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

WEIGHT DECREASED ( 76 FDA reports)
NAUSEA ( 64 FDA reports)
BLOOD GLUCOSE INCREASED ( 62 FDA reports)
FATIGUE ( 32 FDA reports)
PAIN ( 32 FDA reports)
VOMITING ( 31 FDA reports)
DIARRHOEA ( 28 FDA reports)
BLOOD PRESSURE INCREASED ( 27 FDA reports)
DRUG INEFFECTIVE ( 27 FDA reports)
OEDEMA PERIPHERAL ( 27 FDA reports)
DYSPNOEA ( 26 FDA reports)
BLOOD GLUCOSE DECREASED ( 24 FDA reports)
ASTHENIA ( 23 FDA reports)
PNEUMONIA ( 21 FDA reports)
DECREASED APPETITE ( 20 FDA reports)
MYOCARDIAL INFARCTION ( 20 FDA reports)
FEELING ABNORMAL ( 19 FDA reports)
FALL ( 18 FDA reports)
MALAISE ( 18 FDA reports)
ARTHRALGIA ( 16 FDA reports)
DIZZINESS ( 16 FDA reports)
HEADACHE ( 16 FDA reports)
PAIN IN EXTREMITY ( 16 FDA reports)
PYREXIA ( 15 FDA reports)
COUGH ( 14 FDA reports)
DEATH ( 14 FDA reports)
LOSS OF CONSCIOUSNESS ( 14 FDA reports)
PANCREATITIS ( 14 FDA reports)
SOMNOLENCE ( 14 FDA reports)
ABASIA ( 12 FDA reports)
ABDOMINAL DISTENSION ( 12 FDA reports)
ABDOMINAL PAIN UPPER ( 12 FDA reports)
INJECTION SITE PAIN ( 12 FDA reports)
RENAL FAILURE ( 12 FDA reports)
TREMOR ( 12 FDA reports)
HYPOAESTHESIA ( 11 FDA reports)
MUSCULAR WEAKNESS ( 11 FDA reports)
RASH ( 11 FDA reports)
RENAL IMPAIRMENT ( 11 FDA reports)
WEIGHT INCREASED ( 11 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 10 FDA reports)
BRONCHITIS ( 10 FDA reports)
CHEST PAIN ( 10 FDA reports)
CONSTIPATION ( 10 FDA reports)
CONVULSION ( 10 FDA reports)
HYPERSENSITIVITY ( 10 FDA reports)
INSOMNIA ( 10 FDA reports)
MEMORY IMPAIRMENT ( 10 FDA reports)
RENAL FAILURE ACUTE ( 10 FDA reports)
ROAD TRAFFIC ACCIDENT ( 10 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 9 FDA reports)
ERYTHEMA ( 9 FDA reports)
HEPATIC ENZYME INCREASED ( 9 FDA reports)
INJECTION SITE HAEMORRHAGE ( 9 FDA reports)
URTICARIA ( 9 FDA reports)
ARTHRITIS ( 8 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 8 FDA reports)
CARDIAC ARREST ( 8 FDA reports)
CARDIAC DISORDER ( 8 FDA reports)
CONFUSIONAL STATE ( 8 FDA reports)
DEHYDRATION ( 8 FDA reports)
DRUG HYPERSENSITIVITY ( 8 FDA reports)
EARLY SATIETY ( 8 FDA reports)
GAIT DISTURBANCE ( 8 FDA reports)
HYPERHIDROSIS ( 8 FDA reports)
HYPOTENSION ( 8 FDA reports)
PLATELET COUNT DECREASED ( 8 FDA reports)
PRURITUS ( 8 FDA reports)
VISUAL ACUITY REDUCED ( 8 FDA reports)
CEREBROVASCULAR ACCIDENT ( 7 FDA reports)
CHEST DISCOMFORT ( 7 FDA reports)
DISORIENTATION ( 7 FDA reports)
DRUG EFFECT DECREASED ( 7 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 7 FDA reports)
HALLUCINATION ( 7 FDA reports)
HEART RATE INCREASED ( 7 FDA reports)
HYPERTENSION ( 7 FDA reports)
MULTI-ORGAN FAILURE ( 7 FDA reports)
MYALGIA ( 7 FDA reports)
PLEURAL EFFUSION ( 7 FDA reports)
RIB FRACTURE ( 7 FDA reports)
ANXIETY ( 6 FDA reports)
COLD SWEAT ( 6 FDA reports)
DEPRESSION ( 6 FDA reports)
DIVERTICULITIS ( 6 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 6 FDA reports)
HYPERSOMNIA ( 6 FDA reports)
HYPOGLYCAEMIA ( 6 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 6 FDA reports)
NECK PAIN ( 6 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 6 FDA reports)
NO ADVERSE EVENT ( 6 FDA reports)
PRURITUS GENERALISED ( 6 FDA reports)
PULMONARY OEDEMA ( 6 FDA reports)
RESPIRATORY FAILURE ( 6 FDA reports)
SLEEP DISORDER ( 6 FDA reports)
ANAEMIA ( 5 FDA reports)
ANOREXIA ( 5 FDA reports)
BLOOD CREATININE INCREASED ( 5 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 5 FDA reports)
BLOOD PRESSURE DECREASED ( 5 FDA reports)
CHILLS ( 5 FDA reports)
CORONARY ARTERY OCCLUSION ( 5 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 5 FDA reports)
DRY SKIN ( 5 FDA reports)
DYSKINESIA ( 5 FDA reports)
FEELING HOT ( 5 FDA reports)
FLATULENCE ( 5 FDA reports)
GOUT ( 5 FDA reports)
HOT FLUSH ( 5 FDA reports)
ILEUS PARALYTIC ( 5 FDA reports)
INJURY ( 5 FDA reports)
