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

RENAL FAILURE ( 28 FDA reports)
PAIN ( 27 FDA reports)
ANXIETY ( 26 FDA reports)
FEAR ( 26 FDA reports)
INJURY ( 26 FDA reports)
UNEVALUABLE EVENT ( 26 FDA reports)
EMOTIONAL DISTRESS ( 19 FDA reports)
RENAL INJURY ( 18 FDA reports)
ANHEDONIA ( 17 FDA reports)
STRESS ( 15 FDA reports)
RENAL IMPAIRMENT ( 13 FDA reports)
DEPRESSION ( 12 FDA reports)
MULTI-ORGAN FAILURE ( 8 FDA reports)
DEATH ( 6 FDA reports)
ANGIOEDEMA ( 4 FDA reports)
CARDIAC ARREST ( 4 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
CONVULSION ( 4 FDA reports)
DYSPNOEA ( 4 FDA reports)
MYALGIA ( 4 FDA reports)
NERVOUSNESS ( 4 FDA reports)
POST PROCEDURAL COMPLICATION ( 4 FDA reports)
ARTHRALGIA ( 3 FDA reports)
CARDIOMYOPATHY ( 3 FDA reports)
COMA ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
DYSKINESIA ( 3 FDA reports)
FACE OEDEMA ( 3 FDA reports)
FALL ( 3 FDA reports)
FEMORAL NECK FRACTURE ( 3 FDA reports)
GENERALISED OEDEMA ( 3 FDA reports)
HEAD INJURY ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 3 FDA reports)
JOINT SWELLING ( 3 FDA reports)
OROPHARYNGEAL BLISTERING ( 3 FDA reports)
PARKINSON'S DISEASE ( 3 FDA reports)
PNEUMONIA ASPIRATION ( 3 FDA reports)
UPPER LIMB FRACTURE ( 3 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
APNOEA ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD PRESSURE ABNORMAL ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
FEAR OF DEATH ( 2 FDA reports)
HYPOTHYROIDISM ( 2 FDA reports)
LACERATION ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
NO ADVERSE EVENT ( 2 FDA reports)
PAIN IN JAW ( 2 FDA reports)
PULSE ABNORMAL ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
RESPIRATORY RATE DECREASED ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
ACCIDENT ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANAESTHETIC COMPLICATION NEUROLOGICAL ( 1 FDA reports)
ANOXIA ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
AURA ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BRADYKINESIA ( 1 FDA reports)
BRAIN DEATH ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHOKING ( 1 FDA reports)
COMPLEX PARTIAL SEIZURES ( 1 FDA reports)
COUGH ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DISABILITY ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INTERACTION INHIBITION ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HYPERCAPNIA ( 1 FDA reports)
HYPOVENTILATION ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 1 FDA reports)
INJURY ASPHYXIATION ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
NEUROMUSCULAR BLOCK PROLONGED ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
POISONING ( 1 FDA reports)
PRIAPISM ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PSYCHIATRIC SYMPTOM ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RESUSCITATION ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
TRISMUS ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
VENTRICULAR TACHYARRHYTHMIA ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VOMITING ( 1 FDA reports)

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