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

BLOOD GLUCOSE INCREASED ( 608 FDA reports)
HYPOGLYCAEMIA ( 270 FDA reports)
HYPERGLYCAEMIA ( 215 FDA reports)
DRUG INEFFECTIVE ( 207 FDA reports)
PRODUCT QUALITY ISSUE ( 188 FDA reports)
BLOOD GLUCOSE DECREASED ( 175 FDA reports)
DIABETIC KETOACIDOSIS ( 149 FDA reports)
WRONG DRUG ADMINISTERED ( 135 FDA reports)
VOMITING ( 124 FDA reports)
MALAISE ( 116 FDA reports)
NAUSEA ( 115 FDA reports)
DIZZINESS ( 105 FDA reports)
DYSPNOEA ( 99 FDA reports)
ASTHENIA ( 89 FDA reports)
HEADACHE ( 80 FDA reports)
WEIGHT DECREASED ( 77 FDA reports)
FATIGUE ( 74 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 69 FDA reports)
DEATH ( 68 FDA reports)
FALL ( 68 FDA reports)
HYPERHIDROSIS ( 67 FDA reports)
WEIGHT INCREASED ( 67 FDA reports)
CONFUSIONAL STATE ( 64 FDA reports)
VISUAL IMPAIRMENT ( 62 FDA reports)
FEELING ABNORMAL ( 60 FDA reports)
MYOCARDIAL INFARCTION ( 59 FDA reports)
PRURITUS ( 59 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 58 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 56 FDA reports)
DIARRHOEA ( 55 FDA reports)
PAIN ( 55 FDA reports)
PAIN IN EXTREMITY ( 55 FDA reports)
ANAEMIA ( 52 FDA reports)
CARDIAC FAILURE ( 52 FDA reports)
CATARACT ( 52 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 52 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 51 FDA reports)
DEVICE MALFUNCTION ( 49 FDA reports)
OEDEMA PERIPHERAL ( 49 FDA reports)
PNEUMONIA ( 49 FDA reports)
VISION BLURRED ( 47 FDA reports)
CONDITION AGGRAVATED ( 45 FDA reports)
DIABETIC NEUROPATHY ( 45 FDA reports)
TREMOR ( 44 FDA reports)
CEREBRAL HAEMORRHAGE ( 42 FDA reports)
CEREBRAL INFARCTION ( 42 FDA reports)
LOSS OF CONSCIOUSNESS ( 42 FDA reports)
OVERDOSE ( 42 FDA reports)
RENAL FAILURE ( 42 FDA reports)
MEDICATION ERROR ( 41 FDA reports)
ABDOMINAL PAIN ( 40 FDA reports)
BACK PAIN ( 40 FDA reports)
HYPERTENSION ( 38 FDA reports)
KETOACIDOSIS ( 38 FDA reports)
DECREASED APPETITE ( 37 FDA reports)
HOSPITALISATION ( 37 FDA reports)
INJECTION SITE PAIN ( 37 FDA reports)
CHEST PAIN ( 36 FDA reports)
DEHYDRATION ( 36 FDA reports)
RENAL FAILURE ACUTE ( 36 FDA reports)
CEREBROVASCULAR ACCIDENT ( 35 FDA reports)
RASH ( 35 FDA reports)
CONVULSION ( 34 FDA reports)
SOMNOLENCE ( 33 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 31 FDA reports)
COUGH ( 31 FDA reports)
HYPOGLYCAEMIC COMA ( 31 FDA reports)
HYPOTENSION ( 30 FDA reports)
PYREXIA ( 30 FDA reports)
ARTHRITIS ( 28 FDA reports)
ABDOMINAL PAIN UPPER ( 27 FDA reports)
PALPITATIONS ( 27 FDA reports)
POLLAKIURIA ( 27 FDA reports)
BRADYCARDIA ( 26 FDA reports)
HYPOAESTHESIA ( 26 FDA reports)
SEPSIS ( 26 FDA reports)
BLOOD PRESSURE INCREASED ( 25 FDA reports)
EXPIRED DRUG ADMINISTERED ( 25 FDA reports)
KIDNEY INFECTION ( 25 FDA reports)
MYALGIA ( 25 FDA reports)
VISUAL ACUITY REDUCED ( 25 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 25 FDA reports)
ROAD TRAFFIC ACCIDENT ( 24 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 23 FDA reports)
PARAESTHESIA ( 23 FDA reports)
SUICIDE ATTEMPT ( 23 FDA reports)
HYPERSENSITIVITY ( 22 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 22 FDA reports)
URTICARIA ( 22 FDA reports)
ABDOMINAL DISCOMFORT ( 21 FDA reports)
BLOOD CREATININE INCREASED ( 21 FDA reports)
BLOOD PH DECREASED ( 21 FDA reports)
ERYTHEMA ( 21 FDA reports)
GAIT DISTURBANCE ( 21 FDA reports)
AMNESIA ( 20 FDA reports)
ANION GAP INCREASED ( 20 FDA reports)
ARTHRALGIA ( 20 FDA reports)
BACTERIURIA ( 20 FDA reports)
BLOOD BICARBONATE DECREASED ( 20 FDA reports)
BLOOD GASES ABNORMAL ( 20 FDA reports)
BLOOD KETONE BODY INCREASED ( 20 FDA reports)
BLOOD UREA INCREASED ( 20 FDA reports)
BRONCHITIS ( 20 FDA reports)
CARBON DIOXIDE DECREASED ( 20 FDA reports)
DRUG DOSE OMISSION ( 20 FDA reports)
IMPAIRED HEALING ( 20 FDA reports)
INJECTION SITE HAEMORRHAGE ( 20 FDA reports)
MUSCLE SPASMS ( 20 FDA reports)
PCO2 DECREASED ( 20 FDA reports)
PREMATURE BABY ( 20 FDA reports)
PROTEIN URINE PRESENT ( 20 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 20 FDA reports)
STAPHYLOCOCCAL INFECTION ( 20 FDA reports)
SYNCOPE ( 20 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 20 FDA reports)
ANXIETY ( 19 FDA reports)
BURNING SENSATION ( 19 FDA reports)
CYSTITIS ( 19 FDA reports)
DIABETES MELLITUS ( 19 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 19 FDA reports)
KNEE OPERATION ( 19 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 18 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 18 FDA reports)
UNEVALUABLE EVENT ( 18 FDA reports)
CELLULITIS ( 17 FDA reports)
COMA ( 17 FDA reports)
DRUG ADMINISTRATION ERROR ( 17 FDA reports)
FEELING HOT ( 17 FDA reports)
HALLUCINATION ( 17 FDA reports)
HEART RATE INCREASED ( 17 FDA reports)
KETOSIS ( 17 FDA reports)
STRESS ( 17 FDA reports)
EYE HAEMORRHAGE ( 16 FDA reports)
INCORRECT DOSE ADMINISTERED ( 16 FDA reports)
MUSCULAR WEAKNESS ( 16 FDA reports)
