 1 FDA reports)
ALPHA GLOBULIN INCREASED ( 1 FDA reports)
ALVEOLITIS ( 1 FDA reports)
AMAUROSIS FUGAX ( 1 FDA reports)
AMNIOTIC CAVITY DISORDER ( 1 FDA reports)
AMNIOTIC FLUID VOLUME DECREASED ( 1 FDA reports)
ANAL DISCOMFORT ( 1 FDA reports)
ANAL INJURY ( 1 FDA reports)
ANAL PRURITUS ( 1 FDA reports)
ANAL SPHINCTER ATONY ( 1 FDA reports)
ANALGESIA ( 1 FDA reports)
ANALGESIC DRUG LEVEL DECREASED ( 1 FDA reports)
ANALGESIC DRUG LEVEL INCREASED ( 1 FDA reports)
ANDROGEN INSENSITIVITY SYNDROME ( 1 FDA reports)
ANIMAL BITE ( 1 FDA reports)
ANION GAP INCREASED ( 1 FDA reports)
ANKYLOGLOSSIA CONGENITAL ( 1 FDA reports)
ANORGASMIA ( 1 FDA reports)
ANTEPARTUM HAEMORRHAGE ( 1 FDA reports)
ANTERIOR SPINAL ARTERY SYNDROME ( 1 FDA reports)
ANTI-HBC IGM ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 1 FDA reports)
ANTIBODY TEST ABNORMAL ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT TOXICITY ( 1 FDA reports)
ANTIMITOCHONDRIAL ANTIBODY POSITIVE ( 1 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 1 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 1 FDA reports)
AORTIC CALCIFICATION ( 1 FDA reports)
AORTIC EMBOLUS ( 1 FDA reports)
AORTIC THROMBOSIS ( 1 FDA reports)
AORTIC VALVE REPAIR ( 1 FDA reports)
APGAR SCORE LOW ( 1 FDA reports)
APLASIA PURE RED CELL ( 1 FDA reports)
APPENDIX DISORDER ( 1 FDA reports)
APPLICATION SITE DISCHARGE ( 1 FDA reports)
APPLICATION SITE INDURATION ( 1 FDA reports)
APPLICATION SITE INFLAMMATION ( 1 FDA reports)
APPLICATION SITE NODULE ( 1 FDA reports)
ARACHNOID CYST ( 1 FDA reports)
ARTERIOGRAM CORONARY ( 1 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 1 FDA reports)
ASEPTIC NECROSIS BONE ( 1 FDA reports)
ASPIRATION BIOPSY ( 1 FDA reports)
ASPIRATION BRONCHIAL ( 1 FDA reports)
ASPIRATION TRACHEAL ( 1 FDA reports)
ASPIRATION TRACHEAL ABNORMAL ( 1 FDA reports)
ASTIGMATISM ( 1 FDA reports)
ATRIAL PRESSURE INCREASED ( 1 FDA reports)
ATRIAL THROMBOSIS ( 1 FDA reports)
ATROPHIC VULVOVAGINITIS ( 1 FDA reports)
AURA ( 1 FDA reports)
AUTOIMMUNE MYOCARDITIS ( 1 FDA reports)
AZOOSPERMIA ( 1 FDA reports)
B-CELL LYMPHOMA ( 1 FDA reports)
BACTERIA STOOL IDENTIFIED ( 1 FDA reports)
BACTERIA URINE ( 1 FDA reports)
BACTERIAL PYELONEPHRITIS ( 1 FDA reports)
BACTEROIDES BACTERAEMIA ( 1 FDA reports)
BAND NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
BAND NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
BASE EXCESS NEGATIVE ( 1 FDA reports)
BEHCET'S SYNDROME ( 1 FDA reports)
BENIGN LYMPH NODE NEOPLASM ( 1 FDA reports)
BENIGN NEOPLASM OF ADRENAL GLAND ( 1 FDA reports)
BENIGN NEOPLASM OF PINEAL GLAND ( 1 FDA reports)
BILIARY DILATATION ( 1 FDA reports)
BINGE EATING ( 1 FDA reports)
BIOPSY BREAST ABNORMAL ( 1 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 1 FDA reports)
BIOPSY SITE UNSPECIFIED ABNORMAL ( 1 FDA reports)
BIPOLAR I DISORDER ( 1 FDA reports)
BIPOLAR II DISORDER ( 1 FDA reports)
BLADDER DISCOMFORT ( 1 FDA reports)
BLADDER IRRITATION ( 1 FDA reports)
BLADDER NEOPLASM SURGERY ( 1 FDA reports)
BLASTOMYCOSIS ( 1 FDA reports)
BLEPHAROSPASM ( 1 FDA reports)
BLIGHTED OVUM ( 1 FDA reports)
BLISTER INFECTED ( 1 FDA reports)
BLOOD BICARBONATE ABNORMAL ( 1 FDA reports)
BLOOD BILIRUBIN DECREASED ( 1 FDA reports)
BLOOD CHROMOGRANIN A INCREASED ( 1 FDA reports)
BLOOD CORTISOL DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ( 1 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 1 FDA reports)
BLOOD ETHANOL INCREASED ( 1 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 1 FDA reports)
BLOOD FOLLICLE STIMULATING HORMONE DECREASED ( 1 FDA reports)
BLOOD HIV RNA ( 1 FDA reports)
BLOOD IRON INCREASED ( 1 FDA reports)
BLOOD LUTEINISING HORMONE DECREASED ( 1 FDA reports)
BLOOD METHAEMOGLOBIN PRESENT ( 1 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 1 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 1 FDA reports)
BLOOD POTASSIUM ( 1 FDA reports)
BLOOD PROLACTIN INCREASED ( 1 FDA reports)
BLOOD PYRUVIC ACID DECREASED ( 1 FDA reports)
BLOOD SODIUM ABNORMAL ( 1 FDA reports)
BLOOD URIC ACID ABNORMAL ( 1 FDA reports)
BLOOD URINE ( 1 FDA reports)
BLOOD VISCOSITY INCREASED ( 1 FDA reports)
BLOODY DISCHARGE ( 1 FDA reports)
BODY FAT DISORDER ( 1 FDA reports)
BODY HEIGHT ( 1 FDA reports)
BODY MASS INDEX INCREASED ( 1 FDA reports)
BORDERLINE GLAUCOMA ( 1 FDA reports)
BRAIN DEATH ( 1 FDA reports)
