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

APPLICATION SITE ERYTHEMA ( 19 FDA reports)
APPLICATION SITE IRRITATION ( 18 FDA reports)
DEPRESSION ( 18 FDA reports)
PAIN ( 18 FDA reports)
APPLICATION SITE PRURITUS ( 17 FDA reports)
FATIGUE ( 16 FDA reports)
PRECOCIOUS PUBERTY ( 16 FDA reports)
ABDOMINAL PAIN ( 15 FDA reports)
ABNORMAL BEHAVIOUR ( 15 FDA reports)
DRUG INEFFECTIVE ( 15 FDA reports)
AGGRESSION ( 14 FDA reports)
ASTHENIA ( 14 FDA reports)
BACK PAIN ( 14 FDA reports)
APPLICATION SITE RASH ( 13 FDA reports)
CONDITION AGGRAVATED ( 13 FDA reports)
PNEUMONIA ( 13 FDA reports)
RENAL FAILURE ACUTE ( 13 FDA reports)
ARTHRALGIA ( 12 FDA reports)
DIARRHOEA ( 12 FDA reports)
ERECTILE DYSFUNCTION ( 12 FDA reports)
HAIR GROWTH ABNORMAL ( 12 FDA reports)
INSOMNIA ( 12 FDA reports)
NAUSEA ( 12 FDA reports)
URINARY TRACT INFECTION ( 12 FDA reports)
ACCIDENTAL EXPOSURE ( 11 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 11 FDA reports)
CONFUSIONAL STATE ( 11 FDA reports)
DYSPNOEA ( 11 FDA reports)
OEDEMA PERIPHERAL ( 11 FDA reports)
ANGER ( 10 FDA reports)
APPLICATION SITE SWELLING ( 10 FDA reports)
DEATH ( 10 FDA reports)
SUICIDAL IDEATION ( 10 FDA reports)
WEIGHT DECREASED ( 10 FDA reports)
AGITATION ( 9 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 9 FDA reports)
DRUG INTERACTION ( 9 FDA reports)
HEPATIC CONGESTION ( 9 FDA reports)
HYPERTENSION ( 9 FDA reports)
LOSS OF CONSCIOUSNESS ( 9 FDA reports)
MUSCULAR WEAKNESS ( 9 FDA reports)
ACNE ( 8 FDA reports)
APPLICATION SITE BURN ( 8 FDA reports)
BONE DEVELOPMENT ABNORMAL ( 8 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 8 FDA reports)
GAIT DISTURBANCE ( 8 FDA reports)
MYOCARDIAL INFARCTION ( 8 FDA reports)
PULMONARY CONGESTION ( 8 FDA reports)
SCREAMING ( 8 FDA reports)
THROMBOCYTOPENIA ( 8 FDA reports)
THYROID DISORDER ( 8 FDA reports)
ANXIETY ( 7 FDA reports)
DIZZINESS ( 7 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 7 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 7 FDA reports)
HAEMOGLOBIN DECREASED ( 7 FDA reports)
HALLUCINATION ( 7 FDA reports)
MALAISE ( 7 FDA reports)
OVERDOSE ( 7 FDA reports)
VOMITING ( 7 FDA reports)
ANAEMIA ( 6 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 6 FDA reports)
CELLULITIS ( 6 FDA reports)
COLON OPERATION ( 6 FDA reports)
CRYING ( 6 FDA reports)
DECREASED APPETITE ( 6 FDA reports)
FLUSHING ( 6 FDA reports)
GASTROINTESTINAL DISORDER ( 6 FDA reports)
GROWTH RETARDATION ( 6 FDA reports)
HYPERSENSITIVITY ( 6 FDA reports)
INFECTION ( 6 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 6 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 6 FDA reports)
PYREXIA ( 6 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 6 FDA reports)
ABDOMINAL DISTENSION ( 5 FDA reports)
ADVERSE DRUG REACTION ( 5 FDA reports)
BALANCE DISORDER ( 5 FDA reports)
CEREBROVASCULAR ACCIDENT ( 5 FDA reports)
CONVULSION ( 5 FDA reports)
DEEP VEIN THROMBOSIS ( 5 FDA reports)
DEHYDRATION ( 5 FDA reports)
EMOTIONAL DISTRESS ( 5 FDA reports)
EPISTAXIS ( 5 FDA reports)
FALL ( 5 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 5 FDA reports)
HAEMATOCRIT DECREASED ( 5 FDA reports)
HEADACHE ( 5 FDA reports)
HYPOXIA ( 5 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 5 FDA reports)
OSTEOARTHRITIS ( 5 FDA reports)
PAIN IN EXTREMITY ( 5 FDA reports)
PARAESTHESIA ( 5 FDA reports)
PLATELET COUNT DECREASED ( 5 FDA reports)
PRODUCT QUALITY ISSUE ( 5 FDA reports)