PULMONARY EMBOLISM ( 16 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 15 FDA reports)
ANGINA PECTORIS ( 15 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 15 FDA reports)
ERUCTATION ( 15 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 15 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 15 FDA reports)
INJECTION SITE HAEMATOMA ( 15 FDA reports)
MEMORY IMPAIRMENT ( 15 FDA reports)
NEUROPATHY PERIPHERAL ( 15 FDA reports)
RESPIRATORY FAILURE ( 15 FDA reports)
RETINOPATHY ( 15 FDA reports)
ACUTE RESPIRATORY FAILURE ( 14 FDA reports)
BODY TEMPERATURE INCREASED ( 14 FDA reports)
DEEP VEIN THROMBOSIS ( 14 FDA reports)
DIABETIC RETINOPATHY ( 14 FDA reports)
HAEMOGLOBIN DECREASED ( 14 FDA reports)
HYPERVENTILATION ( 14 FDA reports)
INJECTION SITE ERYTHEMA ( 14 FDA reports)
INSULIN RESISTANCE ( 14 FDA reports)
LABORATORY TEST ABNORMAL ( 14 FDA reports)
THROMBOSIS ( 14 FDA reports)
VERTIGO ( 14 FDA reports)
BALANCE DISORDER ( 13 FDA reports)
BLINDNESS UNILATERAL ( 13 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 13 FDA reports)
CHEST DISCOMFORT ( 13 FDA reports)
CORONARY ARTERY DISEASE ( 13 FDA reports)
GLAUCOMA ( 13 FDA reports)
HYPERKALAEMIA ( 13 FDA reports)
INFLUENZA LIKE ILLNESS ( 13 FDA reports)
INSOMNIA ( 13 FDA reports)
INTENTIONAL OVERDOSE ( 13 FDA reports)
SINUS TACHYCARDIA ( 13 FDA reports)
TREATMENT NONCOMPLIANCE ( 13 FDA reports)
URINARY TRACT INFECTION ( 13 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 13 FDA reports)
ABDOMINAL DISTENSION ( 12 FDA reports)
ABDOMINAL TENDERNESS ( 12 FDA reports)
ACCIDENTAL OVERDOSE ( 12 FDA reports)
ANTI-INSULIN ANTIBODY POSITIVE ( 12 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 12 FDA reports)
BLINDNESS ( 12 FDA reports)
BLISTER ( 12 FDA reports)
CATARACT OPERATION ( 12 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 12 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 12 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 12 FDA reports)
INFECTION ( 12 FDA reports)
OFF LABEL USE ( 12 FDA reports)
RENAL IMPAIRMENT ( 12 FDA reports)
SLEEP APNOEA SYNDROME ( 12 FDA reports)
SPEECH DISORDER ( 12 FDA reports)
TACHYCARDIA ( 12 FDA reports)
ABORTION SPONTANEOUS ( 11 FDA reports)
BRADYKINESIA ( 11 FDA reports)
DEVICE FAILURE ( 11 FDA reports)
DIABETIC HYPERGLYCAEMIC COMA ( 11 FDA reports)
DRUG DISPENSING ERROR ( 11 FDA reports)
DRUG INTERACTION ( 11 FDA reports)
EMPHYSEMA ( 11 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 11 FDA reports)
MENTAL STATUS CHANGES ( 11 FDA reports)
METASTASES TO LIVER ( 11 FDA reports)
SOPOR ( 11 FDA reports)
SWELLING ( 11 FDA reports)
ADVERSE EVENT ( 10 FDA reports)
ASTHMA ( 10 FDA reports)
ATELECTASIS ( 10 FDA reports)
BRADYPHRENIA ( 10 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 10 FDA reports)
COLD SWEAT ( 10 FDA reports)
DELIRIUM ( 10 FDA reports)
DIPLOPIA ( 10 FDA reports)
DYSGEUSIA ( 10 FDA reports)
GASTRIC DISORDER ( 10 FDA reports)
HAEMORRHAGE ( 10 FDA reports)
HEAD INJURY ( 10 FDA reports)
HYPONATRAEMIA ( 10 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 10 FDA reports)
MACULAR OEDEMA ( 10 FDA reports)
NECK INJURY ( 10 FDA reports)
PANCREATIC CARCINOMA STAGE IV ( 10 FDA reports)
PANCREATITIS ( 10 FDA reports)
PULMONARY OEDEMA ( 10 FDA reports)
RETINAL HAEMORRHAGE ( 10 FDA reports)
ATRIAL FIBRILLATION ( 9 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 9 FDA reports)
BLOOD PRESSURE DECREASED ( 9 FDA reports)
DEPRESSION ( 9 FDA reports)
DIABETIC NEPHROPATHY ( 9 FDA reports)
LACTIC ACIDOSIS ( 9 FDA reports)
MACULAR DEGENERATION ( 9 FDA reports)
MELAENA ( 9 FDA reports)
SALIVARY HYPERSECRETION ( 9 FDA reports)
SWELLING FACE ( 9 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 8 FDA reports)
CARDIAC DISORDER ( 8 FDA reports)
CARDIO-RESPIRATORY ARREST ( 8 FDA reports)
DIALYSIS ( 8 FDA reports)
DYSPEPSIA ( 8 FDA reports)
DYSPHAGIA ( 8 FDA reports)
ECZEMA ( 8 FDA reports)
FEELING COLD ( 8 FDA reports)
FLUID RETENTION ( 8 FDA reports)
FLUSHING ( 8 FDA reports)
HAEMOPTYSIS ( 8 FDA reports)
HEPATIC STEATOSIS ( 8 FDA reports)
HYPOKINESIA ( 8 FDA reports)
INJECTION SITE BRUISING ( 8 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 8 FDA reports)
MOBILITY DECREASED ( 8 FDA reports)
NON-CARDIAC CHEST PAIN ( 8 FDA reports)
PANCREATIC CARCINOMA ( 8 FDA reports)
PLEURAL EFFUSION ( 8 FDA reports)
PROTEINURIA ( 8 FDA reports)
PYELONEPHRITIS ( 8 FDA reports)
RENAL DISORDER ( 8 FDA reports)
RESPIRATORY DISTRESS ( 8 FDA reports)
RETINAL DETACHMENT ( 8 FDA reports)
SUICIDAL IDEATION ( 8 FDA reports)
THIRST ( 8 FDA reports)
BLOOD URINE PRESENT ( 7 FDA reports)
DIABETIC COMA ( 7 FDA reports)
EPILEPSY ( 7 FDA reports)
HEAD DISCOMFORT ( 7 FDA reports)
HUNGER ( 7 FDA reports)
HYPERBILIRUBINAEMIA ( 7 FDA reports)
INFLUENZA ( 7 FDA reports)
JOINT INJURY ( 7 FDA reports)
LUNG DISORDER ( 7 FDA reports)
METABOLIC DISORDER ( 7 FDA reports)
NO ADVERSE EVENT ( 7 FDA reports)
NODULE ( 7 FDA reports)
PANCREATIC DISORDER ( 7 FDA reports)
