MedsFacts Reports covering NOROXIN
Directory listing ordered by most common adverse events for NOROXIN
Please choose an event type to view the corresponding MedsFacts report:
HEPATITIS ( 113 FDA reports)
TENDON DISORDER ( 101 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 99 FDA reports)
MYOPATHY ( 98 FDA reports)
INJECTION SITE RASH ( 90 FDA reports)
DRUG INTERACTION ( 56 FDA reports)
PYREXIA ( 45 FDA reports)
CONFUSIONAL STATE ( 40 FDA reports)
BURSITIS ( 33 FDA reports)
DIARRHOEA ( 33 FDA reports)
RENAL FAILURE ACUTE ( 33 FDA reports)
VOMITING ( 32 FDA reports)
ARTHRITIS ( 31 FDA reports)
ASTHENIA ( 31 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 31 FDA reports)
CYTOLYTIC HEPATITIS ( 30 FDA reports)
DYSPNOEA ( 30 FDA reports)
URINARY TRACT INFECTION ( 30 FDA reports)
ANAEMIA ( 29 FDA reports)
ARTHRALGIA ( 29 FDA reports)
JAUNDICE ( 29 FDA reports)
NAUSEA ( 29 FDA reports)
CHOLESTASIS ( 28 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 28 FDA reports)
ABDOMINAL PAIN ( 26 FDA reports)
HYPONATRAEMIA ( 26 FDA reports)
MYALGIA ( 25 FDA reports)
PRURITUS ( 25 FDA reports)
TENDONITIS ( 24 FDA reports)
THROMBOCYTOPENIA ( 24 FDA reports)
DRUG ERUPTION ( 23 FDA reports)
FALL ( 23 FDA reports)
PANCREATITIS ACUTE ( 23 FDA reports)
PYELONEPHRITIS ( 23 FDA reports)
RENAL FAILURE ( 23 FDA reports)
NEUTROPENIA ( 21 FDA reports)
OEDEMA PERIPHERAL ( 21 FDA reports)
MALAISE ( 20 FDA reports)
OVERDOSE ( 20 FDA reports)
RASH MACULO-PAPULAR ( 20 FDA reports)
AGRANULOCYTOSIS ( 19 FDA reports)
TOXIC SKIN ERUPTION ( 19 FDA reports)
ANOREXIA ( 18 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 18 FDA reports)
RHABDOMYOLYSIS ( 18 FDA reports)
DEHYDRATION ( 17 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 17 FDA reports)
RASH ( 17 FDA reports)
SOMNOLENCE ( 17 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 16 FDA reports)
BLOOD BILIRUBIN INCREASED ( 16 FDA reports)
DEATH ( 16 FDA reports)
DERMATITIS BULLOUS ( 16 FDA reports)
ESCHERICHIA INFECTION ( 16 FDA reports)
PAIN ( 16 FDA reports)
PANCYTOPENIA ( 16 FDA reports)
ABNORMAL BEHAVIOUR ( 15 FDA reports)
BACTERIAL PYELONEPHRITIS ( 15 FDA reports)
HAEMATOMA ( 15 FDA reports)
BLOOD CREATININE INCREASED ( 14 FDA reports)
ERYTHEMA ( 14 FDA reports)
PURPURA ( 14 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 13 FDA reports)
CONDITION AGGRAVATED ( 13 FDA reports)
CONSTIPATION ( 13 FDA reports)
FATIGUE ( 13 FDA reports)
HYPOKALAEMIA ( 13 FDA reports)
TACHYCARDIA ( 13 FDA reports)
CEREBROVASCULAR ACCIDENT ( 12 FDA reports)
DEPRESSION ( 12 FDA reports)
EPILEPSY ( 12 FDA reports)
EPISTAXIS ( 12 FDA reports)
PLATELET COUNT DECREASED ( 12 FDA reports)
STEVENS-JOHNSON SYNDROME ( 12 FDA reports)
TREMOR ( 12 FDA reports)
ANGIOEDEMA ( 11 FDA reports)
ANXIETY ( 11 FDA reports)
HEADACHE ( 11 FDA reports)
ODYNOPHAGIA ( 11 FDA reports)
PAIN IN EXTREMITY ( 11 FDA reports)
URTICARIA ( 11 FDA reports)
VASCULAR PURPURA ( 11 FDA reports)
ASCITES ( 10 FDA reports)
BLOOD PRESSURE DECREASED ( 10 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 10 FDA reports)
DIZZINESS ( 10 FDA reports)
EOSINOPHILIA ( 10 FDA reports)
GINGIVAL BLEEDING ( 10 FDA reports)
HAEMATURIA ( 10 FDA reports)
HYPERKALAEMIA ( 10 FDA reports)
HYPERTONIA ( 10 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 10 FDA reports)
LEUKOPENIA ( 10 FDA reports)
MUSCULAR WEAKNESS ( 10 FDA reports)
PARAESTHESIA ( 10 FDA reports)
SUBDURAL HAEMATOMA ( 10 FDA reports)
VISUAL IMPAIRMENT ( 10 FDA reports)
ABORTION INDUCED ( 9 FDA reports)
AGGRESSION ( 9 FDA reports)
BRADYCARDIA ( 9 FDA reports)
CHEST PAIN ( 9 FDA reports)
DECREASED APPETITE ( 9 FDA reports)
FACE OEDEMA ( 9 FDA reports)
HAEMOGLOBIN DECREASED ( 9 FDA reports)
HAEMOLYTIC ANAEMIA ( 9 FDA reports)
HEPATIC FAILURE ( 9 FDA reports)
HYPERSENSITIVITY ( 9 FDA reports)
LACTIC ACIDOSIS ( 9 FDA reports)
LOSS OF CONSCIOUSNESS ( 9 FDA reports)
NECK PAIN ( 9 FDA reports)
OFF LABEL USE ( 9 FDA reports)
PEMPHIGOID ( 9 FDA reports)
PNEUMONIA ( 9 FDA reports)
ABDOMINAL PAIN UPPER ( 8 FDA reports)
DRUG TOXICITY ( 8 FDA reports)
EYELID OEDEMA ( 8 FDA reports)
GASTROENTERITIS ( 8 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 8 FDA reports)
HEPATOCELLULAR DAMAGE ( 8 FDA reports)
HEPATOCELLULAR INJURY ( 8 FDA reports)
HYPERTHERMIA ( 8 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 8 FDA reports)
MOTOR DYSFUNCTION ( 8 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 8 FDA reports)
PULMONARY EMBOLISM ( 8 FDA reports)
RESPIRATORY FAILURE ( 8 FDA reports)
SKIN DISORDER ( 8 FDA reports)
SKIN EXFOLIATION ( 8 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 8 FDA reports)
WEIGHT DECREASED ( 8 FDA reports)
ASTERIXIS ( 7 FDA reports)
ATRIAL FIBRILLATION ( 7 FDA reports)
DEEP VEIN THROMBOSIS ( 7 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 7 FDA reports)
DRUG INEFFECTIVE ( 7 FDA reports)
HALLUCINATION ( 7 FDA reports)
HEPATIC ENCEPHALOPATHY ( 7 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 7 FDA reports)
HYPERHIDROSIS ( 7 FDA reports)
HYPOXIA ( 7 FDA reports)
INTERSTITIAL LUNG DISEASE ( 7 FDA reports)
MOUTH ULCERATION ( 7 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 7 FDA reports)
MYOCARDIAL INFARCTION ( 7 FDA reports)
NERVOUS SYSTEM DISORDER ( 7 FDA reports)
PALLOR ( 7 FDA reports)
RASH ERYTHEMATOUS ( 7 FDA reports)
RENAL IMPAIRMENT ( 7 FDA reports)
SYNCOPE ( 7 FDA reports)
TRANSAMINASES INCREASED ( 7 FDA reports)
ABDOMINAL DISTENSION ( 6 FDA reports)
ACUTE PULMONARY OEDEMA ( 6 FDA reports)
AFFECTIVE DISORDER ( 6 FDA reports)
AGITATION ( 6 FDA reports)
BACK PAIN ( 6 FDA reports)
BLOOD AMYLASE INCREASED ( 6 FDA reports)
CEREBRAL ATROPHY ( 6 FDA reports)
CHROMATURIA ( 6 FDA reports)
COGWHEEL RIGIDITY ( 6 FDA reports)
COMA ( 6 FDA reports)
CONVULSION ( 6 FDA reports)
DIABETES MELLITUS ( 6 FDA reports)
DISORIENTATION ( 6 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 6 FDA reports)
DYSPHAGIA ( 6 FDA reports)
ENCEPHALOPATHY ( 6 FDA reports)
FOETOR HEPATICUS ( 6 FDA reports)
HAEMORRHAGE ( 6 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 6 FDA reports)
HEPATITIS FULMINANT ( 6 FDA reports)
HYPERAESTHESIA ( 6 FDA reports)
HYPOTENSION ( 6 FDA reports)
LYMPHADENOPATHY ( 6 FDA reports)
MELAENA ( 6 FDA reports)
MYOCLONUS ( 6 FDA reports)
PORTAL VEIN THROMBOSIS ( 6 FDA reports)
RASH MORBILLIFORM ( 6 FDA reports)
RECTAL HAEMORRHAGE ( 6 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 6 FDA reports)
SEPTIC SHOCK ( 6 FDA reports)
URINARY RETENTION ( 6 FDA reports)
VIRAL LOAD INCREASED ( 6 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 6 FDA reports)
ADVERSE EVENT ( 5 FDA reports)