PULMONARY EMBOLISM ( 5 FDA reports)
RASH ( 5 FDA reports)
RESPIRATORY DISTRESS ( 5 FDA reports)
ROTATOR CUFF SYNDROME ( 5 FDA reports)
SINUSITIS ( 5 FDA reports)
SYNCOPE ( 5 FDA reports)
TACHYCARDIA ( 5 FDA reports)
URTICARIA ( 5 FDA reports)
VISION BLURRED ( 5 FDA reports)
ACROMEGALY ( 4 FDA reports)
ACUTE CORONARY SYNDROME ( 4 FDA reports)
ANGINA UNSTABLE ( 4 FDA reports)
APPLICATION SITE DRYNESS ( 4 FDA reports)
APPLICATION SITE VESICLES ( 4 FDA reports)
BLOOD GLUCOSE INCREASED ( 4 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 4 FDA reports)
BODY HEIGHT INCREASED ( 4 FDA reports)
BURSITIS ( 4 FDA reports)
CAFE AU LAIT SPOTS ( 4 FDA reports)
CHEST WALL PAIN ( 4 FDA reports)
CORONARY ARTERY DISEASE ( 4 FDA reports)
DELUSION ( 4 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 4 FDA reports)
DYSLIPIDAEMIA ( 4 FDA reports)
DYSPEPSIA ( 4 FDA reports)
EAR INFECTION ( 4 FDA reports)
FEAR ( 4 FDA reports)
GASTRIC HAEMORRHAGE ( 4 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 4 FDA reports)
GRANULOMA ( 4 FDA reports)
HAEMORRHAGE ( 4 FDA reports)
HEPATIC ENZYME INCREASED ( 4 FDA reports)
HEPATITIS ACUTE ( 4 FDA reports)
HYDRONEPHROSIS ( 4 FDA reports)
HYPERTRICHOSIS ( 4 FDA reports)
HYPOKALAEMIA ( 4 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 4 FDA reports)
INCREASED APPETITE ( 4 FDA reports)
INTENTIONAL DRUG MISUSE ( 4 FDA reports)
INTERSTITIAL LUNG DISEASE ( 4 FDA reports)
JOINT SWELLING ( 4 FDA reports)
LEUKOPENIA ( 4 FDA reports)
LIVER DISORDER ( 4 FDA reports)
LYMPHOCYTOSIS ( 4 FDA reports)
MENTAL DISORDER ( 4 FDA reports)
NEOPLASM RECURRENCE ( 4 FDA reports)
NEPHROLITHIASIS ( 4 FDA reports)
NEUROPATHY PERIPHERAL ( 4 FDA reports)
PANCREATITIS ( 4 FDA reports)
RENAL DISORDER ( 4 FDA reports)
RENAL FAILURE ( 4 FDA reports)
RENAL IMPAIRMENT ( 4 FDA reports)
RETROPERITONEAL HAEMATOMA ( 4 FDA reports)
SEPSIS ( 4 FDA reports)
SKIN ODOUR ABNORMAL ( 4 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 4 FDA reports)
THIRST ( 4 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 4 FDA reports)
TRANSAMINASES INCREASED ( 4 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 4 FDA reports)
ULCER ( 4 FDA reports)
UROSEPSIS ( 4 FDA reports)
VISUAL DISTURBANCE ( 4 FDA reports)
WHEEZING ( 4 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 4 FDA reports)
ADENOMA BENIGN ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
APPLICATION SITE REACTION ( 3 FDA reports)
ASTHMA ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 3 FDA reports)
BONE PAIN ( 3 FDA reports)
BRADYCARDIA ( 3 FDA reports)
CARDIOVASCULAR DISORDER ( 3 FDA reports)
CARPAL TUNNEL SYNDROME ( 3 FDA reports)
CHEST DISCOMFORT ( 3 FDA reports)
CHOLECYSTITIS CHRONIC ( 3 FDA reports)
COLONIC POLYP ( 3 FDA reports)
CONJUNCTIVITIS ( 3 FDA reports)
CONSTIPATION ( 3 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 3 FDA reports)
DERMATITIS CONTACT ( 3 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 3 FDA reports)
DIALYSIS ( 3 FDA reports)
DRUG ABUSE ( 3 FDA reports)
DRUG ADMINISTRATION ERROR ( 3 FDA reports)
ENDOMETRIAL CANCER STAGE I ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
EYE PAIN ( 3 FDA reports)
HYPOCALCAEMIA ( 3 FDA reports)
HYPOGLYCAEMIA ( 3 FDA reports)
HYPOMAGNESAEMIA ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
INCORRECT DOSE ADMINISTERED ( 3 FDA reports)
INJURY ( 3 FDA reports)
IRON DEFICIENCY ANAEMIA ( 3 FDA reports)
JAUNDICE CHOLESTATIC ( 3 FDA reports)
