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

DIARRHOEA ( 5 FDA reports)
NAUSEA ( 4 FDA reports)
VOMITING ( 4 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
BACK PAIN ( 3 FDA reports)
DRUG HYPERSENSITIVITY ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
MYALGIA ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
RENAL FAILURE ACUTE ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
ABDOMINAL DISCOMFORT ( 2 FDA reports)
ABSCESS ( 2 FDA reports)
ACTINIC KERATOSIS ( 2 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 2 FDA reports)
ADRENAL INSUFFICIENCY ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 2 FDA reports)
ANAEMIA POSTOPERATIVE ( 2 FDA reports)
ANXIETY DISORDER ( 2 FDA reports)
ARTERIAL BRUIT ( 2 FDA reports)
ARTHRITIS ( 2 FDA reports)
ARTHROPATHY ( 2 FDA reports)
BLINDNESS ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD CULTURE POSITIVE ( 2 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 2 FDA reports)
BRONCHITIS CHRONIC ( 2 FDA reports)
BURSITIS ( 2 FDA reports)
CARBUNCLE ( 2 FDA reports)
CERVICAL SPINAL STENOSIS ( 2 FDA reports)
COLITIS ( 2 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 2 FDA reports)
DIVERTICULITIS ( 2 FDA reports)
DYSTHYMIC DISORDER ( 2 FDA reports)
ESSENTIAL HYPERTENSION ( 2 FDA reports)
EYE IRRITATION ( 2 FDA reports)
FACE INJURY ( 2 FDA reports)
FACIAL PALSY ( 2 FDA reports)
FALL ( 2 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 2 FDA reports)
FEMUR FRACTURE ( 2 FDA reports)
FIBROMYALGIA ( 2 FDA reports)
FURUNCLE ( 2 FDA reports)
GOITRE ( 2 FDA reports)
HERPES ZOSTER ( 2 FDA reports)
HIP FRACTURE ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
HYPOTHYROIDISM ( 2 FDA reports)
INCREASED APPETITE ( 2 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 2 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 2 FDA reports)
IRRITABLE BOWEL SYNDROME ( 2 FDA reports)
LABORATORY TEST ABNORMAL ( 2 FDA reports)
LUMBAR RADICULOPATHY ( 2 FDA reports)
LUMBAR SPINAL STENOSIS ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MALIGNANT HYPERTENSION ( 2 FDA reports)
MENISCUS LESION ( 2 FDA reports)
MITRAL VALVE DISEASE MIXED ( 2 FDA reports)
MIXED HYPERLIPIDAEMIA ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
MYOPATHY ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
NEOPLASM SKIN ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
OCULAR HYPERTENSION ( 2 FDA reports)
OSTEOARTHRITIS ( 2 FDA reports)
OSTEOPENIA ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PARONYCHIA ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
POLLAKIURIA ( 2 FDA reports)
POLYARTHRITIS ( 2 FDA reports)
POLYMYALGIA RHEUMATICA ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
RETINAL TEAR ( 2 FDA reports)
RHEUMATOID ARTHRITIS ( 2 FDA reports)
ROTATOR CUFF SYNDROME ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 2 FDA reports)
TUMOUR LYSIS SYNDROME ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 1 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA RECURRENT ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ADRENAL DISORDER ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANURIA ( 1 FDA reports)
AORTIC VALVE SCLEROSIS ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 1 FDA reports)
ARTHRITIS BACTERIAL ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
AXILLARY PAIN ( 1 FDA reports)
BENIGN UTERINE NEOPLASM ( 1 FDA reports)
BEZOAR ( 1 FDA reports)
BLOOD ALUMINIUM INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
BONE METABOLISM DISORDER ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CAECITIS ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CAPILLARY LEAK SYNDROME ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CATHETER SITE PAIN ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
CHOLECYSTITIS CHRONIC ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
COLLAPSE OF LUNG ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CORYNEBACTERIUM INFECTION ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DEVELOPMENTAL DELAY ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DROOLING ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ENDOMETRIAL ATROPHY ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FEEDING DISORDER ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GLIOSIS ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HAND FRACTURE ( 1 FDA reports)
HEPATIC FIBROSIS ( 1 FDA reports)
HEPATOSPLENOMEGALY ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
ILEUS ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INSULINOMA ( 1 FDA reports)
JOINT STIFFNESS ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIPIDS DECREASED ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
LOWER LIMB FRACTURE ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
MACULAR HOLE ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MICROANGIOPATHY ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
OESOPHAGEAL DILATATION ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
OVARIAN ATROPHY ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PARATHYROID DISORDER ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PERITONEAL HAEMORRHAGE ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RENAL HAEMORRHAGE ( 1 FDA reports)
RETINAL NEOPLASM ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SINUS CONGESTION ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STEM CELL TRANSPLANT ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
THIRST ( 1 FDA reports)
THYROID ATROPHY ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TREMOR ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VENOOCCLUSIVE DISEASE ( 1 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 1 FDA reports)

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