ATELECTASIS ( 5 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 5 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 5 FDA reports)
BONE PAIN ( 5 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 5 FDA reports)
COLITIS ( 5 FDA reports)
COUGH ( 5 FDA reports)
CUTANEOUS VASCULITIS ( 5 FDA reports)
CYSTITIS ( 5 FDA reports)
DISTURBANCE IN ATTENTION ( 5 FDA reports)
DIVERTICULUM INTESTINAL ( 5 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 5 FDA reports)
HEPATIC STEATOSIS ( 5 FDA reports)
HEPATITIS ACUTE ( 5 FDA reports)
HYPERTENSION ( 5 FDA reports)
HYPOAESTHESIA ( 5 FDA reports)
IMPAIRED SELF-CARE ( 5 FDA reports)
INJURY ( 5 FDA reports)
INSOMNIA ( 5 FDA reports)
LIPASE INCREASED ( 5 FDA reports)
LIVER DISORDER ( 5 FDA reports)
MOUTH HAEMORRHAGE ( 5 FDA reports)
MUSCLE SPASMS ( 5 FDA reports)
OEDEMA ( 5 FDA reports)
PARALYSIS ( 5 FDA reports)
PETIT MAL EPILEPSY ( 5 FDA reports)
PHLEBITIS ( 5 FDA reports)
PLEURAL EFFUSION ( 5 FDA reports)
RASH GENERALISED ( 5 FDA reports)
STAPHYLOCOCCAL INFECTION ( 5 FDA reports)
STREPTOCOCCAL SEPSIS ( 5 FDA reports)
TENDON RUPTURE ( 5 FDA reports)
THROMBOSIS ( 5 FDA reports)
UPPER LIMB FRACTURE ( 5 FDA reports)
VERTIGO ( 5 FDA reports)
ACTINOMYCOSIS ( 4 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 4 FDA reports)
ANAEMIA MACROCYTIC ( 4 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 4 FDA reports)
BACTERIAL TEST POSITIVE ( 4 FDA reports)
BILE DUCT OBSTRUCTION ( 4 FDA reports)
BIOPSY BONE ABNORMAL ( 4 FDA reports)
BLOOD URINE PRESENT ( 4 FDA reports)
BONE DISORDER ( 4 FDA reports)
BUNION ( 4 FDA reports)
CARDIAC ARREST ( 4 FDA reports)
CARDIOGENIC SHOCK ( 4 FDA reports)
CELL DEATH ( 4 FDA reports)
CHILLS ( 4 FDA reports)
CHOLELITHIASIS ( 4 FDA reports)
CLOSTRIDIUM COLITIS ( 4 FDA reports)
DIALYSIS ( 4 FDA reports)
DISEASE PROGRESSION ( 4 FDA reports)
DRUG HYPERSENSITIVITY ( 4 FDA reports)
DYSGEUSIA ( 4 FDA reports)
DYSKINESIA ( 4 FDA reports)
DYSPAREUNIA ( 4 FDA reports)
DYSURIA ( 4 FDA reports)
EOSINOPHIL COUNT INCREASED ( 4 FDA reports)
EOSINOPHILIC PNEUMONIA ( 4 FDA reports)
FOOT DEFORMITY ( 4 FDA reports)
GALLBLADDER DISORDER ( 4 FDA reports)
HEART DISEASE CONGENITAL ( 4 FDA reports)
HEPATIC CYST ( 4 FDA reports)
HIATUS HERNIA ( 4 FDA reports)
HYPERCALCAEMIA ( 4 FDA reports)
HYPOKINESIA ( 4 FDA reports)
HYPOVOLAEMIC SHOCK ( 4 FDA reports)
IMPAIRED HEALING ( 4 FDA reports)
INTENTIONAL OVERDOSE ( 4 FDA reports)
LACRIMATION INCREASED ( 4 FDA reports)
LEUKOCYTOSIS ( 4 FDA reports)
LIMB MALFORMATION ( 4 FDA reports)
LIPOMA ( 4 FDA reports)
MASS ( 4 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 4 FDA reports)
MEMORY IMPAIRMENT ( 4 FDA reports)
MENISCUS LESION ( 4 FDA reports)
METABOLIC ACIDOSIS ( 4 FDA reports)
MICTURITION URGENCY ( 4 FDA reports)
MIGRAINE ( 4 FDA reports)
MUCOUS MEMBRANE DISORDER ( 4 FDA reports)
MULTI-ORGAN FAILURE ( 4 FDA reports)
MULTIPLE MYELOMA ( 4 FDA reports)
MUSCLE FATIGUE ( 4 FDA reports)
MUSCLE INJURY ( 4 FDA reports)
NEURITIS ( 4 FDA reports)
OESOPHAGEAL DISORDER ( 4 FDA reports)
ONYCHOMYCOSIS ( 4 FDA reports)
OSTEONECROSIS OF JAW ( 4 FDA reports)
OSTEOPENIA ( 4 FDA reports)
PEPTIC ULCER ( 4 FDA reports)
PHOTOSENSITIVITY REACTION ( 4 FDA reports)
PRESCRIBED OVERDOSE ( 4 FDA reports)
RENAL TUBULAR NECROSIS ( 4 FDA reports)
SKIN DISCOLOURATION ( 4 FDA reports)
SKIN LESION ( 4 FDA reports)
SKIN TEST NEGATIVE ( 4 FDA reports)
SPINAL OSTEOARTHRITIS ( 4 FDA reports)
STATUS EPILEPTICUS ( 4 FDA reports)
SUICIDE ATTEMPT ( 4 FDA reports)
TENDON PAIN ( 4 FDA reports)
THROMBOCYTHAEMIA ( 4 FDA reports)
TONGUE EXFOLIATION ( 4 FDA reports)
URINARY INCONTINENCE ( 4 FDA reports)
UROSEPSIS ( 4 FDA reports)
VULVOVAGINAL DRYNESS ( 4 FDA reports)
ABASIA ( 3 FDA reports)
ACUTE CORONARY SYNDROME ( 3 FDA reports)
AGEUSIA ( 3 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 3 FDA reports)
ANAPHYLACTIC REACTION ( 3 FDA reports)
ANAPHYLACTIC SHOCK ( 3 FDA reports)
ARRHYTHMIA ( 3 FDA reports)
BLOOD GLUCOSE INCREASED ( 3 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 3 FDA reports)
BLOOD SODIUM DECREASED ( 3 FDA reports)
BONE MARROW FAILURE ( 3 FDA reports)
CANDIDIASIS ( 3 FDA reports)
CAPILLARY DISORDER ( 3 FDA reports)
CARDIAC MURMUR ( 3 FDA reports)
CIRCULATORY COLLAPSE ( 3 FDA reports)
CONJUNCTIVITIS ( 3 FDA reports)
DISEASE RECURRENCE ( 3 FDA reports)
ECZEMA ( 3 FDA reports)
ENTHESOPATHY ( 3 FDA reports)
ERYTHEMA NODOSUM ( 3 FDA reports)
FEAR ( 3 FDA reports)
FEELING ABNORMAL ( 3 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 3 FDA reports)
HAEMODYNAMIC INSTABILITY ( 3 FDA reports)
HAEMORRHOIDS ( 3 FDA reports)
HALLUCINATION, VISUAL ( 3 FDA reports)
HELICOBACTER GASTRITIS ( 3 FDA reports)
HEMIPLEGIA ( 3 FDA reports)
HEPATIC TRAUMA ( 3 FDA reports)
HYPOTONIA ( 3 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 3 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 3 FDA reports)
INFECTION ( 3 FDA reports)
INFUSION SITE RASH ( 3 FDA reports)
INTRA-UTERINE DEATH ( 3 FDA reports)
JOINT SWELLING ( 3 FDA reports)
LETHARGY ( 3 FDA reports)
LUNG INFECTION ( 3 FDA reports)
MACROCYTOSIS ( 3 FDA reports)
MALABSORPTION ( 3 FDA reports)
MENINGORRHAGIA ( 3 FDA reports)
MUCOSAL INFLAMMATION ( 3 FDA reports)
MUSCLE RIGIDITY ( 3 FDA reports)
MUSCULOSKELETAL PAIN ( 3 FDA reports)
MYDRIASIS ( 3 FDA reports)
MYOCARDIAL ISCHAEMIA ( 3 FDA reports)
NEPHRITIS INTERSTITIAL ( 3 FDA reports)
NEUROPATHY PERIPHERAL ( 3 FDA reports)
PELVIC PAIN ( 3 FDA reports)
PEMPHIGUS ( 3 FDA reports)
PERIARTHRITIS ( 3 FDA reports)
PETECHIAE ( 3 FDA reports)
POLYMYALGIA RHEUMATICA ( 3 FDA reports)
PROTEINURIA ( 3 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 3 FDA reports)
RASH MACULAR ( 3 FDA reports)
RASH PRURITIC ( 3 FDA reports)
RESTLESSNESS ( 3 FDA reports)
SEROTONIN SYNDROME ( 3 FDA reports)
SHOCK HAEMORRHAGIC ( 3 FDA reports)
SHOULDER PAIN ( 3 FDA reports)
SPINA BIFIDA ( 3 FDA reports)
STUPOR ( 3 FDA reports)
SUICIDAL IDEATION ( 3 FDA reports)
THROMBOCYTOPENIC PURPURA ( 3 FDA reports)
URINE ABNORMALITY ( 3 FDA reports)
VISION BLURRED ( 3 FDA reports)
VISUAL ACUITY REDUCED ( 3 FDA reports)
VITAMIN B12 DEFICIENCY ( 3 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 3 FDA reports)
ABORTION MISSED ( 2 FDA reports)
ABORTION SPONTANEOUS ( 2 FDA reports)
ACUTE ABDOMEN ( 2 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 2 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 2 FDA reports)
AMMONIA INCREASED ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
ANGIONEUROTIC OEDEMA ( 2 FDA reports)
ANGIOPATHY ( 2 FDA reports)
ANISOCYTOSIS ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
APHASIA ( 2 FDA reports)
APHTHOUS STOMATITIS ( 2 FDA reports)
