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

MYOCARDIAL INFARCTION ( 5 FDA reports)
FALL ( 4 FDA reports)
HYPOAESTHESIA ( 4 FDA reports)
CHILLS ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
MUSCULAR WEAKNESS ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
VOMITING ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ALOPECIA ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
COUGH ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DELAYED SLEEP PHASE ( 2 FDA reports)
DRUG ADMINISTRATION ERROR ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
ERECTILE DYSFUNCTION ( 2 FDA reports)
FAECAL INCONTINENCE ( 2 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 2 FDA reports)
INCREASED TENDENCY TO BRUISE ( 2 FDA reports)
INFLUENZA ( 2 FDA reports)
MELAS SYNDROME ( 2 FDA reports)
MULTIPLE MYELOMA ( 2 FDA reports)
MULTIPLE SCLEROSIS ( 2 FDA reports)
MUSCLE ATROPHY ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
NASAL CONGESTION ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
OSTEOLYSIS ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PSEUDOMONAS INFECTION ( 2 FDA reports)
RESPIRATORY DISORDER ( 2 FDA reports)
SPINAL OSTEOARTHRITIS ( 2 FDA reports)
URINARY INCONTINENCE ( 2 FDA reports)
VIRAL INFECTION ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
AMNESIA ( 1 FDA reports)
ANGIOMYOLIPOMA ( 1 FDA reports)
APPLICATION SITE INFLAMMATION ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
BREAKTHROUGH PAIN ( 1 FDA reports)
BREAST CANCER IN SITU ( 1 FDA reports)
BREAST TENDERNESS ( 1 FDA reports)
CARDIAC FLUTTER ( 1 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DEPRESSION SUICIDAL ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
ERUCTATION ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HYPERREFLEXIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
ILEUS PARALYTIC ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LOSS OF LIBIDO ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OESOPHAGEAL PAIN ( 1 FDA reports)
OLFACTORY NERVE DISORDER ( 1 FDA reports)
ORAL PRURITUS ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PAIN OF SKIN ( 1 FDA reports)
PAROSMIA ( 1 FDA reports)
PERICARDIAL DISEASE ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPINAL COLUMN STENOSIS ( 1 FDA reports)
SPINAL FRACTURE ( 1 FDA reports)
STRESS CARDIOMYOPATHY ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
TOOTH ABSCESS ( 1 FDA reports)
TOOTH FRACTURE ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TREMOR ( 1 FDA reports)
WALKING AID USER ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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