PLATELET COUNT DECREASED ( 7 FDA reports)
UNRESPONSIVE TO STIMULI ( 7 FDA reports)
VISUAL DISTURBANCE ( 7 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 7 FDA reports)
ABNORMAL BEHAVIOUR ( 6 FDA reports)
ANTI-INSULIN ANTIBODY INCREASED ( 6 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 6 FDA reports)
CONSTIPATION ( 6 FDA reports)
CONTUSION ( 6 FDA reports)
CORONARY ARTERY OCCLUSION ( 6 FDA reports)
DRUG HYPERSENSITIVITY ( 6 FDA reports)
DRUG TOLERANCE INCREASED ( 6 FDA reports)
DYSARTHRIA ( 6 FDA reports)
EYE DISORDER ( 6 FDA reports)
EYE SWELLING ( 6 FDA reports)
FAECES DISCOLOURED ( 6 FDA reports)
FOOT FRACTURE ( 6 FDA reports)
GASTRIC CANCER ( 6 FDA reports)
HUMERUS FRACTURE ( 6 FDA reports)
HYPOPHAGIA ( 6 FDA reports)
INCISION SITE INFECTION ( 6 FDA reports)
INJECTION SITE ABSCESS ( 6 FDA reports)
INJECTION SITE INFECTION ( 6 FDA reports)
INJECTION SITE NODULE ( 6 FDA reports)
JAUNDICE ( 6 FDA reports)
JOINT DISLOCATION ( 6 FDA reports)
LIVER DISORDER ( 6 FDA reports)
MEDICAL DEVICE COMPLICATION ( 6 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 6 FDA reports)
NASOPHARYNGITIS ( 6 FDA reports)
NERVOUSNESS ( 6 FDA reports)
NO ADVERSE DRUG EFFECT ( 6 FDA reports)
OEDEMA ( 6 FDA reports)
OSTEOARTHRITIS ( 6 FDA reports)
PANCREATIC CYST ( 6 FDA reports)
PELVIC FRACTURE ( 6 FDA reports)
PERFORATED ULCER ( 6 FDA reports)
RENAL FAILURE CHRONIC ( 6 FDA reports)
SCHIZOPHRENIA ( 6 FDA reports)
SHOULDER OPERATION ( 6 FDA reports)
SKIN ULCER ( 6 FDA reports)
SOMNAMBULISM ( 6 FDA reports)
THROMBOCYTOPENIA ( 6 FDA reports)
ULCERATIVE KERATITIS ( 6 FDA reports)
WEGENER'S GRANULOMATOSIS ( 6 FDA reports)
ABASIA ( 5 FDA reports)
AGITATION ( 5 FDA reports)
ANAPHYLACTIC SHOCK ( 5 FDA reports)
ANGIOEDEMA ( 5 FDA reports)
BLOOD POTASSIUM DECREASED ( 5 FDA reports)
BRONCHOPNEUMONIA ( 5 FDA reports)
CARDIOMYOPATHY ( 5 FDA reports)
CERVICOBRACHIAL SYNDROME ( 5 FDA reports)
CHILLS ( 5 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 5 FDA reports)
COGNITIVE DISORDER ( 5 FDA reports)
DEPRESSED MOOD ( 5 FDA reports)
DISTURBANCE IN ATTENTION ( 5 FDA reports)
DRUG PRESCRIBING ERROR ( 5 FDA reports)
DRUG WITHDRAWAL CONVULSIONS ( 5 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 5 FDA reports)
DRY MOUTH ( 5 FDA reports)
DYSURIA ( 5 FDA reports)
ECCHYMOSIS ( 5 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 5 FDA reports)
EMOTIONAL DISORDER ( 5 FDA reports)
EMOTIONAL DISTRESS ( 5 FDA reports)
EPISTAXIS ( 5 FDA reports)
FLATULENCE ( 5 FDA reports)
GLOSSODYNIA ( 5 FDA reports)
GOITRE ( 5 FDA reports)
HEPATIC ENZYME INCREASED ( 5 FDA reports)
HEPATIC FAILURE ( 5 FDA reports)
HOT FLUSH ( 5 FDA reports)
HYPOAESTHESIA ORAL ( 5 FDA reports)
INCONTINENCE ( 5 FDA reports)
INJECTION SITE IRRITATION ( 5 FDA reports)
INJECTION SITE PRURITUS ( 5 FDA reports)
INJURY ( 5 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 5 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 5 FDA reports)
ISCHAEMIC STROKE ( 5 FDA reports)
LIP SWELLING ( 5 FDA reports)
LOWER LIMB FRACTURE ( 5 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 5 FDA reports)
METABOLIC ENCEPHALOPATHY ( 5 FDA reports)
OSTEONECROSIS ( 5 FDA reports)
OVARIAN CANCER ( 5 FDA reports)
PANIC ATTACK ( 5 FDA reports)
POLYHYDRAMNIOS ( 5 FDA reports)
PRURITUS GENERALISED ( 5 FDA reports)
RASH MACULAR ( 5 FDA reports)
RASH PRURITIC ( 5 FDA reports)
RHABDOMYOLYSIS ( 5 FDA reports)
SENSORY DISTURBANCE ( 5 FDA reports)
SLEEP DISORDER ( 5 FDA reports)
SLEEP TALKING ( 5 FDA reports)
SPINAL OSTEOARTHRITIS ( 5 FDA reports)
STEVENS-JOHNSON SYNDROME ( 5 FDA reports)
STOMACH DISCOMFORT ( 5 FDA reports)
TENDONITIS ( 5 FDA reports)
THROAT TIGHTNESS ( 5 FDA reports)
TINNITUS ( 5 FDA reports)
VITREOUS HAEMORRHAGE ( 5 FDA reports)
ACIDOSIS ( 4 FDA reports)
ALOPECIA ( 4 FDA reports)
ANGINA UNSTABLE ( 4 FDA reports)
ARRHYTHMIA ( 4 FDA reports)
ASCITES ( 4 FDA reports)
ATRIAL SEPTAL DEFECT ( 4 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 4 FDA reports)
BIPOLAR DISORDER ( 4 FDA reports)
BLADDER DISORDER ( 4 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 4 FDA reports)
BLOOD POTASSIUM INCREASED ( 4 FDA reports)
BLOOD TEST ( 4 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 4 FDA reports)
BREAST CANCER ( 4 FDA reports)
BURSITIS ( 4 FDA reports)
CARDIAC FAILURE ACUTE ( 4 FDA reports)
CARDIAC TAMPONADE ( 4 FDA reports)
CARDIOVASCULAR DISORDER ( 4 FDA reports)
COAGULATION TIME PROLONGED ( 4 FDA reports)
CONDUCT DISORDER ( 4 FDA reports)
DELUSION ( 4 FDA reports)
DISORIENTATION ( 4 FDA reports)
DIVERTICULITIS ( 4 FDA reports)
DRUG EFFECT DECREASED ( 4 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 4 FDA reports)
DYSKINESIA ( 4 FDA reports)
ECONOMIC PROBLEM ( 4 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 4 FDA reports)
EOSINOPHILIA ( 4 FDA reports)
EYE IRRITATION ( 4 FDA reports)
FEAR ( 4 FDA reports)
FEBRILE NEUTROPENIA ( 4 FDA reports)
FEELING JITTERY ( 4 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 4 FDA reports)
