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

URTICARIA ( 5 FDA reports)
ASTHENIA ( 4 FDA reports)
LIP SWELLING ( 3 FDA reports)
DYSPEPSIA ( 3 FDA reports)
CHILLS ( 3 FDA reports)
DROOLING ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
URINARY HESITATION ( 2 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 2 FDA reports)
MALAISE ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
DRUG ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
COUGH ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
EAR HAEMORRHAGE ( 1 FDA reports)
EROSIVE OESOPHAGITIS ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HYPERCAPNIA ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NEUTROPENIC SEPSIS ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TRANSFUSION REACTION ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
VOMITING ( 1 FDA reports)

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