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

DIARRHOEA ( 121 FDA reports)
FATIGUE ( 113 FDA reports)
NAUSEA ( 87 FDA reports)
PAIN ( 79 FDA reports)
PAIN IN EXTREMITY ( 77 FDA reports)
ARTHRALGIA ( 74 FDA reports)
DYSPNOEA ( 71 FDA reports)
PYREXIA ( 66 FDA reports)
HEADACHE ( 64 FDA reports)
ABDOMINAL PAIN ( 62 FDA reports)
DIZZINESS ( 60 FDA reports)
OEDEMA PERIPHERAL ( 60 FDA reports)
ASTHENIA ( 55 FDA reports)
DRUG INEFFECTIVE ( 51 FDA reports)
VOMITING ( 44 FDA reports)
FEELING ABNORMAL ( 42 FDA reports)
INSOMNIA ( 41 FDA reports)
ABDOMINAL PAIN UPPER ( 40 FDA reports)
MUSCLE SPASMS ( 39 FDA reports)
GAIT DISTURBANCE ( 37 FDA reports)
BACK PAIN ( 34 FDA reports)
CONTUSION ( 34 FDA reports)
DEPRESSION ( 33 FDA reports)
ANXIETY ( 32 FDA reports)
DECREASED APPETITE ( 32 FDA reports)
HAEMOGLOBIN DECREASED ( 32 FDA reports)
MALAISE ( 32 FDA reports)
MUSCULAR WEAKNESS ( 32 FDA reports)
RASH ( 32 FDA reports)
WEIGHT DECREASED ( 32 FDA reports)
INJURY ( 31 FDA reports)
DEHYDRATION ( 30 FDA reports)
FLATULENCE ( 30 FDA reports)
BLOOD PRESSURE INCREASED ( 29 FDA reports)
FALL ( 29 FDA reports)
INJECTION SITE PAIN ( 29 FDA reports)
URINARY TRACT INFECTION ( 29 FDA reports)
CONSTIPATION ( 28 FDA reports)
MUSCULOSKELETAL PAIN ( 28 FDA reports)
MYALGIA ( 28 FDA reports)
COUGH ( 27 FDA reports)
HAEMORRHAGE ( 27 FDA reports)
HYPERHIDROSIS ( 27 FDA reports)
HYPOAESTHESIA ( 27 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 26 FDA reports)
CHEST PAIN ( 26 FDA reports)
SOMNOLENCE ( 26 FDA reports)
TREMOR ( 26 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 25 FDA reports)
CHILLS ( 25 FDA reports)
CHOLECYSTITIS CHRONIC ( 25 FDA reports)
ERYTHEMA ( 25 FDA reports)
ABDOMINAL DISTENSION ( 24 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 24 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 24 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 23 FDA reports)
CROHN'S DISEASE ( 23 FDA reports)
LETHARGY ( 23 FDA reports)
ANAEMIA ( 22 FDA reports)
BLOOD GLUCOSE INCREASED ( 22 FDA reports)
ATRIAL FIBRILLATION ( 21 FDA reports)
CHOLELITHIASIS ( 21 FDA reports)
DYSPHAGIA ( 21 FDA reports)
HAEMATOCRIT DECREASED ( 21 FDA reports)
HYPERTENSION ( 21 FDA reports)
PARAESTHESIA ( 21 FDA reports)
PNEUMONIA ( 21 FDA reports)
CONVULSION ( 20 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 20 FDA reports)
RIB FRACTURE ( 20 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 20 FDA reports)
CONFUSIONAL STATE ( 19 FDA reports)
DRUG INTERACTION ( 19 FDA reports)
DYSPEPSIA ( 19 FDA reports)
HOSPITALISATION ( 19 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 19 FDA reports)
PRURITUS ( 19 FDA reports)
RENAL FAILURE ACUTE ( 19 FDA reports)
WEIGHT INCREASED ( 19 FDA reports)
BURNING SENSATION ( 18 FDA reports)
DEEP VEIN THROMBOSIS ( 18 FDA reports)
MIGRAINE ( 18 FDA reports)
OSTEOPOROSIS ( 18 FDA reports)
PULMONARY EMBOLISM ( 18 FDA reports)
BLOOD ALBUMIN DECREASED ( 17 FDA reports)
BLOOD MAGNESIUM DECREASED ( 17 FDA reports)
GINGIVAL BLEEDING ( 17 FDA reports)
HAEMATURIA ( 17 FDA reports)
INJECTION SITE HAEMATOMA ( 17 FDA reports)
MENTAL DISORDER ( 17 FDA reports)
NEPHROLITHIASIS ( 17 FDA reports)
PLATELET COUNT INCREASED ( 17 FDA reports)
PLEURISY ( 17 FDA reports)
VASCULITIS ( 17 FDA reports)
CEREBROVASCULAR ACCIDENT ( 16 FDA reports)
CHORIOAMNIONITIS ( 16 FDA reports)
INJECTION SITE IRRITATION ( 16 FDA reports)
PHLEBITIS ( 16 FDA reports)
PLACENTAL INFARCTION ( 16 FDA reports)
PLACENTAL INSUFFICIENCY ( 16 FDA reports)
RED BLOOD CELL MORPHOLOGY ABNORMAL ( 16 FDA reports)
SKELETAL INJURY ( 16 FDA reports)
UMBILICAL CORD ABNORMALITY ( 16 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 15 FDA reports)
AMNESIA ( 15 FDA reports)
HERPES ZOSTER ( 15 FDA reports)
HYPERSENSITIVITY ( 15 FDA reports)
HYPERSOMNIA ( 15 FDA reports)
JOINT SWELLING ( 15 FDA reports)
ALOPECIA ( 14 FDA reports)
ARTHRITIS ( 14 FDA reports)
CHEST DISCOMFORT ( 14 FDA reports)
EMOTIONAL DISORDER ( 14 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 14 FDA reports)
INFECTION ( 14 FDA reports)
INFLUENZA LIKE ILLNESS ( 14 FDA reports)
OSTEOARTHRITIS ( 14 FDA reports)
ASTHMA ( 13 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 13 FDA reports)
CONDITION AGGRAVATED ( 13 FDA reports)
ECONOMIC PROBLEM ( 13 FDA reports)
EMOTIONAL DISTRESS ( 13 FDA reports)
FAECES DISCOLOURED ( 13 FDA reports)
LOSS OF CONSCIOUSNESS ( 13 FDA reports)
NASOPHARYNGITIS ( 13 FDA reports)
NECK PAIN ( 13 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 13 FDA reports)
RECTAL HAEMORRHAGE ( 13 FDA reports)
VISION BLURRED ( 13 FDA reports)
BONE PAIN ( 12 FDA reports)
CARDIAC ARREST ( 12 FDA reports)
DYSPHONIA ( 12 FDA reports)
EPISTAXIS ( 12 FDA reports)
FLUSHING ( 12 FDA reports)
GASTROINTESTINAL DISORDER ( 12 FDA reports)
HEART RATE INCREASED ( 12 FDA reports)
HYPOTENSION ( 12 FDA reports)
JAW DISORDER ( 12 FDA reports)
NEUROPATHY PERIPHERAL ( 12 FDA reports)
POLLAKIURIA ( 12 FDA reports)
RENAL FAILURE ( 12 FDA reports)
ANOREXIA ( 11 FDA reports)
BLOOD PRESSURE DECREASED ( 11 FDA reports)
BRONCHITIS ( 11 FDA reports)
CELLULITIS ( 11 FDA reports)
DEATH ( 11 FDA reports)
FEELING HOT ( 11 FDA reports)
ILL-DEFINED DISORDER ( 11 FDA reports)
INFLUENZA ( 11 FDA reports)
INJECTION SITE ERYTHEMA ( 11 FDA reports)
ORAL INFECTION ( 11 FDA reports)
PNEUMONIA ASPIRATION ( 11 FDA reports)
RESPIRATORY FAILURE ( 11 FDA reports)
SENSITIVITY OF TEETH ( 11 FDA reports)
SWELLING ( 11 FDA reports)
SWELLING FACE ( 11 FDA reports)
BALANCE DISORDER ( 10 FDA reports)