HAEMATOMA ( 4 FDA reports)
HEART RATE IRREGULAR ( 4 FDA reports)
HEPATIC CONGESTION ( 4 FDA reports)
HEREDITARY ANGIOEDEMA ( 4 FDA reports)
HYPOTHYROIDISM ( 4 FDA reports)
HYPOTONIA ( 4 FDA reports)
IMMUNE SYSTEM DISORDER ( 4 FDA reports)
INCORRECT STORAGE OF DRUG ( 4 FDA reports)
INJECTION SITE SWELLING ( 4 FDA reports)
INJECTION SITE WARMTH ( 4 FDA reports)
INTENTIONAL DRUG MISUSE ( 4 FDA reports)
KERATITIS ( 4 FDA reports)
LACERATION ( 4 FDA reports)
LARYNGEAL OEDEMA ( 4 FDA reports)
LETHARGY ( 4 FDA reports)
LIMB DISCOMFORT ( 4 FDA reports)
LIMB INJURY ( 4 FDA reports)
LUNG INFECTION ( 4 FDA reports)
LUNG NEOPLASM MALIGNANT ( 4 FDA reports)
LYMPHOMA ( 4 FDA reports)
MACULOPATHY ( 4 FDA reports)
METABOLIC ACIDOSIS ( 4 FDA reports)
MOVEMENT DISORDER ( 4 FDA reports)
MULTI-ORGAN FAILURE ( 4 FDA reports)
NASAL CONGESTION ( 4 FDA reports)
OCULAR ICTERUS ( 4 FDA reports)
PARKINSON'S DISEASE ( 4 FDA reports)
PERICARDIAL EFFUSION ( 4 FDA reports)
PHOTOSENSITIVITY REACTION ( 4 FDA reports)
POLYNEUROPATHY ( 4 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 4 FDA reports)
QRS AXIS ABNORMAL ( 4 FDA reports)
SCIATICA ( 4 FDA reports)
SINUSITIS ( 4 FDA reports)
SKIN DISCOLOURATION ( 4 FDA reports)
SKIN EXFOLIATION ( 4 FDA reports)
SUDDEN DEATH ( 4 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 4 FDA reports)
SURGICAL PROCEDURE REPEATED ( 4 FDA reports)
TARDIVE DYSKINESIA ( 4 FDA reports)
THROAT IRRITATION ( 4 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 4 FDA reports)
TRIGGER FINGER ( 4 FDA reports)
UNDERDOSE ( 4 FDA reports)
UPPER LIMB FRACTURE ( 4 FDA reports)
URETHRITIS ( 4 FDA reports)
URINE ALBUMIN/CREATININE RATIO INCREASED ( 4 FDA reports)
URINE ANALYSIS ABNORMAL ( 4 FDA reports)
VARICOSE VEIN ( 4 FDA reports)
WRIST FRACTURE ( 4 FDA reports)
YELLOW SKIN ( 4 FDA reports)
ABORTION INDUCED ( 3 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 3 FDA reports)
ADVERSE DRUG REACTION ( 3 FDA reports)
AMPUTATION ( 3 FDA reports)
ANGER ( 3 FDA reports)
APHASIA ( 3 FDA reports)
APPENDICECTOMY ( 3 FDA reports)
APPLICATION SITE ERYTHEMA ( 3 FDA reports)
ARTERIOSCLEROSIS ( 3 FDA reports)
ARTHRITIS BACTERIAL ( 3 FDA reports)
ATAXIA ( 3 FDA reports)
BACK INJURY ( 3 FDA reports)
BACTERIAL INFECTION ( 3 FDA reports)
BENIGN LUNG NEOPLASM ( 3 FDA reports)
BLOOD IRON DECREASED ( 3 FDA reports)
BLOOD SODIUM DECREASED ( 3 FDA reports)
BREAST MASS ( 3 FDA reports)
CARDIAC MURMUR ( 3 FDA reports)
CHEMOTHERAPY ( 3 FDA reports)
CHOLELITHIASIS ( 3 FDA reports)
COMPLETED SUICIDE ( 3 FDA reports)
CORNEAL TRANSPLANT ( 3 FDA reports)
COSTOCHONDRITIS ( 3 FDA reports)
DEAFNESS UNILATERAL ( 3 FDA reports)
DEFAECATION URGENCY ( 3 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 3 FDA reports)
DERMATITIS BULLOUS ( 3 FDA reports)
DISCOMFORT ( 3 FDA reports)
DISEASE PROGRESSION ( 3 FDA reports)
DRY SKIN ( 3 FDA reports)
EATING DISORDER ( 3 FDA reports)
ENCEPHALOPATHY ( 3 FDA reports)
ENDOMETRIAL CANCER ( 3 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 3 FDA reports)
EYE OPERATION ( 3 FDA reports)
EYE PRURITUS ( 3 FDA reports)
FLUID OVERLOAD ( 3 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 3 FDA reports)
GASTROENTERITIS ( 3 FDA reports)
GASTROENTERITIS VIRAL ( 3 FDA reports)
GOUT ( 3 FDA reports)
HAEMATEMESIS ( 3 FDA reports)
HEPATITIS ( 3 FDA reports)
HEPATITIS ACUTE ( 3 FDA reports)
HEPATITIS C ( 3 FDA reports)
HERPES ZOSTER ( 3 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 3 FDA reports)
INJECTION SITE RASH ( 3 FDA reports)
INJECTION SITE REACTION ( 3 FDA reports)
INJECTION SITE SCAR ( 3 FDA reports)
INJECTION SITE URTICARIA ( 3 FDA reports)
INTERSTITIAL LUNG DISEASE ( 3 FDA reports)
JOINT STIFFNESS ( 3 FDA reports)
KNEE ARTHROPLASTY ( 3 FDA reports)
LEUKOPENIA ( 3 FDA reports)
LOCALISED INFECTION ( 3 FDA reports)
MENSTRUAL DISORDER ( 3 FDA reports)
METABOLIC SYNDROME ( 3 FDA reports)
MUSCLE STRAIN ( 3 FDA reports)
MUSCULOSKELETAL PAIN ( 3 FDA reports)
NECK PAIN ( 3 FDA reports)
NERVE COMPRESSION ( 3 FDA reports)
NERVOUS SYSTEM DISORDER ( 3 FDA reports)
NEUTROPHIL COUNT DECREASED ( 3 FDA reports)
NOCTURIA ( 3 FDA reports)
OEDEMA MOUTH ( 3 FDA reports)
PERICARDITIS ( 3 FDA reports)
PHARYNGEAL OEDEMA ( 3 FDA reports)
PHARYNGITIS ( 3 FDA reports)
PREGNANCY ( 3 FDA reports)
RASH PAPULAR ( 3 FDA reports)
REGURGITATION OF FOOD ( 3 FDA reports)
RENAL TRANSPLANT ( 3 FDA reports)
RESTLESSNESS ( 3 FDA reports)
RETINAL DISORDER ( 3 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 3 FDA reports)
RIB FRACTURE ( 3 FDA reports)
SHOCK HYPOGLYCAEMIC ( 3 FDA reports)
SKIN LESION ( 3 FDA reports)
SPINAL COLUMN STENOSIS ( 3 FDA reports)
STREPTOCOCCAL SEPSIS ( 3 FDA reports)
SUBDURAL HAEMATOMA ( 3 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 3 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 3 FDA reports)
TOXIC SKIN ERUPTION ( 3 FDA reports)
URINE KETONE BODY PRESENT ( 3 FDA reports)
