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

RHABDOMYOLYSIS ( 5 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 5 FDA reports)
HYPONATRAEMIA ( 4 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 4 FDA reports)
ABDOMINAL DISTENSION ( 3 FDA reports)
AFFECTIVE DISORDER ( 3 FDA reports)
WEIGHT DECREASED ( 3 FDA reports)
URINARY RETENTION ( 3 FDA reports)
TACHYCARDIA ( 3 FDA reports)
SHOCK ( 3 FDA reports)
BLISTER ( 3 FDA reports)
RASH PRURITIC ( 3 FDA reports)
POSTURE ABNORMAL ( 3 FDA reports)
BODY TEMPERATURE DECREASED ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 3 FDA reports)
LEUKAEMIA ( 3 FDA reports)
ILEUS ( 3 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 3 FDA reports)
HEART RATE DECREASED ( 3 FDA reports)
HEAD INJURY ( 3 FDA reports)
HAEMATURIA ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 3 FDA reports)
FALL ( 3 FDA reports)
EYE INJURY ( 3 FDA reports)
GINGIVAL HYPERTROPHY ( 2 FDA reports)
FAECAL INCONTINENCE ( 2 FDA reports)
AORTIC DISSECTION ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
URINARY INCONTINENCE ( 2 FDA reports)
COUGH ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
HEART RATE IRREGULAR ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 2 FDA reports)
COMMUNICATION DISORDER ( 2 FDA reports)
QUADRIPLEGIA ( 2 FDA reports)
PULSE PRESSURE DECREASED ( 2 FDA reports)
BLOOD URINE PRESENT ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
BRONCHITIS ACUTE ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
CHILLS ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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