ARTERIOPATHIC DISEASE ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 2 FDA reports)
ATRIAL FLUTTER ( 2 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 2 FDA reports)
AUTOMATISM ( 2 FDA reports)
BACILLUS INFECTION ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
BLADDER DYSFUNCTION ( 2 FDA reports)
BLOOD CHLORIDE DECREASED ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
BONE DEBRIDEMENT ( 2 FDA reports)
BONE DENSITY ABNORMAL ( 2 FDA reports)
BONE MARROW DEPRESSION ( 2 FDA reports)
BONE MARROW TOXICITY ( 2 FDA reports)
BRADYPNOEA ( 2 FDA reports)
BRAIN MALFORMATION ( 2 FDA reports)
BRONCHOSPASM ( 2 FDA reports)
CAESAREAN SECTION ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 2 FDA reports)
CEREBRAL ISCHAEMIA ( 2 FDA reports)
CERVICAL SPINAL STENOSIS ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
CHOLESTATIC LIVER INJURY ( 2 FDA reports)
CHONDROPATHY ( 2 FDA reports)
CHROMOSOME ABNORMALITY ( 2 FDA reports)
CIRRHOSIS ALCOHOLIC ( 2 FDA reports)
CITROBACTER INFECTION ( 2 FDA reports)
CLEFT PALATE ( 2 FDA reports)
CLOSTRIDIAL INFECTION ( 2 FDA reports)
COAGULATION FACTOR X LEVEL INCREASED ( 2 FDA reports)
COLONIC OBSTRUCTION ( 2 FDA reports)
COLONIC POLYP ( 2 FDA reports)
COMPLETED SUICIDE ( 2 FDA reports)
CORONARY ARTERY STENOSIS ( 2 FDA reports)
CORONARY ARTERY THROMBOSIS ( 2 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 2 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 2 FDA reports)
DEAFNESS UNILATERAL ( 2 FDA reports)
DELUSION ( 2 FDA reports)
DERMATITIS EXFOLIATIVE ( 2 FDA reports)
DISCOMFORT ( 2 FDA reports)
DISSOCIATION ( 2 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 2 FDA reports)
DRY SKIN ( 2 FDA reports)
DYSMORPHISM ( 2 FDA reports)
DYSPHONIA ( 2 FDA reports)
DYSTONIA ( 2 FDA reports)
ECCHYMOSIS ( 2 FDA reports)
ECHOLALIA ( 2 FDA reports)
ECONOMIC PROBLEM ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
EMOTIONAL DISORDER ( 2 FDA reports)
EMOTIONAL DISTRESS ( 2 FDA reports)
EPIGASTRIC DISCOMFORT ( 2 FDA reports)
ERYTHROSIS ( 2 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 2 FDA reports)
FACIAL DYSMORPHISM ( 2 FDA reports)
FAECAL VOMITING ( 2 FDA reports)
FAECALOMA ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 2 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 2 FDA reports)
GOITRE ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HAEMORRHAGIC ANAEMIA ( 2 FDA reports)
HEAD INJURY ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
HEPATIC ATROPHY ( 2 FDA reports)
HEPATITIS CHOLESTATIC ( 2 FDA reports)
HEPATOMEGALY ( 2 FDA reports)
HEPATOTOXICITY ( 2 FDA reports)
HYPERAMMONAEMIA ( 2 FDA reports)
HYPERLIPIDAEMIA ( 2 FDA reports)
HYPERREFLEXIA ( 2 FDA reports)
HYPERTENSIVE CRISIS ( 2 FDA reports)
HYPOALBUMINAEMIA ( 2 FDA reports)
HYPOCHLORAEMIA ( 2 FDA reports)
HYPOCHROMASIA ( 2 FDA reports)
HYPOVOLAEMIA ( 2 FDA reports)
IIIRD NERVE PARALYSIS ( 2 FDA reports)
INFARCTION ( 2 FDA reports)
INFLAMMATION ( 2 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 2 FDA reports)
INTESTINAL ISCHAEMIA ( 2 FDA reports)
JAUNDICE NEONATAL ( 2 FDA reports)
JOINT EFFUSION ( 2 FDA reports)
LACUNAR INFARCTION ( 2 FDA reports)
LIP HAEMORRHAGE ( 2 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
LYME DISEASE ( 2 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 2 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 2 FDA reports)
METABOLIC ENCEPHALOPATHY ( 2 FDA reports)
MICROANGIOPATHY ( 2 FDA reports)
MIOSIS ( 2 FDA reports)
MOBILITY DECREASED ( 2 FDA reports)
MULTI-ORGAN DISORDER ( 2 FDA reports)
MUSCLE ATROPHY ( 2 FDA reports)
MUSCLE NECROSIS ( 2 FDA reports)
MUSCLE RUPTURE ( 2 FDA reports)
MUTISM ( 2 FDA reports)
MYOSITIS ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
NEUROLOGICAL SYMPTOM ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
OESOPHAGEAL PAIN ( 2 FDA reports)
ORAL CANDIDIASIS ( 2 FDA reports)
ORAL MUCOSAL ERUPTION ( 2 FDA reports)
ORGAN FAILURE ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PANIC DISORDER ( 2 FDA reports)
PCO2 DECREASED ( 2 FDA reports)
PERITONITIS BACTERIAL ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 2 FDA reports)
PROSTATE CANCER ( 2 FDA reports)
PSYCHOMOTOR RETARDATION ( 2 FDA reports)
PYELONEPHRITIS ACUTE ( 2 FDA reports)
RASH PAPULAR ( 2 FDA reports)
RASH SCARLATINIFORM ( 2 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 2 FDA reports)
RESPIRATORY TRACT CONGESTION ( 2 FDA reports)
RETCHING ( 2 FDA reports)
RHEUMATOID ARTHRITIS ( 2 FDA reports)
ROAD TRAFFIC ACCIDENT ( 2 FDA reports)
SALMONELLA SEPSIS ( 2 FDA reports)
SALMONELLOSIS ( 2 FDA reports)
SARCOIDOSIS ( 2 FDA reports)
SEPTIC ARTHRITIS STAPHYLOCOCCAL ( 2 FDA reports)
SEPTIC ENCEPHALOPATHY ( 2 FDA reports)
SERUM SICKNESS ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
SKIN NECROSIS ( 2 FDA reports)
SKIN REACTION ( 2 FDA reports)
SLEEP-RELATED EATING DISORDER ( 2 FDA reports)
STAPHYLOCOCCAL OSTEOMYELITIS ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 2 FDA reports)
THINKING ABNORMAL ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 2 FDA reports)
ULNA FRACTURE ( 2 FDA reports)
VASCULAR DEMENTIA ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ACUTE PSYCHOSIS ( 1 FDA reports)
ALCOHOL INTERACTION ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
AMNIOTIC BAND SYNDROME ( 1 FDA reports)
ANAESTHETIC COMPLICATION ( 1 FDA reports)
ANHEDONIA ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
ANURIA ( 1 FDA reports)
AORTIC VALVE STENOSIS ( 1 FDA reports)
APATHY ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ARTERIOSPASM CORONARY ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
ATRIAL SEPTAL DEFECT ( 1 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 1 FDA reports)
AURA ( 1 FDA reports)
BACTERIURIA ( 1 FDA reports)
BASAL CELL CARCINOMA ( 1 FDA reports)
BICYTOPENIA ( 1 FDA reports)
BILIARY CIRRHOSIS ( 1 FDA reports)
BILIARY CYST ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD OSMOLARITY DECREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BONE DEVELOPMENT ABNORMAL ( 1 FDA reports)
BONE MARROW DISORDER ( 1 FDA reports)
BRAIN DAMAGE ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BREAST DISORDER ( 1 FDA reports)
BRONCHIAL OBSTRUCTION ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
CANDIDURIA ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CAUDA EQUINA SYNDROME ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM ABSCESS ( 1 FDA reports)
CEREBRAL HAEMATOMA ( 1 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 1 FDA reports)
CERVICOBRACHIAL SYNDROME ( 1 FDA reports)
CHEILITIS ( 1 FDA reports)
CHOLANGITIS ( 1 FDA reports)
CHOLANGITIS SCLEROSING ( 1 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COLON ADENOMA ( 1 FDA reports)