NEUROPATHY PERIPHERAL ( 5 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 5 FDA reports)
PHARYNGEAL OEDEMA ( 5 FDA reports)
RECTAL HAEMORRHAGE ( 5 FDA reports)
SWELLING ( 5 FDA reports)
SWOLLEN TONGUE ( 5 FDA reports)
VISUAL IMPAIRMENT ( 5 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 5 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 5 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
ADVERSE EVENT ( 4 FDA reports)
ANDROPAUSE ( 4 FDA reports)
ANGIOEDEMA ( 4 FDA reports)
ANHEDONIA ( 4 FDA reports)
ARTERIOSCLEROSIS ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
ASTHMA ( 4 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 4 FDA reports)
CATARACT ( 4 FDA reports)
CHROMATURIA ( 4 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 4 FDA reports)
COMA ( 4 FDA reports)
CRYING ( 4 FDA reports)
DECUBITUS ULCER ( 4 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 4 FDA reports)
DRUG INTERACTION ( 4 FDA reports)
DRY MOUTH ( 4 FDA reports)
DYSGEUSIA ( 4 FDA reports)
DYSPEPSIA ( 4 FDA reports)
DYSPHAGIA ( 4 FDA reports)
EATING DISORDER ( 4 FDA reports)
EMOTIONAL DISTRESS ( 4 FDA reports)
EYE SWELLING ( 4 FDA reports)
FEAR ( 4 FDA reports)
FEELING COLD ( 4 FDA reports)
FLUID RETENTION ( 4 FDA reports)
GASTRITIS ( 4 FDA reports)
HUNGER ( 4 FDA reports)
IMPAIRED HEALING ( 4 FDA reports)
INJECTION SITE RASH ( 4 FDA reports)
LIP SWELLING ( 4 FDA reports)
PALPITATIONS ( 4 FDA reports)
PROTEINURIA ( 4 FDA reports)
PULMONARY EMBOLISM ( 4 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 4 FDA reports)
RENAL CYST ( 4 FDA reports)
RENAL INJURY ( 4 FDA reports)
SINUSITIS ( 4 FDA reports)
STRESS ( 4 FDA reports)
SYNCOPE ( 4 FDA reports)
THROMBOCYTOPENIA ( 4 FDA reports)
UNEVALUABLE EVENT ( 4 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ANAPHYLACTIC REACTION ( 3 FDA reports)
ANGINA PECTORIS ( 3 FDA reports)
ATELECTASIS ( 3 FDA reports)
BEDRIDDEN ( 3 FDA reports)
BLINDNESS UNILATERAL ( 3 FDA reports)
BLOOD OSMOLARITY INCREASED ( 3 FDA reports)
BLOOD POTASSIUM INCREASED ( 3 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 3 FDA reports)
BRONCHIOLITIS ( 3 FDA reports)
BURNING SENSATION ( 3 FDA reports)
CHOLELITHIASIS ( 3 FDA reports)
CYSTITIS ( 3 FDA reports)
DRY EYE ( 3 FDA reports)
DYSARTHRIA ( 3 FDA reports)
DYSPHONIA ( 3 FDA reports)
EYE DISORDER ( 3 FDA reports)
FEELING DRUNK ( 3 FDA reports)
FLUID OVERLOAD ( 3 FDA reports)
GALLBLADDER DISORDER ( 3 FDA reports)
GASTRIC ILEUS ( 3 FDA reports)
HAEMORRHAGE ( 3 FDA reports)
HEPATIC FAILURE ( 3 FDA reports)
HYPERGLYCAEMIA ( 3 FDA reports)
IMPLANTABLE DEFIBRILLATOR MALFUNCTION ( 3 FDA reports)
INCORRECT DOSE ADMINISTERED ( 3 FDA reports)
INJECTION SITE DISCOMFORT ( 3 FDA reports)
INJECTION SITE INFECTION ( 3 FDA reports)
INJECTION SITE MASS ( 3 FDA reports)
INJECTION SITE PRURITUS ( 3 FDA reports)
INJECTION SITE ULCER ( 3 FDA reports)
IRRITABILITY ( 3 FDA reports)
JAUNDICE ( 3 FDA reports)
LYMPHADENOPATHY ( 3 FDA reports)
MIDDLE EAR EFFUSION ( 3 FDA reports)
MOBILITY DECREASED ( 3 FDA reports)
MUSCLE SPASMS ( 3 FDA reports)
NIGHT SWEATS ( 3 FDA reports)
OBESITY ( 3 FDA reports)
ORAL PAIN ( 3 FDA reports)
OSTEOMYELITIS ( 3 FDA reports)
PARKINSON'S DISEASE ( 3 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 3 FDA reports)
PYELONEPHRITIS ( 3 FDA reports)
RESPIRATORY RATE INCREASED ( 3 FDA reports)
RHEUMATOID ARTHRITIS ( 3 FDA reports)
ROTATOR CUFF SYNDROME ( 3 FDA reports)
SECRETION DISCHARGE ( 3 FDA reports)
SINUS DISORDER ( 3 FDA reports)
SKIN DISCOLOURATION ( 3 FDA reports)
SLEEP APNOEA SYNDROME ( 3 FDA reports)
SPINAL CORD OEDEMA ( 3 FDA reports)
STENT OCCLUSION ( 3 FDA reports)
STEVENS-JOHNSON SYNDROME ( 3 FDA reports)
SWELLING FACE ( 3 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 3 FDA reports)
TACHYCARDIA ( 3 FDA reports)
THROAT TIGHTNESS ( 3 FDA reports)
THROMBOSIS ( 3 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 3 FDA reports)
