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

UROSEPSIS ( 2 FDA reports)
SKIN ULCER ( 2 FDA reports)
RESPIRATORY DISTRESS ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
ATELECTASIS ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
BRONCHIECTASIS ( 2 FDA reports)
CHORIORETINOPATHY ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
BRONCHIAL WALL THICKENING ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
GESTATIONAL DIABETES ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
MENINGITIS VIRAL ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
PAIN ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
PRE-ECLAMPSIA ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
RETINAL PIGMENT EPITHELIOPATHY ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
AGITATION ( 1 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WEANING FAILURE ( 1 FDA reports)

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