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

COMPLETED SUICIDE ( 15 FDA reports)
DRUG INTERACTION ( 13 FDA reports)
INJURY ASPHYXIATION ( 8 FDA reports)
MALAISE ( 8 FDA reports)
TREATMENT NONCOMPLIANCE ( 8 FDA reports)
CARDIAC ARREST ( 7 FDA reports)
DRUG TOXICITY ( 7 FDA reports)
ENCEPHALITIS ( 7 FDA reports)
TACHYCARDIA ( 7 FDA reports)
THYROIDITIS ( 7 FDA reports)
HYPONATRAEMIA ( 6 FDA reports)
BLOOD OSMOLARITY DECREASED ( 5 FDA reports)
CIRCULATORY COLLAPSE ( 5 FDA reports)
CONFUSIONAL STATE ( 5 FDA reports)
DIZZINESS ( 5 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 5 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 5 FDA reports)
RESPIRATORY DISORDER ( 5 FDA reports)
DRY MOUTH ( 4 FDA reports)
FEELING ABNORMAL ( 4 FDA reports)
HAEMOGLOBIN DECREASED ( 4 FDA reports)
HYPERHIDROSIS ( 4 FDA reports)
INSOMNIA ( 4 FDA reports)
MYOCLONUS ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
NIGHTMARE ( 4 FDA reports)
SCREAMING ( 4 FDA reports)
VERTIGO ( 4 FDA reports)
BLOOD CALCIUM DECREASED ( 3 FDA reports)
CEREBRAL ATROPHY ( 3 FDA reports)
DRUG LEVEL INCREASED ( 3 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 3 FDA reports)
FALL ( 3 FDA reports)
HEPATIC CYST ( 3 FDA reports)
HEPATITIS TOXIC ( 3 FDA reports)
NEUTROPHIL COUNT DECREASED ( 3 FDA reports)
PALPITATIONS ( 3 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 3 FDA reports)
SYNCOPE ( 3 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 3 FDA reports)
WEIGHT DECREASED ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 2 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 2 FDA reports)
AORTIC VALVE SCLEROSIS ( 2 FDA reports)
APGAR SCORE LOW ( 2 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 2 FDA reports)
BACTERIAL INFECTION ( 2 FDA reports)
CEREBROSPINAL FLUID RETENTION ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 2 FDA reports)
CONVULSION NEONATAL ( 2 FDA reports)
DACRYOCYSTITIS INFECTIVE ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
EPILEPSY ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
HEAD INJURY ( 2 FDA reports)
HEPATOMEGALY ( 2 FDA reports)
HYPOCALCAEMIA ( 2 FDA reports)
LIMB INJURY ( 2 FDA reports)
MUSCLE HAEMORRHAGE ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
NEONATAL ASPHYXIA ( 2 FDA reports)
OPHTHALMIA NEONATORUM ( 2 FDA reports)
ORAL CANDIDIASIS ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PREGNANCY ( 2 FDA reports)
PREMATURE BABY ( 2 FDA reports)
PREMATURE LABOUR ( 2 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 2 FDA reports)
PULMONARY HAEMORRHAGE ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
RESPIRATORY RATE INCREASED ( 2 FDA reports)
ABNORMAL FAECES ( 1 FDA reports)
ABORTION ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
AGITATION POSTOPERATIVE ( 1 FDA reports)
ANOXIA ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BRAIN STEM SYNDROME ( 1 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CONFUSION POSTOPERATIVE ( 1 FDA reports)
ENCEPHALITIS POST VARICELLA ( 1 FDA reports)
FEEDING DISORDER NEONATAL ( 1 FDA reports)
HYPERACUSIS ( 1 FDA reports)
HYPOTONIA NEONATAL ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INFECTION ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MENINGITIS ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
NEONATAL CANDIDA INFECTION ( 1 FDA reports)
NEONATAL TACHYCARDIA ( 1 FDA reports)
NO ADVERSE DRUG EFFECT ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
POLYDACTYLY ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TREMOR NEONATAL ( 1 FDA reports)
WOUND HAEMORRHAGE ( 1 FDA reports)

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