JOINT EFFUSION ( 3 FDA reports)
KIDNEY INFECTION ( 3 FDA reports)
LOBAR PNEUMONIA ( 3 FDA reports)
LUNG CANCER METASTATIC ( 3 FDA reports)
MENISCUS LESION ( 3 FDA reports)
MITRAL VALVE INCOMPETENCE ( 3 FDA reports)
MOBILITY DECREASED ( 3 FDA reports)
MUSCLE RUPTURE ( 3 FDA reports)
MUSCULOSKELETAL PAIN ( 3 FDA reports)
NASAL CONGESTION ( 3 FDA reports)
NEUTROPENIA ( 3 FDA reports)
OBESITY ( 3 FDA reports)
OSTEONECROSIS ( 3 FDA reports)
PANCYTOPENIA ( 3 FDA reports)
PITUITARY TUMOUR BENIGN ( 3 FDA reports)
PLEURAL FIBROSIS ( 3 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 3 FDA reports)
PROSTATE CANCER ( 3 FDA reports)
PROTHROMBIN TIME PROLONGED ( 3 FDA reports)
PULMONARY HYPERTENSION ( 3 FDA reports)
RETINAL DISORDER ( 3 FDA reports)
RHEUMATOID ARTHRITIS ( 3 FDA reports)
ROAD TRAFFIC ACCIDENT ( 3 FDA reports)
SELF-INJURIOUS IDEATION ( 3 FDA reports)
SHOCK ( 3 FDA reports)
SLEEP APNOEA SYNDROME ( 3 FDA reports)
TENDON PAIN ( 3 FDA reports)
TENDON RUPTURE ( 3 FDA reports)
TENDONITIS ( 3 FDA reports)
TOOTH ABSCESS ( 3 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 3 FDA reports)
UNEVALUABLE EVENT ( 3 FDA reports)
UNRESPONSIVE TO STIMULI ( 3 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 3 FDA reports)
VERTIGO ( 3 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 2 FDA reports)
ALCOHOLISM ( 2 FDA reports)
ANTISOCIAL BEHAVIOUR ( 2 FDA reports)
APPENDICECTOMY ( 2 FDA reports)
APPLICATION SITE EXFOLIATION ( 2 FDA reports)
APPLICATION SITE INDURATION ( 2 FDA reports)
ARTERIOSCLEROSIS ( 2 FDA reports)
ATAXIA ( 2 FDA reports)
ATELECTASIS ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
BASAL CELL CARCINOMA ( 2 FDA reports)
BLOOD CALCIUM DECREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 2 FDA reports)
BLOOD TESTOSTERONE FREE DECREASED ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 2 FDA reports)
BLOOD URINE PRESENT ( 2 FDA reports)
BODY HEIGHT DECREASED ( 2 FDA reports)
BONE MARROW DISORDER ( 2 FDA reports)
BONE NEOPLASM ( 2 FDA reports)
BRONCHIOLITIS ( 2 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CARDIAC ENZYMES INCREASED ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CARDIAC OUTPUT DECREASED ( 2 FDA reports)
CARDIOMEGALY ( 2 FDA reports)
CARDIOMYOPATHY ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CHROMATURIA ( 2 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 2 FDA reports)
CIRCULATORY COLLAPSE ( 2 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 2 FDA reports)
COORDINATION ABNORMAL ( 2 FDA reports)
CUSHINGOID ( 2 FDA reports)
DEMENTIA ( 2 FDA reports)
DENTAL CARIES ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DEPRESSION SUICIDAL ( 2 FDA reports)
DEREALISATION ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DRUG ABUSER ( 2 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 2 FDA reports)
DRUG DISPENSING ERROR ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
DUODENITIS ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
EARLY SATIETY ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 2 FDA reports)
EROSIVE DUODENITIS ( 2 FDA reports)
EXFOLIATIVE RASH ( 2 FDA reports)
FAILURE TO THRIVE ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
FEELING HOT ( 2 FDA reports)
FIBROMYALGIA ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
FLUID RETENTION ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
GINGIVAL BLEEDING ( 2 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
