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

RENAL FAILURE ( 5 FDA reports)
PNEUMONIA ( 3 FDA reports)
MUSCLE RIGIDITY ( 3 FDA reports)
METABOLIC ACIDOSIS ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
TENSION ( 2 FDA reports)
RESPIRATORY RATE INCREASED ( 2 FDA reports)
POOR QUALITY SLEEP ( 2 FDA reports)
POLYCYTHAEMIA ( 2 FDA reports)
PHLEBITIS ( 2 FDA reports)
NIGHTMARE ( 2 FDA reports)
BLOOD UREA DECREASED ( 2 FDA reports)
NIGHT SWEATS ( 2 FDA reports)
NEONATAL PNEUMONIA ( 2 FDA reports)
NEONATAL INFECTION ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
MIDDLE INSOMNIA ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
HYPERREFLEXIA ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
CONFUSION POSTOPERATIVE ( 1 FDA reports)
HYPOVENTILATION ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MENINGITIS ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 1 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 1 FDA reports)
CATHETER SITE PHLEBITIS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
CATHETER RELATED COMPLICATION ( 1 FDA reports)
NEONATAL DISORDER ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
BRAIN STEM SYNDROME ( 1 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAIN ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
ASPHYXIA ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ANOXIA ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
AGITATION POSTOPERATIVE ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
TONGUE PARALYSIS ( 1 FDA reports)
TREMOR ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
WOUND HAEMORRHAGE ( 1 FDA reports)

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