COMA HEPATIC ( 1 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
CYSTITIS NONINFECTIVE ( 1 FDA reports)
CYSTOPEXY ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DEJA VU ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DENTAL CARIES ( 1 FDA reports)
DEPERSONALISATION ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DIABETIC KETOACIDOTIC HYPERGLYCAEMIC COMA ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISABILITY ( 1 FDA reports)
DISSEMINATED TUBERCULOSIS ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 1 FDA reports)
DYSPNOEA EXACERBATED ( 1 FDA reports)
EATING DISORDER SYMPTOM ( 1 FDA reports)
ECZEMA INFECTED ( 1 FDA reports)
EFFUSION ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 1 FDA reports)
EPICONDYLITIS ( 1 FDA reports)
EPIDERMOLYSIS ( 1 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EYELID PTOSIS ( 1 FDA reports)
FEBRILE BONE MARROW APLASIA ( 1 FDA reports)
FEBRILE INFECTION ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FLIGHT OF IDEAS ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FOAMING AT MOUTH ( 1 FDA reports)
FOLATE DEFICIENCY ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
FRACTURE DELAYED UNION ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GESTATIONAL DIABETES ( 1 FDA reports)
GESTATIONAL HYPERTENSION ( 1 FDA reports)
GINGIVAL DISORDER ( 1 FDA reports)
GLYCOSURIA ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
GRANULOCYTE COUNT INCREASED ( 1 FDA reports)
GRUNTING ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT RECURRENT ( 1 FDA reports)
HEPATIC PAIN ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYDROCEPHALUS ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERBILIRUBINAEMIA NEONATAL ( 1 FDA reports)
HYPERPLASIA ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
HYPOPROTHROMBINAEMIA ( 1 FDA reports)
HYPOSPADIAS ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMMUNODEFICIENCY ( 1 FDA reports)
IMPRISONMENT ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INFECTIOUS PERITONITIS ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
IRRITABLE BOWEL SYNDROME ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
KYPHOSIS ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LARYNGEAL DISORDER ( 1 FDA reports)
LAXATIVE ABUSE ( 1 FDA reports)
LIBIDO DECREASED ( 1 FDA reports)
LICHENOID KERATOSIS ( 1 FDA reports)
LIPIDS INCREASED ( 1 FDA reports)
LOOSE STOOLS ( 1 FDA reports)
LOSS OF EMPLOYMENT ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 1 FDA reports)
LYMPHOCYTOSIS ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
METAPLASIA ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
MILIARY PNEUMONIA ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
MULTIPLE INJURIES ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
NEONATAL HEPATOMEGALY ( 1 FDA reports)
NEONATAL RESPIRATORY DEPRESSION ( 1 FDA reports)
NEONATAL TACHYPNOEA ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEUROENDOCRINE TUMOUR ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
NODULE ( 1 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 1 FDA reports)
OCULAR ICTERUS ( 1 FDA reports)
OCULAR TOXICITY ( 1 FDA reports)
ODDI'S SPHINCTER CONSTRICTION ( 1 FDA reports)
OESOPHAGEAL ULCER ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
OPEN WOUND ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PAINFUL RESPIRATION ( 1 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 1 FDA reports)
PALPABLE PURPURA ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PELVIC FRACTURE ( 1 FDA reports)
PEPTOSTREPTOCOCCUS TEST POSITIVE ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PERITONEAL HAEMORRHAGE ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PHYSICAL ASSAULT ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POLYCYTHAEMIA ( 1 FDA reports)
POLYP COLORECTAL ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POSTICTAL STATE ( 1 FDA reports)
POTENTIATING DRUG INTERACTION ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PRODUCT SOLUBILITY ABNORMAL ( 1 FDA reports)
PROLONGED PREGNANCY ( 1 FDA reports)
PROSTATITIS ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 1 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 1 FDA reports)
PRURIGO ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 1 FDA reports)
PULMONARY ARTERY STENOSIS ( 1 FDA reports)
PULMONARY ARTERY STENOSIS CONGENITAL ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PYONEPHROSIS ( 1 FDA reports)
QUALITY OF LIFE DECREASED ( 1 FDA reports)
RALES ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
RECTAL PROLAPSE ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL NEOPLASM ( 1 FDA reports)
RENAL TUBULAR DISORDER ( 1 FDA reports)
RENAL VESSEL DISORDER ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RETINAL DETACHMENT ( 1 FDA reports)
ROTATOR CUFF REPAIR ( 1 FDA reports)
ROTATOR CUFF SYNDROME ( 1 FDA reports)
SCAN ABNORMAL ( 1 FDA reports)
SCIATICA ( 1 FDA reports)
SCREAMING ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SENSATION OF PRESSURE ( 1 FDA reports)
SENSORIMOTOR DISORDER ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SJOGREN'S SYNDROME ( 1 FDA reports)
SKIN WARM ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPINAL MYELOGRAM ABNORMAL ( 1 FDA reports)
STARING ( 1 FDA reports)
STRESS ( 1 FDA reports)
STRESS POLYCYTHAEMIA ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUBILEUS ( 1 FDA reports)
SUPERINFECTION ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TARDIVE DYSKINESIA ( 1 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TONGUE GEOGRAPHIC ( 1 FDA reports)
TONIC CLONIC MOVEMENTS ( 1 FDA reports)
TONIC CONVULSION ( 1 FDA reports)
TOOTH FRACTURE ( 1 FDA reports)
TOOTH LOSS ( 1 FDA reports)
TRISMUS ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
TYPE 1 DIABETES MELLITUS ( 1 FDA reports)
TYPE I HYPERSENSITIVITY ( 1 FDA reports)
TYPE II HYPERSENSITIVITY ( 1 FDA reports)
ULCER ( 1 FDA reports)
UMBILICAL HERNIA ( 1 FDA reports)
URINARY TRACT DISORDER ( 1 FDA reports)
URINARY TRACT OBSTRUCTION ( 1 FDA reports)
URINE ELECTROLYTES INCREASED ( 1 FDA reports)
URINE OSMOLARITY DECREASED ( 1 FDA reports)
URINE SODIUM DECREASED ( 1 FDA reports)
URTICARIA PAPULAR ( 1 FDA reports)
VAGINAL ERYTHEMA ( 1 FDA reports)
VAGINAL HAEMATOMA ( 1 FDA reports)
VARICES OESOPHAGEAL ( 1 FDA reports)
VASCULITIC RASH ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VENOUS THROMBOSIS ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VESTIBULAR NEURONITIS ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VULVITIS ( 1 FDA reports)
VULVOVAGINAL DISCOMFORT ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