ACIDOSIS HYPERCHLORAEMIC ( 2 FDA reports)
ACNE ( 2 FDA reports)
ACUTE HEPATIC FAILURE ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
AGGRESSION ( 2 FDA reports)
AMMONIA INCREASED ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
ANGIONEUROTIC OEDEMA ( 2 FDA reports)
ANTI-INSULIN ANTIBODY ( 2 FDA reports)
APNOEA ( 2 FDA reports)
APPLICATION SITE PRURITUS ( 2 FDA reports)
ARTERIAL BYPASS OPERATION ( 2 FDA reports)
ARTHROPATHY ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK ( 2 FDA reports)
AUTOIMMUNE HEPATITIS ( 2 FDA reports)
BARRETT'S OESOPHAGUS ( 2 FDA reports)
BASAL CELL CARCINOMA ( 2 FDA reports)
BILIARY DILATATION ( 2 FDA reports)
BILIARY TRACT DISORDER ( 2 FDA reports)
BILIARY TRACT INFECTION ( 2 FDA reports)
BLADDER CANCER ( 2 FDA reports)
BLINDNESS TRANSIENT ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD CREATINE INCREASED ( 2 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 2 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 2 FDA reports)
BLOOD URIC ACID INCREASED ( 2 FDA reports)
BODY MASS INDEX INCREASED ( 2 FDA reports)
BRADYARRHYTHMIA ( 2 FDA reports)
BREAST PAIN ( 2 FDA reports)
BREECH PRESENTATION ( 2 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CAESAREAN SECTION ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CARDIAC SEPTAL DEFECT ( 2 FDA reports)
CARDIOMEGALY ( 2 FDA reports)
CAROTID BRUIT ( 2 FDA reports)
CHOLECYSTITIS INFECTIVE ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
CLOSTRIDIAL INFECTION ( 2 FDA reports)
COAGULOPATHY ( 2 FDA reports)
COLLAPSE OF LUNG ( 2 FDA reports)
COLON CANCER STAGE IV ( 2 FDA reports)
COLONIC POLYP ( 2 FDA reports)
CONGENITAL ANOMALY ( 2 FDA reports)
CONGENITAL MUSCULOSKELETAL ANOMALY ( 2 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 2 FDA reports)
CONJUNCTIVAL DISCOLOURATION ( 2 FDA reports)
CORONARY ARTERY BYPASS ( 2 FDA reports)
CORONARY ARTERY STENOSIS ( 2 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 2 FDA reports)
CUSHING'S SYNDROME ( 2 FDA reports)
DEAFNESS ( 2 FDA reports)
DERMAL CYST ( 2 FDA reports)
DERMATITIS ACNEIFORM ( 2 FDA reports)
DERMATITIS ALLERGIC ( 2 FDA reports)
DEVICE DIFFICULT TO USE ( 2 FDA reports)
DEVICE OCCLUSION ( 2 FDA reports)
DIABETIC FOOT ( 2 FDA reports)
DILATATION ATRIAL ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
DRUG EFFECT INCREASED ( 2 FDA reports)
DRY EYE ( 2 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 2 FDA reports)
DYSLALIA ( 2 FDA reports)
DYSLIPIDAEMIA ( 2 FDA reports)
DYSPHONIA ( 2 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 2 FDA reports)
ENTEROCOLITIS ( 2 FDA reports)
EXOSTOSIS ( 2 FDA reports)
EYE INFLAMMATION ( 2 FDA reports)
FACE OEDEMA ( 2 FDA reports)
FEMUR FRACTURE ( 2 FDA reports)
FIBROMYALGIA ( 2 FDA reports)
FLANK PAIN ( 2 FDA reports)
FOCAL NODULAR HYPERPLASIA ( 2 FDA reports)
GASTRIC BYPASS ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
GENERALISED OEDEMA ( 2 FDA reports)
GOUTY ARTHRITIS ( 2 FDA reports)
GUILLAIN-BARRE SYNDROME ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HALLUCINATION, VISUAL ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HEMIPLEGIA ( 2 FDA reports)
HEPATIC ENCEPHALOPATHY ( 2 FDA reports)
HEPATIC FIBROSIS ( 2 FDA reports)
HEPATIC NECROSIS ( 2 FDA reports)
HEPATIC NEOPLASM ( 2 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 2 FDA reports)
HEPATIC PAIN ( 2 FDA reports)
HERPES SIMPLEX ( 2 FDA reports)
HERPES ZOSTER DISSEMINATED ( 2 FDA reports)
HIATUS HERNIA ( 2 FDA reports)
HYPERGLYCAEMIC SEIZURE ( 2 FDA reports)
HYPERSOMNIA ( 2 FDA reports)
HYPOGLYCAEMIA UNAWARENESS ( 2 FDA reports)
HYPOHIDROSIS ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
ICHTHYOSIS ( 2 FDA reports)
ILEUS PARALYTIC ( 2 FDA reports)
INCREASED APPETITE ( 2 FDA reports)
INFERIOR VENA CAVA DILATATION ( 2 FDA reports)
INFLAMMATION ( 2 FDA reports)
INJECTION SITE EXTRAVASATION ( 2 FDA reports)
INJECTION SITE INJURY ( 2 FDA reports)
INJECTION SITE OEDEMA ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 2 FDA reports)
INTERSTITIAL GRANULOMATOUS DERMATITIS ( 2 FDA reports)
INTERVERTEBRAL DISC INJURY ( 2 FDA reports)
INTRA-UTERINE DEATH ( 2 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 2 FDA reports)
IRON DEFICIENCY ANAEMIA ( 2 FDA reports)
IRRITABILITY ( 2 FDA reports)
JOINT SWELLING ( 2 FDA reports)
LARYNGITIS ( 2 FDA reports)
LIP INJURY ( 2 FDA reports)
LIPASE INCREASED ( 2 FDA reports)
LIPODYSTROPHY ACQUIRED ( 2 FDA reports)
LIQUID PRODUCT PHYSICAL ISSUE ( 2 FDA reports)
LIVER INJURY ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
MACROSOMIA ( 2 FDA reports)
MENTAL DISORDER ( 2 FDA reports)
MENTAL IMPAIRMENT ( 2 FDA reports)
MIOSIS ( 2 FDA reports)
MITRAL VALVE CALCIFICATION ( 2 FDA reports)
MOOD ALTERED ( 2 FDA reports)
MOTION SICKNESS ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 2 FDA reports)
MULTIPLE INJURIES ( 2 FDA reports)
MUSCLE RUPTURE ( 2 FDA reports)
MUSCLE TWITCHING ( 2 FDA reports)
MUSCULOSKELETAL DISORDER ( 2 FDA reports)