BRAIN SCAN ABNORMAL ( 1 FDA reports)
BREAST CALCIFICATIONS ( 1 FDA reports)
BREAST CANCER STAGE I ( 1 FDA reports)
BREAST CANCER STAGE II ( 1 FDA reports)
BREAST CELLULITIS ( 1 FDA reports)
BREAST DISCOMFORT ( 1 FDA reports)
BREAST DISORDER ( 1 FDA reports)
BREAST ENLARGEMENT ( 1 FDA reports)
BREAST HAEMORRHAGE ( 1 FDA reports)
BREAST RECONSTRUCTION ( 1 FDA reports)
BREAST SWELLING ( 1 FDA reports)
BRONCHIAL DISORDER ( 1 FDA reports)
BRONCHIAL IRRITATION ( 1 FDA reports)
BRONCHIAL SECRETION RETENTION ( 1 FDA reports)
BRONCHIOLITIS ( 1 FDA reports)
BUNDLE BRANCH BLOCK BILATERAL ( 1 FDA reports)
BURKHOLDERIA CEPACIA COMPLEX INFECTION ( 1 FDA reports)
BURN OESOPHAGEAL ( 1 FDA reports)
BURNOUT SYNDROME ( 1 FDA reports)
BURNS THIRD DEGREE ( 1 FDA reports)
CAFFEINE CONSUMPTION ( 1 FDA reports)
CALCIUM DEFICIENCY ( 1 FDA reports)
CANCER PAIN ( 1 FDA reports)
CARBON DIOXIDE DECREASED ( 1 FDA reports)
CARDIAC ANEURYSM ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
CARDIAC HYPERTROPHY ( 1 FDA reports)
CARDIAC NEOPLASM UNSPECIFIED ( 1 FDA reports)
CARDIAC VALVE VEGETATION ( 1 FDA reports)
CARDIAC VENTRICULOGRAM RIGHT ABNORMAL ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 1 FDA reports)
CAROTID ARTERY ATHEROMA ( 1 FDA reports)
CAROTID ARTERY DISSECTION ( 1 FDA reports)
CAROTID ARTERY STENT INSERTION ( 1 FDA reports)
CAROTID ARTERY THROMBOSIS ( 1 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 1 FDA reports)
CATARACT CORTICAL ( 1 FDA reports)
CATARACT NUCLEAR ( 1 FDA reports)
CATARACT SUBCAPSULAR ( 1 FDA reports)
CATHETER RELATED COMPLICATION ( 1 FDA reports)
CATHETER SITE DISCHARGE ( 1 FDA reports)
CELLULITIS ORBITAL ( 1 FDA reports)
CENTRAL LINE INFECTION ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM STIMULATION ( 1 FDA reports)
CENTRAL PAIN SYNDROME ( 1 FDA reports)
CEREBELLAR ATROPHY ( 1 FDA reports)
CEREBELLAR TUMOUR ( 1 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 1 FDA reports)
CEREBRAL HAEMATOMA ( 1 FDA reports)
CEREBRAL HYPOPERFUSION ( 1 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 1 FDA reports)
CEREBRAL THROMBOSIS ( 1 FDA reports)
CEREBROVASCULAR INSUFFICIENCY ( 1 FDA reports)
CERVIX CARCINOMA ( 1 FDA reports)
CERVIX CARCINOMA STAGE 0 ( 1 FDA reports)
CHEMICAL ABUSER ( 1 FDA reports)
CHEMICAL INJURY ( 1 FDA reports)
CHEMICAL POISONING ( 1 FDA reports)
CHEST WALL PAIN ( 1 FDA reports)
CHONDROMALACIA ( 1 FDA reports)
CHORDAE TENDINAE RUPTURE ( 1 FDA reports)
CHOROID MELANOMA ( 1 FDA reports)
CHROMATOPSIA ( 1 FDA reports)
CHRONIC HEPATIC FAILURE ( 1 FDA reports)
COAGULATION FACTOR INCREASED ( 1 FDA reports)
COAGULATION FACTOR IX LEVEL DECREASED ( 1 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 1 FDA reports)
COAGULATION FACTOR VII LEVEL DECREASED ( 1 FDA reports)
COAGULATION FACTOR VIII LEVEL INCREASED ( 1 FDA reports)
COCCIDIOIDOMYCOSIS ( 1 FDA reports)
COCCYDYNIA ( 1 FDA reports)
COITAL BLEEDING ( 1 FDA reports)
COLECTOMY ( 1 FDA reports)
COLLAGEN-VASCULAR DISEASE ( 1 FDA reports)
COLOBOMA ( 1 FDA reports)
COLON CANCER METASTATIC ( 1 FDA reports)
COMPLEMENT FACTOR C3 DECREASED ( 1 FDA reports)
COMPLEMENT FACTOR C4 DECREASED ( 1 FDA reports)
COMPLICATION OF DEVICE INSERTION ( 1 FDA reports)
COMPLICATION OF PREGNANCY ( 1 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 1 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 1 FDA reports)
CONGENITAL ATRIAL SEPTAL DEFECT ( 1 FDA reports)
CONGENITAL CENTRAL NERVOUS SYSTEM ANOMALY ( 1 FDA reports)
CONGENITAL CHOROID PLEXUS CYST ( 1 FDA reports)
CONGENITAL TONGUE ANOMALY ( 1 FDA reports)
CONGENITAL VESICOURETERIC REFLUX ( 1 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 1 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 1 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 1 FDA reports)
CORONARY ARTERY THROMBOSIS ( 1 FDA reports)
COXSACKIE VIRAL INFECTION ( 1 FDA reports)
CRACKLES LUNG ( 1 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CSF BACTERIA IDENTIFIED ( 1 FDA reports)
CSF VIRUS IDENTIFIED ( 1 FDA reports)
CULTURE WOUND POSITIVE ( 1 FDA reports)
CYSTITIS ESCHERICHIA ( 1 FDA reports)
DACRYOCYSTORHINOSTOMY ( 1 FDA reports)
DARK CIRCLES UNDER EYES ( 1 FDA reports)
DEAFNESS TRANSITORY ( 1 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 1 FDA reports)
DENERVATION ATROPHY ( 1 FDA reports)