CATHETERISATION CARDIAC ( 10 FDA reports)
COGNITIVE DISORDER ( 10 FDA reports)
EXERCISE TOLERANCE DECREASED ( 10 FDA reports)
FEELING JITTERY ( 10 FDA reports)
FUNGAL INFECTION ( 10 FDA reports)
GASTRITIS ( 10 FDA reports)
HAEMATOCHEZIA ( 10 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 10 FDA reports)
OSTEONECROSIS ( 10 FDA reports)
OVERDOSE ( 10 FDA reports)
PAIN IN JAW ( 10 FDA reports)
ROTATOR CUFF SYNDROME ( 10 FDA reports)
UNEVALUABLE EVENT ( 10 FDA reports)
ANHEDONIA ( 9 FDA reports)
AORTIC STENOSIS ( 9 FDA reports)
BLADDER DISORDER ( 9 FDA reports)
DYSGEUSIA ( 9 FDA reports)
GALLBLADDER DISORDER ( 9 FDA reports)
HIP ARTHROPLASTY ( 9 FDA reports)
INJECTION SITE HAEMORRHAGE ( 9 FDA reports)
MITRAL VALVE INCOMPETENCE ( 9 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 9 FDA reports)
MYOCARDIAL INFARCTION ( 9 FDA reports)
OROPHARYNGEAL PAIN ( 9 FDA reports)
THROMBOCYTOPENIA ( 9 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 9 FDA reports)
VIRAL INFECTION ( 9 FDA reports)
WHEEZING ( 9 FDA reports)
AGITATION ( 8 FDA reports)
BLOOD CALCIUM INCREASED ( 8 FDA reports)
BLOOD GLUCOSE DECREASED ( 8 FDA reports)
CARDIAC DISORDER ( 8 FDA reports)
DIVERTICULUM ( 8 FDA reports)
DRY MOUTH ( 8 FDA reports)
DYSURIA ( 8 FDA reports)
GASTROENTERITIS ( 8 FDA reports)
HALLUCINATION ( 8 FDA reports)
INJECTION SITE RASH ( 8 FDA reports)
IRON DEFICIENCY ANAEMIA ( 8 FDA reports)
IRRITABLE BOWEL SYNDROME ( 8 FDA reports)
JOINT INJURY ( 8 FDA reports)
MELANOCYTIC NAEVUS ( 8 FDA reports)
MENTAL IMPAIRMENT ( 8 FDA reports)
NASAL CONGESTION ( 8 FDA reports)
NERVOUSNESS ( 8 FDA reports)
NEUTROPENIA ( 8 FDA reports)
RESTLESSNESS ( 8 FDA reports)
SEPSIS ( 8 FDA reports)
SKIN DISCOLOURATION ( 8 FDA reports)
SUICIDAL IDEATION ( 8 FDA reports)
TACHYCARDIA ( 8 FDA reports)
TENDON RUPTURE ( 8 FDA reports)
TINNITUS ( 8 FDA reports)
ABDOMINAL DISCOMFORT ( 7 FDA reports)
ANTI-THYROID ANTIBODY POSITIVE ( 7 FDA reports)
BREAST CANCER ( 7 FDA reports)
CARDIAC STRESS TEST ( 7 FDA reports)
CHOLECYSTECTOMY ( 7 FDA reports)
CLOSTRIDIAL INFECTION ( 7 FDA reports)
CRYING ( 7 FDA reports)
CYSTITIS ( 7 FDA reports)
DEAFNESS ( 7 FDA reports)
EATING DISORDER ( 7 FDA reports)
ERUCTATION ( 7 FDA reports)
EXOSTOSIS ( 7 FDA reports)
EYE IRRITATION ( 7 FDA reports)
FEELING DRUNK ( 7 FDA reports)
FEMUR FRACTURE ( 7 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 7 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 7 FDA reports)
HEARING IMPAIRED ( 7 FDA reports)
HEPATIC ENZYME INCREASED ( 7 FDA reports)
HIP FRACTURE ( 7 FDA reports)
HYPERGLYCAEMIA ( 7 FDA reports)
HYPERLIPIDAEMIA ( 7 FDA reports)
IMPAIRED HEALING ( 7 FDA reports)
INCONTINENCE ( 7 FDA reports)
INTESTINAL OBSTRUCTION ( 7 FDA reports)
IRRITABILITY ( 7 FDA reports)
MEMORY IMPAIRMENT ( 7 FDA reports)
NEURALGIA ( 7 FDA reports)
OSTEOMYELITIS ( 7 FDA reports)
PERICARDIAL EFFUSION ( 7 FDA reports)
PHARYNGEAL OEDEMA ( 7 FDA reports)
ROAD TRAFFIC ACCIDENT ( 7 FDA reports)
SKIN DISORDER ( 7 FDA reports)
SLEEP APNOEA SYNDROME ( 7 FDA reports)
SPINAL COLUMN STENOSIS ( 7 FDA reports)
SURGERY ( 7 FDA reports)
SYNCOPE ( 7 FDA reports)
TENDON DISORDER ( 7 FDA reports)
VISUAL IMPAIRMENT ( 7 FDA reports)
AGGRESSION ( 6 FDA reports)
APNOEA ( 6 FDA reports)
AUTOIMMUNE THYROIDITIS ( 6 FDA reports)
BLOOD CALCIUM DECREASED ( 6 FDA reports)
BONE LESION ( 6 FDA reports)
BURSITIS ( 6 FDA reports)
CHOLECYSTITIS ACUTE ( 6 FDA reports)
CHRONIC SINUSITIS ( 6 FDA reports)
COMMUNICATION DISORDER ( 6 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 6 FDA reports)
DRUG DOSE OMISSION ( 6 FDA reports)
DRY SKIN ( 6 FDA reports)
EYE INJURY ( 6 FDA reports)
FEAR ( 6 FDA reports)
FIBROMYALGIA ( 6 FDA reports)
HEART RATE DECREASED ( 6 FDA reports)
HYPOXIA ( 6 FDA reports)
IMMOBILE ( 6 FDA reports)
INCREASED TENDENCY TO BRUISE ( 6 FDA reports)
INFLAMMATION ( 6 FDA reports)
INFUSION RELATED REACTION ( 6 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 6 FDA reports)
ISCHAEMIA ( 6 FDA reports)
LIMB DISCOMFORT ( 6 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 6 FDA reports)
MEDICATION ERROR ( 6 FDA reports)
MUSCLE ATROPHY ( 6 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 6 FDA reports)
OEDEMA MOUTH ( 6 FDA reports)
ONYCHOCLASIS ( 6 FDA reports)
ORAL MUCOSAL DISCOLOURATION ( 6 FDA reports)
OSTEONECROSIS OF JAW ( 6 FDA reports)
OXYGEN SATURATION DECREASED ( 6 FDA reports)
PALPITATIONS ( 6 FDA reports)
PANCREATITIS ( 6 FDA reports)
POLYDIPSIA ( 6 FDA reports)
PRODUCTIVE COUGH ( 6 FDA reports)
PULMONARY HYPERTENSION ( 6 FDA reports)
SINUS DISORDER ( 6 FDA reports)
SINUSITIS ( 6 FDA reports)
SLEEP DISORDER ( 6 FDA reports)
SPINAL OSTEOARTHRITIS ( 6 FDA reports)
SPONDYLOLISTHESIS ( 6 FDA reports)
STOMACH DISCOMFORT ( 6 FDA reports)
STRESS ( 6 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 6 FDA reports)
TENDERNESS ( 6 FDA reports)
TREATMENT NONCOMPLIANCE ( 6 FDA reports)
URINARY INCONTINENCE ( 6 FDA reports)
URTICARIA ( 6 FDA reports)
VASCULAR INJURY ( 6 FDA reports)
VENTRICULAR TACHYCARDIA ( 6 FDA reports)
VERTIGO ( 6 FDA reports)
WHEELCHAIR USER ( 6 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 6 FDA reports)
ABSCESS ( 5 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 5 FDA reports)
AORTIC VALVE CALCIFICATION ( 5 FDA reports)
BACK DISORDER ( 5 FDA reports)
BILIARY DYSKINESIA ( 5 FDA reports)
BLOOD CREATININE INCREASED ( 5 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 5 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 5 FDA reports)
