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

HEADACHE ( 11 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 10 FDA reports)
CONGENITAL VESICOURETERIC REFLUX ( 8 FDA reports)
PALPITATIONS ( 8 FDA reports)
PSYCHOMOTOR RETARDATION ( 8 FDA reports)
HYPERHIDROSIS ( 7 FDA reports)
ANXIETY ( 6 FDA reports)
BACK PAIN ( 6 FDA reports)
CARDIAC ARREST ( 6 FDA reports)
DEPRESSION ( 6 FDA reports)
FATIGUE ( 6 FDA reports)
PARAESTHESIA ( 6 FDA reports)
SEROTONIN SYNDROME ( 6 FDA reports)
WEIGHT INCREASED ( 6 FDA reports)
CHEST PAIN ( 5 FDA reports)
DRY MOUTH ( 5 FDA reports)
MALAISE ( 5 FDA reports)
SUICIDAL IDEATION ( 5 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 4 FDA reports)
FALL ( 4 FDA reports)
MYALGIA ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
OEDEMA PERIPHERAL ( 4 FDA reports)
PYREXIA ( 4 FDA reports)
RASH GENERALISED ( 4 FDA reports)
RESTLESSNESS ( 4 FDA reports)
SYNCOPE ( 4 FDA reports)
VISUAL ACUITY REDUCED ( 4 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 4 FDA reports)
ABSCESS JAW ( 3 FDA reports)
ANHEDONIA ( 3 FDA reports)
BONE DISORDER ( 3 FDA reports)
BONE TRIMMING ( 3 FDA reports)
CAESAREAN SECTION ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
DECREASED INTEREST ( 3 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
EATING DISORDER ( 3 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 3 FDA reports)
FACE OEDEMA ( 3 FDA reports)
FISTULA ( 3 FDA reports)
HALLUCINATION, AUDITORY ( 3 FDA reports)
HYPOACUSIS ( 3 FDA reports)
IMPAIRED HEALING ( 3 FDA reports)
INFECTION ( 3 FDA reports)
JAW DISORDER ( 3 FDA reports)
MASTICATION DISORDER ( 3 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 3 FDA reports)
MEMORY IMPAIRMENT ( 3 FDA reports)
MORBID THOUGHTS ( 3 FDA reports)
OSTEONECROSIS ( 3 FDA reports)
PAIN ( 3 FDA reports)
PAIN IN JAW ( 3 FDA reports)
PERIODONTITIS ( 3 FDA reports)
PRIMARY SEQUESTRUM ( 3 FDA reports)
PSYCHOTIC DISORDER ( 3 FDA reports)
SWELLING ( 3 FDA reports)
TOOTH DISORDER ( 3 FDA reports)
TOOTH EXTRACTION ( 3 FDA reports)
TRISMUS ( 3 FDA reports)
VOMITING ( 3 FDA reports)
WOUND DEHISCENCE ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
AUTISM ( 2 FDA reports)
BONE DEVELOPMENT ABNORMAL ( 2 FDA reports)
CRYING ( 2 FDA reports)
DENTAL CARIES ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DISTURBANCE IN ATTENTION ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
INFLUENZA ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
MYOCLONUS ( 2 FDA reports)
NERVOUSNESS ( 2 FDA reports)
PHOTOPHOBIA ( 2 FDA reports)
RASH ERYTHEMATOUS ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
TEARFULNESS ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CORONARY ARTERY THROMBOSIS ( 1 FDA reports)
COUGH ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
HAIR TEXTURE ABNORMAL ( 1 FDA reports)
HEPATIC CONGESTION ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOTRICHOSIS ( 1 FDA reports)
IMPAIRED DRIVING ABILITY ( 1 FDA reports)
INJURY ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
RADIATION INJURY ( 1 FDA reports)
SCHIZOPHRENIA ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SOMATIC DELUSION ( 1 FDA reports)
SUBCUTANEOUS ABSCESS ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
THYROXINE INCREASED ( 1 FDA reports)
TRACHEAL HAEMORRHAGE ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)

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