HAEMATOCHEZIA ( 2 FDA reports)
HAEMORRHOIDS ( 2 FDA reports)
HEAD INJURY ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HEPATIC ADENOMA ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HEPATITIS ALCOHOLIC ( 2 FDA reports)
HIP ARTHROPLASTY ( 2 FDA reports)
HIRSUTISM ( 2 FDA reports)
HOT FLUSH ( 2 FDA reports)
HYPERBILIRUBINAEMIA ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
HYPOPHOSPHATAEMIA ( 2 FDA reports)
HYPOTHYROIDISM ( 2 FDA reports)
INCREASED TENDENCY TO BRUISE ( 2 FDA reports)
INFUSION RELATED REACTION ( 2 FDA reports)
INSULIN RESISTANCE ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 2 FDA reports)
JOINT INJURY ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
LIBIDO DECREASED ( 2 FDA reports)
LIMB INJURY ( 2 FDA reports)
LOSS OF LIBIDO ( 2 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 2 FDA reports)
LYMPHANGITIS ( 2 FDA reports)
MALIGNANT MELANOMA ( 2 FDA reports)
METASTATIC NEOPLASM ( 2 FDA reports)
MITRAL VALVE CALCIFICATION ( 2 FDA reports)
MOOD SWINGS ( 2 FDA reports)
MULTIPLE INJURIES ( 2 FDA reports)
MULTIPLE SCLEROSIS ( 2 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 2 FDA reports)
MUSCLE TIGHTNESS ( 2 FDA reports)
MYCOBACTERIAL INFECTION ( 2 FDA reports)
MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
NECROSIS ( 2 FDA reports)
NOCTURIA ( 2 FDA reports)
OESOPHAGEAL SPASM ( 2 FDA reports)
OPPORTUNISTIC INFECTION ( 2 FDA reports)
OSTEOLYSIS ( 2 FDA reports)
PEMPHIGUS ( 2 FDA reports)
PERIODONTAL DISEASE ( 2 FDA reports)
PERIPHERAL ARTERY ANEURYSM ( 2 FDA reports)
PETECHIAE ( 2 FDA reports)
PITUITARY TUMOUR ( 2 FDA reports)
PNEUMONIA BACTERIAL ( 2 FDA reports)
PROTEIN URINE PRESENT ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PSORIASIS ( 2 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 2 FDA reports)
PULMONARY FIBROSIS ( 2 FDA reports)
PULMONARY MASS ( 2 FDA reports)
PURPURA ( 2 FDA reports)
RASH ERYTHEMATOUS ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
RESPIRATORY TRACT INFECTION ( 2 FDA reports)
ROSACEA ( 2 FDA reports)
SENSATION OF PRESSURE ( 2 FDA reports)
SKIN DEPIGMENTATION ( 2 FDA reports)
SKIN INFLAMMATION ( 2 FDA reports)
SKIN REACTION ( 2 FDA reports)
SKIN TIGHTNESS ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
SPINAL COMPRESSION FRACTURE ( 2 FDA reports)
SPINAL CORD COMPRESSION ( 2 FDA reports)
SPINAL CORD OEDEMA ( 2 FDA reports)
SPINAL FRACTURE ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
STASIS DERMATITIS ( 2 FDA reports)
SUBDURAL HAEMATOMA ( 2 FDA reports)
SYSTEMIC SCLEROSIS ( 2 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 2 FDA reports)
THINKING ABNORMAL ( 2 FDA reports)
THROAT IRRITATION ( 2 FDA reports)
THROMBOCYTOSIS ( 2 FDA reports)
THYROID CANCER ( 2 FDA reports)
TOOTH FRACTURE ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
TREMOR ( 2 FDA reports)
URINE ABNORMALITY ( 2 FDA reports)
URINE ODOUR ABNORMAL ( 2 FDA reports)
VASCULITIS ( 2 FDA reports)
VITILIGO ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
WITHDRAWAL SYNDROME ( 2 FDA reports)
X-RAY ABNORMAL ( 2 FDA reports)
ABDOMINAL HERNIA ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABSCESS DRAINAGE ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ADRENAL ADENOMA ( 1 FDA reports)
ADRENOMEGALY ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
AFFECT LABILITY ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANDROGEN DEFICIENCY ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANGIOFIBROMA ( 1 FDA reports)