DEPRESSION SUICIDAL ( 1 FDA reports)
DEREALISATION ( 1 FDA reports)
DERMATITIS HERPETIFORMIS ( 1 FDA reports)
DETOXIFICATION ( 1 FDA reports)
DEVICE DISLOCATION ( 1 FDA reports)
DIABETIC FOOT ( 1 FDA reports)
DIABETIC NEUROPATHY ( 1 FDA reports)
DIAPHRAGMATIC HERNIA ( 1 FDA reports)
DIFFICULT TO WEAN FROM VENTILATOR ( 1 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 1 FDA reports)
DISEASE COMPLICATION ( 1 FDA reports)
DISSOCIATION ( 1 FDA reports)
DIVORCED ( 1 FDA reports)
DREAMY STATE ( 1 FDA reports)
DROOLING ( 1 FDA reports)
DRUG ADDICT ( 1 FDA reports)
DRUG EFFECT PROLONGED ( 1 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 1 FDA reports)
DRUG LABEL CONFUSION ( 1 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 1 FDA reports)
DRUG WITHDRAWAL CONVULSIONS ( 1 FDA reports)
DRUG-INDUCED LIVER INJURY ( 1 FDA reports)
DUODENITIS HAEMORRHAGIC ( 1 FDA reports)
DUPUYTREN'S CONTRACTURE ( 1 FDA reports)
DYSLOGIA ( 1 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 1 FDA reports)
DYSSOMNIA ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
DYSTROPHIC CALCIFICATION ( 1 FDA reports)
EAR INJURY ( 1 FDA reports)
EAR OPERATION COMPLICATION ( 1 FDA reports)
ECTOPIC PREGNANCY ( 1 FDA reports)
EDUCATIONAL PROBLEM ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM QT INTERVAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROLYTE DEPLETION ( 1 FDA reports)
ENDOMETRIAL METAPLASIA ( 1 FDA reports)
ENDOTRACHEAL INTUBATION ( 1 FDA reports)
ENLARGED UVULA ( 1 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 1 FDA reports)
ENTEROVESICAL FISTULA ( 1 FDA reports)
ENURESIS ( 1 FDA reports)
EOSINOPHIL COUNT DECREASED ( 1 FDA reports)
EOSINOPHILIC CELLULITIS ( 1 FDA reports)
EOSINOPHILIC PNEUMONIA ( 1 FDA reports)
EPHELIDES ( 1 FDA reports)
EPIGLOTTIC OEDEMA ( 1 FDA reports)
EPIGLOTTITIS ( 1 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 1 FDA reports)
ESCHERICHIA BACTERAEMIA ( 1 FDA reports)
ETHMOID SINUS SURGERY ( 1 FDA reports)
EXCITABILITY ( 1 FDA reports)
EXPOSED BONE IN JAW ( 1 FDA reports)
EXTRADURAL HAEMATOMA ( 1 FDA reports)
EXTRAOCULAR MUSCLE PARESIS ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EXTREMITY NECROSIS ( 1 FDA reports)
EYE BURNS ( 1 FDA reports)
EYE PENETRATION ( 1 FDA reports)
EYE REDNESS ( 1 FDA reports)
EYELASH DISCOLOURATION ( 1 FDA reports)
EYELID BLEEDING ( 1 FDA reports)
FACIAL LESION EXCISION ( 1 FDA reports)
FACIAL WASTING ( 1 FDA reports)
FALLOPIAN TUBE DISORDER ( 1 FDA reports)
FAMILY STRESS ( 1 FDA reports)
FANCONI SYNDROME ( 1 FDA reports)
FASCIECTOMY ( 1 FDA reports)
FAT TISSUE INCREASED ( 1 FDA reports)
FEBRILE BONE MARROW APLASIA ( 1 FDA reports)
FEEDING DISORDER NEONATAL ( 1 FDA reports)
FEEDING TUBE COMPLICATION ( 1 FDA reports)
FEELING HOT AND COLD ( 1 FDA reports)
FEMALE GENITAL-DIGESTIVE TRACT FISTULA ( 1 FDA reports)
FEMORAL ARTERY DISSECTION ( 1 FDA reports)
FEMORAL NECK FRACTURE ( 1 FDA reports)
FIBROADENOMA OF BREAST ( 1 FDA reports)
FINGER DEFORMITY ( 1 FDA reports)
FLIGHT OF IDEAS ( 1 FDA reports)
FOETAL HEART RATE ABNORMAL ( 1 FDA reports)
FOETAL MALPRESENTATION ( 1 FDA reports)
FOLLICULAR THYROID CANCER ( 1 FDA reports)
FOLLICULITIS ( 1 FDA reports)
FONTANELLE BULGING ( 1 FDA reports)
FOOD ALLERGY ( 1 FDA reports)
FORAMINOTOMY ( 1 FDA reports)
FOREARM FRACTURE ( 1 FDA reports)
FRACTURE NONUNION ( 1 FDA reports)
FRACTURE TREATMENT ( 1 FDA reports)
GALLBLADDER OEDEMA ( 1 FDA reports)
GALLOP RHYTHM PRESENT ( 1 FDA reports)
GANGLION ( 1 FDA reports)
GASTRIC ANTRAL VASCULAR ECTASIA ( 1 FDA reports)
GASTRIC OUTLET OBSTRUCTION ( 1 FDA reports)
GASTRIC PERFORATION ( 1 FDA reports)
GASTRIC ULCER HELICOBACTER ( 1 FDA reports)
GASTROENTERITIS ROTAVIRUS ( 1 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 1 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL SURGERY ( 1 FDA reports)
GASTROSTOMY TUBE INSERTION ( 1 FDA reports)
GENITAL BURNING SENSATION ( 1 FDA reports)
GENITAL DISORDER FEMALE ( 1 FDA reports)
GENITAL PAIN ( 1 FDA reports)
GENITAL PRURITUS FEMALE ( 1 FDA reports)
GENITAL RASH ( 1 FDA reports)
GINGIVAL ERYTHEMA ( 1 FDA reports)
GINGIVAL HYPERPLASIA ( 1 FDA reports)
GLIOMA ( 1 FDA reports)
GLOBAL AMNESIA ( 1 FDA reports)
GLOBULINS INCREASED ( 1 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 1 FDA reports)
GLOMERULONEPHRITIS RAPIDLY PROGRESSIVE ( 1 FDA reports)