BLOOD URINE PRESENT ( 5 FDA reports)
BONE GIANT CELL TUMOUR ( 5 FDA reports)
BONE MARROW OEDEMA ( 5 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 5 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 5 FDA reports)
CHOKING ( 5 FDA reports)
COLITIS ( 5 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 5 FDA reports)
CONCUSSION ( 5 FDA reports)
CULTURE URINE POSITIVE ( 5 FDA reports)
DECREASED INTEREST ( 5 FDA reports)
DEPRESSED MOOD ( 5 FDA reports)
DEVICE FAILURE ( 5 FDA reports)
DISABILITY ( 5 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 5 FDA reports)
ESSENTIAL HYPERTENSION ( 5 FDA reports)
EYE DISORDER ( 5 FDA reports)
FLUID RETENTION ( 5 FDA reports)
GINGIVAL DISORDER ( 5 FDA reports)
ILIOTIBIAL BAND SYNDROME ( 5 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 5 FDA reports)
LACTOSE INTOLERANCE ( 5 FDA reports)
LIBIDO DECREASED ( 5 FDA reports)
LIMB INJURY ( 5 FDA reports)
LIP SWELLING ( 5 FDA reports)
LOBAR PNEUMONIA ( 5 FDA reports)
LUMBAR RADICULOPATHY ( 5 FDA reports)
MASTICATION DISORDER ( 5 FDA reports)
MENORRHAGIA ( 5 FDA reports)
MYOSITIS ( 5 FDA reports)
NEUROMA ( 5 FDA reports)
NEUTROPENIC SEPSIS ( 5 FDA reports)
ORGANISING PNEUMONIA ( 5 FDA reports)
OSTEITIS DEFORMANS ( 5 FDA reports)
OSTEOPENIA ( 5 FDA reports)
OSTEOSCLEROSIS ( 5 FDA reports)
PLATELET COUNT DECREASED ( 5 FDA reports)
RESPIRATORY ARREST ( 5 FDA reports)
RETCHING ( 5 FDA reports)
RHINORRHOEA ( 5 FDA reports)
SINUS POLYP ( 5 FDA reports)
SKIN ULCER ( 5 FDA reports)
SOFT TISSUE DISORDER ( 5 FDA reports)
SPEECH DISORDER ( 5 FDA reports)
STAPHYLOCOCCAL INFECTION ( 5 FDA reports)
TENDONITIS ( 5 FDA reports)
TENSION ( 5 FDA reports)
THYROID DISORDER ( 5 FDA reports)
UPPER LIMB FRACTURE ( 5 FDA reports)
UTERINE LEIOMYOMA ( 5 FDA reports)
VENTRICULAR FIBRILLATION ( 5 FDA reports)
WEIGHT FLUCTUATION ( 5 FDA reports)
ADVERSE DRUG REACTION ( 4 FDA reports)
ANOSMIA ( 4 FDA reports)
ANOXIC ENCEPHALOPATHY ( 4 FDA reports)
ARTHROPATHY ( 4 FDA reports)
BASAL CELL CARCINOMA ( 4 FDA reports)
BLOOD POTASSIUM DECREASED ( 4 FDA reports)
BRADYCARDIA ( 4 FDA reports)
CACHEXIA ( 4 FDA reports)
CARDIOMYOPATHY ( 4 FDA reports)
CEREBRAL ISCHAEMIA ( 4 FDA reports)
CHOLECYSTITIS ( 4 FDA reports)
CHROMATURIA ( 4 FDA reports)
DECUBITUS ULCER ( 4 FDA reports)
DEMENTIA ( 4 FDA reports)
DEPENDENCE ( 4 FDA reports)
DIALYSIS ( 4 FDA reports)
DISCOMFORT ( 4 FDA reports)
DISTURBANCE IN ATTENTION ( 4 FDA reports)
DRUG INTOLERANCE ( 4 FDA reports)
DRY EYE ( 4 FDA reports)
EYE PRURITUS ( 4 FDA reports)
EYELID DISORDER ( 4 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 4 FDA reports)
GINGIVAL RECESSION ( 4 FDA reports)
GOITRE ( 4 FDA reports)
HAEMATEMESIS ( 4 FDA reports)
HEART RATE IRREGULAR ( 4 FDA reports)
HEMIPLEGIA ( 4 FDA reports)
HOT FLUSH ( 4 FDA reports)
HYPOAESTHESIA FACIAL ( 4 FDA reports)
HYPOKALAEMIA ( 4 FDA reports)
HYPOTHYROIDISM ( 4 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 4 FDA reports)
INCORRECT DOSE ADMINISTERED ( 4 FDA reports)
INJECTION SITE REACTION ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 4 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 4 FDA reports)
LYMPHADENOPATHY ( 4 FDA reports)
MULTIPLE MYELOMA ( 4 FDA reports)
MUSCLE CRAMP ( 4 FDA reports)
MYOPATHY ( 4 FDA reports)
OBESITY ( 4 FDA reports)
ORAL INTAKE REDUCED ( 4 FDA reports)
PANCYTOPENIA ( 4 FDA reports)
PANIC ATTACK ( 4 FDA reports)
PARANOIA ( 4 FDA reports)
PELVIC PAIN ( 4 FDA reports)
PHARYNGITIS ( 4 FDA reports)
PLEURAL EFFUSION ( 4 FDA reports)
PRESCRIBED OVERDOSE ( 4 FDA reports)
RASH PRURITIC ( 4 FDA reports)
RENAL DISORDER ( 4 FDA reports)
RESPIRATORY TRACT INFECTION ( 4 FDA reports)
RHEUMATOID ARTHRITIS ( 4 FDA reports)
RHINITIS ( 4 FDA reports)
SCAR ( 4 FDA reports)
SENSATION OF HEAVINESS ( 4 FDA reports)
SINUS HEADACHE ( 4 FDA reports)
SKIN BURNING SENSATION ( 4 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 4 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 4 FDA reports)
SYNOVITIS ( 4 FDA reports)
TEMPERATURE INTOLERANCE ( 4 FDA reports)
THIRST ( 4 FDA reports)
TINEA PEDIS ( 4 FDA reports)
TYPE 2 DIABETES MELLITUS ( 4 FDA reports)
URINARY RETENTION ( 4 FDA reports)
VAGINAL HAEMORRHAGE ( 4 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 4 FDA reports)
VITAMIN D DECREASED ( 4 FDA reports)
ACCIDENTAL NEEDLE STICK ( 3 FDA reports)
ADRENAL INSUFFICIENCY ( 3 FDA reports)
ADVERSE REACTION ( 3 FDA reports)
ANORECTAL DISCOMFORT ( 3 FDA reports)
ANORECTAL DISORDER ( 3 FDA reports)
APPLICATION SITE HAEMATOMA ( 3 FDA reports)
ATRIAL FLUTTER ( 3 FDA reports)
BACK INJURY ( 3 FDA reports)
BLINDNESS ( 3 FDA reports)
BLOOD BICARBONATE DECREASED ( 3 FDA reports)
BLOOD BILIRUBIN INCREASED ( 3 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 3 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 3 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 3 FDA reports)
BODY TEMPERATURE INCREASED ( 3 FDA reports)
BONE CYST ( 3 FDA reports)
BONE DISORDER ( 3 FDA reports)
BONE EROSION ( 3 FDA reports)
BREATH ODOUR ( 3 FDA reports)
BREECH PRESENTATION ( 3 FDA reports)
CANDIDIASIS ( 3 FDA reports)
CARDIAC OPERATION ( 3 FDA reports)
CARDIO-RESPIRATORY ARREST ( 3 FDA reports)
CATARACT ( 3 FDA reports)
CHEST X-RAY ABNORMAL ( 3 FDA reports)
CLOSTRIDIUM COLITIS ( 3 FDA reports)
COLLAPSE OF LUNG ( 3 FDA reports)
COMA ( 3 FDA reports)
CONDUCTION DISORDER ( 3 FDA reports)
COORDINATION ABNORMAL ( 3 FDA reports)
CORONARY ARTERY OCCLUSION ( 3 FDA reports)
DENTAL DISCOMFORT ( 3 FDA reports)
DERMATITIS ACNEIFORM ( 3 FDA reports)