TRISOMY 21 ( 3 FDA reports)
TYPE 2 DIABETES MELLITUS ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
WEIGHT FLUCTUATION ( 3 FDA reports)
ABDOMINAL DISCOMFORT ( 2 FDA reports)
ABDOMINAL RIGIDITY ( 2 FDA reports)
ABNORMAL DREAMS ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
ADRENAL NEOPLASM ( 2 FDA reports)
AGITATION ( 2 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 2 FDA reports)
ANGINA UNSTABLE ( 2 FDA reports)
ANKLE FRACTURE ( 2 FDA reports)
AORTIC ANEURYSM ( 2 FDA reports)
APHTHOUS STOMATITIS ( 2 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 2 FDA reports)
AXILLARY PAIN ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
BLOOD COUNT ABNORMAL ( 2 FDA reports)
BLOOD PRESSURE ABNORMAL ( 2 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
BREAST CANCER ( 2 FDA reports)
BREAST CANCER STAGE I ( 2 FDA reports)
BREAST PAIN ( 2 FDA reports)
CARDIAC CIRRHOSIS ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CARDIOMYOPATHY ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
CHOKING ( 2 FDA reports)
CHOLECYSTECTOMY ( 2 FDA reports)
CIRCULATORY COLLAPSE ( 2 FDA reports)
COAGULOPATHY ( 2 FDA reports)
COLONIC ATONY ( 2 FDA reports)
CONJUNCTIVITIS VIRAL ( 2 FDA reports)
CORONARY ARTERY DISEASE ( 2 FDA reports)
CORONARY ARTERY REOCCLUSION ( 2 FDA reports)
COSTOCHONDRITIS ( 2 FDA reports)
DEVICE MALFUNCTION ( 2 FDA reports)
DIABETIC FOOT ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
EAR PAIN ( 2 FDA reports)
EJECTION FRACTION DECREASED ( 2 FDA reports)
EPIDURAL ANAESTHESIA ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
ERECTILE DYSFUNCTION ( 2 FDA reports)
EYE INFECTION STAPHYLOCOCCAL ( 2 FDA reports)
EYE IRRITATION ( 2 FDA reports)
EYE ROLLING ( 2 FDA reports)
FEELING JITTERY ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 2 FDA reports)
GENERALISED ERYTHEMA ( 2 FDA reports)
GRANULOCYTOPENIA ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
HAEMOGLOBIN ABNORMAL ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
HEPATIC ENCEPHALOPATHY ( 2 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 2 FDA reports)
HERNIA ( 2 FDA reports)
HIP FRACTURE ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
HYSTERECTOMY ( 2 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 2 FDA reports)
INFLAMMATION ( 2 FDA reports)
INFLUENZA ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 2 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 2 FDA reports)
KNEE ARTHROPLASTY ( 2 FDA reports)
LIP DISORDER ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
LOCALISED INFECTION ( 2 FDA reports)
MACULAR DEGENERATION ( 2 FDA reports)
MACULAR HOLE ( 2 FDA reports)
MASS ( 2 FDA reports)
MEDICAL DEVICE COMPLICATION ( 2 FDA reports)
MEDICAL OBSERVATION ( 2 FDA reports)
MENTAL DISORDER ( 2 FDA reports)
MOOD SWINGS ( 2 FDA reports)
MUSCLE TWITCHING ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
MYDRIASIS ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
NEOPLASM ( 2 FDA reports)
OBSTRUCTION GASTRIC ( 2 FDA reports)
OCULAR HYPERAEMIA ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 2 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 2 FDA reports)
OSTEONECROSIS ( 2 FDA reports)
OSTEOPOROSIS ( 2 FDA reports)
OTITIS MEDIA VIRAL ( 2 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PERITONITIS ( 2 FDA reports)
POLYURIA ( 2 FDA reports)
POOR PERIPHERAL CIRCULATION ( 2 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
RASH MACULAR ( 2 FDA reports)
RASH PRURITIC ( 2 FDA reports)
RASH PUSTULAR ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
SCOTOMA ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
SKIN EXFOLIATION ( 2 FDA reports)
SKIN WRINKLING ( 2 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
SPINAL COLUMN STENOSIS ( 2 FDA reports)
SPINAL DISORDER ( 2 FDA reports)
SUTURE INSERTION ( 2 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 2 FDA reports)
