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

PAIN ( 34 FDA reports)
HYPERTENSION ( 28 FDA reports)
NAUSEA ( 27 FDA reports)
BACK PAIN ( 26 FDA reports)
PAIN IN EXTREMITY ( 25 FDA reports)
WEIGHT DECREASED ( 25 FDA reports)
ANAEMIA ( 23 FDA reports)
HEADACHE ( 23 FDA reports)
DEPRESSION ( 22 FDA reports)
URINARY TRACT INFECTION ( 22 FDA reports)
BLOOD PRESSURE INCREASED ( 21 FDA reports)
DRUG INEFFECTIVE ( 21 FDA reports)
HYPOAESTHESIA ( 21 FDA reports)
PNEUMONIA ( 21 FDA reports)
BLOOD GLUCOSE INCREASED ( 20 FDA reports)
FALL ( 20 FDA reports)
ARTHRALGIA ( 19 FDA reports)
DYSPNOEA ( 19 FDA reports)
COUGH ( 18 FDA reports)
DIABETES MELLITUS ( 18 FDA reports)
MUSCLE SPASMS ( 18 FDA reports)
SYNCOPE ( 18 FDA reports)
VOMITING ( 18 FDA reports)
WEIGHT INCREASED ( 18 FDA reports)
ASTHENIA ( 17 FDA reports)
NEUROPATHY PERIPHERAL ( 17 FDA reports)
ABDOMINAL PAIN ( 16 FDA reports)
FATIGUE ( 16 FDA reports)
PARAESTHESIA ( 16 FDA reports)
DIARRHOEA ( 15 FDA reports)
DIZZINESS ( 15 FDA reports)
HAEMOGLOBIN DECREASED ( 15 FDA reports)
OSTEONECROSIS OF JAW ( 15 FDA reports)
PALPITATIONS ( 15 FDA reports)
TREMOR ( 15 FDA reports)
CHEST PAIN ( 14 FDA reports)
DEHYDRATION ( 14 FDA reports)
DYSPEPSIA ( 14 FDA reports)
HYPONATRAEMIA ( 14 FDA reports)
INSOMNIA ( 14 FDA reports)
MALAISE ( 14 FDA reports)
ANXIETY ( 13 FDA reports)
BLOOD GLUCOSE DECREASED ( 13 FDA reports)
FEELING ABNORMAL ( 13 FDA reports)
NEOPLASM MALIGNANT ( 13 FDA reports)
OVERDOSE ( 13 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 12 FDA reports)
HYPOTENSION ( 12 FDA reports)
OEDEMA PERIPHERAL ( 12 FDA reports)
SLEEP APNOEA SYNDROME ( 12 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 11 FDA reports)
BLOOD POTASSIUM DECREASED ( 11 FDA reports)
BRONCHITIS ( 11 FDA reports)
CHEST DISCOMFORT ( 11 FDA reports)
CONSTIPATION ( 11 FDA reports)
DEATH ( 11 FDA reports)
DEFORMITY ( 11 FDA reports)
INFECTION ( 11 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 11 FDA reports)
PARTNER STRESS ( 11 FDA reports)
RADICULOPATHY ( 11 FDA reports)
VISION BLURRED ( 11 FDA reports)
ATRIAL FIBRILLATION ( 10 FDA reports)
HAEMATURIA ( 10 FDA reports)
HEART RATE INCREASED ( 10 FDA reports)
HEART RATE IRREGULAR ( 10 FDA reports)
HYPERTENSIVE EMERGENCY ( 10 FDA reports)
ARTHRITIS ( 9 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 9 FDA reports)
DYSURIA ( 9 FDA reports)
ESSENTIAL HYPERTENSION ( 9 FDA reports)
LYMPHOMA ( 9 FDA reports)
MEMORY IMPAIRMENT ( 9 FDA reports)
MYOCARDIAL INFARCTION ( 9 FDA reports)
PANIC ATTACK ( 9 FDA reports)
POLYDIPSIA ( 9 FDA reports)
RENAL FAILURE ( 9 FDA reports)
ABASIA ( 8 FDA reports)
BURNING SENSATION ( 8 FDA reports)
CEREBROVASCULAR ACCIDENT ( 8 FDA reports)
CONDITION AGGRAVATED ( 8 FDA reports)
DECREASED APPETITE ( 8 FDA reports)
HAEMATOCRIT DECREASED ( 8 FDA reports)
HAEMORRHAGE ( 8 FDA reports)
HEPATOMEGALY ( 8 FDA reports)
MUSCULAR WEAKNESS ( 8 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 8 FDA reports)
NEPHROLITHIASIS ( 8 FDA reports)
OSTEOLYSIS ( 8 FDA reports)
PULMONARY EMBOLISM ( 8 FDA reports)
SEPSIS ( 8 FDA reports)
THROMBOCYTOPENIA ( 8 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 8 FDA reports)
ATELECTASIS ( 7 FDA reports)
BALANCE DISORDER ( 7 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 7 FDA reports)
GASTRIC DISORDER ( 7 FDA reports)
GOUT ( 7 FDA reports)
HAEMOPTYSIS ( 7 FDA reports)
HAEMORRHAGE URINARY TRACT ( 7 FDA reports)