DEVICE MISUSE ( 3 FDA reports)
DIFFICULTY IN WALKING ( 3 FDA reports)
DISEASE PROGRESSION ( 3 FDA reports)
DIVERTICULITIS ( 3 FDA reports)
DRUG ADMINISTRATION ERROR ( 3 FDA reports)
DRUG ERUPTION ( 3 FDA reports)
DYSSTASIA ( 3 FDA reports)
EAR DISCOMFORT ( 3 FDA reports)
ECZEMA ( 3 FDA reports)
EJECTION FRACTION DECREASED ( 3 FDA reports)
FASCIITIS ( 3 FDA reports)
FEELING COLD ( 3 FDA reports)
FLANK PAIN ( 3 FDA reports)
GASTRIC DISORDER ( 3 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 3 FDA reports)
GLAUCOMA ( 3 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 3 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 3 FDA reports)
HAEMORRHOIDS ( 3 FDA reports)
HAIR TEXTURE ABNORMAL ( 3 FDA reports)
HEAD INJURY ( 3 FDA reports)
HEPATIC STEATOSIS ( 3 FDA reports)
HEPATITIS C ( 3 FDA reports)
HEPATOMEGALY ( 3 FDA reports)
HIATUS HERNIA ( 3 FDA reports)
HYPERAESTHESIA ( 3 FDA reports)
HYPOVOLAEMIA ( 3 FDA reports)
IMMUNE SYSTEM DISORDER ( 3 FDA reports)
INFECTIVE THROMBOSIS ( 3 FDA reports)
INJECTION SITE INFECTION ( 3 FDA reports)
INTENTIONAL DRUG MISUSE ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 3 FDA reports)
INTESTINAL PERFORATION ( 3 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 3 FDA reports)
JAUNDICE ( 3 FDA reports)
JUGULAR VEIN THROMBOSIS ( 3 FDA reports)
KLEBSIELLA INFECTION ( 3 FDA reports)
KNEE OPERATION ( 3 FDA reports)
LIGAMENT LAXITY ( 3 FDA reports)
LOCAL SWELLING ( 3 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
LOWER LIMB FRACTURE ( 3 FDA reports)
LUNG NEOPLASM ( 3 FDA reports)
MASS ( 3 FDA reports)
MEDICAL DEVICE COMPLICATION ( 3 FDA reports)
MENSTRUATION IRREGULAR ( 3 FDA reports)
MENTAL STATUS CHANGES ( 3 FDA reports)
MOOD SWINGS ( 3 FDA reports)
MULTIPLE SCLEROSIS ( 3 FDA reports)
MUSCLE ABSCESS ( 3 FDA reports)
MUSCLE DISORDER ( 3 FDA reports)
MUSCULOSKELETAL DISORDER ( 3 FDA reports)
MYOCARDIAL ISCHAEMIA ( 3 FDA reports)
NAIL BED BLEEDING ( 3 FDA reports)
NARCOLEPSY ( 3 FDA reports)
NECK INJURY ( 3 FDA reports)
NEUROGENIC BLADDER ( 3 FDA reports)
OESOPHAGITIS ( 3 FDA reports)
ONYCHOMYCOSIS ( 3 FDA reports)
OVARIAN CYST ( 3 FDA reports)
PAIN THRESHOLD DECREASED ( 3 FDA reports)
PATHOLOGICAL GAMBLING ( 3 FDA reports)
PERIRECTAL ABSCESS ( 3 FDA reports)
PNEUMONITIS ( 3 FDA reports)
POLYP ( 3 FDA reports)
PREGNANCY ( 3 FDA reports)
PROCEDURAL COMPLICATION ( 3 FDA reports)
PROCEDURAL NAUSEA ( 3 FDA reports)
PROCEDURAL VOMITING ( 3 FDA reports)
PRODUCT QUALITY ISSUE ( 3 FDA reports)
PRURITUS GENERALISED ( 3 FDA reports)
PSORIASIS ( 3 FDA reports)
PULMONARY INFARCTION ( 3 FDA reports)
PULMONARY OEDEMA ( 3 FDA reports)
RALES ( 3 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 3 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 3 FDA reports)
SENSORY DISTURBANCE ( 3 FDA reports)
SENSORY LOSS ( 3 FDA reports)
SKIN EXFOLIATION ( 3 FDA reports)
SKIN INJURY ( 3 FDA reports)
SKIN LESION ( 3 FDA reports)
SKIN WARM ( 3 FDA reports)
SKIN WRINKLING ( 3 FDA reports)
SOFT TISSUE MASS ( 3 FDA reports)
SPINAL COMPRESSION FRACTURE ( 3 FDA reports)
TESTICULAR SWELLING ( 3 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 3 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 3 FDA reports)
THERAPY NON-RESPONDER ( 3 FDA reports)
THYROID NEOPLASM ( 3 FDA reports)
TRACHEOBRONCHITIS ( 3 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 3 FDA reports)
VASCULAR CALCIFICATION ( 3 FDA reports)
VISUAL ACUITY REDUCED ( 3 FDA reports)
VITAMIN D DEFICIENCY ( 3 FDA reports)
WOUND ( 3 FDA reports)
ABASIA ( 2 FDA reports)
ABDOMINAL PAIN LOWER ( 2 FDA reports)
ACNE ( 2 FDA reports)
ACOUSTIC NEUROMA ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 2 FDA reports)
AGORAPHOBIA ( 2 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
ANASTOMOTIC COMPLICATION ( 2 FDA reports)
ANKLE FRACTURE ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
ARTERIAL BYPASS OPERATION ( 2 FDA reports)
ARTERIAL DISORDER ( 2 FDA reports)
ARTERIAL THERAPEUTIC PROCEDURE ( 2 FDA reports)
ARTERIOSCLEROSIS ( 2 FDA reports)
ASCITES ( 2 FDA reports)
ATAXIA ( 2 FDA reports)
ATELECTASIS ( 2 FDA reports)
ATRIAL TACHYCARDIA ( 2 FDA reports)
BACTERIA STOOL IDENTIFIED ( 2 FDA reports)
BACTERIAL INFECTION ( 2 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 2 FDA reports)
BIOPSY LIP ( 2 FDA reports)
BIPOLAR DISORDER ( 2 FDA reports)
BLADDER CANCER ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD CORTISOL INCREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 2 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 2 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 2 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 2 FDA reports)
BODY HEIGHT DECREASED ( 2 FDA reports)
BRAIN INJURY ( 2 FDA reports)
BRAIN OEDEMA ( 2 FDA reports)
BRONCHIOLOALVEOLAR CARCINOMA ( 2 FDA reports)
CARCINOMA IN SITU OF TRACHEA ( 2 FDA reports)
CARDIAC ASTHMA ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CARDIAC FIBRILLATION ( 2 FDA reports)
CAROTID ARTERY STENOSIS ( 2 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
CERUMEN IMPACTION ( 2 FDA reports)
CHOLANGITIS ( 2 FDA reports)
CLAVICLE FRACTURE ( 2 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 2 FDA reports)
COLITIS ULCERATIVE ( 2 FDA reports)
COMPULSIVE SHOPPING ( 2 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 2 FDA reports)
CONJUNCTIVITIS ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
DECREASED ACTIVITY ( 2 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 2 FDA reports)
DIARRHOEA INFECTIOUS ( 2 FDA reports)