WHITE BLOOD CELLS URINE ( 1 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)
TENDON DISORDER ( 101 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 99 FDA reports)
MYOPATHY ( 98 FDA reports)
INJECTION SITE RASH ( 90 FDA reports)
DRUG INTERACTION ( 56 FDA reports)
PYREXIA ( 45 FDA reports)
CONFUSIONAL STATE ( 40 FDA reports)
BURSITIS ( 33 FDA reports)
DIARRHOEA ( 33 FDA reports)
RENAL FAILURE ACUTE ( 33 FDA reports)
VOMITING ( 32 FDA reports)
ARTHRITIS ( 31 FDA reports)
ASTHENIA ( 31 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 31 FDA reports)
CYTOLYTIC HEPATITIS ( 30 FDA reports)
DYSPNOEA ( 30 FDA reports)
URINARY TRACT INFECTION ( 30 FDA reports)
ANAEMIA ( 29 FDA reports)
ARTHRALGIA ( 29 FDA reports)
JAUNDICE ( 29 FDA reports)
NAUSEA ( 29 FDA reports)
CHOLESTASIS ( 28 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 28 FDA reports)
ABDOMINAL PAIN ( 26 FDA reports)
HYPONATRAEMIA ( 26 FDA reports)
MYALGIA ( 25 FDA reports)
PRURITUS ( 25 FDA reports)
TENDONITIS ( 24 FDA reports)
THROMBOCYTOPENIA ( 24 FDA reports)
DRUG ERUPTION ( 23 FDA reports)
FALL ( 23 FDA reports)
PANCREATITIS ACUTE ( 23 FDA reports)
PYELONEPHRITIS ( 23 FDA reports)
RENAL FAILURE ( 23 FDA reports)
NEUTROPENIA ( 21 FDA reports)
OEDEMA PERIPHERAL ( 21 FDA reports)
MALAISE ( 20 FDA reports)
OVERDOSE ( 20 FDA reports)
RASH MACULO-PAPULAR ( 20 FDA reports)
AGRANULOCYTOSIS ( 19 FDA reports)
TOXIC SKIN ERUPTION ( 19 FDA reports)
ANOREXIA ( 18 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 18 FDA reports)
RHABDOMYOLYSIS ( 18 FDA reports)
DEHYDRATION ( 17 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 17 FDA reports)
RASH ( 17 FDA reports)
SOMNOLENCE ( 17 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 16 FDA reports)
BLOOD BILIRUBIN INCREASED ( 16 FDA reports)
DEATH ( 16 FDA reports)
DERMATITIS BULLOUS ( 16 FDA reports)
ESCHERICHIA INFECTION ( 16 FDA reports)
PAIN ( 16 FDA reports)
PANCYTOPENIA ( 16 FDA reports)
ABNORMAL BEHAVIOUR ( 15 FDA reports)
BACTERIAL PYELONEPHRITIS ( 15 FDA reports)
HAEMATOMA ( 15 FDA reports)
BLOOD CREATININE INCREASED ( 14 FDA reports)
ERYTHEMA ( 14 FDA reports)
PURPURA ( 14 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 13 FDA reports)
CONDITION AGGRAVATED ( 13 FDA reports)
CONSTIPATION ( 13 FDA reports)
FATIGUE ( 13 FDA reports)
HYPOKALAEMIA ( 13 FDA reports)
TACHYCARDIA ( 13 FDA reports)
CEREBROVASCULAR ACCIDENT ( 12 FDA reports)
DEPRESSION ( 12 FDA reports)
EPILEPSY ( 12 FDA reports)
EPISTAXIS ( 12 FDA reports)
PLATELET COUNT DECREASED ( 12 FDA reports)
STEVENS-JOHNSON SYNDROME ( 12 FDA reports)
TREMOR ( 12 FDA reports)
ANGIOEDEMA ( 11 FDA reports)
ANXIETY ( 11 FDA reports)
HEADACHE ( 11 FDA reports)
ODYNOPHAGIA ( 11 FDA reports)
PAIN IN EXTREMITY ( 11 FDA reports)
URTICARIA ( 11 FDA reports)
VASCULAR PURPURA ( 11 FDA reports)
ASCITES ( 10 FDA reports)
BLOOD PRESSURE DECREASED ( 10 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 10 FDA reports)
DIZZINESS ( 10 FDA reports)
EOSINOPHILIA ( 10 FDA reports)
GINGIVAL BLEEDING ( 10 FDA reports)
HAEMATURIA ( 10 FDA reports)
HYPERKALAEMIA ( 10 FDA reports)
HYPERTONIA ( 10 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 10 FDA reports)
LEUKOPENIA ( 10 FDA reports)
MUSCULAR WEAKNESS ( 10 FDA reports)
PARAESTHESIA ( 10 FDA reports)
SUBDURAL HAEMATOMA ( 10 FDA reports)
VISUAL IMPAIRMENT ( 10 FDA reports)
ABORTION INDUCED ( 9 FDA reports)
AGGRESSION ( 9 FDA reports)
BRADYCARDIA ( 9 FDA reports)
CHEST PAIN ( 9 FDA reports)
DECREASED APPETITE ( 9 FDA reports)
FACE OEDEMA ( 9 FDA reports)
HAEMOGLOBIN DECREASED ( 9 FDA reports)
HAEMOLYTIC ANAEMIA ( 9 FDA reports)
HEPATIC FAILURE ( 9 FDA reports)
HYPERSENSITIVITY ( 9 FDA reports)
LACTIC ACIDOSIS ( 9 FDA reports)
LOSS OF CONSCIOUSNESS ( 9 FDA reports)
NECK PAIN ( 9 FDA reports)
OFF LABEL USE ( 9 FDA reports)
PEMPHIGOID ( 9 FDA reports)
PNEUMONIA ( 9 FDA reports)
ABDOMINAL PAIN UPPER ( 8 FDA reports)
DRUG TOXICITY ( 8 FDA reports)
EYELID OEDEMA ( 8 FDA reports)
GASTROENTERITIS ( 8 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 8 FDA reports)
HEPATOCELLULAR DAMAGE ( 8 FDA reports)
HEPATOCELLULAR INJURY ( 8 FDA reports)
HYPERTHERMIA ( 8 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 8 FDA reports)
MOTOR DYSFUNCTION ( 8 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 8 FDA reports)
PULMONARY EMBOLISM ( 8 FDA reports)
RESPIRATORY FAILURE ( 8 FDA reports)
SKIN DISORDER ( 8 FDA reports)
SKIN EXFOLIATION ( 8 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 8 FDA reports)
WEIGHT DECREASED ( 8 FDA reports)
ASTERIXIS ( 7 FDA reports)
ATRIAL FIBRILLATION ( 7 FDA reports)
DEEP VEIN THROMBOSIS ( 7 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 7 FDA reports)
DRUG INEFFECTIVE ( 7 FDA reports)
HALLUCINATION ( 7 FDA reports)
HEPATIC ENCEPHALOPATHY ( 7 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 7 FDA reports)
HYPERHIDROSIS ( 7 FDA reports)
HYPOXIA ( 7 FDA reports)
INTERSTITIAL LUNG DISEASE ( 7 FDA reports)
MOUTH ULCERATION ( 7 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 7 FDA reports)
MYOCARDIAL INFARCTION ( 7 FDA reports)
NERVOUS SYSTEM DISORDER ( 7 FDA reports)
PALLOR ( 7 FDA reports)
RASH ERYTHEMATOUS ( 7 FDA reports)
RENAL IMPAIRMENT ( 7 FDA reports)
SYNCOPE ( 7 FDA reports)
TRANSAMINASES INCREASED ( 7 FDA reports)
ABDOMINAL DISTENSION ( 6 FDA reports)
ACUTE PULMONARY OEDEMA ( 6 FDA reports)
AFFECTIVE DISORDER ( 6 FDA reports)
AGITATION ( 6 FDA reports)
BACK PAIN ( 6 FDA reports)
BLOOD AMYLASE INCREASED ( 6 FDA reports)
CEREBRAL ATROPHY ( 6 FDA reports)
CHROMATURIA ( 6 FDA reports)
COGWHEEL RIGIDITY ( 6 FDA reports)
COMA ( 6 FDA reports)
CONVULSION ( 6 FDA reports)
DIABETES MELLITUS ( 6 FDA reports)
DISORIENTATION ( 6 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 6 FDA reports)
DYSPHAGIA ( 6 FDA reports)
ENCEPHALOPATHY ( 6 FDA reports)
FOETOR HEPATICUS ( 6 FDA reports)
HAEMORRHAGE ( 6 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 6 FDA reports)
HEPATITIS FULMINANT ( 6 FDA reports)
HYPERAESTHESIA ( 6 FDA reports)
HYPOTENSION ( 6 FDA reports)
LYMPHADENOPATHY ( 6 FDA reports)
MELAENA ( 6 FDA reports)
MYOCLONUS ( 6 FDA reports)
PORTAL VEIN THROMBOSIS ( 6 FDA reports)
RASH MORBILLIFORM ( 6 FDA reports)
RECTAL HAEMORRHAGE ( 6 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 6 FDA reports)
SEPTIC SHOCK ( 6 FDA reports)
URINARY RETENTION ( 6 FDA reports)
VIRAL LOAD INCREASED ( 6 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 6 FDA reports)
ADVERSE EVENT ( 5 FDA reports)
ATELECTASIS ( 5 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 5 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 5 FDA reports)