GLOMERULOSCLEROSIS ( 1 FDA reports)
GLOMUS TUMOUR ( 1 FDA reports)
GLYCOSURIA ( 1 FDA reports)
GRAFT COMPLICATION ( 1 FDA reports)
GRANDIOSITY ( 1 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 1 FDA reports)
GRIP STRENGTH DECREASED ( 1 FDA reports)
GROWTH OF EYELASHES ( 1 FDA reports)
GRUNTING ( 1 FDA reports)
HABITUAL ABORTION ( 1 FDA reports)
HAEMATOCOLPOS ( 1 FDA reports)
HAEMOCHROMATOSIS ( 1 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 1 FDA reports)
HAEMORRHAGIC INFARCTION ( 1 FDA reports)
HAEMORRHAGIC OVARIAN CYST ( 1 FDA reports)
HAIR COLOUR CHANGES ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
HAMARTOMA ( 1 FDA reports)
HAPTOGLOBIN INCREASED ( 1 FDA reports)
HEADACHE POSTOPERATIVE ( 1 FDA reports)
HEART SOUNDS ABNORMAL ( 1 FDA reports)
HEART VALVE REPLACEMENT ( 1 FDA reports)
HEAT RASH ( 1 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
HEMIANOPIA ( 1 FDA reports)
HEPATIC ENZYME ABNORMAL ( 1 FDA reports)
HEPATIC INFECTION ( 1 FDA reports)
HEPATIC NEOPLASM ( 1 FDA reports)
HEPATIC TRAUMA ( 1 FDA reports)
HEPATITIS C VIRUS ( 1 FDA reports)
HEPATITIS E ANTIBODY POSITIVE ( 1 FDA reports)
HERNIA HIATUS REPAIR ( 1 FDA reports)
HICCUPS ( 1 FDA reports)
HIP SURGERY ( 1 FDA reports)
HIV WASTING SYNDROME ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HYDROCELE ( 1 FDA reports)
HYPERAMMONAEMIA ( 1 FDA reports)
HYPERCALCIURIA ( 1 FDA reports)
HYPERCHLORAEMIA ( 1 FDA reports)
HYPERKERATOSIS PALMARIS AND PLANTARIS ( 1 FDA reports)
HYPERTENSIVE EMERGENCY ( 1 FDA reports)
HYPERVIGILANCE ( 1 FDA reports)
HYPNOPOMPIC HALLUCINATION ( 1 FDA reports)
HYPOCHLORAEMIA ( 1 FDA reports)
HYPOCHROMIC ANAEMIA ( 1 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 1 FDA reports)
HYPOGEUSIA ( 1 FDA reports)
HYPOGONADISM ( 1 FDA reports)
HYPOMENORRHOEA ( 1 FDA reports)
HYPOPHONESIS ( 1 FDA reports)
HYPOPNOEA ( 1 FDA reports)
HYPOSMIA ( 1 FDA reports)
HYPOVITAMINOSIS ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
ILEAL STENOSIS ( 1 FDA reports)
ILIAC ARTERY THROMBOSIS ( 1 FDA reports)
IMMUNOGLOBULINS INCREASED ( 1 FDA reports)
IMPAIRED FASTING GLUCOSE ( 1 FDA reports)
IMPAIRED SELF-CARE ( 1 FDA reports)
IMPINGEMENT SYNDROME ( 1 FDA reports)
IMPLANT SITE CELLULITIS ( 1 FDA reports)
IMPLANT SITE HAEMORRHAGE ( 1 FDA reports)
IMPLANT SITE INFECTION ( 1 FDA reports)
IMPLANT SITE REACTION ( 1 FDA reports)
IMPRISONMENT ( 1 FDA reports)
INADEQUATE LUBRICATION ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INCREASED BRONCHIAL SECRETION ( 1 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
INHALATION THERAPY ( 1 FDA reports)
INJECTION SITE ABSCESS STERILE ( 1 FDA reports)
INJECTION SITE ANAESTHESIA ( 1 FDA reports)
INJECTION SITE ATROPHY ( 1 FDA reports)
INJECTION SITE EXTRAVASATION ( 1 FDA reports)
INJECTION SITE JOINT PAIN ( 1 FDA reports)
INJECTION SITE NERVE DAMAGE ( 1 FDA reports)
INJECTION SITE RECALL REACTION ( 1 FDA reports)
INJECTION SITE ULCER ( 1 FDA reports)
INJECTION SITE URTICARIA ( 1 FDA reports)
INJECTION SITE WARMTH ( 1 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
INTERMITTENT EXPLOSIVE DISORDER ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 1 FDA reports)
INTERTRIGO ( 1 FDA reports)
INTERVERTEBRAL DISC INJURY ( 1 FDA reports)
INTESTINAL DILATATION ( 1 FDA reports)
INTESTINAL FISTULA ( 1 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 1 FDA reports)
INTESTINAL GANGRENE ( 1 FDA reports)
INTESTINAL STENOSIS ( 1 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 1 FDA reports)
INTRAOCULAR LENS IMPLANT ( 1 FDA reports)
IRIDOCYCLITIS ( 1 FDA reports)
IUCD COMPLICATION ( 1 FDA reports)
JC VIRUS INFECTION ( 1 FDA reports)
JOB DISSATISFACTION ( 1 FDA reports)
JOINT ADHESION ( 1 FDA reports)
JOINT ARTHROPLASTY ( 1 FDA reports)
JOINT DESTRUCTION ( 1 FDA reports)
JOINT WARMTH ( 1 FDA reports)
JUDGEMENT IMPAIRED ( 1 FDA reports)
JUGULAR VEIN THROMBOSIS ( 1 FDA reports)
KETOACIDOSIS ( 1 FDA reports)
KLEBSIELLA BACTERAEMIA ( 1 FDA reports)
LABELLED DRUG-DISEASE INTERACTION MEDICATION ERROR ( 1 FDA reports)
LABILE HYPERTENSION ( 1 FDA reports)
LACRIMATION DECREASED ( 1 FDA reports)
LAPAROSCOPY NORMAL ( 1 FDA reports)
LARGE FOR DATES BABY ( 1 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 1 FDA reports)
LARGE INTESTINAL ULCER ( 1 FDA reports)
LARYNGEAL GRANULOMA ( 1 FDA reports)