TOE AMPUTATION ( 2 FDA reports)
TRANSFUSION REACTION ( 2 FDA reports)
TUBERCULOSIS OF GENITOURINARY SYSTEM ( 2 FDA reports)
TUMOUR ASSOCIATED FEVER ( 2 FDA reports)
UNRESPONSIVE TO STIMULI ( 2 FDA reports)
URINARY INCONTINENCE ( 2 FDA reports)
URINE FLOW DECREASED ( 2 FDA reports)
VENTRICULAR FIBRILLATION ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
VITAMIN B12 DEFICIENCY ( 2 FDA reports)
WHEEZING ( 2 FDA reports)
WOUND DRAINAGE ( 2 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ABORTION ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
ACCIDENT ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ADENOCARCINOMA PANCREAS ( 1 FDA reports)
ADRENAL MASS ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ALLERGY TEST POSITIVE ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANAPLASTIC LARGE CELL LYMPHOMA T- AND NULL-CELL TYPES ( 1 FDA reports)
ANGER ( 1 FDA reports)
ANGIODYSPLASIA ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
APPLICATION SITE HAEMATOMA ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 1 FDA reports)
ARTERIOSPASM CORONARY ( 1 FDA reports)
ARTHROPOD BITE ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ASPHYXIA ( 1 FDA reports)
AUTOIMMUNE HEPATITIS ( 1 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 1 FDA reports)
BACTERIAL TEST POSITIVE ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BRADYKINESIA ( 1 FDA reports)
BREATH SOUNDS ( 1 FDA reports)
CARCINOID TUMOUR ( 1 FDA reports)
CARDIAC INFECTION ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOTOXICITY ( 1 FDA reports)
CAROTID ARTERY DISEASE ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHOLECYSTITIS CHRONIC ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COLITIS ( 1 FDA reports)
COLONIC POLYP ( 1 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 1 FDA reports)
CONCUSSION ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 1 FDA reports)
CORONARY ARTERY BYPASS ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
CRYPTOGENIC CIRRHOSIS ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIABETIC COMPLICATION ( 1 FDA reports)
DIABETIC RETINOPATHY ( 1 FDA reports)
DISABILITY ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DYSLIPIDAEMIA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
EJACULATION FAILURE ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 1 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
EPIGASTRIC DISCOMFORT ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
ERUCTATION ( 1 FDA reports)
EXPIRED DRUG ADMINISTERED ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
EYELASH THICKENING ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FANCONI SYNDROME ACQUIRED ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
FOOT DEFORMITY ( 1 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 1 FDA reports)
FURUNCLE ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GAS POISONING ( 1 FDA reports)
GASTRIC BYPASS ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTRIC ULCER PERFORATION ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL OEDEMA ( 1 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GENITAL DISORDER MALE ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
GLOSSITIS ( 1 FDA reports)
GLYCOSURIA ( 1 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 1 FDA reports)
HAEMORRHOID OPERATION ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HAND FRACTURE ( 1 FDA reports)
HEAD DISCOMFORT ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HELICOBACTER INFECTION ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HIP ARTHROPLASTY ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HOSTILITY ( 1 FDA reports)
HYPERADRENALISM ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERCHLORHYDRIA ( 1 FDA reports)