HEARING IMPAIRED ( 7 FDA reports)
HODGKIN'S DISEASE STAGE IV ( 7 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 7 FDA reports)
JOINT SWELLING ( 7 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 7 FDA reports)
METASTASES TO LUNG ( 7 FDA reports)
METASTASES TO SPINE ( 7 FDA reports)
MYALGIA ( 7 FDA reports)
NASAL ULCER ( 7 FDA reports)
NERVOUSNESS ( 7 FDA reports)
PANCREATITIS ACUTE ( 7 FDA reports)
POLLAKIURIA ( 7 FDA reports)
PROSTATITIS ( 7 FDA reports)
PROSTATOMEGALY ( 7 FDA reports)
PRURITUS ( 7 FDA reports)
RASH ( 7 FDA reports)
SPLENOMEGALY ( 7 FDA reports)
SWELLING ( 7 FDA reports)
TESTICULAR MASS ( 7 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 7 FDA reports)
URETHRAL STENOSIS ( 7 FDA reports)
ADVERSE EVENT ( 6 FDA reports)
APPARENT DEATH ( 6 FDA reports)
APPENDIX DISORDER ( 6 FDA reports)
BLOOD CREATININE INCREASED ( 6 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 6 FDA reports)
CARDIAC DISORDER ( 6 FDA reports)
DIVERTICULUM INTESTINAL ( 6 FDA reports)
FACIAL PALSY ( 6 FDA reports)
HYPERLIPIDAEMIA ( 6 FDA reports)
HYPERSENSITIVITY ( 6 FDA reports)
HYPOKALAEMIA ( 6 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 6 FDA reports)
MEDICATION RESIDUE ( 6 FDA reports)
METASTASES TO BONE ( 6 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 6 FDA reports)
NEURALGIA ( 6 FDA reports)
PERIODONTAL DISEASE ( 6 FDA reports)
POOR DENTAL CONDITION ( 6 FDA reports)
SACRALISATION ( 6 FDA reports)
SOMNOLENCE ( 6 FDA reports)
ULCER HAEMORRHAGE ( 6 FDA reports)
URETHRITIS ( 6 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
ANGINA PECTORIS ( 5 FDA reports)
BLADDER DISORDER ( 5 FDA reports)
BREAST CANCER ( 5 FDA reports)
CARDIAC FAILURE ( 5 FDA reports)
DIABETIC KETOACIDOSIS ( 5 FDA reports)
DRUG HYPERSENSITIVITY ( 5 FDA reports)
DRUG INTERACTION ( 5 FDA reports)
FEELING HOT ( 5 FDA reports)
GAIT DISTURBANCE ( 5 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 5 FDA reports)
HAEMORRHOIDS ( 5 FDA reports)
INJURY ( 5 FDA reports)
LOSS OF CONSCIOUSNESS ( 5 FDA reports)
MENTAL DISORDER ( 5 FDA reports)
MOBILITY DECREASED ( 5 FDA reports)
OFF LABEL USE ( 5 FDA reports)
OSTEONECROSIS ( 5 FDA reports)
PYREXIA ( 5 FDA reports)
RECTAL HAEMORRHAGE ( 5 FDA reports)
RENAL FAILURE ACUTE ( 5 FDA reports)
SURGERY ( 5 FDA reports)
TACHYCARDIA ( 5 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 5 FDA reports)
TYPE 2 DIABETES MELLITUS ( 5 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 5 FDA reports)
ABDOMINAL DISTENSION ( 4 FDA reports)
ABSCESS ( 4 FDA reports)
ABSCESS ORAL ( 4 FDA reports)
ARTHRODESIS ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
ASTHMA ( 4 FDA reports)
ATRIAL SEPTAL DEFECT ( 4 FDA reports)
BASEDOW'S DISEASE ( 4 FDA reports)
BLINDNESS ( 4 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 4 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 4 FDA reports)
BLOOD UREA INCREASED ( 4 FDA reports)
BODY TINEA ( 4 FDA reports)
BRONCHITIS CHRONIC ( 4 FDA reports)
CARDIO-RESPIRATORY ARREST ( 4 FDA reports)
CATARACT OPERATION ( 4 FDA reports)
CELLULITIS ( 4 FDA reports)
CEREBRAL HAEMORRHAGE ( 4 FDA reports)
CEREBRAL ISCHAEMIA ( 4 FDA reports)
CONGENITAL ANOMALY ( 4 FDA reports)
DRUG ADMINISTRATION ERROR ( 4 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 4 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 4 FDA reports)
DYSARTHRIA ( 4 FDA reports)
DYSLIPIDAEMIA ( 4 FDA reports)
