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DYSPNOEA ( 34 FDA reports)
FATIGUE ( 30 FDA reports)
ARTHRALGIA ( 24 FDA reports)
CHEST PAIN ( 19 FDA reports)
HEADACHE ( 19 FDA reports)
HYPOAESTHESIA ( 19 FDA reports)
FACE OEDEMA ( 18 FDA reports)
MUSCULAR WEAKNESS ( 18 FDA reports)
ASTHMA ( 17 FDA reports)
INJECTION SITE REACTION ( 17 FDA reports)
PERONEAL NERVE PALSY ( 17 FDA reports)
TYPE I HYPERSENSITIVITY ( 17 FDA reports)
INJECTION SITE PRURITUS ( 16 FDA reports)
RHINORRHOEA ( 16 FDA reports)
SNEEZING ( 16 FDA reports)
WHEEZING ( 16 FDA reports)
FOOD ALLERGY ( 14 FDA reports)
GAIT DISTURBANCE ( 14 FDA reports)
PAIN IN EXTREMITY ( 14 FDA reports)
RASH MACULAR ( 13 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 12 FDA reports)
NAUSEA ( 12 FDA reports)
URTICARIA ( 12 FDA reports)
INSOMNIA ( 11 FDA reports)
OEDEMA PERIPHERAL ( 11 FDA reports)
ABDOMINAL PAIN UPPER ( 10 FDA reports)
ABORTION SPONTANEOUS ( 10 FDA reports)
CHILLS ( 10 FDA reports)
ERYTHEMA INFECTIOSUM ( 10 FDA reports)
GINGIVAL BLEEDING ( 10 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 10 FDA reports)
INJECTION SITE PAIN ( 10 FDA reports)
INTERMITTENT CLAUDICATION ( 10 FDA reports)
PETECHIAE ( 10 FDA reports)
PURPURA ( 10 FDA reports)
PYREXIA ( 10 FDA reports)
SERUM SICKNESS ( 10 FDA reports)
VOMITING ( 10 FDA reports)
BRAIN CONTUSION ( 8 FDA reports)
CONVULSION ( 8 FDA reports)
EAR HAEMORRHAGE ( 8 FDA reports)
FEELING HOT ( 8 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 8 FDA reports)
SKULL FRACTURE ( 8 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 8 FDA reports)
PRURITUS ( 7 FDA reports)
DEEP VEIN THROMBOSIS ( 6 FDA reports)
DYSGEUSIA ( 6 FDA reports)
FACIAL PALSY ( 6 FDA reports)
MUSCLE SPASMS ( 6 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 6 FDA reports)
PAIN ( 6 FDA reports)
PARAESTHESIA ( 6 FDA reports)
ANAEMIA ( 5 FDA reports)
ERYTHEMA ( 5 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 5 FDA reports)
RASH MACULO-PAPULAR ( 5 FDA reports)
ANXIETY ( 4 FDA reports)
EMOTIONAL DISTRESS ( 4 FDA reports)
PHARYNGEAL OEDEMA ( 4 FDA reports)
PRE-ECLAMPSIA ( 4 FDA reports)
PREMATURE LABOUR ( 4 FDA reports)
THROMBOCYTOPENIA ( 4 FDA reports)
VACCINATION SITE INFLAMMATION ( 4 FDA reports)
BLISTER ( 3 FDA reports)
COUGH ( 3 FDA reports)
DYSPHONIA ( 3 FDA reports)
INFLAMMATION ( 3 FDA reports)
NASAL CONGESTION ( 3 FDA reports)
OPEN WOUND ( 3 FDA reports)
PERTUSSIS ( 3 FDA reports)
TENDERNESS ( 3 FDA reports)
VACCINATION FAILURE ( 3 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BURNING SENSATION ( 2 FDA reports)
CELLULITIS ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
CHOLECYSTITIS CHRONIC ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
DISTURBANCE IN ATTENTION ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
EXTENSIVE SWELLING OF VACCINATED LIMB ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INJECTION SITE INDURATION ( 2 FDA reports)
INJURY ( 2 FDA reports)
LOCAL SWELLING ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
MITRAL VALVE DISEASE ( 2 FDA reports)
MITRAL VALVE INCOMPETENCE ( 2 FDA reports)
NODULE ( 2 FDA reports)
PRODUCT QUALITY ISSUE ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
VACCINATION SITE CELLULITIS ( 2 FDA reports)
VACCINATION SITE PAIN ( 2 FDA reports)
VACCINATION SITE REACTION ( 2 FDA reports)
BILIARY DYSKINESIA ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BODY MASS INDEX INCREASED ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 1 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
CRYING ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
ERYTHEMA OF EYELID ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GESTATIONAL DIABETES ( 1 FDA reports)
HAEMORRHAGIC ANAEMIA ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HORDEOLUM ( 1 FDA reports)
HYPERACUSIS ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INJECTION SITE OEDEMA ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 1 FDA reports)
JUGULAR VEIN THROMBOSIS ( 1 FDA reports)
LUNG ADENOCARCINOMA STAGE IV ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
METASTATIC NEOPLASM ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
PALATAL OEDEMA ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PLEURAL FIBROSIS ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
SECRETION DISCHARGE ( 1 FDA reports)
SENSATION OF PRESSURE ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TEMPERATURE INTOLERANCE ( 1 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 1 FDA reports)
URINARY HESITATION ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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