BONE PAIN ( 5 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 5 FDA reports)
COLITIS ( 5 FDA reports)
COUGH ( 5 FDA reports)
CUTANEOUS VASCULITIS ( 5 FDA reports)
CYSTITIS ( 5 FDA reports)
DISTURBANCE IN ATTENTION ( 5 FDA reports)
DIVERTICULUM INTESTINAL ( 5 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 5 FDA reports)
HEPATIC STEATOSIS ( 5 FDA reports)
HEPATITIS ACUTE ( 5 FDA reports)
HYPERTENSION ( 5 FDA reports)
HYPOAESTHESIA ( 5 FDA reports)
IMPAIRED SELF-CARE ( 5 FDA reports)
INJURY ( 5 FDA reports)
INSOMNIA ( 5 FDA reports)
LIPASE INCREASED ( 5 FDA reports)
LIVER DISORDER ( 5 FDA reports)
MOUTH HAEMORRHAGE ( 5 FDA reports)
MUSCLE SPASMS ( 5 FDA reports)
OEDEMA ( 5 FDA reports)
PARALYSIS ( 5 FDA reports)
PETIT MAL EPILEPSY ( 5 FDA reports)
PHLEBITIS ( 5 FDA reports)
PLEURAL EFFUSION ( 5 FDA reports)
RASH GENERALISED ( 5 FDA reports)
STAPHYLOCOCCAL INFECTION ( 5 FDA reports)
STREPTOCOCCAL SEPSIS ( 5 FDA reports)
TENDON RUPTURE ( 5 FDA reports)
THROMBOSIS ( 5 FDA reports)
UPPER LIMB FRACTURE ( 5 FDA reports)
VERTIGO ( 5 FDA reports)
ACTINOMYCOSIS ( 4 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 4 FDA reports)
ANAEMIA MACROCYTIC ( 4 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 4 FDA reports)
BACTERIAL TEST POSITIVE ( 4 FDA reports)
BILE DUCT OBSTRUCTION ( 4 FDA reports)
BIOPSY BONE ABNORMAL ( 4 FDA reports)
BLOOD URINE PRESENT ( 4 FDA reports)
BONE DISORDER ( 4 FDA reports)
BUNION ( 4 FDA reports)
CARDIAC ARREST ( 4 FDA reports)
CARDIOGENIC SHOCK ( 4 FDA reports)
CELL DEATH ( 4 FDA reports)
CHILLS ( 4 FDA reports)
CHOLELITHIASIS ( 4 FDA reports)
CLOSTRIDIUM COLITIS ( 4 FDA reports)
DIALYSIS ( 4 FDA reports)
DISEASE PROGRESSION ( 4 FDA reports)
DRUG HYPERSENSITIVITY ( 4 FDA reports)
DYSGEUSIA ( 4 FDA reports)
DYSKINESIA ( 4 FDA reports)
DYSPAREUNIA ( 4 FDA reports)
DYSURIA ( 4 FDA reports)
EOSINOPHIL COUNT INCREASED ( 4 FDA reports)
EOSINOPHILIC PNEUMONIA ( 4 FDA reports)
FOOT DEFORMITY ( 4 FDA reports)
GALLBLADDER DISORDER ( 4 FDA reports)
HEART DISEASE CONGENITAL ( 4 FDA reports)
HEPATIC CYST ( 4 FDA reports)
HIATUS HERNIA ( 4 FDA reports)
HYPERCALCAEMIA ( 4 FDA reports)
HYPOKINESIA ( 4 FDA reports)
HYPOVOLAEMIC SHOCK ( 4 FDA reports)
IMPAIRED HEALING ( 4 FDA reports)
INTENTIONAL OVERDOSE ( 4 FDA reports)
LACRIMATION INCREASED ( 4 FDA reports)
LEUKOCYTOSIS ( 4 FDA reports)
LIMB MALFORMATION ( 4 FDA reports)
LIPOMA ( 4 FDA reports)
MASS ( 4 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 4 FDA reports)
MEMORY IMPAIRMENT ( 4 FDA reports)
MENISCUS LESION ( 4 FDA reports)
METABOLIC ACIDOSIS ( 4 FDA reports)
MICTURITION URGENCY ( 4 FDA reports)
MIGRAINE ( 4 FDA reports)
MUCOUS MEMBRANE DISORDER ( 4 FDA reports)
MULTI-ORGAN FAILURE ( 4 FDA reports)
MULTIPLE MYELOMA ( 4 FDA reports)
MUSCLE FATIGUE ( 4 FDA reports)
MUSCLE INJURY ( 4 FDA reports)
NEURITIS ( 4 FDA reports)
OESOPHAGEAL DISORDER ( 4 FDA reports)
ONYCHOMYCOSIS ( 4 FDA reports)
OSTEONECROSIS OF JAW ( 4 FDA reports)
OSTEOPENIA ( 4 FDA reports)
PEPTIC ULCER ( 4 FDA reports)
PHOTOSENSITIVITY REACTION ( 4 FDA reports)
PRESCRIBED OVERDOSE ( 4 FDA reports)
RENAL TUBULAR NECROSIS ( 4 FDA reports)
SKIN DISCOLOURATION ( 4 FDA reports)
SKIN LESION ( 4 FDA reports)
SKIN TEST NEGATIVE ( 4 FDA reports)
SPINAL OSTEOARTHRITIS ( 4 FDA reports)
STATUS EPILEPTICUS ( 4 FDA reports)
SUICIDE ATTEMPT ( 4 FDA reports)
TENDON PAIN ( 4 FDA reports)
THROMBOCYTHAEMIA ( 4 FDA reports)
TONGUE EXFOLIATION ( 4 FDA reports)
URINARY INCONTINENCE ( 4 FDA reports)
UROSEPSIS ( 4 FDA reports)
VULVOVAGINAL DRYNESS ( 4 FDA reports)
ABASIA ( 3 FDA reports)
ACUTE CORONARY SYNDROME ( 3 FDA reports)
AGEUSIA ( 3 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 3 FDA reports)
ANAPHYLACTIC REACTION ( 3 FDA reports)
ANAPHYLACTIC SHOCK ( 3 FDA reports)
ARRHYTHMIA ( 3 FDA reports)
BLOOD GLUCOSE INCREASED ( 3 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 3 FDA reports)
BLOOD SODIUM DECREASED ( 3 FDA reports)
BONE MARROW FAILURE ( 3 FDA reports)
CANDIDIASIS ( 3 FDA reports)
CAPILLARY DISORDER ( 3 FDA reports)
CARDIAC MURMUR ( 3 FDA reports)
CIRCULATORY COLLAPSE ( 3 FDA reports)
CONJUNCTIVITIS ( 3 FDA reports)
DISEASE RECURRENCE ( 3 FDA reports)
ECZEMA ( 3 FDA reports)
ENTHESOPATHY ( 3 FDA reports)
ERYTHEMA NODOSUM ( 3 FDA reports)
FEAR ( 3 FDA reports)
FEELING ABNORMAL ( 3 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 3 FDA reports)
HAEMODYNAMIC INSTABILITY ( 3 FDA reports)
HAEMORRHOIDS ( 3 FDA reports)
HALLUCINATION, VISUAL ( 3 FDA reports)
HELICOBACTER GASTRITIS ( 3 FDA reports)
HEMIPLEGIA ( 3 FDA reports)
HEPATIC TRAUMA ( 3 FDA reports)
HYPOTONIA ( 3 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 3 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 3 FDA reports)
INFECTION ( 3 FDA reports)
INFUSION SITE RASH ( 3 FDA reports)
INTRA-UTERINE DEATH ( 3 FDA reports)
JOINT SWELLING ( 3 FDA reports)
LETHARGY ( 3 FDA reports)
LUNG INFECTION ( 3 FDA reports)
MACROCYTOSIS ( 3 FDA reports)
MALABSORPTION ( 3 FDA reports)
MENINGORRHAGIA ( 3 FDA reports)
MUCOSAL INFLAMMATION ( 3 FDA reports)
MUSCLE RIGIDITY ( 3 FDA reports)
MUSCULOSKELETAL PAIN ( 3 FDA reports)
MYDRIASIS ( 3 FDA reports)
MYOCARDIAL ISCHAEMIA ( 3 FDA reports)
NEPHRITIS INTERSTITIAL ( 3 FDA reports)
NEUROPATHY PERIPHERAL ( 3 FDA reports)
PELVIC PAIN ( 3 FDA reports)
PEMPHIGUS ( 3 FDA reports)
PERIARTHRITIS ( 3 FDA reports)
PETECHIAE ( 3 FDA reports)
POLYMYALGIA RHEUMATICA ( 3 FDA reports)
PROTEINURIA ( 3 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 3 FDA reports)
RASH MACULAR ( 3 FDA reports)
RASH PRURITIC ( 3 FDA reports)
RESTLESSNESS ( 3 FDA reports)
SEROTONIN SYNDROME ( 3 FDA reports)
SHOCK HAEMORRHAGIC ( 3 FDA reports)
SHOULDER PAIN ( 3 FDA reports)
SPINA BIFIDA ( 3 FDA reports)
STUPOR ( 3 FDA reports)
SUICIDAL IDEATION ( 3 FDA reports)
THROMBOCYTOPENIC PURPURA ( 3 FDA reports)
URINE ABNORMALITY ( 3 FDA reports)
VISION BLURRED ( 3 FDA reports)
VISUAL ACUITY REDUCED ( 3 FDA reports)
VITAMIN B12 DEFICIENCY ( 3 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 3 FDA reports)
ABORTION MISSED ( 2 FDA reports)
ABORTION SPONTANEOUS ( 2 FDA reports)
ACUTE ABDOMEN ( 2 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 2 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 2 FDA reports)
AMMONIA INCREASED ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
ANGIONEUROTIC OEDEMA ( 2 FDA reports)
ANGIOPATHY ( 2 FDA reports)
ANISOCYTOSIS ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
APHASIA ( 2 FDA reports)
APHTHOUS STOMATITIS ( 2 FDA reports)
ARTERIOPATHIC DISEASE ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 2 FDA reports)
ATRIAL FLUTTER ( 2 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 2 FDA reports)
