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RETINAL DETACHMENT ( 8 FDA reports)
CARDIO-RESPIRATORY ARREST ( 7 FDA reports)
DISORIENTATION ( 6 FDA reports)
EYE EXCISION ( 6 FDA reports)
HYPERTENSION ( 6 FDA reports)
RETINOBLASTOMA ( 6 FDA reports)
VITREOUS HAEMORRHAGE ( 6 FDA reports)
ABNORMAL BEHAVIOUR ( 5 FDA reports)
CARDIAC ARREST ( 5 FDA reports)
PULMONARY OEDEMA ( 5 FDA reports)
CRANIAL NERVE PARALYSIS ( 4 FDA reports)
DRUG INTERACTION ( 4 FDA reports)
DYSPNOEA ( 4 FDA reports)
ERYTHEMA ( 4 FDA reports)
OXYGEN SATURATION DECREASED ( 4 FDA reports)
PAIN ( 4 FDA reports)
RETINAL PIGMENT EPITHELIOPATHY ( 4 FDA reports)
ANAEMIA ( 3 FDA reports)
BLINDNESS UNILATERAL ( 3 FDA reports)
CARDIAC MURMUR FUNCTIONAL ( 3 FDA reports)
CHOLELITHIASIS ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
DEBRIDEMENT ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
EPISTAXIS ( 3 FDA reports)
IIIRD NERVE PARALYSIS ( 3 FDA reports)
JAW OPERATION ( 3 FDA reports)
MECHANICAL VENTILATION ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
OFF LABEL USE ( 3 FDA reports)
OSTEOMYELITIS ( 3 FDA reports)
PAIN IN JAW ( 3 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 3 FDA reports)
RESPIRATORY FAILURE ( 3 FDA reports)
SEASONAL ALLERGY ( 3 FDA reports)
SUDDEN DEATH ( 3 FDA reports)
SURGERY ( 3 FDA reports)
TACHYCARDIA ( 3 FDA reports)
TOOTH EXTRACTION ( 3 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 3 FDA reports)
VENOUS INSUFFICIENCY ( 3 FDA reports)
ABDOMINAL INFECTION ( 2 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
AGITATION ( 2 FDA reports)
ANAPHYLACTIC SHOCK ( 2 FDA reports)
ANGIOEDEMA ( 2 FDA reports)
APGAR SCORE LOW ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BRADYCARDIA FOETAL ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CATARACT ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CRANIAL NERVE DISORDER ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
DRUG DISPENSING ERROR ( 2 FDA reports)
DRUG EFFECT DECREASED ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
GALLBLADDER INJURY ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
HYPOTONIA ( 2 FDA reports)
INCISIONAL DRAINAGE ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 2 FDA reports)
KERATOCONUS ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
MYDRIASIS ( 2 FDA reports)
OESOPHAGEAL CARCINOMA ( 2 FDA reports)
OSTEONECROSIS ( 2 FDA reports)
PANCREATITIS ACUTE ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
RESPIRATORY DISTRESS ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
SWELLING ( 2 FDA reports)
TRANSPLANT REJECTION ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
WRONG DRUG ADMINISTERED ( 2 FDA reports)
ABNORMAL LABOUR ( 1 FDA reports)
ABSCESS INTESTINAL ( 1 FDA reports)
ABSCESS LIMB ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
AIRWAY PEAK PRESSURE INCREASED ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANURIA ( 1 FDA reports)
APPENDICITIS ( 1 FDA reports)
APPENDIX DISORDER ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ASPERGILLOMA ( 1 FDA reports)
ASPERGILLOSIS ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIOVERSION ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHOLECYSTITIS CHRONIC ( 1 FDA reports)
COMA ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
DEFAECATION URGENCY ( 1 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 1 FDA reports)
DENTAL CARIES ( 1 FDA reports)
DENTAL PLAQUE ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DRUG EFFECT PROLONGED ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FALLOPIAN TUBE OPERATION ( 1 FDA reports)
FEAR ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FOETAL DISORDER ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GENITAL DISORDER FEMALE ( 1 FDA reports)
GINGIVAL INFECTION ( 1 FDA reports)
GINGIVAL SWELLING ( 1 FDA reports)
GINGIVITIS ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMORRHAGIC ANAEMIA ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPOPERFUSION ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
HYPOVENTILATION ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
HYSTERECTOMY ( 1 FDA reports)
ILEUS ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTESTINAL PERFORATION ( 1 FDA reports)
INTESTINAL STRANGULATION ( 1 FDA reports)
INTRA-AORTIC BALLOON PLACEMENT ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
INTUBATION ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
JAW DISORDER ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
LIGAMENT DISORDER ( 1 FDA reports)
LOOSE TOOTH ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LUNG LOBECTOMY ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
MEDICAL DIET ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OOPHORECTOMY ( 1 FDA reports)
OPEN WOUND ( 1 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 1 FDA reports)
ORAL SURGERY ( 1 FDA reports)
ORBITAL OEDEMA ( 1 FDA reports)
OSTEONECROSIS OF JAW ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PLACENTAL DISORDER ( 1 FDA reports)
PLACENTAL INFARCTION ( 1 FDA reports)
PLASMACYTOMA ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PREMATURE LABOUR ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
PULMONARY VASCULAR DISORDER ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
PUPILS UNEQUAL ( 1 FDA reports)
PURULENT DISCHARGE ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
REFLUX OESOPHAGITIS ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RESPIRATORY ACIDOSIS ( 1 FDA reports)
RESUSCITATION ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
STRESS CARDIOMYOPATHY ( 1 FDA reports)
TOOTH DISCOLOURATION ( 1 FDA reports)
TOOTH INFECTION ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
TOXIC ENCEPHALOPATHY ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TRISMUS ( 1 FDA reports)
TUMOUR LYSIS SYNDROME ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
URETHRAL STENT INSERTION ( 1 FDA reports)
URINE COLOUR ABNORMAL ( 1 FDA reports)
UTERINE ATONY ( 1 FDA reports)
UTERINE DISORDER ( 1 FDA reports)
UTERINE HAEMORRHAGE ( 1 FDA reports)
UTERINE HYPERTONUS ( 1 FDA reports)
UTERINE HYPOTONUS ( 1 FDA reports)
VASODILATATION ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WOUND TREATMENT ( 1 FDA reports)

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