LARYNGEAL OBSTRUCTION ( 1 FDA reports)
LEFT ATRIAL DILATATION ( 1 FDA reports)
LEGIONELLA TEST ( 1 FDA reports)
LENTIGO ( 1 FDA reports)
LICE INFESTATION ( 1 FDA reports)
LIMB ASYMMETRY ( 1 FDA reports)
LIMB CRUSHING INJURY ( 1 FDA reports)
LIMB OPERATION ( 1 FDA reports)
LIP EXFOLIATION ( 1 FDA reports)
LIP HAEMORRHAGE ( 1 FDA reports)
LIP NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 1 FDA reports)
LIPIDS DECREASED ( 1 FDA reports)
LIPIDS INCREASED ( 1 FDA reports)
LIPOMATOSIS ( 1 FDA reports)
LIPOMATOUS HYPERTROPHY OF THE INTERATRIAL SEPTUM ( 1 FDA reports)
LIVEDO RETICULARIS ( 1 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 1 FDA reports)
LOOSE ASSOCIATIONS ( 1 FDA reports)
LOSS OF LIBIDO ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE II ( 1 FDA reports)
LUNG CREPITATION ( 1 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 1 FDA reports)
LYME DISEASE ( 1 FDA reports)
LYMPHOCYTE COUNT ABNORMAL ( 1 FDA reports)
LYMPHOCYTIC DERMATITIS ( 1 FDA reports)
LYMPHOID TISSUE HYPERPLASIA ( 1 FDA reports)
MACROGNATHIA ( 1 FDA reports)
MACULAR FIBROSIS ( 1 FDA reports)
MACULE ( 1 FDA reports)
MALIGNANT TUMOUR EXCISION ( 1 FDA reports)
MARASMUS ( 1 FDA reports)
MASTOID DISORDER ( 1 FDA reports)
MATERNAL EXPOSURE BEFORE PREGNANCY ( 1 FDA reports)
MAXILLOFACIAL SINUS NEOPLASM ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 1 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 1 FDA reports)
MEDIASTINAL CYST ( 1 FDA reports)
MEDIASTINUM NEOPLASM ( 1 FDA reports)
MEDICAL DEVICE CHANGE ( 1 FDA reports)
MEDICAL DEVICE DISCOMFORT ( 1 FDA reports)
MEGAKARYOCYTES INCREASED ( 1 FDA reports)
MENINGITIS MENINGOCOCCAL ( 1 FDA reports)
MENINGOCOCCAL INFECTION ( 1 FDA reports)
MENSTRUAL DISCOMFORT ( 1 FDA reports)
METABOLIC ENCEPHALOPATHY ( 1 FDA reports)
METAMORPHOPSIA ( 1 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 1 FDA reports)
METASTASES TO GASTROINTESTINAL TRACT ( 1 FDA reports)
METASTASES TO PLEURA ( 1 FDA reports)
METASTASES TO SMALL INTESTINE ( 1 FDA reports)
METASTASES TO THORAX ( 1 FDA reports)
MICTURITION DISORDER ( 1 FDA reports)
MICTURITION FREQUENCY DECREASED ( 1 FDA reports)
MIDDLE EAR EFFUSION ( 1 FDA reports)
MIGRAINE WITHOUT AURA ( 1 FDA reports)
MITRAL VALVE REPAIR ( 1 FDA reports)
MIXED INCONTINENCE ( 1 FDA reports)
MOANING ( 1 FDA reports)
MODIFIED RADICAL MASTECTOMY ( 1 FDA reports)
MOLLUSCUM CONTAGIOSUM ( 1 FDA reports)
MONOCYTE COUNT ABNORMAL ( 1 FDA reports)
MONOCYTE COUNT DECREASED ( 1 FDA reports)
MONOCYTOSIS ( 1 FDA reports)
MONOPARESIS ( 1 FDA reports)
MORAXELLA INFECTION ( 1 FDA reports)
MORGANELLA INFECTION ( 1 FDA reports)
MORPHOEA ( 1 FDA reports)
MOUTH BREATHING ( 1 FDA reports)
MUCOSAL DISCOLOURATION ( 1 FDA reports)
MUCOSAL DRYNESS ( 1 FDA reports)
MUCOSAL EXFOLIATION ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 1 FDA reports)
MUMPS ( 1 FDA reports)
MUSCLE HAEMORRHAGE ( 1 FDA reports)
MUSCLE SWELLING ( 1 FDA reports)
MYCOPLASMA SEROLOGY POSITIVE ( 1 FDA reports)
MYELITIS ( 1 FDA reports)
MYELITIS TRANSVERSE ( 1 FDA reports)
MYELOFIBROSIS ( 1 FDA reports)
MYELOMA RECURRENCE ( 1 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 1 FDA reports)
MYOCARDIAL RUPTURE ( 1 FDA reports)
MYRINGOPLASTY ( 1 FDA reports)
MYRINGOTOMY ( 1 FDA reports)
NASAL NEOPLASM ( 1 FDA reports)
NASAL POLYPS ( 1 FDA reports)
NASAL SEPTUM DISORDER ( 1 FDA reports)
NASOPHARYNGEAL DISORDER ( 1 FDA reports)
NECK MASS ( 1 FDA reports)
NECROSIS ISCHAEMIC ( 1 FDA reports)
NEOPLASM RECURRENCE ( 1 FDA reports)
NEPHROCALCINOSIS ( 1 FDA reports)
NEPHROGENIC ANAEMIA ( 1 FDA reports)
NEURAL TUBE DEFECT ( 1 FDA reports)
NEUROENDOCRINE CARCINOMA ( 1 FDA reports)
NEUROGENIC BLADDER ( 1 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
NEUROMYOPATHY ( 1 FDA reports)
NEUROTRANSMITTER LEVEL ALTERED ( 1 FDA reports)
NEUTROPHIL TOXIC GRANULATION PRESENT ( 1 FDA reports)
NICOTINE DEPENDENCE ( 1 FDA reports)
NIPPLE PAIN ( 1 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
NOCTURNAL DYSPNOEA ( 1 FDA reports)
NODAL ARRHYTHMIA ( 1 FDA reports)
NODAL OSTEOARTHRITIS ( 1 FDA reports)
NODAL RHYTHM ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE III ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA UNSPECIFIED HISTOLOGY AGGRESSIVE ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IV ( 1 FDA reports)