DYSPHAGIA ( 4 FDA reports)
DYSPNOEA EXERTIONAL ( 4 FDA reports)
DYSSTASIA ( 4 FDA reports)
ERECTILE DYSFUNCTION ( 4 FDA reports)
EYE PAIN ( 4 FDA reports)
GASTRITIS EROSIVE ( 4 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 4 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 4 FDA reports)
HAND DEFORMITY ( 4 FDA reports)
HEAD INJURY ( 4 FDA reports)
HERPES SIMPLEX ( 4 FDA reports)
HERPES SIMPLEX OPHTHALMIC ( 4 FDA reports)
HORDEOLUM ( 4 FDA reports)
HYPOGLYCAEMIA ( 4 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 4 FDA reports)
INFLUENZA ( 4 FDA reports)
LETHARGY ( 4 FDA reports)
LIMB MALFORMATION ( 4 FDA reports)
METABOLIC SYNDROME ( 4 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 4 FDA reports)
OBESITY ( 4 FDA reports)
ORTHOPNOEA ( 4 FDA reports)
OTITIS MEDIA ACUTE ( 4 FDA reports)
PARKINSONISM ( 4 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 4 FDA reports)
PHARYNGITIS ( 4 FDA reports)
PLEURISY ( 4 FDA reports)
POLYURIA ( 4 FDA reports)
POST PROCEDURAL COMPLICATION ( 4 FDA reports)
PRESYNCOPE ( 4 FDA reports)
RENAL NEOPLASM ( 4 FDA reports)
SENSORY LOSS ( 4 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 4 FDA reports)
THYROIDITIS ( 4 FDA reports)
TOOTHACHE ( 4 FDA reports)
VENTRICULAR FIBRILLATION ( 4 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 4 FDA reports)
VERTIGO ( 4 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 3 FDA reports)
AMNESIA ( 3 FDA reports)
ANAL SPHINCTER ATONY ( 3 FDA reports)
ANGINA UNSTABLE ( 3 FDA reports)
ANGIOEDEMA ( 3 FDA reports)
ANOREXIA ( 3 FDA reports)
APHAGIA ( 3 FDA reports)
ARRHYTHMIA ( 3 FDA reports)
ARTHRITIS INFECTIVE ( 3 FDA reports)
BLADDER NEOPLASM ( 3 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 3 FDA reports)
BLOOD IRON DECREASED ( 3 FDA reports)
BONE LESION ( 3 FDA reports)
CARDIAC ARREST ( 3 FDA reports)
CATARACT ( 3 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
CONGENITAL HEART VALVE DISORDER ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
CORONARY ARTERY DISEASE ( 3 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 3 FDA reports)
DIABETIC NEPHROPATHY ( 3 FDA reports)
DIZZINESS POSTURAL ( 3 FDA reports)
DRUG DEPENDENCE ( 3 FDA reports)
EATING DISORDER ( 3 FDA reports)
EXPOSED BONE IN JAW ( 3 FDA reports)
FACIAL PARESIS ( 3 FDA reports)
FLUSHING ( 3 FDA reports)
FUNGAL INFECTION ( 3 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 3 FDA reports)
GLYCOSURIA ( 3 FDA reports)
HAEMATEMESIS ( 3 FDA reports)
HEPATITIS ( 3 FDA reports)
HYPERCHLORHYDRIA ( 3 FDA reports)
HYPERTENSIVE CRISIS ( 3 FDA reports)
IMPAIRED WORK ABILITY ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 3 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 3 FDA reports)
LABYRINTHITIS ( 3 FDA reports)
METABOLIC ACIDOSIS ( 3 FDA reports)
MIGRAINE ( 3 FDA reports)
NEUTROPHIL COUNT INCREASED ( 3 FDA reports)
NO ADVERSE EVENT ( 3 FDA reports)
OSTEOARTHRITIS ( 3 FDA reports)
PANCREATITIS ( 3 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 3 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 3 FDA reports)
PLEURAL EFFUSION ( 3 FDA reports)
PROTEINURIA ( 3 FDA reports)
STAPHYLOCOCCAL INFECTION ( 3 FDA reports)
TOBACCO USER ( 3 FDA reports)
TONGUE OEDEMA ( 3 FDA reports)
TORSADE DE POINTES ( 3 FDA reports)
UNEVALUABLE EVENT ( 3 FDA reports)
VISUAL IMPAIRMENT ( 3 FDA reports)