AUTOMATISM ( 2 FDA reports)
BACILLUS INFECTION ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
BLADDER DYSFUNCTION ( 2 FDA reports)
BLOOD CHLORIDE DECREASED ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
BONE DEBRIDEMENT ( 2 FDA reports)
BONE DENSITY ABNORMAL ( 2 FDA reports)
BONE MARROW DEPRESSION ( 2 FDA reports)
BONE MARROW TOXICITY ( 2 FDA reports)
BRADYPNOEA ( 2 FDA reports)
BRAIN MALFORMATION ( 2 FDA reports)
BRONCHOSPASM ( 2 FDA reports)
CAESAREAN SECTION ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 2 FDA reports)
CEREBRAL ISCHAEMIA ( 2 FDA reports)
CERVICAL SPINAL STENOSIS ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
CHOLESTATIC LIVER INJURY ( 2 FDA reports)
CHONDROPATHY ( 2 FDA reports)
CHROMOSOME ABNORMALITY ( 2 FDA reports)
CIRRHOSIS ALCOHOLIC ( 2 FDA reports)
CITROBACTER INFECTION ( 2 FDA reports)
CLEFT PALATE ( 2 FDA reports)
CLOSTRIDIAL INFECTION ( 2 FDA reports)
COAGULATION FACTOR X LEVEL INCREASED ( 2 FDA reports)
COLONIC OBSTRUCTION ( 2 FDA reports)
COLONIC POLYP ( 2 FDA reports)
COMPLETED SUICIDE ( 2 FDA reports)
CORONARY ARTERY STENOSIS ( 2 FDA reports)
CORONARY ARTERY THROMBOSIS ( 2 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 2 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 2 FDA reports)
DEAFNESS UNILATERAL ( 2 FDA reports)
DELUSION ( 2 FDA reports)
DERMATITIS EXFOLIATIVE ( 2 FDA reports)
DISCOMFORT ( 2 FDA reports)
DISSOCIATION ( 2 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 2 FDA reports)
DRY SKIN ( 2 FDA reports)
DYSMORPHISM ( 2 FDA reports)
DYSPHONIA ( 2 FDA reports)
DYSTONIA ( 2 FDA reports)
ECCHYMOSIS ( 2 FDA reports)
ECHOLALIA ( 2 FDA reports)
ECONOMIC PROBLEM ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
EMOTIONAL DISORDER ( 2 FDA reports)
EMOTIONAL DISTRESS ( 2 FDA reports)
EPIGASTRIC DISCOMFORT ( 2 FDA reports)
ERYTHROSIS ( 2 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 2 FDA reports)
FACIAL DYSMORPHISM ( 2 FDA reports)
FAECAL VOMITING ( 2 FDA reports)
FAECALOMA ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 2 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 2 FDA reports)
GOITRE ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HAEMORRHAGIC ANAEMIA ( 2 FDA reports)
HEAD INJURY ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
HEPATIC ATROPHY ( 2 FDA reports)
HEPATITIS CHOLESTATIC ( 2 FDA reports)
HEPATOMEGALY ( 2 FDA reports)
HEPATOTOXICITY ( 2 FDA reports)
HYPERAMMONAEMIA ( 2 FDA reports)
HYPERLIPIDAEMIA ( 2 FDA reports)
HYPERREFLEXIA ( 2 FDA reports)
HYPERTENSIVE CRISIS ( 2 FDA reports)
HYPOALBUMINAEMIA ( 2 FDA reports)
HYPOCHLORAEMIA ( 2 FDA reports)
HYPOCHROMASIA ( 2 FDA reports)
HYPOVOLAEMIA ( 2 FDA reports)
IIIRD NERVE PARALYSIS ( 2 FDA reports)
INFARCTION ( 2 FDA reports)
INFLAMMATION ( 2 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 2 FDA reports)
INTESTINAL ISCHAEMIA ( 2 FDA reports)
JAUNDICE NEONATAL ( 2 FDA reports)
JOINT EFFUSION ( 2 FDA reports)
LACUNAR INFARCTION ( 2 FDA reports)
LIP HAEMORRHAGE ( 2 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
LYME DISEASE ( 2 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 2 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 2 FDA reports)
METABOLIC ENCEPHALOPATHY ( 2 FDA reports)
MICROANGIOPATHY ( 2 FDA reports)
MIOSIS ( 2 FDA reports)
MOBILITY DECREASED ( 2 FDA reports)
MULTI-ORGAN DISORDER ( 2 FDA reports)
MUSCLE ATROPHY ( 2 FDA reports)
MUSCLE NECROSIS ( 2 FDA reports)
MUSCLE RUPTURE ( 2 FDA reports)
MUTISM ( 2 FDA reports)
MYOSITIS ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
NEUROLOGICAL SYMPTOM ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
OESOPHAGEAL PAIN ( 2 FDA reports)
ORAL CANDIDIASIS ( 2 FDA reports)
ORAL MUCOSAL ERUPTION ( 2 FDA reports)
ORGAN FAILURE ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PANIC DISORDER ( 2 FDA reports)
PCO2 DECREASED ( 2 FDA reports)
PERITONITIS BACTERIAL ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 2 FDA reports)
PROSTATE CANCER ( 2 FDA reports)
PSYCHOMOTOR RETARDATION ( 2 FDA reports)
PYELONEPHRITIS ACUTE ( 2 FDA reports)
RASH PAPULAR ( 2 FDA reports)
RASH SCARLATINIFORM ( 2 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 2 FDA reports)
RESPIRATORY TRACT CONGESTION ( 2 FDA reports)
RETCHING ( 2 FDA reports)
RHEUMATOID ARTHRITIS ( 2 FDA reports)
ROAD TRAFFIC ACCIDENT ( 2 FDA reports)
SALMONELLA SEPSIS ( 2 FDA reports)
SALMONELLOSIS ( 2 FDA reports)
SARCOIDOSIS ( 2 FDA reports)
SEPTIC ARTHRITIS STAPHYLOCOCCAL ( 2 FDA reports)
SEPTIC ENCEPHALOPATHY ( 2 FDA reports)
SERUM SICKNESS ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
SKIN NECROSIS ( 2 FDA reports)
SKIN REACTION ( 2 FDA reports)
SLEEP-RELATED EATING DISORDER ( 2 FDA reports)
STAPHYLOCOCCAL OSTEOMYELITIS ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 2 FDA reports)
THINKING ABNORMAL ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 2 FDA reports)
ULNA FRACTURE ( 2 FDA reports)
VASCULAR DEMENTIA ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ACUTE PSYCHOSIS ( 1 FDA reports)
ALCOHOL INTERACTION ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
AMNIOTIC BAND SYNDROME ( 1 FDA reports)
ANAESTHETIC COMPLICATION ( 1 FDA reports)
ANHEDONIA ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
ANURIA ( 1 FDA reports)
AORTIC VALVE STENOSIS ( 1 FDA reports)
APATHY ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ARTERIOSPASM CORONARY ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
ATRIAL SEPTAL DEFECT ( 1 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 1 FDA reports)
AURA ( 1 FDA reports)
BACTERIURIA ( 1 FDA reports)
BASAL CELL CARCINOMA ( 1 FDA reports)
BICYTOPENIA ( 1 FDA reports)
BILIARY CIRRHOSIS ( 1 FDA reports)
BILIARY CYST ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD OSMOLARITY DECREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BONE DEVELOPMENT ABNORMAL ( 1 FDA reports)
BONE MARROW DISORDER ( 1 FDA reports)
BRAIN DAMAGE ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BREAST DISORDER ( 1 FDA reports)
BRONCHIAL OBSTRUCTION ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
CANDIDURIA ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CAUDA EQUINA SYNDROME ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM ABSCESS ( 1 FDA reports)
CEREBRAL HAEMATOMA ( 1 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 1 FDA reports)
CERVICOBRACHIAL SYNDROME ( 1 FDA reports)
CHEILITIS ( 1 FDA reports)
CHOLANGITIS ( 1 FDA reports)
CHOLANGITIS SCLEROSING ( 1 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COLON ADENOMA ( 1 FDA reports)
COMA HEPATIC ( 1 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