NORMAL NEWBORN ( 1 FDA reports)
NORMAL TENSION GLAUCOMA ( 1 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 1 FDA reports)
OESOPHAGEAL ACHALASIA ( 1 FDA reports)
OESOPHAGEAL IRRITATION ( 1 FDA reports)
OESOPHAGEAL OEDEMA ( 1 FDA reports)
OESOPHAGEAL STENOSIS ( 1 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 1 FDA reports)
OPEN ANGLE GLAUCOMA ( 1 FDA reports)
OPEN FRACTURE ( 1 FDA reports)
OPHTHALMOPLEGIA ( 1 FDA reports)
OPTIC ATROPHY ( 1 FDA reports)
OPTIC NERVE CUPPING ( 1 FDA reports)
OPTIC NERVE DISORDER ( 1 FDA reports)
ORAL MUCOSA EROSION ( 1 FDA reports)
ORAL MUCOSAL DISORDER ( 1 FDA reports)
ORAL MUCOSAL ERUPTION ( 1 FDA reports)
ORAL PRURITUS ( 1 FDA reports)
ORBITAL OEDEMA ( 1 FDA reports)
OSMOPHOBIA ( 1 FDA reports)
OSTEOARTHROPATHY ( 1 FDA reports)
OSTEOMYELITIS FUNGAL ( 1 FDA reports)
OVARIAN CYSTECTOMY ( 1 FDA reports)
OVERGROWTH BACTERIAL ( 1 FDA reports)
PAIN MANAGEMENT ( 1 FDA reports)
PALATAL DISORDER ( 1 FDA reports)
PALATAL DYSPLASIA ( 1 FDA reports)
PALATAL OEDEMA ( 1 FDA reports)
PANCREATIC CYST ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PARACENTESIS EYE ABNORMAL ( 1 FDA reports)
PARANEOPLASTIC SYNDROME ( 1 FDA reports)
PARAPHARYNGEAL ABSCESS ( 1 FDA reports)
PARAPLEGIA ( 1 FDA reports)
PARASOMNIA ( 1 FDA reports)
PARATHYROID DISORDER ( 1 FDA reports)
PARATHYROID GLAND ENLARGEMENT ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PAROTID ABSCESS ( 1 FDA reports)
PARVOVIRUS INFECTION ( 1 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 1 FDA reports)
PELVIC FLUID COLLECTION ( 1 FDA reports)
PEMPHIGOID ( 1 FDA reports)
PENILE HAEMORRHAGE ( 1 FDA reports)
PEPTIC ULCER PERFORATION ( 1 FDA reports)
PERIDIVERTICULAR ABSCESS ( 1 FDA reports)
PERINEPHRIC EFFUSION ( 1 FDA reports)
PERIOSTITIS ( 1 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
PERIPHERAL EMBOLISM ( 1 FDA reports)
PERITONEAL ADHESIONS ( 1 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 1 FDA reports)
PERITONEAL FLUID ANALYSIS ABNORMAL ( 1 FDA reports)
PERITONEAL HAEMATOMA ( 1 FDA reports)
PERONEAL NERVE PALSY POSTOPERATIVE ( 1 FDA reports)
PH URINE DECREASED ( 1 FDA reports)
PHANTOM PAIN ( 1 FDA reports)
PHARYNGEAL DISORDER ( 1 FDA reports)
PHARYNGEAL LESION ( 1 FDA reports)
PHARYNGEAL MASS ( 1 FDA reports)
PHARYNGOLARYNGEAL DISCOMFORT ( 1 FDA reports)
PHLEBECTOMY ( 1 FDA reports)
PHYSICAL BREAST EXAMINATION ABNORMAL ( 1 FDA reports)
PILOERECTION ( 1 FDA reports)
PITUITARY TUMOUR ( 1 FDA reports)
PITUITARY TUMOUR BENIGN ( 1 FDA reports)
PLANTAR ERYTHEMA ( 1 FDA reports)
PLASMODIUM FALCIPARUM INFECTION ( 1 FDA reports)
PLATELET AGGREGATION DECREASED ( 1 FDA reports)
PLATELET COUNT ABNORMAL ( 1 FDA reports)
PLATELET MORPHOLOGY ABNORMAL ( 1 FDA reports)
PLEURAL CALCIFICATION ( 1 FDA reports)
PLEUROPERICARDITIS ( 1 FDA reports)
PNEUMATOSIS ( 1 FDA reports)
PNEUMOCOCCAL BACTERAEMIA ( 1 FDA reports)
PNEUMOCYSTIS CARINII INFECTION ( 1 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 1 FDA reports)
PNEUMONIA HAEMOPHILUS ( 1 FDA reports)
PNEUMONIA LIPOID ( 1 FDA reports)
PNEUMONIA MYCOPLASMAL ( 1 FDA reports)
PNEUMONIA PARAINFLUENZAE VIRAL ( 1 FDA reports)
POLYCYSTIC OVARIES ( 1 FDA reports)
POLYP COLORECTAL ( 1 FDA reports)
POOR PERIPHERAL CIRCULATION ( 1 FDA reports)
PORTAL VEIN THROMBOSIS ( 1 FDA reports)
POSITIVE ROMBERGISM ( 1 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 1 FDA reports)
POST CONCUSSION SYNDROME ( 1 FDA reports)
POST PROCEDURAL HAEMATOMA ( 1 FDA reports)
POST PROCEDURAL INFECTION ( 1 FDA reports)
POST PROCEDURAL NAUSEA ( 1 FDA reports)
POST PROCEDURAL SWELLING ( 1 FDA reports)
POST PROCEDURAL VOMITING ( 1 FDA reports)
POST-TRAUMATIC HEADACHE ( 1 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 1 FDA reports)
POSTICTAL STATE ( 1 FDA reports)
POSTOPERATIVE FEVER ( 1 FDA reports)
POTENTIATING DRUG INTERACTION ( 1 FDA reports)
POVERTY OF SPEECH ( 1 FDA reports)
PRE-ECLAMPSIA ( 1 FDA reports)
PREDISPOSITION TO DISEASE ( 1 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 1 FDA reports)
PREGNANCY WITH INJECTABLE CONTRACEPTIVE ( 1 FDA reports)
PROCEDURAL SITE REACTION ( 1 FDA reports)
PRODUCT COLOUR ISSUE ( 1 FDA reports)
PRODUCT CONTAMINATION PHYSICAL ( 1 FDA reports)
PRODUCT LABEL CONFUSION ( 1 FDA reports)
PRODUCT LABEL ON WRONG PRODUCT ( 1 FDA reports)
PRODUCT MEASURED POTENCY ISSUE ( 1 FDA reports)
