Training Manual for Preventive Malaria - Ministry of Health

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WHO SHOULD REPORT ADRS IN GHANA FOR SP IN IPT • The patient (usually to the CBS/CHO/MCH Centre/Health Centre/ Hospital). • Community Based Supports (CBSs) • Health care workers (e.g. Clinic attendants) Health professionals should fill the SP/IPT reporting form on behalf of patients and submit it to the next level. WHAT SHOULD BE REPORTED? All suspected reactions to SP on SP/IPT forms and all drugs on National Reporting Form – blue colour, including minor ones. In addition, drug-drug, drug-food, or drug-food supplements interactions (including herbal and complementary products) should also be reported. The following should also be reported; • Overdose or medication error • Lack of efficacy or when the drug is suspected to be defective, substandard, counterfeit or not giving the “expected” response. • Any other reaction that the patient is sufficiently concerned about to report to the health professional. Remember “if the patient is concerned enough to report a reaction to you, you must also be concerned to report to the NMCP/NCPv. ADVERSE EVENT REPORTING FORM (specimen at the appendix) A copy of the National Spontaneous Reporting Form is shown in Appendix. The form consists four main parts as follows: Patient Details Name Age, Weight Address Reaction Details What happened – description of the event or problem When – date of event What was done – treatment given to the patient or whether the drug was withdrawn (dechallenge) and/or reintroduced (rechallenge) What was the outcome – outcomes attributed to adverse event i.e. was the patient hospitalized? If so, for how long? Did the patient die? How long did the reaction last? Drug Details o Suspected agent (brand names if known or else generic name) o Lot/batch number, expiry date etc. if known o Dose, frequency and route used o Date of intake o Was patient on SP for IPT? 58
o Other medical products (drugs, herbal medicines etc) taken within the preceding two weeks Reporter Details • Name, address and telephone number • Profession • Specialty (if applicable) • Date of Reporting • Signature 59
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INTERMITTENT PREVENTIVE TREATMENT (
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curative treatment doses of an effe
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TABLE OF CONTENTS CONTENT PAGE COVE
Page 7 and 8: INTRODUCTION Background Malaria is
Page 9 and 10: • Cover doors and windows with wi
Page 11 and 12: cells. About 1 to 2 weeks later, th
Page 13 and 14: 1.4: INTERACTION BETWEEN HIV/AIDS A
Page 15 and 16: ROLE-PLAY: MALARIA DURING PREGNANCY
Page 17 and 18: 2a.1: FOCUSED ANTENATAL CARE Focuse
Page 19 and 20: 2A.3: SCHEDULING OF VISITS It is re
Page 21 and 22: UNIT 2B COMMUNICATION AND COUNSELLI
Page 23 and 24: 2B.3: BIRTH PREPAREDNESS AND COMPLI
Page 25 and 26: I will make sure she finds out how
Page 27 and 28: i. Explain all procedures/actions a
Page 29 and 30: These effects are caused by malaria
Page 31 and 32: Step 2 ° Give pregnant woman 1 st
Page 33 and 34: ALTERNATIVE MEASURES FOR THOSE WHO
Page 35 and 36: UNIT 4 CASE MANAGEMENT This unit ou
Page 37 and 38: Table: Treatment of Uncomplicated M
Page 39 and 40: Oral Administration Oral Quinine at
Page 41 and 42: CASE STUDY : TREATING A CLIENT WHO
Page 43 and 44: -- Begin treatment for uncomplicate
Page 45 and 46: (If the diluted volume is more than
Page 47 and 48: LEARNING GUIDE FOR TREATMENT OF UNC
Page 49 and 50: 16. If she has any of the danger sy
Page 51 and 52: - % of antenatal clinic staff train
Page 53 and 54: CASE STUDY: RECORD KEEPING Directio
Page 55 and 56: UNIT 5B ADVERSE DRUG REACTION MONIT
Page 57: 5B.4: MONITORING OF ADVERSE EFFECTS
Page 61 and 62: Delivery (Maternity) Book This reco
Page 63 and 64: Addendum to Midwifery Monthly Retur
Page 65 and 66: IN STRICT CONFIDENCE Adverse Event
Page 67 and 68: APPENDIX F: MONITORING AND EVALUATI
Page 69 and 70: ADD UP TO 20 QUESTIONS 69
Page 71 and 72: C. Check the gestational age of the
Page 73: A. Oedema B. Dark coloured-urine C.
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Training Manual for Preventive Malaria - Ministry of Health

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