MYDRIASIS ( 2 FDA reports)
NASAL DISCOMFORT ( 2 FDA reports)
NEOPLASM MALIGNANT ( 2 FDA reports)
NEPHROLITHIASIS ( 2 FDA reports)
NEPHROPATHY TOXIC ( 2 FDA reports)
NEURODERMATITIS ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
NIGHTMARE ( 2 FDA reports)
NO ADVERSE EFFECT ( 2 FDA reports)
OCULAR HYPERAEMIA ( 2 FDA reports)
OESOPHAGEAL ATRESIA ( 2 FDA reports)
ORGANISING PNEUMONIA ( 2 FDA reports)
OROPHARYNGEAL SWELLING ( 2 FDA reports)
OVARIAN NEOPLASM ( 2 FDA reports)
PALATAL DISORDER ( 2 FDA reports)
PANCREATITIS ACUTE ( 2 FDA reports)
PARALYSIS FLACCID ( 2 FDA reports)
PARONYCHIA ( 2 FDA reports)
PAROSMIA ( 2 FDA reports)
PERIARTHRITIS ( 2 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
PIGMENTATION DISORDER ( 2 FDA reports)
PITUITARY TUMOUR ( 2 FDA reports)
POLYOMAVIRUS TEST POSITIVE ( 2 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 2 FDA reports)
POST CONCUSSION SYNDROME ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
POST PROCEDURAL DRAINAGE ( 2 FDA reports)
POSTURE ABNORMAL ( 2 FDA reports)
PRE-ECLAMPSIA ( 2 FDA reports)
PRESYNCOPE ( 2 FDA reports)
PROSTATE CANCER ( 2 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
RASH MACULO-PAPULAR ( 2 FDA reports)
RASH PUSTULAR ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 2 FDA reports)
RENAL CANCER ( 2 FDA reports)
RENAL INJURY ( 2 FDA reports)
RENAL TUBULAR NECROSIS ( 2 FDA reports)
RHINORRHOEA ( 2 FDA reports)
SCAR ( 2 FDA reports)
SCRATCH ( 2 FDA reports)
SEDATION ( 2 FDA reports)
SENSORY LOSS ( 2 FDA reports)
SKIN DISORDER ( 2 FDA reports)
SKIN HAEMORRHAGE ( 2 FDA reports)
SKIN LACERATION ( 2 FDA reports)
SKIN ODOUR ABNORMAL ( 2 FDA reports)
SKIN PLAQUE ( 2 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 2 FDA reports)
SNORING ( 2 FDA reports)
SPINAL COMPRESSION FRACTURE ( 2 FDA reports)
SQUAMOUS CELL CARCINOMA ( 2 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 2 FDA reports)
STILLBIRTH ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
SUFFOCATION FEELING ( 2 FDA reports)
SURGERY ( 2 FDA reports)
SWOLLEN TONGUE ( 2 FDA reports)
TACHYPHRENIA ( 2 FDA reports)
TEMPERATURE INTOLERANCE ( 2 FDA reports)
TENDON DISORDER ( 2 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 2 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 2 FDA reports)
THINKING ABNORMAL ( 2 FDA reports)
THYROID CANCER ( 2 FDA reports)
TONGUE BITING ( 2 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 2 FDA reports)
TRISOMY 21 ( 2 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 2 FDA reports)
TYPE 2 DIABETES MELLITUS ( 2 FDA reports)
ULCER HAEMORRHAGE ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
URINE ODOUR ABNORMAL ( 2 FDA reports)
UTERINE CANCER ( 2 FDA reports)
VIRAEMIA ( 2 FDA reports)
VISUAL FIELD DEFECT ( 2 FDA reports)
WOUND HAEMORRHAGE ( 2 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABDOMINAL RIGIDITY ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ABNORMAL PRODUCT OF CONCEPTION ( 1 FDA reports)
ABNORMAL SENSATION IN EYE ( 1 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 1 FDA reports)
ABSCESS DRAINAGE ( 1 FDA reports)
ABSCESS LIMB ( 1 FDA reports)
ACCIDENTAL NEEDLE STICK ( 1 FDA reports)
ACETONAEMIA ( 1 FDA reports)
ACNE CYSTIC ( 1 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ADDISON'S DISEASE ( 1 FDA reports)
ADHESION ( 1 FDA reports)
ADJUSTMENT DISORDER ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
AKINESIA ( 1 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 1 FDA reports)
AMENORRHOEA ( 1 FDA reports)
ANHEDONIA ( 1 FDA reports)
ANIMAL BITE ( 1 FDA reports)
ANKLE FRACTURE ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANTI-INSULIN RECEPTOR ANTIBODY POSITIVE ( 1 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
ANURIA ( 1 FDA reports)
AORTIC VALVE REPLACEMENT ( 1 FDA reports)
AORTIC VALVE SCLEROSIS ( 1 FDA reports)
AORTIC VALVE STENOSIS ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
APPENDICITIS PERFORATED ( 1 FDA reports)
APPLICATION SITE IRRITATION ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ARTHROPOD BITE ( 1 FDA reports)
ASTHENOPIA ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
AURICULAR SWELLING ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BILE DUCT CANCER ( 1 FDA reports)
BILIARY DYSKINESIA ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 1 FDA reports)
BLOOD KETONE BODY ( 1 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 1 FDA reports)
BLOOD UREA ABNORMAL ( 1 FDA reports)
BLOOD URIC ACID ABNORMAL ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE ABNORMAL ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
BRAIN STEM HAEMORRHAGE ( 1 FDA reports)
BREAST DISCOMFORT ( 1 FDA reports)
BREAST LUMP REMOVAL ( 1 FDA reports)
BREATH ODOUR ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 1 FDA reports)
C-REACTIVE PROTEIN ABNORMAL ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIAC FLUTTER ( 1 FDA reports)