PRODUCT TAMPERING ( 1 FDA reports)
PROSTATIC ACID PHOSPHATASE INCREASED ( 1 FDA reports)
PROTEIN C DECREASED ( 1 FDA reports)
PROTEIN URINE ( 1 FDA reports)
PROTEUS INFECTION ( 1 FDA reports)
PRURITUS ALLERGIC ( 1 FDA reports)
PSEUDARTHROSIS ( 1 FDA reports)
PSYCHOMOTOR SEIZURES ( 1 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 1 FDA reports)
PULMONARY INTERSTITIAL EMPHYSEMA SYNDROME ( 1 FDA reports)
PULMONARY MYCOSIS ( 1 FDA reports)
PULMONARY TOXICITY ( 1 FDA reports)
PUPIL FIXED ( 1 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 1 FDA reports)
PUPILS UNEQUAL ( 1 FDA reports)
PYURIA ( 1 FDA reports)
RADIATION FIBROSIS - LUNG ( 1 FDA reports)
RADICAL NECK DISSECTION ( 1 FDA reports)
RASH PSORIAFORM ( 1 FDA reports)
REACTION TO PRESERVATIVES ( 1 FDA reports)
REBOUND EFFECT ( 1 FDA reports)
RECTAL SPASM ( 1 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 1 FDA reports)
RED BLOOD CELLS CSF POSITIVE ( 1 FDA reports)
RED BLOOD CELLS SEMEN ( 1 FDA reports)
RED MAN SYNDROME ( 1 FDA reports)
REFUSAL OF EXAMINATION ( 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 ATROPHY ( 1 FDA reports)
RENAL CORTICAL NECROSIS ( 1 FDA reports)
RENAL ISCHAEMIA ( 1 FDA reports)
RENAL MASS ( 1 FDA reports)
RENAL STONE REMOVAL ( 1 FDA reports)
RENAL TUBULAR ATROPHY ( 1 FDA reports)
REOCCLUSION ( 1 FDA reports)
REPERFUSION ARRHYTHMIA ( 1 FDA reports)
RESPIRATION ABNORMAL ( 1 FDA reports)
RESPIRATORY TRACT INFECTION BACTERIAL ( 1 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 1 FDA reports)
RETICULOCYTE COUNT ABNORMAL ( 1 FDA reports)
RETINAL PIGMENT EPITHELIOPATHY ( 1 FDA reports)
RETINAL TEAR ( 1 FDA reports)
RETINAL VASCULAR DISORDER ( 1 FDA reports)
RETINAL VEIN THROMBOSIS ( 1 FDA reports)
RETINOPATHY ( 1 FDA reports)
RETROGRADE EJACULATION ( 1 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 1 FDA reports)
RHINALGIA ( 1 FDA reports)
RHINOLARYNGITIS ( 1 FDA reports)
RHINOVIRUS INFECTION ( 1 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE DECREASED ( 1 FDA reports)
RUPTURED ECTOPIC PREGNANCY ( 1 FDA reports)
SALMONELLOSIS ( 1 FDA reports)
SCAN ABDOMEN ABNORMAL ( 1 FDA reports)
SCAPULA FRACTURE ( 1 FDA reports)
SCAR PAIN ( 1 FDA reports)
SCARLET FEVER ( 1 FDA reports)
SCHIZOPHRENIA ( 1 FDA reports)
SCIATIC NERVE INJURY ( 1 FDA reports)
SCLERAL DISORDER ( 1 FDA reports)
SCROTAL DISORDER ( 1 FDA reports)
SCROTAL MASS ( 1 FDA reports)
SCROTAL OEDEMA ( 1 FDA reports)
SCROTAL PAIN ( 1 FDA reports)
SCROTAL SWELLING ( 1 FDA reports)
SEBACEOUS GLAND INFECTION ( 1 FDA reports)
SECONDARY ADRENOCORTICAL INSUFFICIENCY ( 1 FDA reports)
SENILE DEMENTIA ( 1 FDA reports)
SEXUAL ABUSE ( 1 FDA reports)
SIGMOIDITIS ( 1 FDA reports)
SIMILAR REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
SIMPLE PARTIAL SEIZURES ( 1 FDA reports)
SINUS ANTROSTOMY ( 1 FDA reports)
SKIN BACTERIAL INFECTION ( 1 FDA reports)
SKIN CHAPPED ( 1 FDA reports)
SKIN DEPIGMENTATION ( 1 FDA reports)
SKIN EROSION ( 1 FDA reports)
SKIN GRAFT ( 1 FDA reports)
SKIN HAEMORRHAGE ( 1 FDA reports)
SKIN HYPERTROPHY ( 1 FDA reports)
SKIN INFECTION ( 1 FDA reports)
SKIN INFLAMMATION ( 1 FDA reports)
SKIN MASS ( 1 FDA reports)
SKIN NODULE ( 1 FDA reports)
SKIN ODOUR ABNORMAL ( 1 FDA reports)
SKIN SWELLING ( 1 FDA reports)
SLEEP STUDY ABNORMAL ( 1 FDA reports)
SLEEP TERROR ( 1 FDA reports)
SLEEP-RELATED EATING DISORDER ( 1 FDA reports)
SMALL BOWEL ANGIOEDEMA ( 1 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 1 FDA reports)
SMOKER ( 1 FDA reports)
SMOOTH MUSCLE ANTIBODY POSITIVE ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
SOFT TISSUE INFECTION ( 1 FDA reports)
SOLITARY KIDNEY ( 1 FDA reports)
SOMNAMBULISM ( 1 FDA reports)
SPINAL CORD DISORDER ( 1 FDA reports)
SPINAL LAMINECTOMY ( 1 FDA reports)
SPLEEN DISORDER ( 1 FDA reports)
SPLENIC GRANULOMA ( 1 FDA reports)
SPLENIC RUPTURE ( 1 FDA reports)
SPLINT APPLICATION ( 1 FDA reports)
SPONDYLOLISTHESIS ACQUIRED ( 1 FDA reports)
SPONTANEOUS HAEMATOMA ( 1 FDA reports)
STARVATION ( 1 FDA reports)
STEAL PHENOMENON ( 1 FDA reports)
STEAL SYNDROME ( 1 FDA reports)
STOMACH MASS ( 1 FDA reports)
STOMATITIS HAEMORRHAGIC ( 1 FDA reports)
STRESS AT WORK ( 1 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SUBSTANCE ABUSE ( 1 FDA reports)
SUPPRESSED LACTATION ( 1 FDA reports)