ANKLE FRACTURE ( 1 FDA reports)
ANORGASMIA ( 1 FDA reports)
AORTIC ANEURYSM ( 1 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APNOEA ( 1 FDA reports)
APPLICATION SITE DERMATITIS ( 1 FDA reports)
APPLICATION SITE EXCORIATION ( 1 FDA reports)
APPLICATION SITE HYPERSENSITIVITY ( 1 FDA reports)
APPLICATION SITE NECROSIS ( 1 FDA reports)
APPLICATION SITE PAIN ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 1 FDA reports)
ATRIOVENTRICULAR DISSOCIATION ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BARRETT'S OESOPHAGUS ( 1 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BENIGN SOFT TISSUE NEOPLASM ( 1 FDA reports)
BILIARY DILATATION ( 1 FDA reports)
BIPOLAR I DISORDER ( 1 FDA reports)
BLEPHARITIS ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD ALBUMIN INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD BICARBONATE INCREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CHLORIDE INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD INSULIN INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BONE INFECTION ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BRONCHIECTASIS ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
BURNS SECOND DEGREE ( 1 FDA reports)
BURNS THIRD DEGREE ( 1 FDA reports)
CALCULUS URETERIC ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CAUSTIC INJURY ( 1 FDA reports)
CEREBRAL CALCIFICATION ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CHONDROMALACIA ( 1 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 1 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
CONJUNCTIVAL DISCOLOURATION ( 1 FDA reports)
CONNECTIVE TISSUE DISORDER ( 1 FDA reports)
DEATH OF RELATIVE ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DEVICE ADHESION ISSUE ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DIVERTICULUM INTESTINAL ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRUG WITHDRAWAL CONVULSIONS ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DUODENAL NEOPLASM ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
EJACULATION DISORDER ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ENTHESOPATHY ( 1 FDA reports)
EOSINOPHILIC MYOCARDITIS ( 1 FDA reports)
EROSIVE OESOPHAGITIS ( 1 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 1 FDA reports)
ESSENTIAL TREMOR ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
GASTRIC FLUID ANALYSIS ABNORMAL ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GENITAL HERPES ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
GOUT ( 1 FDA reports)
GYNAECOMASTIA ( 1 FDA reports)
HAEMANGIOMA ( 1 FDA reports)
HAEMATOCRIT INCREASED ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HEAD AND NECK CANCER ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC HAEMORRHAGE ( 1 FDA reports)
HEPATIC RUPTURE ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HERNIA REPAIR ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
HYPERCAPNIA ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERPARATHYROIDISM ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERTENSIVE HEART DISEASE ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 1 FDA reports)
INHIBITORY DRUG INTERACTION ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
JOINT STIFFNESS ( 1 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
LEGAL PROBLEM ( 1 FDA reports)
LIGAMENT INJURY ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LIPOMA ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