DRUG EFFECT DECREASED ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
DRUG PRESCRIBING ERROR ( 2 FDA reports)
DUODENITIS ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
DYSMENORRHOEA ( 2 FDA reports)
DYSPNOEA EXERTIONAL ( 2 FDA reports)
DYSTONIA ( 2 FDA reports)
EARLY SATIETY ( 2 FDA reports)
EJECTION FRACTION ABNORMAL ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
ENDOCRINE OPHTHALMOPATHY ( 2 FDA reports)
ENDODONTIC PROCEDURE ( 2 FDA reports)
ENDOPHTHALMITIS ( 2 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 2 FDA reports)
EYE DISCHARGE ( 2 FDA reports)
EYE SWELLING ( 2 FDA reports)
FACIAL PALSY ( 2 FDA reports)
FAECES HARD ( 2 FDA reports)
FIBULA FRACTURE ( 2 FDA reports)
FINGER DEFORMITY ( 2 FDA reports)
FOOT FRACTURE ( 2 FDA reports)
FRACTURED COCCYX ( 2 FDA reports)
FULL BLOOD COUNT DECREASED ( 2 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 2 FDA reports)
GALLBLADDER INJURY ( 2 FDA reports)
GALLBLADDER OPERATION ( 2 FDA reports)
GASTRIC ULCER ( 2 FDA reports)
GASTROINTESTINAL INFECTION ( 2 FDA reports)
GASTROINTESTINAL OEDEMA ( 2 FDA reports)
GINGIVAL INJURY ( 2 FDA reports)
GLOSSODYNIA ( 2 FDA reports)
GLUCOSE URINE PRESENT ( 2 FDA reports)
GRAVITATIONAL OEDEMA ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
HAEMOLYTIC ANAEMIA ( 2 FDA reports)
HAEMORRHAGIC DISORDER ( 2 FDA reports)
HAEMOTHORAX ( 2 FDA reports)
HEART VALVE REPLACEMENT ( 2 FDA reports)
HELICOBACTER INFECTION ( 2 FDA reports)
HEMIANOPIA HOMONYMOUS ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HEPATIC CIRRHOSIS ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HYPERTONIC BLADDER ( 2 FDA reports)
HYPERVENTILATION ( 2 FDA reports)
HYPOACUSIS ( 2 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 2 FDA reports)
HYPOMAGNESAEMIA ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
HYPOPHAGIA ( 2 FDA reports)
HYPOTONIA ( 2 FDA reports)
HYPOVENTILATION ( 2 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 2 FDA reports)
IMPAIRED SELF-CARE ( 2 FDA reports)
IMPLANT SITE INFLAMMATION ( 2 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 2 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 2 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 2 FDA reports)
INCORRECT STORAGE OF DRUG ( 2 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 2 FDA reports)
INFECTIOUS PERITONITIS ( 2 FDA reports)
INGROWING NAIL ( 2 FDA reports)
INJECTION SITE INFLAMMATION ( 2 FDA reports)
INJECTION SITE SWELLING ( 2 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 2 FDA reports)
INTESTINAL STENOSIS ( 2 FDA reports)
JAW OPERATION ( 2 FDA reports)
JOINT DISLOCATION ( 2 FDA reports)
JOINT LOCK ( 2 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 2 FDA reports)
LUNG ABSCESS ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
MALNUTRITION ( 2 FDA reports)
MELAENA ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
METASTASIS ( 2 FDA reports)
MIDDLE INSOMNIA ( 2 FDA reports)
MOBILITY DECREASED ( 2 FDA reports)
MUCOUS STOOLS ( 2 FDA reports)
NAIL GROWTH ABNORMAL ( 2 FDA reports)
NERVE COMPRESSION ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
NIGHT SWEATS ( 2 FDA reports)
NIGHTMARE ( 2 FDA reports)
NODAL ARRHYTHMIA ( 2 FDA reports)
NODULE ON EXTREMITY ( 2 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
OESOPHAGEAL CARCINOMA ( 2 FDA reports)
OESOPHAGEAL INJURY ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
ORAL DISORDER ( 2 FDA reports)
ORAL HERPES ( 2 FDA reports)
ORAL PAIN ( 2 FDA reports)
ORAL PRURITUS ( 2 FDA reports)
OROPHARYNGEAL SWELLING ( 2 FDA reports)
OSTEOMYELITIS FUNGAL ( 2 FDA reports)
PARALYSIS ( 2 FDA reports)
PARKINSON'S DISEASE ( 2 FDA reports)
PAROSMIA ( 2 FDA reports)
PERITONEAL EFFUSION ( 2 FDA reports)
PERONEAL NERVE PALSY ( 2 FDA reports)
PH URINE INCREASED ( 2 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 2 FDA reports)
PLANTAR FASCIITIS ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
PRESYNCOPE ( 2 FDA reports)
PROCTITIS ( 2 FDA reports)
PROSTATIC DISORDER ( 2 FDA reports)
PROTEIN URINE PRESENT ( 2 FDA reports)
PSEUDOMONAS INFECTION ( 2 FDA reports)
PSYCHOLOGICAL TRAUMA ( 2 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 2 FDA reports)
PULMONARY FIBROSIS ( 2 FDA reports)
PULSE ABSENT ( 2 FDA reports)
PYELONEPHRITIS ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
RASH MACULAR ( 2 FDA reports)
RENAL FAILURE CHRONIC ( 2 FDA reports)
RENAL PAIN ( 2 FDA reports)
RESPIRATORY DISORDER ( 2 FDA reports)
RESPIRATORY TRACT CONGESTION ( 2 FDA reports)
RESTLESS LEGS SYNDROME ( 2 FDA reports)
RHONCHI ( 2 FDA reports)
ROTATOR CUFF REPAIR ( 2 FDA reports)
SCIATICA ( 2 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 2 FDA reports)
SELF-MEDICATION ( 2 FDA reports)
SENILE DEMENTIA ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
SEROMA ( 2 FDA reports)
SHOCK ( 2 FDA reports)
SINUS OPERATION ( 2 FDA reports)
SKIN INDURATION ( 2 FDA reports)
SNEEZING ( 2 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 2 FDA reports)
STASIS DERMATITIS ( 2 FDA reports)
STENT PLACEMENT ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
STRESS SYMPTOMS ( 2 FDA reports)
SUDDEN CARDIAC DEATH ( 2 FDA reports)
SWOLLEN TONGUE ( 2 FDA reports)
TACHYPHRENIA ( 2 FDA reports)
THROAT IRRITATION ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
TONGUE DISCOLOURATION ( 2 FDA reports)
TONSILLITIS ( 2 FDA reports)
TOOTHACHE ( 2 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 2 FDA reports)
TROPONIN INCREASED ( 2 FDA reports)