SURGICAL FAILURE ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
SUTURE INSERTION ( 1 FDA reports)
SWEAT DISCOLOURATION ( 1 FDA reports)
SYSTEMIC MASTOCYTOSIS ( 1 FDA reports)
SYSTEMIC SCLEROSIS ( 1 FDA reports)
TABLET ISSUE ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
TARSAL TUNNEL SYNDROME ( 1 FDA reports)
TENDON RUPTURE ( 1 FDA reports)
TERMINAL INSOMNIA ( 1 FDA reports)
TETANY ( 1 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 1 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 1 FDA reports)
THROAT CANCER ( 1 FDA reports)
THROAT LESION ( 1 FDA reports)
THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
THROMBOEMBOLIC STROKE ( 1 FDA reports)
THROMBOLYSIS ( 1 FDA reports)
THYROID CANCER METASTATIC ( 1 FDA reports)
THYROID GLAND CANCER ( 1 FDA reports)
THYROIDECTOMY ( 1 FDA reports)
THYROIDITIS SUBACUTE ( 1 FDA reports)
TINEA INFECTION ( 1 FDA reports)
TOBACCO USER ( 1 FDA reports)
TONGUE HAEMATOMA ( 1 FDA reports)
TONIC CLONIC MOVEMENTS ( 1 FDA reports)
TONSILLAR ULCER ( 1 FDA reports)
TOOTH INJURY ( 1 FDA reports)
TOOTH REPAIR ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 1 FDA reports)
TOXIC SHOCK SYNDROME STAPHYLOCOCCAL ( 1 FDA reports)
TOXOPLASMA SEROLOGY POSITIVE ( 1 FDA reports)
TRACHEOSTOMY ( 1 FDA reports)
TRANSFERRIN DECREASED ( 1 FDA reports)
TRAUMATIC ARTHRITIS ( 1 FDA reports)
TRIFASCICULAR BLOCK ( 1 FDA reports)
TROPONIN ( 1 FDA reports)
TRYPTASE INCREASED ( 1 FDA reports)
TUMOUR MARKER INCREASED ( 1 FDA reports)
TURNER'S SYNDROME ( 1 FDA reports)
TYMPANIC MEMBRANE HYPERAEMIA ( 1 FDA reports)
TYPE III IMMUNE COMPLEX MEDIATED REACTION ( 1 FDA reports)
ULNAR NERVE INJURY ( 1 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 1 FDA reports)
ULTRASOUND PELVIS ABNORMAL ( 1 FDA reports)
UNDERDOSE ( 1 FDA reports)
UNINTENDED PREGNANCY ( 1 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 1 FDA reports)
URETERAL SPASM ( 1 FDA reports)
URETERAL STENT INSERTION ( 1 FDA reports)
URETERIC STENOSIS ( 1 FDA reports)
URETHRAL HAEMORRHAGE ( 1 FDA reports)
URETHRAL STRICTURE POSTOPERATIVE ( 1 FDA reports)
URINARY BLADDER ADENOMA ( 1 FDA reports)
URINE BARBITURATES INCREASED ( 1 FDA reports)
URINE CANNABINOIDS INCREASED ( 1 FDA reports)
URINE COLOUR ABNORMAL ( 1 FDA reports)
URINE KETONE BODY ( 1 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 1 FDA reports)
URINE OUTPUT INCREASED ( 1 FDA reports)
UROBILIN URINE ( 1 FDA reports)
UROBILIN URINE PRESENT ( 1 FDA reports)
UTERINE DILATION AND CURETTAGE ( 1 FDA reports)
UVEITIS ( 1 FDA reports)
VACCINATION COMPLICATION ( 1 FDA reports)
VAGINAL CANCER ( 1 FDA reports)
VAGINAL EROSION ( 1 FDA reports)
VAGINAL ERYTHEMA ( 1 FDA reports)
VAGINAL LESION ( 1 FDA reports)
VAGINAL MUCOSAL BLISTERING ( 1 FDA reports)
VAGINITIS BACTERIAL ( 1 FDA reports)
VANISHING BILE DUCT SYNDROME ( 1 FDA reports)
VARICELLA ZOSTER VIRUS SEROLOGY POSITIVE ( 1 FDA reports)
VASCULAR COMPLICATION ASSOCIATED WITH DEVICE ( 1 FDA reports)
VASCULAR OCCLUSION ( 1 FDA reports)
VASCULAR RUPTURE ( 1 FDA reports)
VASCULAR STENOSIS ( 1 FDA reports)
VASCULITIS CEREBRAL ( 1 FDA reports)
VASODILATATION ( 1 FDA reports)
VASOSPASM ( 1 FDA reports)
VEIN DISCOLOURATION ( 1 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 1 FDA reports)
VENOUS HAEMORRHAGE ( 1 FDA reports)
VENOUS OCCLUSION ( 1 FDA reports)
VENOUS THROMBOSIS LIMB ( 1 FDA reports)
VERTEBRAL ARTERY STENOSIS ( 1 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 1 FDA reports)
VERY LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
VESTIBULAR NEURONITIS ( 1 FDA reports)
VIRAEMIA ( 1 FDA reports)
VIRAL MYOCARDITIS ( 1 FDA reports)
VISUAL BRIGHTNESS ( 1 FDA reports)
VITAL CAPACITY DECREASED ( 1 FDA reports)
VITAMIN B12 DECREASED ( 1 FDA reports)
VOCAL CORD DISORDER ( 1 FDA reports)
VOCAL CORD PARALYSIS ( 1 FDA reports)
VOLUME BLOOD DECREASED ( 1 FDA reports)
VOMITING IN PREGNANCY ( 1 FDA reports)
VULVAL ABSCESS ( 1 FDA reports)
VULVAR EROSION ( 1 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 1 FDA reports)
WALLENBERG SYNDROME ( 1 FDA reports)
WERNICKE'S ENCEPHALOPATHY ( 1 FDA reports)
WITHDRAWAL BLEED ( 1 FDA reports)
WOUND COMPLICATION ( 1 FDA reports)
WOUND HAEMORRHAGE ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)
XEROSIS ( 1 FDA reports)
YELLOW SKIN ( 1 FDA reports)

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