WOUND TREATMENT ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ABNORMAL DREAMS ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
ADMINISTRATION SITE REACTION ( 2 FDA reports)
AGGRESSION ( 2 FDA reports)
AGITATION ( 2 FDA reports)
ANGIOPATHY ( 2 FDA reports)
ANHEDONIA ( 2 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 2 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BLOOD MAGNESIUM DECREASED ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
BONE DISORDER ( 2 FDA reports)
BRAIN NEOPLASM ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CARDIOMEGALY ( 2 FDA reports)
CAROTID ARTERY STENOSIS ( 2 FDA reports)
CEREBROVASCULAR DISORDER ( 2 FDA reports)
CHOKING ( 2 FDA reports)
COLITIS ( 2 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 2 FDA reports)
CYSTITIS ( 2 FDA reports)
DIABETIC NEUROPATHY ( 2 FDA reports)
DIABETIC ULCER ( 2 FDA reports)
DISTURBANCE IN ATTENTION ( 2 FDA reports)
DRUG DOSE OMISSION ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
EMOTIONAL DISTRESS ( 2 FDA reports)
EMPHYSEMA ( 2 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 2 FDA reports)
FEAR ( 2 FDA reports)
GENERALISED ANXIETY DISORDER ( 2 FDA reports)
GINGIVAL EROSION ( 2 FDA reports)
GINGIVITIS ( 2 FDA reports)
HALLUCINATION, AUDITORY ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 2 FDA reports)
HEPATIC STEATOSIS ( 2 FDA reports)
HIP ARTHROPLASTY ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 2 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 2 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 2 FDA reports)
JOINT ANKYLOSIS ( 2 FDA reports)
JOINT DISLOCATION ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
LIMB OPERATION ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
LUPUS-LIKE SYNDROME ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
MITRAL VALVE DISEASE ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
MULTIPLE ALLERGIES ( 2 FDA reports)
MULTIPLE FRACTURES ( 2 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 2 FDA reports)
MUSCLE RIGIDITY ( 2 FDA reports)
MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 2 FDA reports)
NYSTAGMUS ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
PANCREATITIS CHRONIC ( 2 FDA reports)
PARALYSIS ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
POLYARTHRITIS ( 2 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
ROAD TRAFFIC ACCIDENT ( 2 FDA reports)
SENSATION OF HEAVINESS ( 2 FDA reports)
SENSE OF OPPRESSION ( 2 FDA reports)
SEROTONIN SYNDROME ( 2 FDA reports)
SHOCK ( 2 FDA reports)
SKIN DISCOLOURATION ( 2 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 2 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 2 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 2 FDA reports)
SPINAL CORD DISORDER ( 2 FDA reports)
STRESS ( 2 FDA reports)
TACHYPNOEA ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
TYPE 1 DIABETES MELLITUS ( 2 FDA reports)
TYPE V HYPERLIPIDAEMIA ( 2 FDA reports)
URINE FLOW DECREASED ( 2 FDA reports)
UROSEPSIS ( 2 FDA reports)
UTERINE LEIOMYOMA ( 2 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
WRIST FRACTURE ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
ADENOMYOSIS ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 1 FDA reports)
ANAL ABSCESS ( 1 FDA reports)
ANEURYSM ( 1 FDA reports)
ANGER ( 1 FDA reports)
ANKLE FRACTURE ( 1 FDA reports)
ANORECTAL DISORDER ( 1 FDA reports)
ANXIETY DISORDER ( 1 FDA reports)