CYSTITIS NONINFECTIVE ( 1 FDA reports)
CYSTOPEXY ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DEJA VU ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DENTAL CARIES ( 1 FDA reports)
DEPERSONALISATION ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DIABETIC KETOACIDOTIC HYPERGLYCAEMIC COMA ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISABILITY ( 1 FDA reports)
DISSEMINATED TUBERCULOSIS ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 1 FDA reports)
DYSPNOEA EXACERBATED ( 1 FDA reports)
EATING DISORDER SYMPTOM ( 1 FDA reports)
ECZEMA INFECTED ( 1 FDA reports)
EFFUSION ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 1 FDA reports)
EPICONDYLITIS ( 1 FDA reports)
EPIDERMOLYSIS ( 1 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EYELID PTOSIS ( 1 FDA reports)
FEBRILE BONE MARROW APLASIA ( 1 FDA reports)
FEBRILE INFECTION ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FLIGHT OF IDEAS ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FOAMING AT MOUTH ( 1 FDA reports)
FOLATE DEFICIENCY ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
FRACTURE DELAYED UNION ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GESTATIONAL DIABETES ( 1 FDA reports)
GESTATIONAL HYPERTENSION ( 1 FDA reports)
GINGIVAL DISORDER ( 1 FDA reports)
GLYCOSURIA ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
GRANULOCYTE COUNT INCREASED ( 1 FDA reports)
GRUNTING ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT RECURRENT ( 1 FDA reports)
HEPATIC PAIN ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYDROCEPHALUS ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERBILIRUBINAEMIA NEONATAL ( 1 FDA reports)
HYPERPLASIA ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
HYPOPROTHROMBINAEMIA ( 1 FDA reports)
HYPOSPADIAS ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMMUNODEFICIENCY ( 1 FDA reports)
IMPRISONMENT ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INFECTIOUS PERITONITIS ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
IRRITABLE BOWEL SYNDROME ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
KYPHOSIS ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LARYNGEAL DISORDER ( 1 FDA reports)
LAXATIVE ABUSE ( 1 FDA reports)
LIBIDO DECREASED ( 1 FDA reports)
LICHENOID KERATOSIS ( 1 FDA reports)
LIPIDS INCREASED ( 1 FDA reports)
LOOSE STOOLS ( 1 FDA reports)
LOSS OF EMPLOYMENT ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 1 FDA reports)
LYMPHOCYTOSIS ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
METAPLASIA ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
MILIARY PNEUMONIA ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
MULTIPLE INJURIES ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
NEONATAL HEPATOMEGALY ( 1 FDA reports)
NEONATAL RESPIRATORY DEPRESSION ( 1 FDA reports)
NEONATAL TACHYPNOEA ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEUROENDOCRINE TUMOUR ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
NODULE ( 1 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 1 FDA reports)
OCULAR ICTERUS ( 1 FDA reports)
OCULAR TOXICITY ( 1 FDA reports)
ODDI'S SPHINCTER CONSTRICTION ( 1 FDA reports)
OESOPHAGEAL ULCER ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
OPEN WOUND ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PAINFUL RESPIRATION ( 1 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 1 FDA reports)
PALPABLE PURPURA ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PELVIC FRACTURE ( 1 FDA reports)
PEPTOSTREPTOCOCCUS TEST POSITIVE ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PERITONEAL HAEMORRHAGE ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PHYSICAL ASSAULT ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POLYCYTHAEMIA ( 1 FDA reports)
POLYP COLORECTAL ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POSTICTAL STATE ( 1 FDA reports)
POTENTIATING DRUG INTERACTION ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PRODUCT SOLUBILITY ABNORMAL ( 1 FDA reports)
PROLONGED PREGNANCY ( 1 FDA reports)
PROSTATITIS ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 1 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 1 FDA reports)
PRURIGO ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 1 FDA reports)
PULMONARY ARTERY STENOSIS ( 1 FDA reports)
PULMONARY ARTERY STENOSIS CONGENITAL ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PYONEPHROSIS ( 1 FDA reports)
QUALITY OF LIFE DECREASED ( 1 FDA reports)
RALES ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
RECTAL PROLAPSE ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL NEOPLASM ( 1 FDA reports)
RENAL TUBULAR DISORDER ( 1 FDA reports)
RENAL VESSEL DISORDER ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RETINAL DETACHMENT ( 1 FDA reports)
ROTATOR CUFF REPAIR ( 1 FDA reports)
ROTATOR CUFF SYNDROME ( 1 FDA reports)
SCAN ABNORMAL ( 1 FDA reports)
SCIATICA ( 1 FDA reports)
SCREAMING ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SENSATION OF PRESSURE ( 1 FDA reports)
SENSORIMOTOR DISORDER ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SJOGREN'S SYNDROME ( 1 FDA reports)
SKIN WARM ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPINAL MYELOGRAM ABNORMAL ( 1 FDA reports)
STARING ( 1 FDA reports)
STRESS ( 1 FDA reports)
STRESS POLYCYTHAEMIA ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUBILEUS ( 1 FDA reports)
SUPERINFECTION ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TARDIVE DYSKINESIA ( 1 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TONGUE GEOGRAPHIC ( 1 FDA reports)
TONIC CLONIC MOVEMENTS ( 1 FDA reports)
TONIC CONVULSION ( 1 FDA reports)
TOOTH FRACTURE ( 1 FDA reports)
TOOTH LOSS ( 1 FDA reports)
TRISMUS ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
TYPE 1 DIABETES MELLITUS ( 1 FDA reports)
TYPE I HYPERSENSITIVITY ( 1 FDA reports)
TYPE II HYPERSENSITIVITY ( 1 FDA reports)
ULCER ( 1 FDA reports)
UMBILICAL HERNIA ( 1 FDA reports)
URINARY TRACT DISORDER ( 1 FDA reports)
URINARY TRACT OBSTRUCTION ( 1 FDA reports)
URINE ELECTROLYTES INCREASED ( 1 FDA reports)
URINE OSMOLARITY DECREASED ( 1 FDA reports)
URINE SODIUM DECREASED ( 1 FDA reports)
URTICARIA PAPULAR ( 1 FDA reports)
VAGINAL ERYTHEMA ( 1 FDA reports)
VAGINAL HAEMATOMA ( 1 FDA reports)
VARICES OESOPHAGEAL ( 1 FDA reports)
VASCULITIC RASH ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VENOUS THROMBOSIS ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VESTIBULAR NEURONITIS ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VULVITIS ( 1 FDA reports)
VULVOVAGINAL DISCOMFORT ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
WHITE BLOOD CELLS URINE ( 1 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)