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

PAIN IN EXTREMITY ( 16 FDA reports)
VOMITING ( 12 FDA reports)
MYALGIA ( 11 FDA reports)
INSOMNIA ( 10 FDA reports)
MYOCARDIAL INFARCTION ( 10 FDA reports)
RETINAL HAEMORRHAGE ( 10 FDA reports)
ABDOMINAL PAIN UPPER ( 7 FDA reports)
HEPATITIS ACUTE ( 7 FDA reports)
MOBILITY DECREASED ( 7 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 7 FDA reports)
OROPHARYNGEAL BLISTERING ( 7 FDA reports)
STRESS ( 7 FDA reports)
TONGUE BLISTERING ( 7 FDA reports)
BLOOD CREATININE INCREASED ( 6 FDA reports)
CONFUSIONAL STATE ( 6 FDA reports)
DYSPEPSIA ( 6 FDA reports)
HAEMATEMESIS ( 6 FDA reports)
HYPOTENSION ( 6 FDA reports)
ORAL PAIN ( 6 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 5 FDA reports)
ANGINA PECTORIS ( 5 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 5 FDA reports)
CARDIAC FAILURE ( 5 FDA reports)
NAUSEA ( 5 FDA reports)
ANOREXIA ( 4 FDA reports)
BALANCE DISORDER ( 4 FDA reports)
CARDIAC ARREST ( 4 FDA reports)
CELLULITIS ( 4 FDA reports)
DEHYDRATION ( 4 FDA reports)
DISORIENTATION ( 4 FDA reports)
DIZZINESS ( 4 FDA reports)
FALL ( 4 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 4 FDA reports)
HEART RATE IRREGULAR ( 4 FDA reports)
HEPATIC STEATOSIS ( 4 FDA reports)
HIP FRACTURE ( 4 FDA reports)
JOINT SWELLING ( 4 FDA reports)
MITRAL VALVE INCOMPETENCE ( 4 FDA reports)
SKIN ULCER ( 4 FDA reports)
TREMOR ( 4 FDA reports)
VENTRICULAR HYPERTROPHY ( 4 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
AGITATION ( 3 FDA reports)
ANXIETY ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
BLOOD POTASSIUM DECREASED ( 3 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 3 FDA reports)
BRONCHITIS ( 3 FDA reports)
CHEST DISCOMFORT ( 3 FDA reports)
CHEST PAIN ( 3 FDA reports)
CONSTIPATION ( 3 FDA reports)
CORONARY ARTERY DISEASE ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
ECZEMA ( 3 FDA reports)
HEART RATE INCREASED ( 3 FDA reports)
HEPATIC NECROSIS ( 3 FDA reports)
HYPERHIDROSIS ( 3 FDA reports)
MELAENA ( 3 FDA reports)
MYOCARDIAL FIBROSIS ( 3 FDA reports)
MYOCARDIAL ISCHAEMIA ( 3 FDA reports)
NECK PAIN ( 3 FDA reports)
OESOPHAGITIS ( 3 FDA reports)
ORAL CANDIDIASIS ( 3 FDA reports)
PHARYNGEAL ERYTHEMA ( 3 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 3 FDA reports)
SHOCK ( 3 FDA reports)
ADRENOCORTICAL INSUFFICIENCY CHRONIC ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BONE MARROW DEPRESSION ( 2 FDA reports)
CATARACT ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
FAECES DISCOLOURED ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HEPATIC FIBROSIS ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
MYOSITIS ( 2 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
RESPIRATORY RATE INCREASED ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 2 FDA reports)
URINE OUTPUT DECREASED ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHILLS ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROENTERITIS HELICOBACTER ( 1 FDA reports)
HELICOBACTER INFECTION ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
PECTUS EXCAVATUM ( 1 FDA reports)
PEPTIC ULCER ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PROCTALGIA ( 1 FDA reports)
PROCTALGIA FUGAX ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SCLERITIS ( 1 FDA reports)
SPINAL FRACTURE ( 1 FDA reports)
SPONDYLOSIS ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TENDON RUPTURE ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
WHEEZING ( 1 FDA reports)

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