LUNG CYST ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
MAJOR DEPRESSION ( 1 FDA reports)
MALIGNANT NEOPLASM OF EYELID ( 1 FDA reports)
MANIA ( 1 FDA reports)
MASTOIDITIS ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MITRAL VALVE DISEASE ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MULTI-ORGAN DISORDER ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
MUSCLE MASS ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NASAL DRYNESS ( 1 FDA reports)
NECK MASS ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NEPHROBLASTOMA ( 1 FDA reports)
NEPHROPATHY ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEUROSIS ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
NODULE ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
OESOPHAGEAL ULCER ( 1 FDA reports)
ONYCHOMYCOSIS ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PERIPHERAL EMBOLISM ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PERIRECTAL ABSCESS ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
PHYSICAL ABUSE ( 1 FDA reports)
PICKWICKIAN SYNDROME ( 1 FDA reports)
PITUITARY TUMOUR RECURRENT ( 1 FDA reports)
PLATELET AGGREGATION INCREASED ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PLEURITIC PAIN ( 1 FDA reports)
PNEUMOCYSTIS CARINII INFECTION ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 1 FDA reports)
POSTNASAL DRIP ( 1 FDA reports)
POSTOPERATIVE INFECTION ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROSTATITIS ( 1 FDA reports)
PROSTATOMEGALY ( 1 FDA reports)
PROTRUSION TONGUE ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PUBIC RAMI FRACTURE ( 1 FDA reports)
PUBIS FRACTURE ( 1 FDA reports)
PULMONARY INFARCTION ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 1 FDA reports)
RECURRENT CANCER ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL INJURY ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RENAL VASCULITIS ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
RHINITIS ALLERGIC ( 1 FDA reports)
SCROTAL SWELLING ( 1 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SEXUAL DYSFUNCTION ( 1 FDA reports)
SEXUALLY INAPPROPRIATE BEHAVIOUR ( 1 FDA reports)
SICK SINUS SYNDROME ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SINUS HEADACHE ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SKIN DESQUAMATION ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 1 FDA reports)
STRABISMUS ( 1 FDA reports)
STRESS ( 1 FDA reports)
SUBENDOCARDIAL ISCHAEMIA ( 1 FDA reports)
TARDIVE DYSKINESIA ( 1 FDA reports)
TESTICULAR PAIN ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THYROID MASS ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TOE DEFORMITY ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TRICUSPID VALVE DISEASE ( 1 FDA reports)
TROPONIN I INCREASED ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
TUMOUR LYSIS SYNDROME ( 1 FDA reports)
TYPE III IMMUNE COMPLEX MEDIATED REACTION ( 1 FDA reports)
ULCER HAEMORRHAGE ( 1 FDA reports)
URETERIC OBSTRUCTION ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URINARY TRACT DISORDER ( 1 FDA reports)
VASCULAR CALCIFICATION ( 1 FDA reports)
VASCULAR PSEUDOANEURYSM ( 1 FDA reports)
VENOUS STASIS ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VENTRICULAR DYSSYNCHRONY ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VITAMIN D DEFICIENCY ( 1 FDA reports)
WOUND ( 1 FDA reports)

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