TUNNEL VISION ( 2 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 2 FDA reports)
URINE ODOUR ABNORMAL ( 2 FDA reports)
UROSEPSIS ( 2 FDA reports)
VAGINAL EROSION ( 2 FDA reports)
VASCULITIS GASTROINTESTINAL ( 2 FDA reports)
VEIN DISORDER ( 2 FDA reports)
VEIN PAIN ( 2 FDA reports)
VISUAL DISTURBANCE ( 2 FDA reports)
VISUAL FIELD DEFECT ( 2 FDA reports)
WALKING AID USER ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
WOUND INFECTION ( 2 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 2 FDA reports)
ABDOMINAL ADHESIONS ( 1 FDA reports)
ABDOMINAL MASS ( 1 FDA reports)
ABDOMINAL RIGIDITY ( 1 FDA reports)
ABDOMINOPLASTY ( 1 FDA reports)
ABNORMAL FAECES ( 1 FDA reports)
ACETABULUM FRACTURE ( 1 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ABNORMAL ( 1 FDA reports)
ACUTE HEPATIC FAILURE ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ACUTE SINUSITIS ( 1 FDA reports)
ADENOMA BENIGN ( 1 FDA reports)
ADHESION ( 1 FDA reports)
ADRENAL DISORDER ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 1 FDA reports)
ANAL ABSCESS ( 1 FDA reports)
ANALGESIC DRUG LEVEL INCREASED ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
ANEURYSM ( 1 FDA reports)
ANGER ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ANORECTAL OPERATION ( 1 FDA reports)
ANTIBODY TEST POSITIVE ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANXIETY DISORDER ( 1 FDA reports)
AORTITIS ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
APHONIA ( 1 FDA reports)
APNOEIC ATTACK ( 1 FDA reports)
APPENDICITIS PERFORATED ( 1 FDA reports)
APPLICATION SITE ERYTHEMA ( 1 FDA reports)
APPLICATION SITE IRRITATION ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ARTERIAL THROMBOSIS ( 1 FDA reports)
ARTHROPOD BITE ( 1 FDA reports)
ARTHROSCOPY ( 1 FDA reports)
ASPHYXIA ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
ASPIRATION TRACHEAL ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
ATROPHIC VULVOVAGINITIS ( 1 FDA reports)
ATROPHY ( 1 FDA reports)
AUTOIMMUNE DISORDER ( 1 FDA reports)
AUTOPSY ( 1 FDA reports)
BACTERIURIA ( 1 FDA reports)
BAND NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
BARRETT'S OESOPHAGUS ( 1 FDA reports)
BEREAVEMENT ( 1 FDA reports)
BILE DUCT CANCER ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BIOPSY BRAIN ABNORMAL ( 1 FDA reports)
BIOPSY LIVER ( 1 FDA reports)
BIOPSY MUSCLE ABNORMAL ( 1 FDA reports)
BLADDER NECK SUSPENSION ( 1 FDA reports)
BLINDNESS TRANSIENT ( 1 FDA reports)
BLOOD CHLORIDE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD CREATININE DECREASED ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BLOOD IRON INCREASED ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BLOOD URIC ACID DECREASED ( 1 FDA reports)
BONE DEBRIDEMENT ( 1 FDA reports)
BONE DENSITY DECREASED ( 1 FDA reports)
BONE FORMATION INCREASED ( 1 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 1 FDA reports)
BOWEL SOUNDS ABNORMAL ( 1 FDA reports)
BRADYPHRENIA ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
BREAST CANCER IN SITU ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 1 FDA reports)
BRONCHITIS CHRONIC ( 1 FDA reports)
BRONCHOSCOPY ( 1 FDA reports)
BUNION ( 1 FDA reports)
BURSA DISORDER ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)
CARBON DIOXIDE DECREASED ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
CARDIAC FAILURE CHRONIC ( 1 FDA reports)
CARDIAC PACEMAKER INSERTION ( 1 FDA reports)
CARDIAC VALVE DISEASE ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CARDIOVERSION ( 1 FDA reports)
CAROTID ARTERY DISEASE ( 1 FDA reports)
CARPAL TUNNEL SYNDROME ( 1 FDA reports)
CATHETER SITE DISCHARGE ( 1 FDA reports)
CATHETER SITE ERYTHEMA ( 1 FDA reports)
CEREBRAL AMYLOID ANGIOPATHY ( 1 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 1 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBRAL DISORDER ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CERVICAL SPINAL STENOSIS ( 1 FDA reports)
CHEILITIS ( 1 FDA reports)
CHOLANGITIS SCLEROSING ( 1 FDA reports)
CHRONIC FATIGUE SYNDROME ( 1 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 1 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COLONIC POLYP ( 1 FDA reports)
COLORECTAL CANCER METASTATIC ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 1 FDA reports)
COMPRESSION FRACTURE ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 1 FDA reports)
CONVERSION DISORDER ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CORRECTIVE LENS USER ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CULTURE STOOL POSITIVE ( 1 FDA reports)
CUSHING'S SYNDROME ( 1 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 1 FDA reports)
CYST RUPTURE ( 1 FDA reports)
DEBRIDEMENT ( 1 FDA reports)
DEFORMITY ( 1 FDA reports)
DEFORMITY THORAX ( 1 FDA reports)
DELUSIONAL PERCEPTION ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DEVICE RELATED SEPSIS ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 1 FDA reports)
DIABETIC NEUROPATHY ( 1 FDA reports)
DIAPHRAGMATIC HERNIA ( 1 FDA reports)
DIASTOLIC DYSFUNCTION ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 1 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 1 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSLIPIDAEMIA ( 1 FDA reports)
DYSPHEMIA ( 1 FDA reports)
EAR INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
ECTOPIC PREGNANCY ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
ENCEPHALITIS ( 1 FDA reports)
ENDOCRINE DISORDER ( 1 FDA reports)
ENTEROBACTER INFECTION ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
EOSINOPHIL COUNT DECREASED ( 1 FDA reports)