CARDIAC OPERATION ( 1 FDA reports)
CARDIAC PACEMAKER INSERTION ( 1 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
CARPAL TUNNEL SYNDROME ( 1 FDA reports)
CATATONIA ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CERVICAL SPINAL STENOSIS ( 1 FDA reports)
CHEST WALL PAIN ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
CHOREA ( 1 FDA reports)
CLUBBING ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
COMPRESSION FRACTURE ( 1 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 1 FDA reports)
CREATININE RENAL CLEARANCE ABNORMAL ( 1 FDA reports)
DARK CIRCLES UNDER EYES ( 1 FDA reports)
DEATH OF RELATIVE ( 1 FDA reports)
DECREASED INTEREST ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DERMATOSIS ( 1 FDA reports)
DEVICE DISLOCATION ( 1 FDA reports)
DEVICE ISSUE ( 1 FDA reports)
DEVICE RELATED SEPSIS ( 1 FDA reports)
DIABETIC GASTROPARESIS ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DIPLEGIA ( 1 FDA reports)
DISABILITY ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DIVERTICULAR PERFORATION ( 1 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG LABEL CONFUSION ( 1 FDA reports)
DRUG TOLERANCE ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 1 FDA reports)
DUODENAL POLYP ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
EAR DISCOMFORT ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
EARLY SATIETY ( 1 FDA reports)
ECLAMPSIA ( 1 FDA reports)
EJECTION FRACTION ABNORMAL ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
EPICONDYLITIS ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
EXCESSIVE EYE BLINKING ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EXTREMITY NECROSIS ( 1 FDA reports)
EYE INFECTION ( 1 FDA reports)
EYE INJURY ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
FACIAL BONES FRACTURE ( 1 FDA reports)
FACIAL PAIN ( 1 FDA reports)
FAT TISSUE INCREASED ( 1 FDA reports)
FEEDING DISORDER ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
FOETAL DAMAGE ( 1 FDA reports)
FOETAL DEATH ( 1 FDA reports)
FORMICATION ( 1 FDA reports)
FREEZING PHENOMENON ( 1 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 1 FDA reports)
FUNGAEMIA ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GALLBLADDER INJURY ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 1 FDA reports)
GANGRENE ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 1 FDA reports)
GENITOURINARY TRACT INFECTION ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
GLUCOSE TOLERANCE INCREASED ( 1 FDA reports)
GRANULOMA ANNULARE ( 1 FDA reports)
GRIMACING ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMOGLOBIN ABNORMAL ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HAEMORRHAGIC ANAEMIA ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
HEART DISEASE CONGENITAL ( 1 FDA reports)
HEART SOUNDS ABNORMAL ( 1 FDA reports)
HEPATITIS FULMINANT ( 1 FDA reports)
HERNIA ( 1 FDA reports)
HICCUPS ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
HYDROPHOBIA ( 1 FDA reports)
HYPERCHLORHYDRIA ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERINSULINAEMIA ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 1 FDA reports)
HYPERTRICHOSIS ( 1 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOPARATHYROIDISM ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
HYSTERECTOMY ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 1 FDA reports)
IMPAIRED SELF-CARE ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 1 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
INADEQUATE DIET ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INFLAMMATION OF WOUND ( 1 FDA reports)
INFUSION SITE EXTRAVASATION ( 1 FDA reports)
INFUSION SITE INFECTION ( 1 FDA reports)
INJECTION SITE DISCOLOURATION ( 1 FDA reports)
INJECTION SITE INFLAMMATION ( 1 FDA reports)
INJECTION SITE LACERATION ( 1 FDA reports)
INJECTION SITE ULCER ( 1 FDA reports)
INJURY CORNEAL ( 1 FDA reports)
INSULIN AUTOIMMUNE SYNDROME ( 1 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 1 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 1 FDA reports)
INTESTINAL ISCHAEMIA ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
INTESTINAL POLYP ( 1 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
JOINT CREPITATION ( 1 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 1 FDA reports)
JUDGEMENT IMPAIRED ( 1 FDA reports)
LABYRINTHITIS ( 1 FDA reports)
LEARNING DISORDER ( 1 FDA reports)
LEFT ATRIAL DILATATION ( 1 FDA reports)
LENS DISORDER ( 1 FDA reports)
LIGAMENT OPERATION ( 1 FDA reports)
LIMB OPERATION ( 1 FDA reports)
LIP EROSION ( 1 FDA reports)
LIPOATROPHY ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LUMBAR SPINAL STENOSIS ( 1 FDA reports)
LUNG CANCER METASTATIC ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
MACULAR HOLE ( 1 FDA reports)
MAJOR DEPRESSION ( 1 FDA reports)
MALLORY-WEISS SYNDROME ( 1 FDA reports)
MEDICATION RESIDUE ( 1 FDA reports)
MENINGITIS BACTERIAL ( 1 FDA reports)
MENISCUS LESION ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