HYPERKERATOSIS ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOGLYCAEMIC COMA ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPOPHOSPHATAEMIA ( 1 FDA reports)
HYPOVITAMINOSIS ( 1 FDA reports)
INADEQUATE ANALGESIA ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INJECTION SITE PAPULE ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INJECTION SITE URTICARIA ( 1 FDA reports)
INJURY ASPHYXIATION ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
JOINT INJURY ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LOCKED-IN SYNDROME ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LYMPH NODE PAIN ( 1 FDA reports)
MACULAR OEDEMA ( 1 FDA reports)
MANIA ( 1 FDA reports)
MENTAL RETARDATION ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 1 FDA reports)
MICROANGIOPATHY ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MONARTHRITIS ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MULTI-ORGAN DISORDER ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
MUSCLE TIGHTNESS ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
MYOCARDITIS ( 1 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NOCTURIA ( 1 FDA reports)
OESOPHAGEAL DISORDER ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OPTIC ATROPHY ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OVARIAN CANCER ( 1 FDA reports)
OVERWEIGHT ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PALATAL OEDEMA ( 1 FDA reports)
PALLANAESTHESIA ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 1 FDA reports)
PANCREATIC CARCINOMA ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PAPILLOEDEMA ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PAROTID GLAND ENLARGEMENT ( 1 FDA reports)
PERIORBITAL OEDEMA ( 1 FDA reports)
PERITONEAL DISORDER ( 1 FDA reports)
PERITONEAL HAEMORRHAGE ( 1 FDA reports)
PERSONALITY CHANGE ( 1 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PLATELET COUNT ABNORMAL ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
PLEURITIC PAIN ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POLYMYALGIA RHEUMATICA ( 1 FDA reports)
PORTAL HYPERTENSION ( 1 FDA reports)
POST PROCEDURAL SWELLING ( 1 FDA reports)
PRESCRIBED OVERDOSE ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
RADIATION INJURY ( 1 FDA reports)
RECTAL POLYP ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 1 FDA reports)
RESUSCITATION ( 1 FDA reports)
RETINOPATHY PROLIFERATIVE ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SCAR ( 1 FDA reports)
SEASONAL ALLERGY ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SEPSIS SYNDROME ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SINUS CONGESTION ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SLUGGISHNESS ( 1 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 1 FDA reports)
SOFT TISSUE INFECTION ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
SPINAL FRACTURE ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
STENT PLACEMENT ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
STRIDOR ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
TARDIVE DYSKINESIA ( 1 FDA reports)
TESTICULAR PAIN ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THERAPEUTIC RESPONSE INCREASED ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THROMBOCYTOSIS ( 1 FDA reports)
TIBIA FRACTURE ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TONGUE GEOGRAPHIC ( 1 FDA reports)
TONGUE ULCERATION ( 1 FDA reports)
TOOTH INJURY ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
TUMOUR LYSIS SYNDROME ( 1 FDA reports)
UPPER LIMB FRACTURE ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
UTERINE DISORDER ( 1 FDA reports)
UTERINE LEIOMYOMA ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VARICES OESOPHAGEAL ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
WALKING AID USER ( 1 FDA reports)
WOUND ( 1 FDA reports)
WRIST FRACTURE ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)
YAWNING ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use