EOSINOPHIL PERCENTAGE DECREASED ( 1 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 1 FDA reports)
ERYTHEMA NODOSUM ( 1 FDA reports)
ESCHAR ( 1 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 1 FDA reports)
EYE ALLERGY ( 1 FDA reports)
EYE EXCISION ( 1 FDA reports)
EYE INFECTION ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
EYELIDS PRURITUS ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FACIAL PAIN ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FANCONI SYNDROME ( 1 FDA reports)
FEEDING DISORDER ( 1 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 1 FDA reports)
FISTULA ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
FOLLICULITIS ( 1 FDA reports)
FONTANELLE BULGING ( 1 FDA reports)
FOOD CRAVING ( 1 FDA reports)
FOOD INTOLERANCE ( 1 FDA reports)
FOOT DEFORMITY ( 1 FDA reports)
FOREIGN BODY ( 1 FDA reports)
FORMICATION ( 1 FDA reports)
FRONTOTEMPORAL DEMENTIA ( 1 FDA reports)
GALLBLADDER PAIN ( 1 FDA reports)
GALLBLADDER POLYP ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTRIC ANTRAL VASCULAR ECTASIA ( 1 FDA reports)
GASTROINTESTINAL SURGERY ( 1 FDA reports)
GENITAL DISORDER MALE ( 1 FDA reports)
GENITAL PAIN ( 1 FDA reports)
GINGIVAL BLISTER ( 1 FDA reports)
GINGIVAL PAIN ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GOUT ( 1 FDA reports)
GROIN PAIN ( 1 FDA reports)
H1N1 INFLUENZA ( 1 FDA reports)
HAEMATOCRIT ABNORMAL ( 1 FDA reports)
HAEMOGLOBIN ABNORMAL ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 1 FDA reports)
HAEMORRHAGIC ANAEMIA ( 1 FDA reports)
HAIR GROWTH ABNORMAL ( 1 FDA reports)
HALLUCINATION, OLFACTORY ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEART INJURY ( 1 FDA reports)
HEMISENSORY NEGLECT ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HEPATIC ENZYME ABNORMAL ( 1 FDA reports)
HEPATIC LESION ( 1 FDA reports)
HEPATITIS TOXIC ( 1 FDA reports)
HEPATOBILIARY SCAN ABNORMAL ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HERNIA HIATUS REPAIR ( 1 FDA reports)
HERNIA OBSTRUCTIVE ( 1 FDA reports)
HERNIA REPAIR ( 1 FDA reports)
HICCUPS ( 1 FDA reports)
HOSPICE CARE ( 1 FDA reports)
HYDROCEPHALUS ( 1 FDA reports)
HYPERCALCIURIA ( 1 FDA reports)
HYPERCOAGULATION ( 1 FDA reports)
HYPERDYNAMIC LEFT VENTRICLE ( 1 FDA reports)
HYPERKERATOSIS ( 1 FDA reports)
HYPERPHAGIA ( 1 FDA reports)
HYPERVIGILANCE ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOPHOSPHATAEMIA ( 1 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 1 FDA reports)
IMMUNOLOGY TEST ABNORMAL ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
INCISION SITE COMPLICATION ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INCREASED APPETITE ( 1 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 1 FDA reports)
INFERTILITY FEMALE ( 1 FDA reports)
INFUSION SITE ERYTHEMA ( 1 FDA reports)
INGROWN HAIR ( 1 FDA reports)
INJECTION SITE BRUISING ( 1 FDA reports)
INJECTION SITE BURNING ( 1 FDA reports)
INJECTION SITE EXTRAVASATION ( 1 FDA reports)
INJECTION SITE HYPERSENSITIVITY ( 1 FDA reports)
INJECTION SITE PAPULE ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJECTION SITE STINGING ( 1 FDA reports)
INJECTION SITE URTICARIA ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
INTESTINAL DILATATION ( 1 FDA reports)
INTESTINAL HAEMORRHAGE ( 1 FDA reports)
INTESTINAL ISCHAEMIA ( 1 FDA reports)
INTESTINAL MUCOSAL HYPERTROPHY ( 1 FDA reports)
INTESTINAL ULCER ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
INTRAOCULAR MELANOMA ( 1 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 1 FDA reports)
IRON DEFICIENCY ( 1 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
KYPHOSIS ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LACTATION DISORDER ( 1 FDA reports)
LAGOPHTHALMOS ( 1 FDA reports)
LARYNGOSPASM ( 1 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
LIGAMENT SPRAIN ( 1 FDA reports)
LIP BLISTER ( 1 FDA reports)
LIVEDO RETICULARIS ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
LUMBAR PUNCTURE ( 1 FDA reports)
LUMBAR SPINAL STENOSIS ( 1 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 1 FDA reports)
LUNG ADENOCARCINOMA ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
LYMPHOEDEMA ( 1 FDA reports)
MASKED FACIES ( 1 FDA reports)
MENINGITIS VIRAL ( 1 FDA reports)
METABOLIC ENCEPHALOPATHY ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
MINI MENTAL STATUS EXAMINATION ABNORMAL ( 1 FDA reports)
MITRAL VALVE DISEASE ( 1 FDA reports)
MITRAL VALVE PROLAPSE ( 1 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MORGANELLA INFECTION ( 1 FDA reports)
MOTOR NEURONE DISEASE ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MULTIPLE INJURIES ( 1 FDA reports)
MUSCLE SPASTICITY ( 1 FDA reports)
MUSCLE STRAIN ( 1 FDA reports)
MUSCLE SWELLING ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MUSCULAR DYSTROPHY ( 1 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 1 FDA reports)
MYCOBACTERIUM MARINUM INFECTION ( 1 FDA reports)
MYELOPATHY ( 1 FDA reports)
MYOPIA ( 1 FDA reports)
NAIL BED DISORDER ( 1 FDA reports)
NAIL DISCOLOURATION ( 1 FDA reports)
NASAL ODOUR ( 1 FDA reports)
NASAL OEDEMA ( 1 FDA reports)
NASOPHARYNGEAL DISORDER ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NERVE INJURY ( 1 FDA reports)
NEUROGENIC BOWEL ( 1 FDA reports)
NOCTURIA ( 1 FDA reports)
NODULE ( 1 FDA reports)
NON-CARDIAC CHEST PAIN ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER ( 1 FDA reports)
NOSOCOMIAL INFECTION ( 1 FDA reports)
NUCHAL RIGIDITY ( 1 FDA reports)
OBSTRUCTION ( 1 FDA reports)