AORTIC DISSECTION ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APLASIA PURE RED CELL ( 1 FDA reports)
APPETITE DISORDER ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
BACK DISORDER ( 1 FDA reports)
BACK INJURY ( 1 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 1 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 1 FDA reports)
BILE DUCT OBSTRUCTION ( 1 FDA reports)
BILIARY NEOPLASM ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BIPOLAR I DISORDER ( 1 FDA reports)
BLOOD COUNT ABNORMAL ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD KETONE BODY PRESENT ( 1 FDA reports)
BLOOD MAGNESIUM ( 1 FDA reports)
BLOOD OSMOLARITY DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 1 FDA reports)
BLOOD UREA ABNORMAL ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
CANDIDA SEPSIS ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIAC DISCOMFORT ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CARTILAGE INJURY ( 1 FDA reports)
CERVICAL SPINAL STENOSIS ( 1 FDA reports)
CERVIX CANCER METASTATIC ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
CHOLECYSTITIS ACUTE ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CHRONIC HEPATITIS ( 1 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COLON ADENOMA ( 1 FDA reports)
COLONIC POLYP ( 1 FDA reports)
COLORECTAL CANCER ( 1 FDA reports)
COLOSTOMY ( 1 FDA reports)
COLOSTOMY CLOSURE ( 1 FDA reports)
COMA ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 1 FDA reports)
CULTURE STOOL POSITIVE ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DEAFNESS NEUROSENSORY ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DEPENDENCE ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 1 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
EMBOLIC STROKE ( 1 FDA reports)
ENDOMETRIOSIS ( 1 FDA reports)
ENERGY INCREASED ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 1 FDA reports)
EXPIRED DRUG ADMINISTERED ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
FACIAL PAIN ( 1 FDA reports)
FAECALOMA ( 1 FDA reports)
FAECES HARD ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FEELING OF RELAXATION ( 1 FDA reports)
FISTULA ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
GAIT SPASTIC ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 1 FDA reports)
GASTROINTESTINAL OEDEMA ( 1 FDA reports)
GINGIVAL OPERATION ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GRANULOCYTE COUNT DECREASED ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEART DISEASE CONGENITAL ( 1 FDA reports)
HELICOBACTER GASTRITIS ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC CONGESTION ( 1 FDA reports)
HEPATIC ENZYME ABNORMAL ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HERNIA ( 1 FDA reports)
HICCUPS ( 1 FDA reports)
HIP SURGERY ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOGONADISM MALE ( 1 FDA reports)
HYPOTRICHOSIS ( 1 FDA reports)
IMPAIRED SELF-CARE ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCREASED APPETITE ( 1 FDA reports)
INCREASED TENDENCY TO BRUISE ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INJECTION SITE ANAESTHESIA ( 1 FDA reports)
INJECTION SITE BRUISING ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE EXTRAVASATION ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE IRRITATION ( 1 FDA reports)
INJECTION SITE OEDEMA ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INJECTION SITE URTICARIA ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
