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

PNEUMONIA ( 7 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 6 FDA reports)
DIABETES MELLITUS ( 6 FDA reports)
DYSPNOEA ( 6 FDA reports)
PLEURISY ( 6 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 6 FDA reports)
STAPHYLOCOCCAL INFECTION ( 6 FDA reports)
THORACIC CAVITY DRAINAGE ( 6 FDA reports)
HEADACHE ( 5 FDA reports)
OEDEMA PERIPHERAL ( 5 FDA reports)
RESPIRATORY DISTRESS ( 5 FDA reports)
SEPTIC SHOCK ( 5 FDA reports)
ANURIA ( 4 FDA reports)
DRUG ADMINISTRATION ERROR ( 4 FDA reports)
HAEMODYNAMIC INSTABILITY ( 4 FDA reports)
HAEMORRHAGIC URTICARIA ( 4 FDA reports)
JOINT SWELLING ( 4 FDA reports)
LUNG DISORDER ( 4 FDA reports)
MULTI-ORGAN FAILURE ( 4 FDA reports)
MYALGIA ( 4 FDA reports)
RENAL FAILURE ( 4 FDA reports)
ANKLE FRACTURE ( 3 FDA reports)
ANKLE OPERATION ( 3 FDA reports)
BRONCHITIS ( 3 FDA reports)
CELLULITIS ( 3 FDA reports)
CEREBROVASCULAR ACCIDENT ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
HYPERGLYCAEMIA ( 3 FDA reports)
MALAISE ( 3 FDA reports)
STRESS ( 3 FDA reports)
THYROID DISORDER ( 3 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
HYPOTHYROIDISM ( 2 FDA reports)
MASS ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 2 FDA reports)
PAIN ( 2 FDA reports)
PROSTATE CANCER ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
SCAB ( 2 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 2 FDA reports)
ABNORMAL FAECES ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANXIETY DISORDER ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASCITES ( 1 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BREAST HAEMORRHAGE ( 1 FDA reports)
BURNING FEET SYNDROME ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
COMA ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
EAR INFECTION ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FOLLICULITIS ( 1 FDA reports)
GALACTORRHOEA ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GOUT ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HEAT EXHAUSTION ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
INFECTIOUS PERITONITIS ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
MYASTHENIA GRAVIS ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PERITONEAL TUBERCULOSIS ( 1 FDA reports)
PHLEBITIS ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SURGERY ( 1 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VERTIGO POSITIONAL ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)

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