OCCULT BLOOD POSITIVE ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 1 FDA reports)
OESOPHAGEAL POLYP ( 1 FDA reports)
OESOPHAGEAL RUPTURE ( 1 FDA reports)
OESOPHAGEAL SPASM ( 1 FDA reports)
OESOPHAGEAL ULCER ( 1 FDA reports)
ONYCHOPHAGIA ( 1 FDA reports)
OPEN WOUND ( 1 FDA reports)
ORAL DISCOMFORT ( 1 FDA reports)
ORAL FUNGAL INFECTION ( 1 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
ORTHOSIS USER ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
PAIN OF SKIN ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 1 FDA reports)
PANCREATIC ENZYMES INCREASED ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PANCREATITIS CHRONIC ( 1 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
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PATHOLOGICAL FRACTURE ( 1 FDA reports)
PELVIC FRACTURE ( 1 FDA reports)
PEPTIC ULCER ( 1 FDA reports)
PERFORMANCE STATUS DECREASED ( 1 FDA reports)
PERIANAL ABSCESS ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PH BODY FLUID ABNORMAL ( 1 FDA reports)
PHARYNGEAL ERYTHEMA ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
PLASMACYTOMA ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
PNEUMONIA HERPES VIRAL ( 1 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POLYP COLORECTAL ( 1 FDA reports)
POLYPECTOMY ( 1 FDA reports)
PORTAL HYPERTENSION ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
POSTICTAL STATE ( 1 FDA reports)
POSTNASAL DRIP ( 1 FDA reports)
POSTOPERATIVE ABSCESS ( 1 FDA reports)
POSTOPERATIVE ADHESION ( 1 FDA reports)
POUCHITIS ( 1 FDA reports)
PRESBYOPIA ( 1 FDA reports)
PRODUCT FORMULATION ISSUE ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 1 FDA reports)
PROTHROMBIN TIME RATIO INCREASED ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 1 FDA reports)
PULMONARY GRANULOMA ( 1 FDA reports)
PULMONARY MYCOSIS ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
QUALITY OF LIFE DECREASED ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RASH VESICULAR ( 1 FDA reports)
REACTION TO AZO-DYES ( 1 FDA reports)
REBOUND EFFECT ( 1 FDA reports)
RECTAL CANCER STAGE III ( 1 FDA reports)
RECTOCELE ( 1 FDA reports)
RED BLOOD CELL ABNORMALITY ( 1 FDA reports)
REFLEXES ABNORMAL ( 1 FDA reports)
REFLUX OESOPHAGITIS ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
REGURGITATION ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RENAL TUBULAR ACIDOSIS ( 1 FDA reports)
REPETITIVE STRAIN INJURY ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
SALMONELLOSIS ( 1 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 1 FDA reports)
SCAPULA FRACTURE ( 1 FDA reports)
SERRATIA INFECTION ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SICK SINUS SYNDROME ( 1 FDA reports)
SKIN CANDIDA ( 1 FDA reports)
SKIN DISCOMFORT ( 1 FDA reports)
SKIN INFECTION ( 1 FDA reports)
SKIN ODOUR ABNORMAL ( 1 FDA reports)
SOCIAL PROBLEM ( 1 FDA reports)
SPIDER VEIN ( 1 FDA reports)
SPINAL CORD COMPRESSION ( 1 FDA reports)
SPINAL DEFORMITY ( 1 FDA reports)
SPINAL FUSION SURGERY ( 1 FDA reports)
SPLENIC INJURY ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
STEATORRHOEA ( 1 FDA reports)
STREPTOCOCCAL IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SUTURE RELATED COMPLICATION ( 1 FDA reports)
SYNCOPE VASOVAGAL ( 1 FDA reports)
SYNOVECTOMY ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
SYSTEMIC MYCOSIS ( 1 FDA reports)
TARDIVE DYSKINESIA ( 1 FDA reports)
TEMPERATURE REGULATION DISORDER ( 1 FDA reports)
TESTICULAR GERM CELL CANCER ( 1 FDA reports)
THERAPY CESSATION ( 1 FDA reports)
THROAT LESION ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
THROMBOCYTOSIS ( 1 FDA reports)
THYROGLOBULIN INCREASED ( 1 FDA reports)
THYROID CANCER ( 1 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 1 FDA reports)
THYROID GLAND CANCER ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TONGUE ULCERATION ( 1 FDA reports)
TOOTH EROSION ( 1 FDA reports)
TOOTH INFECTION ( 1 FDA reports)
TOOTH LOSS ( 1 FDA reports)
TOXIC ENCEPHALOPATHY ( 1 FDA reports)
TRANSFERRIN SATURATION INCREASED ( 1 FDA reports)
TRISMUS ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
UNWANTED AWARENESS DURING ANAESTHESIA ( 1 FDA reports)
UPPER EXTREMITY MASS ( 1 FDA reports)
URETHRAL DISORDER ( 1 FDA reports)
URGE INCONTINENCE ( 1 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 1 FDA reports)
URINE ANALYSIS ABNORMAL ( 1 FDA reports)
URINE KETONE BODY PRESENT ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
URINE SODIUM DECREASED ( 1 FDA reports)
UVEITIS ( 1 FDA reports)
VAGINAL DISCHARGE ( 1 FDA reports)
VAGINAL MUCOSAL BLISTERING ( 1 FDA reports)
VAGINAL MYCOSIS ( 1 FDA reports)
VAGINAL ODOUR ( 1 FDA reports)
VAGINITIS BACTERIAL ( 1 FDA reports)
VARICOPHLEBITIS ( 1 FDA reports)
VARICOSE VEIN ( 1 FDA reports)
VASCULAR RUPTURE ( 1 FDA reports)
VASOMOTOR RHINITIS ( 1 FDA reports)
VENOUS INSUFFICIENCY ( 1 FDA reports)
VENOUS OCCLUSION ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VENTRICULAR INTERNAL DIAMETER ABNORMAL ( 1 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 1 FDA reports)
VERTEBROPLASTY ( 1 FDA reports)
VIBRATION TEST ABNORMAL ( 1 FDA reports)
VITAMIN B12 DEFICIENCY ( 1 FDA reports)
VITAMIN B12 INCREASED ( 1 FDA reports)
VOLVULUS ( 1 FDA reports)
VULVAL OEDEMA ( 1 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 1 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 1 FDA reports)
WITHDRAWAL SYNDROME ( 1 FDA reports)
WOUND DRAINAGE ( 1 FDA reports)
WRIST FRACTURE ( 1 FDA reports)

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