INTESTINAL HAEMORRHAGE ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
JOINT SPRAIN ( 1 FDA reports)
KNEE OPERATION ( 1 FDA reports)
LARGE INTESTINAL ULCER ( 1 FDA reports)
LEG AMPUTATION ( 1 FDA reports)
LEUKOCYTURIA ( 1 FDA reports)
LIBIDO DECREASED ( 1 FDA reports)
LIGAMENT SPRAIN ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LOWER LIMB FRACTURE ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LUNG TRANSPLANT REJECTION ( 1 FDA reports)
LYMPHOEDEMA ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MENOPAUSAL SYMPTOMS ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
METASTASES TO PERITONEUM ( 1 FDA reports)
METASTASES TO SPLEEN ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MITRAL VALVE CALCIFICATION ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
MORGANELLA INFECTION ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MUSCLE CRAMP ( 1 FDA reports)
MUSCLE INJURY ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
NARCISSISTIC PERSONALITY DISORDER ( 1 FDA reports)
NEOPLASM PROSTATE ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NERVE COMPRESSION ( 1 FDA reports)
NERVE ROOT COMPRESSION ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NIPPLE PAIN ( 1 FDA reports)
NODULE ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
OESOPHAGEAL CARCINOMA ( 1 FDA reports)
OPTIC NERVE INFARCTION ( 1 FDA reports)
ORAL SOFT TISSUE DISORDER ( 1 FDA reports)
OVARIAN CANCER ( 1 FDA reports)
OVARIAN DISORDER ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PAROSMIA ( 1 FDA reports)
PATELLA FRACTURE ( 1 FDA reports)
PEMPHIGOID ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PERIPHERAL EMBOLISM ( 1 FDA reports)
PERSONALITY CHANGE ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PHLEBITIS ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
POLYP ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
PROCTITIS ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROSTATE INFECTION ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
PYODERMA GANGRENOSUM ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RECTAL DISCHARGE ( 1 FDA reports)
RECTAL LESION ( 1 FDA reports)
RECTAL POLYP ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL EMBOLISM ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RENAL INJURY ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RETCHING ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
RHINITIS ALLERGIC ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
SCIATICA ( 1 FDA reports)
SCROTAL SWELLING ( 1 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
SPLENIC EMBOLISM ( 1 FDA reports)
SPUTUM PURULENT ( 1 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 1 FDA reports)
SUDDEN CARDIAC DEATH ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
TENDON RUPTURE ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
THYROID MASS ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TOE OPERATION ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URINARY SEDIMENT PRESENT ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VARICOSE VEIN ( 1 FDA reports)
VENOUS STASIS ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VIITH NERVE PARALYSIS ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VITAMIN B12 DEFICIENCY ( 1 FDA reports)
VITAMIN D DECREASED ( 1 FDA reports)
VITAMIN D DEFICIENCY ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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