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MUSCLE SPASMS ( 8 FDA reports)
ARTHRALGIA ( 7 FDA reports)
OEDEMA PERIPHERAL ( 6 FDA reports)
DYSPNOEA ( 5 FDA reports)
ERYTHEMA ( 5 FDA reports)
FATIGUE ( 5 FDA reports)
MIGRAINE ( 5 FDA reports)
BLOOD PRESSURE INCREASED ( 4 FDA reports)
FLUSHING ( 4 FDA reports)
HYPERSENSITIVITY ( 4 FDA reports)
INJECTION SITE PAIN ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
PAIN IN EXTREMITY ( 4 FDA reports)
RASH ( 4 FDA reports)
SINUSITIS ( 4 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
APPLICATION SITE ERYTHEMA ( 3 FDA reports)
APPLICATION SITE IRRITATION ( 3 FDA reports)
APPLICATION SITE PRURITUS ( 3 FDA reports)
APPLICATION SITE REACTION ( 3 FDA reports)
APPLICATION SITE SCAB ( 3 FDA reports)
BIOPSY BREAST ABNORMAL ( 3 FDA reports)
BREAST CANCER ( 3 FDA reports)
BREAST NECROSIS ( 3 FDA reports)
COUGH ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
FEELING HOT ( 3 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 3 FDA reports)
MAMMOGRAM ABNORMAL ( 3 FDA reports)
MUSCULOSKELETAL PAIN ( 3 FDA reports)
NASAL CONGESTION ( 3 FDA reports)
NASAL SEPTUM DEVIATION ( 3 FDA reports)
OSTEOPOROSIS ( 3 FDA reports)
PELVIC PAIN ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
PSORIASIS ( 3 FDA reports)
ROTATOR CUFF SYNDROME ( 3 FDA reports)
SWELLING FACE ( 3 FDA reports)
TOOTH FRACTURE ( 3 FDA reports)
UTERINE LEIOMYOMA ( 3 FDA reports)
VOMITING ( 3 FDA reports)
ABDOMINAL DISCOMFORT ( 2 FDA reports)
ABDOMINAL HERNIA ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
BUNION ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA STAGE 2 ( 2 FDA reports)
CORONARY ARTERY OCCLUSION ( 2 FDA reports)
DRUG DOSE OMISSION ( 2 FDA reports)
FALL ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
FLUID RETENTION ( 2 FDA reports)
FOOD POISONING ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HOT FLUSH ( 2 FDA reports)
INJECTION SITE HAEMORRHAGE ( 2 FDA reports)
JOINT INJURY ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
MALAISE ( 2 FDA reports)
OROPHARYNGEAL PAIN ( 2 FDA reports)
OSTEOARTHRITIS ( 2 FDA reports)
PAIN ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PERIORBITAL OEDEMA ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
PURULENT DISCHARGE ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
SWELLING ( 2 FDA reports)
TREMOR ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
AORTIC VALVE REPLACEMENT ( 1 FDA reports)
ARTERIAL THERAPEUTIC PROCEDURE ( 1 FDA reports)
ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
BACK DISORDER ( 1 FDA reports)
BIOPSY ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BRAIN SCAN ABNORMAL ( 1 FDA reports)
BREAST LUMP REMOVAL ( 1 FDA reports)
CARDIAC PACEMAKER INSERTION ( 1 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHONDROPATHY ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DEVICE FAILURE ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
EYE DISCHARGE ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
FAECES HARD ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GRIP STRENGTH DECREASED ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
METRORRHAGIA ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NASAL DISCOMFORT ( 1 FDA reports)
NASAL OBSTRUCTION ( 1 FDA reports)
NASAL SEPTAL OPERATION ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PITUITARY CYST ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
SEBORRHOEIC KERATOSIS ( 1 FDA reports)
SKELETAL INJURY ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
SURGERY ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
THYROID DISORDER ( 1 FDA reports)
TOOTH REPAIR ( 1 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 1 FDA reports)
VAGINAL CONTRACEPTIVE DEVICE EXPELLED ( 1 FDA reports)
VITAMIN D DECREASED ( 1 FDA reports)

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