MENSTRUATION IRREGULAR ( 1 FDA reports)
METASTASIS ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
MOUTH INJURY ( 1 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 1 FDA reports)
MULTIPLE FRACTURES ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCLE INJURY ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
MYELITIS ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NAIL DISCOLOURATION ( 1 FDA reports)
NAIL DISORDER ( 1 FDA reports)
NEEDLE ISSUE ( 1 FDA reports)
NEONATAL ASPHYXIA ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NERVE INJURY ( 1 FDA reports)
NEUROPATHIC ARTHROPATHY ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
NODAL ARRHYTHMIA ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OBESITY SURGERY ( 1 FDA reports)
OBSESSIVE THOUGHTS ( 1 FDA reports)
OCCULT BLOOD ( 1 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 1 FDA reports)
OESOPHAGEAL HYPOMOTILITY ( 1 FDA reports)
OESOPHAGEAL STENOSIS ( 1 FDA reports)
OLIGOHYDRAMNIOS ( 1 FDA reports)
ONYCHOMYCOSIS ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
ORAL INFECTION ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
OTORRHOEA ( 1 FDA reports)
OVARIAN CYST ( 1 FDA reports)
PAIN OF SKIN ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 1 FDA reports)
PANCREAS INFECTION ( 1 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 1 FDA reports)
PANCREATIC MASS ( 1 FDA reports)
PANCREATITIS CHRONIC ( 1 FDA reports)
PANCREATITIS NECROTISING ( 1 FDA reports)
PANCREATITIS RELAPSING ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PARATHYROID TUMOUR ( 1 FDA reports)
PEMPHIGOID ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PERNICIOUS ANAEMIA ( 1 FDA reports)
PHARYNGEAL DISORDER ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
POLYDIPSIA ( 1 FDA reports)
POLYNEUROPATHY IDIOPATHIC PROGRESSIVE ( 1 FDA reports)
POOR PERSONAL HYGIENE ( 1 FDA reports)
PORTAL HYPERTENSION ( 1 FDA reports)
PORTAL VEIN THROMBOSIS ( 1 FDA reports)
POST HERPETIC NEURALGIA ( 1 FDA reports)
POST PROCEDURAL BILE LEAK ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 1 FDA reports)
POSTOPERATIVE ADHESION ( 1 FDA reports)
PREMATURE LABOUR ( 1 FDA reports)
PRODUCT LABEL ISSUE ( 1 FDA reports)
PRODUCT MEASURED POTENCY ISSUE ( 1 FDA reports)
PRODUCT OUTER PACKAGING ISSUE ( 1 FDA reports)
PRODUCT PACKAGING ISSUE ( 1 FDA reports)
PROGESTERONE DECREASED ( 1 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 1 FDA reports)
PROSTATIC DISORDER ( 1 FDA reports)
PROTRUSION TONGUE ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY HYPERTENSIVE CRISIS ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
PULSE ABNORMAL ( 1 FDA reports)
PYURIA ( 1 FDA reports)
RALES ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH VESICULAR ( 1 FDA reports)
RENAL ARTERY STENT PLACEMENT ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESTING TREMOR ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SENSORIMOTOR DISORDER ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SERUM FERRITIN DECREASED ( 1 FDA reports)
SERUM SICKNESS ( 1 FDA reports)
SHORT-BOWEL SYNDROME ( 1 FDA reports)
SHOULDER PAIN ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SINUS CONGESTION ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SKIN ATROPHY ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SKIN IRRITATION ( 1 FDA reports)
SKIN NODULE ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SKIN SWELLING ( 1 FDA reports)
SMALL FOR DATES BABY ( 1 FDA reports)
SOMATIC HALLUCINATION ( 1 FDA reports)
SPINAL CORD DISORDER ( 1 FDA reports)
SPINAL CORD INJURY ( 1 FDA reports)
SPINAL FRACTURE ( 1 FDA reports)
SPINAL OPERATION ( 1 FDA reports)
STERNAL FRACTURE ( 1 FDA reports)
STRABISMUS ( 1 FDA reports)
SWEAT GLAND DISORDER ( 1 FDA reports)
SYSTEMIC CANDIDA ( 1 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 1 FDA reports)
THERAPY CESSATION ( 1 FDA reports)
TONGUE DISCOLOURATION ( 1 FDA reports)
TONGUE DRY ( 1 FDA reports)
TOOTH FRACTURE ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TRUNCUS ARTERIOSUS PERSISTENT ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URETHRAL STENOSIS ( 1 FDA reports)
URINE ABNORMALITY ( 1 FDA reports)
VAGINAL DISCHARGE ( 1 FDA reports)
VAGINAL SWELLING ( 1 FDA reports)
VARICES OESOPHAGEAL ( 1 FDA reports)
VASCULAR GRAFT ( 1 FDA reports)
VASCULITIS NECROTISING ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VITAMIN D DECREASED ( 1 FDA reports)
VITAMIN D DEFICIENCY ( 1 FDA reports)
VITREOUS FLOATERS ( 1 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 1 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 1 FDA reports)
WEANING FAILURE ( 1 FDA reports)
WEIGHT LOSS POOR ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WITHDRAWAL SYNDROME ( 1 FDA reports)
WOUND ( 1 FDA reports)
WOUND NECROSIS ( 1 FDA reports)
X-RAY OF PELVIS AND HIP ABNORMAL ( 1 FDA reports)

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