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CONDITION AGGRAVATED ( 4 FDA reports)
VISUAL ACUITY REDUCED ( 4 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 3 FDA reports)
CHOROIDAL HAEMORRHAGE ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
MYOCARDIAL INFARCTION ( 3 FDA reports)
RESPIRATORY RATE INCREASED ( 3 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
DILATATION ATRIAL ( 2 FDA reports)
DIPLOPIA ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DYSSTASIA ( 2 FDA reports)
ECONOMIC PROBLEM ( 2 FDA reports)
EYE INFECTION ( 2 FDA reports)
EYE PAIN ( 2 FDA reports)
FACIAL PAIN ( 2 FDA reports)
FALL ( 2 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 2 FDA reports)
JOINT INJURY ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
PAIN ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
SINUS BRADYCARDIA ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
VITH NERVE PARALYSIS ( 2 FDA reports)
AMNESIA ( 1 FDA reports)
ANURIA ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
BACK CRUSHING ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BODY HEIGHT DECREASED ( 1 FDA reports)
BURSITIS ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CONVERSION DISORDER ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
COR PULMONALE ( 1 FDA reports)
CORNEAL DISORDER ( 1 FDA reports)
CORRECTIVE LENS USER ( 1 FDA reports)
COUGH ( 1 FDA reports)
DIABETIC NEUROPATHY ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 1 FDA reports)
EYE DISCHARGE ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FLAT ANTERIOR CHAMBER OF EYE ( 1 FDA reports)
FLUCTUANCE ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
GLYCOSURIA ( 1 FDA reports)
GRIP STRENGTH DECREASED ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
INTRAOCULAR PRESSURE DECREASED ( 1 FDA reports)
LACUNAR INFARCTION ( 1 FDA reports)
LIMB OPERATION ( 1 FDA reports)
LYMPHOEDEMA ( 1 FDA reports)
MASS ( 1 FDA reports)
MEASLES ( 1 FDA reports)
MENOPAUSE ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PENILE SIZE REDUCED ( 1 FDA reports)
POSTOPERATIVE INFECTION ( 1 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 1 FDA reports)
PROSTATIC DISORDER ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
RASH MORBILLIFORM ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SCINTILLATING SCOTOMA ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SICK SINUS SYNDROME ( 1 FDA reports)
SKIN HAEMORRHAGE ( 1 FDA reports)
SPINAL FRACTURE ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
TENDONITIS ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 1 FDA reports)
TRIGGER FINGER ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
WRIST SURGERY ( 1 FDA reports)

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